Page last updated: 2024-10-16

ammonium hydroxide and Hyperammonemia

ammonium hydroxide has been researched along with Hyperammonemia in 486 studies

azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.

Hyperammonemia: Elevated level of AMMONIA in the blood. It is a sign of defective CATABOLISM of AMINO ACIDS or ammonia to UREA.

Research Excerpts

ExcerptRelevanceReference
"Hyperammonemia can occur after acute overdose or chronic use of valproic acid (VPA)."9.41Risk factors of hyperammonemia in epilepsy patients with valproic acid therapy. ( Kim, DW; Kwack, DW, 2023)
"The objective was to evaluate the efficacy and safety of sodium benzoate in the management of hyperammonemia and hepatic encephalopathy (HE) in decompensated chronic liver disease."9.34Efficacy and Safety of Sodium Benzoate in The Management of Hyperammonemia in Decompensated Chronic Liver Disease of the Childhood-A Double-blind Randomized Controlled Trial. ( Alam, S; Khanna, R; Lal, BB; Snehavardhan, P; Sood, V, 2020)
"Intestinal mannitol is as effective and safe as conventional treatment for reducing hyperammonemia, oxidative stress, and hepatic encephalopathy of CLD patients in the emergency room."9.27Impact of intestinal mannitol on hyperammonemia, oxidative stress and severity of hepatic encephalopathy in the ED. ( Cruz-Domínguez, MP; Jara, LJ; Montes-Cortés, DH; Novelo-Del Valle, JL; Olivares-Corichi, IM; Rosas-Barrientos, JV, 2018)
"Valproate (VPA) administration may be associated with adverse metabolic effects, among is hyperammonemia, which could suggest metabolic abnormalities as carnitine deficiency."9.14The risk of asymptomatic hyperammonemia in children with idiopathic epilepsy treated with valproate: relationship to blood carnitine status. ( Abdella, MM; Hamed, SA, 2009)
"Valproic acid (VPA)-induced hyperammonemia (HA) is a rare adverse effect reported even at therapeutic VPA levels."8.31Valproic acid-induced hyperammonemia in neuropsychiatric disorders: a 2-year clinical survey. ( Aghamollaii, V; Ghayyem, H; Hassani, M; Hosseini, H; Mayeli, M; Shafie, M; Shakiba, A, 2023)
"Further research should be conducted into the prevalence and pathophysiology of methamphetamine-induced encephalopathy in the absence of hyperammonemia."8.31Methamphetamine-induced encephalopathy in the absence of hyperammonemia. ( Bowman, J; Dong, F; Fitzgerald, K; Neeki, MM; Rabbany, JM, 2023)
"This study was to investigate the effects of ammonia and manganese in the metabolism of minimal hepatic encephalopathy (MHE)."8.31The interaction of ammonia and manganese in abnormal metabolism of minimal hepatic encephalopathy: A comparison metabolomics study. ( Li, Y; Liu, XF; Lu, JJ; Qiang, JW; Yang, XY, 2023)
" Urea cycle disorders with hyperammonemia remain difficult to treat and eventually necessitate liver transplantation."8.12Glutaminase 2 knockdown reduces hyperammonemia and associated lethality of urea cycle disorder mouse model. ( Burczynski, ME; Chen, H; Cheng, X; Halasz, G; Kim, S; Lin, AZ; Mao, X; Murphy, AJ; Na, E; Okamoto, H; Sleeman, MW, 2022)
"AbstractThe aim of this study was to explore the effect of lamotrigine (LTG) on blood ammonia level in patients with epilepsy and identify risk factors affecting blood ammonia level."8.12Risk factors of elevated blood ammonia level in epilepsy patients treated with lamotrigine. ( Chen, J; Chen, X; Chen, Y; Miao, J; Wang, R; Zeng, J; Zhuang, X, 2022)
"Acetaminophen-induced hepatotoxicity can result in hyperammonemia, but it is not clear if elevated ammonia concentrations predict encephalopathy."8.12Hyperammonemia in acetaminophen toxicity. ( Marino, RT; Sidlak, AM, 2022)
"Routine use of lactulose to treat mild to moderate hyperammonemia in this patient population was not associated with improved outcomes."8.12Use of Lactulose to Treat Hyperammonemia in ICU Patients Without Chronic Liver Disease or Significant Hepatocellular Injury. ( Cutler, NS; MacGregor, DA; Sadowski, BW, 2022)
"Hyperammonemia is a common side effect of valproic acid (VPA) and can occur after generalized seizures, but the clinical significance is unclear."8.02Hyperammonemia in Patients With Status Epilepticus Treated With or Without Valproic Acid. ( Britton, JW; Hocker, SE; Smith, KM; Toledano, M, 2021)
"Hyperammonemia is an important adverse event associated with 5-fluorouracil (5FU) from 5FU metabolite accumulation."7.96Successful management of hyperammonemia with hemodialysis on day 2 during 5-fluorouracil treatment in a patient with gastric cancer: a case report with 5-fluorouracil metabolite analyses. ( Funakoshi, T; Horimatsu, T; Ikeda, A; Imamaki, H; Kataoka, S; Matsubara, T; Muto, M; Nakagawa, S; Nishikawa, Y; Oura, M; Ozaki, Y; Watanabe, N; Yanagita, M; Yonezawa, A, 2020)
"This study was aimed at identifying genetic and non-genetic risk factors for valproic acid (VPA)-induced hyperammonaemia in Chinese paediatric patients with epilepsy."7.88Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy. ( Li, X; Zhang, T; Zhao, L; Zhu, X, 2018)
" The current investigation was designed to evaluate the role of taurine treatment on the brain and liver mitochondrial function in a rat model of hepatic encephalopathy and hyperammonemia."7.85Taurine treatment preserves brain and liver mitochondrial function in a rat model of fulminant hepatic failure and hyperammonemia. ( Abasvali, M; Abdoli, N; Asadi, B; Azarpira, N; Heidari, R; Jafari, F; Jamshidzadeh, A; Khodaei, F; Latifpour, Z; Mardani, E; Najibi, A; Ommati, MM; Yeganeh, Y; Zarei, A; Zarei, M, 2017)
"High-dose 5-fluorouracil (5-FU) containing chemotherapy occasionally causes hyperammonemia and can be lethal."7.85Accumulation of alpha-fluoro-beta-alanine and fluoro mono acetate in a patient with 5-fluorouracil-associated hyperammonemia. ( Funakoshi, T; Horimatsu, T; Matsubara, K; Matsubara, T; Miyamoto, S; Muto, M; Nakagawa, S; Nishikawa, Y; Yanagita, M; Yonezawa, A, 2017)
"Valproic acid (VPA), which is widely used to treat epilepsy, migraine, and bipolar disorder, can causes severe hyperammonemia."7.81Influence of glutamine synthetase gene polymorphisms on the development of hyperammonemia during valproic acid-based therapy. ( Hirai, K; Imai, K; Inoue, K; Inoue, Y; Itoh, K; Suzuki, E; Takahashi, T; Takahashi, Y; Tsuji, D; Yamamoto, Y, 2015)
" L-Carnitine is a vitamin-like substance and several reports have described the usefulness of L-carnitine supplementation in cases of cirrhosis, with confirmed effectiveness against refractory hepatic encephalopathy."7.81Usefulness of Levocarnitine and/or Branched-Chain Amino Acids during Invasive Treatment for Hepatocellular Carcinoma. ( Hasegawa, H; Ishihara, T; Iwasa, M; Kobayashi, Y; Mifuji-Moroka, R; Sekoguchi-Fujikawa, N; Sugimoto, R; Takei, Y; Tanaka, H; Yoshikawa, K, 2015)
"Valproic acid, a branched short-chain fatty acid, has numerous action mechanisms which turn it into a broad spectrum anticonvulsant drug and make its use possible in some other pathologies such as bipolar disorder."7.80Hyperammonemia associated with valproic acid concentrations. ( Alvariza, S; Fagiolino, P; Guevara, N; Ibarra, M; Magallanes, L; Maldonado, C; Olano, I; Olmos, I; Vázquez, M, 2014)
"Valproic acid, which is widely used to treat various types of epilepsy, may cause severe hyperammonemia."7.804217C>A polymorphism in carbamoyl-phosphate synthase 1 gene may not associate with hyperammonemia development during valproic acid-based therapy. ( Hayashi, H; Imai, K; Inoue, K; Inoue, Y; Itoh, K; Miyakawa, K; Suzuki, E; Takahashi, T; Takahashi, Y; Tsuji, D; Yamamoto, Y; Yazawa, R, 2014)
"Hyperammonemia has been reported to be associated with patients who receive valproic acid (VPA) therapy."7.80Risk factors of hyperammonemia in patients with epilepsy under valproic acid therapy. ( Chang, CC; Chang, WN; Chen, NC; Chuang, YC; Huang, CR; Lin, CH; Lu, CH; Lu, YT; Tseng, YL, 2014)
"Combined administration of ornithine and phenylacetate (OP) is proposed as a novel treatment of hyperammonemia and hepatic encephalopathy."7.79Interorgan metabolism of ornithine phenylacetate (OP)--a novel strategy for treatment of hyperammonemia. ( Bak, LK; Dadsetan, S; Jalan, R; Keiding, S; Ott, P; Schousboe, A; Sørensen, M; Vilstrup, H; Waagepetersen, HS, 2013)
" The present study was undertaken to examine the protective influence of rutin, a polyphenolic flavonoid, on oxidative stress during ammonium chloride (AC)-induced hyperammonemia by measuring the levels of oxidative damage as well as antioxidant status."7.78Influence of rutin on biochemical alterations in hyperammonemia in rats. ( Mahmoud, AM, 2012)
"In propionic aciduria and methylmalonic aciduria, hyperammonemia as a symptom of metabolic decompensation is one of the major clinical problems."7.76N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria. ( Donati, MA; Filippi, L; Fiorini, P; Gozzini, E; la Marca, G; Malvagia, S, 2010)
"Adult-onset type II citrullinemia is an inborn error of urea cycle metabolism that can lead to hyperammonemic encephalopathy and coma."7.74Magnetic resonance spectroscopy in adult-onset citrullinemia: elevated glutamine levels in comatose patients. ( Au, WL; Lim, CC; Wong, YC; Xu, M; Ye, J, 2007)
"Fulminant hyperammonaemia as a threshold effect of coma-inducing dose of sodium thiopental has been revealed in rats."7.73Fulminant hyperammonaemia induced by thiopental coma in rats. ( Ivnitsky, JJ; Malakhovsky, VN; Rejniuk, VL; Schäfer, TV, 2006)
"To describe a case of oral valproic acid-induced hyperammonemia and thrombocytopenia in an elderly patient."7.72Valproic acid-induced hyperammonemia and thrombocytopenia in an elderly woman. ( Babin, S; Mallet, L; Morais, JA, 2004)
"Juvenile visceral steatosis (JVS) mouse is an animal model of human primary carnitine deficiency caused by a mutation of the gene encoding carnitine transporter, and suffers from various symptoms, such as fatty liver, growth retardation, hyperammonemia, hypoglycemia, and cardiac hypertrophy."7.71Hyperammonemia in carnitine-deficient adult JVS mice used by starvation. ( Horiuchi, M; Jalil, A; Kobayashi, K; Li, XX; Saheki, T; Yoshida, G, 2002)
"The objective of this study was to evaluate a new method for the treatment of acute hyperammonemia with a helium-oxygen mixture (heliox)."7.71Heliox use in the treatment of acute hyperammonemia. ( Barr, J; Chen-Levy, Z; Eshel, G; Lahat, E, 2001)
"The urea cycle disorders are a group of inherited biochemical diseases caused by a complete or partial deficiency of any one of the enzymes or transport proteins required to convert toxic ammonia into urea and to produce arginine and citrulline."6.58Inborn Errors of Metabolism with Hyperammonemia: Urea Cycle Defects and Related Disorders. ( Mew, NA; Summar, ML, 2018)
"Valproic acid (VPA) is a short-chain fatty acid widely prescribed in the treatment of seizure disorders and epilepsy syndromes, although its therapeutic value may be undermined by its toxicity."5.91Quantitative systems pharmacology Model to characterize valproic acid-induced hyperammonemia and the effect of L-carnitine supplementation. ( Fagiolino, P; Ibarra, M; Maldonado, C; Schiavo, A; Trocóniz, IF; Vázquez, M, 2023)
"Results: Mild cognitive impairment - MCI was diagnosed in 4 patients (28."5.72HYPERAMMONAEMIA AND COGNITIVE IMPAIRMENT IN EPILEPSY PATIENTS TREATED WITH VALPROIC ACID - PRELIMINARY STUDY. ( Dutkiewicz, J; Pilut, D; Szczygieł-Pilut, EE; Zajączkowska-Dutkiewicz, A, 2022)
"Leukoencephalopathy was resolved following the administration of L-arginine and lactulose with a decrease in plasma ammonia levels and glutamine-glutamate peak on magnetic resonance spectroscopy."5.72Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome. ( Fukuyama, T; Hoshino, Y; Kaneko, T; Kodaira, M; Matsuno, A; Sekijima, Y; Takano, K; Yazaki, M, 2022)
" One of the biggest problems of these compounds, however, is their very short bioavailability due to instant metabolism and rapid excretion."5.51Poly(ornithine)-based self-assembling drug for recovery of hyperammonemia and damage in acute liver injury. ( Ibayashi, Y; Lee, Y; Nagasaki, Y; Ngo, DN; Nishikawa, Y; Vong, LB, 2019)
" Of the reported serious adverse events (AEs), which included 11 deaths, none was attributable to study medication."5.48Safety, tolerability, and pharmacokinetics of l-ornithine phenylacetate in patients with acute liver injury/failure and hyperammonemia. ( Bukofzer, S; Clasen, K; Durkalski, V; Fontana, RJ; Ganger, D; Gottfried, M; Hameed, B; Hanje, AJ; Koch, D; Lee, WM; Little, L; Ravis, WR; Sherker, A; Stravitz, RT; Subramanian, RM, 2018)
"Hyperammonemia is a common complication of a wide variety of both inherited and acquired liver diseases."5.48Enhancement of hepatic autophagy increases ureagenesis and protects against hyperammonemia. ( Allegri, G; Annunziata, P; Ballabio, A; Brunetti-Pierri, N; Häberle, J; Melck, D; Motta, A; Nusco, E; Paris, D; Pastore, N; Polishchuk, E; Soria, LR; Thöny, B, 2018)
"Hyperammonemia can occur after acute overdose or chronic use of valproic acid (VPA)."5.41Risk factors of hyperammonemia in epilepsy patients with valproic acid therapy. ( Kim, DW; Kwack, DW, 2023)
"Hyperammonemia is a major etiological toxic factor in the development of hepatic encephalopathy."5.39Brain alanine formation as an ammonia-scavenging pathway during hyperammonemia: effects of glutamine synthetase inhibition in rats and astrocyte-neuron co-cultures. ( Bak, LK; Dadsetan, S; Keiding, S; Kukolj, E; Ott, P; Schousboe, A; Sørensen, M; Vilstrup, H; Waagepetersen, HS, 2013)
"Although hyperammonemia was suspected as the cause of the patient's mental changes, there was no evidence of chronic liver disease."5.38Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency. ( Choi, DE; Lee, KW; Na, KR; Shin, YT, 2012)
"The objective was to evaluate the efficacy and safety of sodium benzoate in the management of hyperammonemia and hepatic encephalopathy (HE) in decompensated chronic liver disease."5.34Efficacy and Safety of Sodium Benzoate in The Management of Hyperammonemia in Decompensated Chronic Liver Disease of the Childhood-A Double-blind Randomized Controlled Trial. ( Alam, S; Khanna, R; Lal, BB; Snehavardhan, P; Sood, V, 2020)
"The diagnosis of hereditary ornithine transcarbamylase deficiency was confirmed by liver biopsy in the immediate post-mortem period."5.31[Fulminant coma: think hyperammonemia and urea cycle disorders]. ( Augris, C; Benabdelmalek, F; Caramella, JP; Jouvet, P; Vauquelin, P, 2002)
"Intestinal mannitol is as effective and safe as conventional treatment for reducing hyperammonemia, oxidative stress, and hepatic encephalopathy of CLD patients in the emergency room."5.27Impact of intestinal mannitol on hyperammonemia, oxidative stress and severity of hepatic encephalopathy in the ED. ( Cruz-Domínguez, MP; Jara, LJ; Montes-Cortés, DH; Novelo-Del Valle, JL; Olivares-Corichi, IM; Rosas-Barrientos, JV, 2018)
"Valproic acid (VPA) has been associated with hyperammonemia with and without encephalopathy."5.14Hyperammonemia following intravenous valproate loading. ( Beasley, MT; Cofield, S; DeWolfe, JL; Faught, E; Knowlton, RC; Limdi, NA, 2009)
"Valproate (VPA) administration may be associated with adverse metabolic effects, among is hyperammonemia, which could suggest metabolic abnormalities as carnitine deficiency."5.14The risk of asymptomatic hyperammonemia in children with idiopathic epilepsy treated with valproate: relationship to blood carnitine status. ( Abdella, MM; Hamed, SA, 2009)
"Arginine treatment is able to reduces attacks of hyperammonemia in boys with late-onset OTCD and to increase their growth."5.12Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency. ( Adachi, M; Kanazawa, M; Kobayashi, K; Kubota, M; Kurokawa, K; Murakami, T; Murayama, K; Nagasaka, H; Ogawa, A; Ogawa, E; Takatani, T; Takayanagi, M; Yamamoto, S; Yorifuji, T, 2006)
"We report the results of a 25-year, open-label, uncontrolled study of sodium phenylacetate and sodium benzoate therapy (Ammonul, Ucyclyd Pharma) in 299 patients with urea-cycle disorders in whom there were 1181 episodes of acute hyperammonemia."5.12Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. ( Berry, GT; Berry, SA; Brusilow, SW; Enns, GM; Hamosh, A; Rhead, WJ, 2007)
" Recent studies provide new evidence for the use of lactulose, probiotics and rifaximin, as well as closure of large portosystemic shunts in the treatment of hepatic encephalopathy."4.90Treatment of hyperammonemia in liver failure. ( Jalan, R; Jover-Cobos, M; Khetan, V, 2014)
"Valproic acid (VPA)-induced hyperammonemia (HA) is a rare adverse effect reported even at therapeutic VPA levels."4.31Valproic acid-induced hyperammonemia in neuropsychiatric disorders: a 2-year clinical survey. ( Aghamollaii, V; Ghayyem, H; Hassani, M; Hosseini, H; Mayeli, M; Shafie, M; Shakiba, A, 2023)
"Further research should be conducted into the prevalence and pathophysiology of methamphetamine-induced encephalopathy in the absence of hyperammonemia."4.31Methamphetamine-induced encephalopathy in the absence of hyperammonemia. ( Bowman, J; Dong, F; Fitzgerald, K; Neeki, MM; Rabbany, JM, 2023)
"Hyperammonemia has been reported following asparaginase administration, consistent with the mechanisms of asparaginase, which catabolizes asparagine to aspartic acid and ammonia, and secondarily converts glutamine to glutamate and ammonia."4.31Treatment and outcomes of symptomatic hyperammonemia following asparaginase therapy in children with acute lymphoblastic leukemia. ( Altintas, B; Eldem, I; Langley, R; Lee, A; Nguyen, H; Shinawi, M; Willis, D, 2023)
"This study was to investigate the effects of ammonia and manganese in the metabolism of minimal hepatic encephalopathy (MHE)."4.31The interaction of ammonia and manganese in abnormal metabolism of minimal hepatic encephalopathy: A comparison metabolomics study. ( Li, Y; Liu, XF; Lu, JJ; Qiang, JW; Yang, XY, 2023)
" Urea cycle disorders with hyperammonemia remain difficult to treat and eventually necessitate liver transplantation."4.12Glutaminase 2 knockdown reduces hyperammonemia and associated lethality of urea cycle disorder mouse model. ( Burczynski, ME; Chen, H; Cheng, X; Halasz, G; Kim, S; Lin, AZ; Mao, X; Murphy, AJ; Na, E; Okamoto, H; Sleeman, MW, 2022)
"We used desflurane and remifentanil for general anesthesia to avoid hyperammonemia and delayed emergence."4.12Desflurane and remifentanil anesthesia in a child with citrin deficiency: A case report. ( Jung, SM; Kim, K, 2022)
"AbstractThe aim of this study was to explore the effect of lamotrigine (LTG) on blood ammonia level in patients with epilepsy and identify risk factors affecting blood ammonia level."4.12Risk factors of elevated blood ammonia level in epilepsy patients treated with lamotrigine. ( Chen, J; Chen, X; Chen, Y; Miao, J; Wang, R; Zeng, J; Zhuang, X, 2022)
"Life-threatening hyperammonemia occurs in both inherited and acquired liver diseases affecting ureagenesis, the main pathway for detoxification of neurotoxic ammonia in mammals."4.12O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis. ( Arena, P; Attanasio, S; Boffa, I; Brunetti-Pierri, N; Cuomo, P; D'Alessio, AM; De Angelis, A; Desviat, LR; Ferenbach, AT; Häberle, J; Lipshutz, GS; Makris, G; Martínez-Pizarro, A; Motta, A; Nitzahn, M; Nusco, E; Paris, D; Pravata, VM; Richard, E; Rüfenacht, V; Soria, LR; van Aalten, DMF, 2022)
"Acetaminophen-induced hepatotoxicity can result in hyperammonemia, but it is not clear if elevated ammonia concentrations predict encephalopathy."4.12Hyperammonemia in acetaminophen toxicity. ( Marino, RT; Sidlak, AM, 2022)
"Routine use of lactulose to treat mild to moderate hyperammonemia in this patient population was not associated with improved outcomes."4.12Use of Lactulose to Treat Hyperammonemia in ICU Patients Without Chronic Liver Disease or Significant Hepatocellular Injury. ( Cutler, NS; MacGregor, DA; Sadowski, BW, 2022)
"We report the case of a 79-year-old male who had undergone surgery for a mucus-secreting, stage-III pancreatic adenocarcinoma 2 years previously, who was recently started on capecitabine monotherapy for radiographic local progression."4.12Capecitabine-induced hyperammonemic encephalopathy. ( Armesto González, EM; Cano Calderero, FX; Cerrella Cano, C; Junquera Alonso, E; Seoane Blanco, L; Terroba Alonso, M, 2022)
"Hyperammonemia is a common side effect of valproic acid (VPA) and can occur after generalized seizures, but the clinical significance is unclear."4.02Hyperammonemia in Patients With Status Epilepticus Treated With or Without Valproic Acid. ( Britton, JW; Hocker, SE; Smith, KM; Toledano, M, 2021)
"Ornithine transcarbamylase deficiency (OTCD) is pleomorphic congenital hyperammonemia, in which the prognosis of the patient is determined both by genotype and environmental factors."3.96Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency. ( Cai, YN; Jiang, MY; Li, XZ; Lin, YT; Liu, L; Mei, HF; Peng, MZ; Shao, YX; Sheng, HY; Su, L; Yin, X, 2020)
"Hyperammonemia is an important adverse event associated with 5-fluorouracil (5FU) from 5FU metabolite accumulation."3.96Successful management of hyperammonemia with hemodialysis on day 2 during 5-fluorouracil treatment in a patient with gastric cancer: a case report with 5-fluorouracil metabolite analyses. ( Funakoshi, T; Horimatsu, T; Ikeda, A; Imamaki, H; Kataoka, S; Matsubara, T; Muto, M; Nakagawa, S; Nishikawa, Y; Oura, M; Ozaki, Y; Watanabe, N; Yanagita, M; Yonezawa, A, 2020)
"Arginase deficiency is caused by biallelic mutations in arginase 1 (ARG1), the final step of the urea cycle, and results biochemically in hyperargininemia and the presence of guanidino compounds, while it is clinically notable for developmental delays, spastic diplegia, psychomotor function loss, and (uncommonly) death."3.91Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency. ( Allegri, G; Burke, KE; Cederbaum, SD; Häberle, J; Lipshutz, GS; Liu, XB; Martini, PGV; Truong, B; Zhu, X, 2019)
"The purpose of the study was to evaluate the influence of establishing a protocol for the use of combined sodium benzoate and sodium phenylacetate (SBSP) (Ammonul®) to treat acute hyperammonemia."3.91Influence of implementing a protocol for an intravenously administered ammonia scavenger on the management of acute hyperammonemia in a pediatric intensive care unit. ( Brossier, D; Goyer, I; Jouvet, P; Marquis, C; Mitchell, G; Ozanne, B; Ziani, L, 2019)
"Patients with neonatal urea cycle defects (UCDs) typically experience severe hyperammonemia during the first days of life, which results in serious neurological injury or death."3.88Prenatal treatment of ornithine transcarbamylase deficiency. ( Akula, VP; Alcorn, D; Benitz, WE; Bernstein, JA; Berquist, WE; Blumenfeld, YJ; Castillo, RO; Concepcion, W; Cowan, TM; Cox, KL; Cusmano, K; Enns, GM; Esquivel, CO; Hintz, SR; Homeyer, M; Hudgins, L; Hurwitz, M; Lyell, DJ; Palma, JP; Schelley, S; Summar, ML; Wilnai, Y, 2018)
"This study was aimed at identifying genetic and non-genetic risk factors for valproic acid (VPA)-induced hyperammonaemia in Chinese paediatric patients with epilepsy."3.88Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy. ( Li, X; Zhang, T; Zhao, L; Zhu, X, 2018)
"The underlying pathophysiology of liver dysfunction in urea cycle disorders (UCDs) is still largely elusive."3.85Metabolically based liver damage pathophysiology in patients with urea cycle disorders - A new hypothesis. ( Garavelli, L; Ivanovski, A; Ivanovski, I; Ivanovski, P; Ješić, M, 2017)
" The current investigation was designed to evaluate the role of taurine treatment on the brain and liver mitochondrial function in a rat model of hepatic encephalopathy and hyperammonemia."3.85Taurine treatment preserves brain and liver mitochondrial function in a rat model of fulminant hepatic failure and hyperammonemia. ( Abasvali, M; Abdoli, N; Asadi, B; Azarpira, N; Heidari, R; Jafari, F; Jamshidzadeh, A; Khodaei, F; Latifpour, Z; Mardani, E; Najibi, A; Ommati, MM; Yeganeh, Y; Zarei, A; Zarei, M, 2017)
", drowsiness, coma) were selected for treatment with l-arginine."3.85L-Arginine in the treatment of valproate overdose - five clinical cases. ( Eyer, F; Felgenhauer, N; Fernando, M; Rabe, C; Schrettl, V, 2017)
"High-dose 5-fluorouracil (5-FU) containing chemotherapy occasionally causes hyperammonemia and can be lethal."3.85Accumulation of alpha-fluoro-beta-alanine and fluoro mono acetate in a patient with 5-fluorouracil-associated hyperammonemia. ( Funakoshi, T; Horimatsu, T; Matsubara, K; Matsubara, T; Miyamoto, S; Muto, M; Nakagawa, S; Nishikawa, Y; Yanagita, M; Yonezawa, A, 2017)
"Hyperammonemia is a common finding in children with methylmalonic acidemia."3.83A neuronal disruption in redox homeostasis elicited by ammonia alters the glycine/glutamate (GABA) cycle and contributes to MMA-induced excitability. ( Braga, DV; da Silva, AM; da Silva, LR; da Silveira Junior, ME; de Oliveira Ferreira, AP; Della-Pace, ID; Dobrachinski, F; Fighera, MR; Furian, AF; Gabbi, P; Grisólia, AB; Marchesan, S; Oliveira, MS; Ribeiro, LR; Rodrigues, FS; Royes, LF; Soares, FA, 2016)
"Valproic acid (VPA), which is widely used to treat epilepsy, migraine, and bipolar disorder, can causes severe hyperammonemia."3.81Influence of glutamine synthetase gene polymorphisms on the development of hyperammonemia during valproic acid-based therapy. ( Hirai, K; Imai, K; Inoue, K; Inoue, Y; Itoh, K; Suzuki, E; Takahashi, T; Takahashi, Y; Tsuji, D; Yamamoto, Y, 2015)
" L-Carnitine is a vitamin-like substance and several reports have described the usefulness of L-carnitine supplementation in cases of cirrhosis, with confirmed effectiveness against refractory hepatic encephalopathy."3.81Usefulness of Levocarnitine and/or Branched-Chain Amino Acids during Invasive Treatment for Hepatocellular Carcinoma. ( Hasegawa, H; Ishihara, T; Iwasa, M; Kobayashi, Y; Mifuji-Moroka, R; Sekoguchi-Fujikawa, N; Sugimoto, R; Takei, Y; Tanaka, H; Yoshikawa, K, 2015)
"Hyperammonemia is a common finding in children with methylmalonic acidemia and propionic acidemia, but its contribution to the development of the neurological symptoms in the affected patients is poorly known."3.80Disruption of redox homeostasis and brain damage caused in vivo by methylmalonic acid and ammonia in cerebral cortex and striatum of developing rats. ( de Oliveira, FH; Grings, M; Hickmann, FH; Leipnitz, G; Monteiro, WO; Sitta, Â; Soares, LE; Viegas, CM; Wajner, M; Zanatta, Â, 2014)
"Valproic acid, a branched short-chain fatty acid, has numerous action mechanisms which turn it into a broad spectrum anticonvulsant drug and make its use possible in some other pathologies such as bipolar disorder."3.80Hyperammonemia associated with valproic acid concentrations. ( Alvariza, S; Fagiolino, P; Guevara, N; Ibarra, M; Magallanes, L; Maldonado, C; Olano, I; Olmos, I; Vázquez, M, 2014)
"Valproic acid, which is widely used to treat various types of epilepsy, may cause severe hyperammonemia."3.804217C>A polymorphism in carbamoyl-phosphate synthase 1 gene may not associate with hyperammonemia development during valproic acid-based therapy. ( Hayashi, H; Imai, K; Inoue, K; Inoue, Y; Itoh, K; Miyakawa, K; Suzuki, E; Takahashi, T; Takahashi, Y; Tsuji, D; Yamamoto, Y; Yazawa, R, 2014)
"Hyperammonemia has been reported to be associated with patients who receive valproic acid (VPA) therapy."3.80Risk factors of hyperammonemia in patients with epilepsy under valproic acid therapy. ( Chang, CC; Chang, WN; Chen, NC; Chuang, YC; Huang, CR; Lin, CH; Lu, CH; Lu, YT; Tseng, YL, 2014)
"Combined administration of ornithine and phenylacetate (OP) is proposed as a novel treatment of hyperammonemia and hepatic encephalopathy."3.79Interorgan metabolism of ornithine phenylacetate (OP)--a novel strategy for treatment of hyperammonemia. ( Bak, LK; Dadsetan, S; Jalan, R; Keiding, S; Ott, P; Schousboe, A; Sørensen, M; Vilstrup, H; Waagepetersen, HS, 2013)
" The present study was undertaken to examine the protective influence of rutin, a polyphenolic flavonoid, on oxidative stress during ammonium chloride (AC)-induced hyperammonemia by measuring the levels of oxidative damage as well as antioxidant status."3.78Influence of rutin on biochemical alterations in hyperammonemia in rats. ( Mahmoud, AM, 2012)
" Current knowledge suggests that hyperammonemia, related to liver failure, is a main factor contributing to the cerebral alterations in HE and that hyperammonemia might impair signal transduction associated with post-translational modification of proteins such as tyrosine-nitration and phosphorylation."3.78Exploratory investigation on nitro- and phospho-proteome cerebellum changes in hyperammonemia and hepatic encephalopathy rat models. ( Airoldi, L; Boix, J; Brunelli, L; Campagna, R; Cauli, O; Felipo, V; Llansola, M; Pastorelli, R, 2012)
" Cyclophosphamide caused hyperammonemia; glutamine/ammonia and urea/ammonia ratios in the blood decreased."3.78Aggravation of cyclophosphamide-induced acute neurological disorders under conditions of artificial acidification of chyme in rats. ( Ivnitsky, JJ; Malakhovsky, VN; Rejuniuk, VL; Schaefer, TV, 2012)
"Hyperammonemia is a frequent side-effect of valproic acid (VPA) therapy, which points to an imbalance between ammoniagenesis and ammonia disposal via the urea cycle."3.77New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoA. ( Aires, CC; de Almeida, IT; Duran, M; Ijlst, L; Silva, MF; van Cruchten, A; Wanders, RJ, 2011)
"Patients with extrahepatic portal vein obstruction have inflammation and hyperammonemia made evident by higher blood TNF-α, IL-6, ammonia, and brain glutamine levels."3.77Pro-inflammatory cytokines are raised in extrahepatic portal venous obstruction, with minimal hepatic encephalopathy. ( Gupta, RK; Saraswat, VA; Srivastava, A; Thomas, MA; Yachha, SK; Yadav, SK, 2011)
"In propionic aciduria and methylmalonic aciduria, hyperammonemia as a symptom of metabolic decompensation is one of the major clinical problems."3.76N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria. ( Donati, MA; Filippi, L; Fiorini, P; Gozzini, E; la Marca, G; Malvagia, S, 2010)
" Significant decrease of myo-inositol in adults is probably due to cellular osmoregulation secondary to long-standing hyperammonemia."3.76Brain MR imaging and 1H-MR spectroscopy changes in patients with extrahepatic portal vein obstruction from early childhood to adulthood. ( Gupta, RK; Rathore, RK; Saksena, S; Saraswat, VA; Srivastava, A; Thomas, MA; Yadav, SK, 2010)
" plantarum strains were administered in ornithine transcarbamoylase-deficient Sparse-fur mice, a model of constitutive hyperammonemia, in a carbon tetrachloride rat model of chronic liver insufficiency and in a thioacetamide-induced acute liver failure mice model."3.74Control of acute, chronic, and constitutive hyperammonemia by wild-type and genetically engineered Lactobacillus plantarum in rodents. ( Demetter, P; Devière, J; Goffin, P; Gustot, T; Hols, P; Moreno, C; Nicaise, C; Prozzi, D; Quertinmont, E; Suain, V; Viaene, E, 2008)
"An infant with a suspected inborn metabolism error was treated with a metabolic cocktail of intravenous sodium phenylacetate (NaPh) and sodium benzoate (NaBz) for hyperammonemia."3.74Phenylacetate and benzoate clearance in a hyperammonemic infant on sequential hemodialysis and hemofiltration. ( Barletta, GM; Bunchman, TE; Crumb, TL; Gardner, JJ; McBryde, KD; Winters, JW, 2007)
"Adult-onset type II citrullinemia is an inborn error of urea cycle metabolism that can lead to hyperammonemic encephalopathy and coma."3.74Magnetic resonance spectroscopy in adult-onset citrullinemia: elevated glutamine levels in comatose patients. ( Au, WL; Lim, CC; Wong, YC; Xu, M; Ye, J, 2007)
"Sodium thiopental in the comatogenic (but not soporogenic) dose caused hyperammoniemia in rats."3.74Hyperammoniemia in rats with barbiturate coma. ( Ivnitskii, YY; Malakhovskii, VN; Ovsep'yan, RV; Reinyuk, VL; Shefer, TV, 2007)
" The resistance of rats to the lethal effect of barbiturate tended to decrease under conditions of experimental hyperammonemia induced by intraperitoneal injection of ammonium acetate in a nonlethal dose (6 mmol/kg)."3.74Effect of atmospheric ammonia on mortality rate of rats with barbiturate intoxication. ( Ivnitsky, JJ; Ovsep'yan, RV; Rejniuk, VL; Schafer, TV, 2007)
"To investigate the incidences of urea cycle defects (UCDs) in the patients with hyperammonemia and study their etiology, clinical and laboratory features."3.73[Clinical and laboratory screening studies on urea cycle defects]. ( Bao, XH; Chang, XZ; Li, L; Li, M; Qi, Y; Qian, N; Qin, J; Song, JQ; Sun, F; Wang, S; Wang, SQ; Wu, XR; Yang, HY; Yang, YL; Zhang, YH, 2005)
"Fulminant hyperammonaemia as a threshold effect of coma-inducing dose of sodium thiopental has been revealed in rats."3.73Fulminant hyperammonaemia induced by thiopental coma in rats. ( Ivnitsky, JJ; Malakhovsky, VN; Rejniuk, VL; Schäfer, TV, 2006)
" ALF pigs developed hyperammonemia and increased glutamine levels, whereas glutamate levels were decreased."3.73Interorgan ammonia, glutamate, and glutamine trafficking in pigs with acute liver failure. ( Davies, NA; Deutz, NE; Hodges, S; Jalan, R; Nedredal, GI; Revhaug, A; Romero-Gomez, M; Rose, C; Sen, S; Ten Have, GA; Williams, R; Ytrebø, LM, 2006)
"To describe a case of oral valproic acid-induced hyperammonemia and thrombocytopenia in an elderly patient."3.72Valproic acid-induced hyperammonemia and thrombocytopenia in an elderly woman. ( Babin, S; Mallet, L; Morais, JA, 2004)
"We compared the effect of hyperammonemia on NADH levels in brain slices and on the rate of oxygen consumption from isolated nonsynaptic brain mitochondria in ammonia-sensitive Wistar rats with that in ammonia-tolerant gulf toadfish (Opsanus beta)."3.71Comparison of the effects of ammonia on brain mitochondrial function in rats and gulf toadfish. ( Pérez-Pinzón, MA; Veauvy, CM; Walsh, PJ; Wang, Y, 2002)
"Juvenile visceral steatosis (JVS) mouse is an animal model of human primary carnitine deficiency caused by a mutation of the gene encoding carnitine transporter, and suffers from various symptoms, such as fatty liver, growth retardation, hyperammonemia, hypoglycemia, and cardiac hypertrophy."3.71Hyperammonemia in carnitine-deficient adult JVS mice used by starvation. ( Horiuchi, M; Jalil, A; Kobayashi, K; Li, XX; Saheki, T; Yoshida, G, 2002)
"The objective of this study was to evaluate a new method for the treatment of acute hyperammonemia with a helium-oxygen mixture (heliox)."3.71Heliox use in the treatment of acute hyperammonemia. ( Barr, J; Chen-Levy, Z; Eshel, G; Lahat, E, 2001)
"Serum or CSF glutamine levels are initially elevated in a majority of patients with suspected VHE, sometimes in the absence of hyperammonemia."3.71Serum and CSF glutamine levels in valproate-related hyperammonemic encephalopathy. ( Cawthon, DF; Caylor, LM; Kraemer, DL; Morgan, JD; Ojemann, LM; Vossler, DG; Wilensky, AJ, 2002)
"Hyperammonemia is a life-threatening condition mainly due to the neurotoxicity of ammonia."3.01Expanding the Spectrum of Extracorporeal Strategies in Small Infants with Hyperammonemia. ( Ceschia, G; Longo, G; Parolin, M; Ronco, C; Vidal, E, 2023)
"An effective and rapid treatment of hyperammonemia is crucial to prevent irreversible neurological damage and it depends on the understanding of the pathophysiology of the diseases, as well as of the available therapeutic approaches."2.82Hyperammonemia in Inherited Metabolic Diseases. ( Deon, M; Lopes, FF; Ribas, GS; Vargas, CR, 2022)
"Pregnancy is an important risk factor for women with CTLN1."2.82Hyperammonemia in a pregnant woman with citrullinemia type I: a case report and literature review. ( Ding, Y; Dou, X; He, R; Zhang, C; Zhou, Y, 2022)
"Isovaleric aciduria (IVA), propionic aciduria (PA) and methylmalonic aciduria (MMA) are inherited organic acidurias (OAs) in which impaired organic acid metabolism induces hyperammonaemia arising partly from secondary deficiency of N-acetylglutamate (NAG) synthase."2.82Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study. ( Baruteau, J; Cano, A; Chakrapani, A; Coker, M; Couce, ML; Del Toro, M; Delgado, MB; Donati, MA; Garcia-Cazorla, A; Gil-Ortega, D; Gomez-de Quero, P; Guffon, N; Hofstede, FC; Kalkan-Ucar, S; Lama-More, R; Le Mouhaer, J; Martinez-Pardo Casanova, M; Molina, A; Papadia, F; Pichard, S; Plisson, C; Rosello, P; Valayannopoulos, V, 2016)
"Hyperammonemia is a feature of liver failure, which is associated with increased risk of infection."2.73Ammonia impairs neutrophil phagocytic function in liver disease. ( Davies, NA; Hodges, SJ; Jalan, R; Pitsillides, AA; Shawcross, DL; Stadlbauer, V; Wheeler-Jones, C; Wright, GA, 2008)
"Minimal hepatic encephalopathy (MHE) is common in cirrhosis but its pathophysiologic basis remains undefined."2.73Role of ammonia and inflammation in minimal hepatic encephalopathy. ( Jalan, R; Olde Damink, SW; Shawcross, DL; Wright, G, 2007)
"Hyperammonemia is a life-threatening condition."2.72Extracorporeal Ammonia Clearance for Hyperammonemia in Critically Ill Patients: A Scoping Review. ( Baldwin, I; Bellomo, R; Eastwood, GM; Naorungroj, T; Yanase, F, 2021)
"Hyperammonemia is a universal finding after gastrointestinal hemorrhage in cirrhosis."2.71Induced hyperammonemia alters neuropsychology, brain MR spectroscopy and magnetization transfer in cirrhosis. ( Balata, S; Deutz, NE; Ferguson, K; Hayes, PC; Jalan, R; Marshall, I; Olde Damink, SW; Wardlaw, J; Williams, R, 2003)
"VPA is widely used for the treatment of generalized epilepsy."2.61[Valproic acid-induced hyperammonemic encephalopathy in a patient receiving valproic acid monotherapy]. ( Araki, M; Mukai, T; Naka, H; Shishido, T; Tokinobu, H; Yamada, H, 2019)
"Sarcopenia is a common complication of cirrhosis with a negative impact on posttransplant outcome, health-related quality of life (HRQOL), and patient survival."2.61L-Ornithine L-Aspartate for the Treatment of Sarcopenia in Chronic Liver Disease: The Taming of a Vicious Cycle. ( Butterworth, RF, 2019)
"The current treatments for hyperammonemia, such as antibiotics or lactulose, are designed to decrease the intestinal production of ammonia and/or its absorption into the body and are not effective, besides being often accompanied by side effects."2.58The Pharmabiotic Approach to Treat Hyperammonemia. ( Chung, HJ; Hong, ST; Kim, HJ; Liu, J; Lkhagva, E, 2018)
"The urea cycle disorders are a group of inherited biochemical diseases caused by a complete or partial deficiency of any one of the enzymes or transport proteins required to convert toxic ammonia into urea and to produce arginine and citrulline."2.58Inborn Errors of Metabolism with Hyperammonemia: Urea Cycle Defects and Related Disorders. ( Mew, NA; Summar, ML, 2018)
"Hyperammonemia is an important cause of cerebral edema in both adults with liver failure and children with inborn errors of metabolism."2.53The Role of RRT in Hyperammonemic Patients. ( Fenves, AZ; Gupta, S; Hootkins, R, 2016)
"Search terms included hepatic encephalopathy, ammonia hypothesis, brain and ammonia, liver failure and ammonia, acute-on-chronic liver failure and ammonia, cirrhosis and ammonia, portosytemic shunt, ammonia and lactulose, rifaximin, zinc, and nutrition."2.52Refining the ammonia hypothesis: a physiology-driven approach to the treatment of hepatic encephalopathy. ( Jiang, ZG; Patwardhan, VR; Tapper, EB, 2015)
"Recent advances in treating hyperammonemia include using synergistic combination treatments, broadening the indication of orphan drugs, and developing novel approaches to regenerate functional liver tissue."2.52Recent advances in the treatment of hyperammonemia. ( Leroux, JC; Matoori, S, 2015)
"Hyperammonemia is necessary for development of the cerebral complications to liver disease including hepatic encephalopathy and cerebral edema but the mechanisms are unclear."2.50Cerebral effects of ammonia in liver disease: current hypotheses. ( Ott, P; Vilstrup, H, 2014)
"Most treatments of hyperammonemia target the organs and metabolic processes involved in ammonia detoxification."2.50Pharmacotherapy for hyperammonemia. ( Hadjihambi, A; Jalan, R; Khetan, V, 2014)
"Hyperammonemia in end-stage acute liver failure (ALF) is often associated with cerebral edema and astrocyte pathology/swelling."2.49Possible treatment of end-stage hyperammonemic encephalopathy by inhibition of glutamine synthetase. ( Cooper, AJ, 2013)
"In patients with acute liver failure cerebral microdialysis studies show a linear correlation between the lactate to pyruvate ratio and the glutamine concentration, as well as to some of the adenosine triphosphate degradation products."2.49Changes in cerebral oxidative metabolism in patients with acute liver failure. ( Bjerring, PN; Larsen, FS, 2013)
" We, therefore, speculate that the beneficial effect of long term intake of BCAA on HE demonstrated in clinical studies may be related to an improved muscle mass and nutritional status rather than to an ammonia lowering effect of BCAA themselves."2.49Branched-chain amino acids and muscle ammonia detoxification in cirrhosis. ( Aagaard, NK; Dam, G; Ott, P; Vilstrup, H, 2013)
"Any delay in recognition and start of treatment of hyperammonemia may have deleterious consequences for the patient."2.47Clinical practice: the management of hyperammonemia. ( Häberle, J, 2011)
"Systemic hyperammonemia has been largely found in patients with cirrhosis and hepatic encephalopathy, and ammonia plays a major role in the pathogenesis of hepatic encephalopathy."2.45Gut ammonia production and its modulation. ( Galán, JJ; Jover, M; Romero-Gómez, M; Ruiz, A, 2009)
"Gene therapy for OTC deficiency is effective in animals, and work is ongoing to improve persistence and safety."2.45Ammonia toxicity and its prevention in inherited defects of the urea cycle. ( Walker, V, 2009)
" Some neuroprotective strategies such as the potential use of NMDA receptor antagonists, nitric oxide inhibitors, creatine and acetyl-l-carnitine have been suggested to counteract these toxic effects."2.44Hyperammonemia-induced toxicity for the developing central nervous system. ( Braissant, O; Cagnon, L, 2007)
"When hyperammonemia is not thought to be the result of liver failure, treatment for an occult disorder of metabolism must begin prior to the confirmation of an etiology."2.44Hyperammonemia in the ICU. ( Clay, AS; Hainline, BE, 2007)
"Hyperammonemic disorders such as acute liver failure (ALF) or urea cycle enzymopathies are associated with hyperexcitability, seizures, brain edema and increased extracellular brain glutamate."2.43Effect of ammonia on astrocytic glutamate uptake/release mechanisms. ( Rose, C, 2006)
"Hepatic encephalopathy has been linked to H."2.42Helicobacter pylori and hepatic encephalopathy. ( Chawla, YK; Dhiman, RK; Duseja, A; Sachdev, A, 2003)
"Symptoms of hyperammonemia are age-dependent and some are reversible."2.42Ammonia toxicity to the brain and creatine. ( Bachmann, C; Boulat, O; Braissant, O; Henry, H; Villard, AM, 2004)
"Hyperammonemia is mainly found in hepatic encephalopathy and in genetic defects of the urea cycle or other pathways of the intermediary metabolism."2.41Mechanisms of hyperammonemia. ( Bachmann, C, 2002)
"Valproic acid (VPA) is a short-chain fatty acid widely prescribed in the treatment of seizure disorders and epilepsy syndromes, although its therapeutic value may be undermined by its toxicity."1.91Quantitative systems pharmacology Model to characterize valproic acid-induced hyperammonemia and the effect of L-carnitine supplementation. ( Fagiolino, P; Ibarra, M; Maldonado, C; Schiavo, A; Trocóniz, IF; Vázquez, M, 2023)
"Ornithine transcarbamylase deficiency is an X-linked disorder which results in the accumulation of ammonia causing irritability and vomiting."1.91Acute onset of ornithine transcarbamylase deficiency after total anomalous pulmonary venous connection repair to a 2-day-old neonate. ( Fuchigami, T; Iwata, Y; Katagiri, J; Yoshida, H, 2023)
"Neonatal hyperammonemia is a disorder of ammonia metabolism that occurs in the neonatal period."1.91[Expert consensus on the diagnosis and treatment of neonatal hyperammonemia]. ( , 2023)
"This can cause neurotoxicity, cerebral edema, and seizures."1.91Treatment of hyperammonemia using in-line renal replacement and hyperosmolar therapies within an extracorporeal membrane oxygenation circuit. ( Grazioli, A; Iacono, A; Krupnik, AS; Madathil, RJ; Podell, JE; Shah, SR, 2023)
"But although the drugs developed to treat hyperammonemia resulting from urea cycle disorders were successfully developed and approved by the FDA, the compound suggested as a treatment for hepatic encephalopathy was unable to attract sufficient interest and investment to be tested for use in humans."1.72Saul Brusilow: Understanding and treating diseases of ammonia toxicity. ( Brusilow, WSA, 2022)
"Acute liver failure was present in 4 (25%) and acute-on-chronic liver failure in 8 (75%)."1.72Ammonia Clearance with Different Continuous Renal Replacement Therapy Techniques in Patients with Liver Failure. ( Baldwin, I; Bellomo, R; Fealy, N; Fisher, C; Naorungroj, T, 2022)
"Propionic acidemia is an inborn error of metabolism caused by a deficiency in the mitochondrial enzyme propionyl-CoA carboxylase that converts the propionyl CoA to methyl malonyl CoA."1.72Interorgan amino acid interchange in propionic acidemia: the missing key to understanding its physiopathology. ( Arrieta, F; Belanger-Quintana, A; Del Valle, M; Fernandez-Felix, BM; Garcia, F; Martinez-Pardo, M; Ruiz-Sala, P; Stanescu, S, 2022)
"Patients who developed encephalopathy had higher median ammonia levels, but there was no association between the severity of hyperammonemia and liver tumor burden or presence of liver insufficiency."1.72Prognostic significance of hyperammonemia in neuroendocrine neoplasm patients with liver metastases. ( Brabander, T; Charehbili, A; de Herder, WW; den Hoed, CM; Feelders, RA; Hofland, J; Langendonk, J; Refardt, J; Zandee, WT, 2022)
"Hyperammonemia is known to cause various neurological dysfunctions such as seizures and cognitive impairment."1.72Ammonia induces amyloidogenesis in astrocytes by promoting amyloid precursor protein translocation into the endoplasmic reticulum. ( Harada, F; Iida, I; Ito, G; Kishikawa, S; Komatsu, A; Maeda, T; Moss, SJ; Nasu, Y; Terunuma, M, 2022)
"Results: Mild cognitive impairment - MCI was diagnosed in 4 patients (28."1.72HYPERAMMONAEMIA AND COGNITIVE IMPAIRMENT IN EPILEPSY PATIENTS TREATED WITH VALPROIC ACID - PRELIMINARY STUDY. ( Dutkiewicz, J; Pilut, D; Szczygieł-Pilut, EE; Zajączkowska-Dutkiewicz, A, 2022)
"The most prevalent UCD detected were ornithine transcarbamylase deficiency, followed by citrullinemia type 1, hyperargininemia, carbamoyl phosphate synthase 1 deficiency, and argininosuccinic aciduria."1.72Clinical findings of patients with hyperammonemia affected by urea cycle disorders with hepatic encephalopathy. ( de Moura Coelho, D; Dos Reis, BG; Faverzani, JL; Lopes, FF; Ribas, GS; Sitta, A; Vargas, CR; Wajner, M, 2022)
"The prednisolone was stopped 5 days before hospital admission."1.72Late-Onset Ornithine Transcarbamylase Deficiency Complicated with Extremely High Serum Ammonia Level: Prompt Induction of Hemodialysis as the Key to Successful Treatment. ( Kakiuchi, T; Kurogi, K; Nishi, TM; Tago, M; Yamamoto, S; Yamashita, S; Yamashita, SI, 2022)
"Hyperammonemia from Ureaplasma parvum septic arthritis has never been reported previously."1.72Hyperammonemia in a septic patient with Ureaplasma parvum arthritis: a case report. ( Huang, X; Mao, M; Pan, L; Pan, X; Qiu, J; Wang, C; Xu, J; Yan, C, 2022)
"Leukoencephalopathy was resolved following the administration of L-arginine and lactulose with a decrease in plasma ammonia levels and glutamine-glutamate peak on magnetic resonance spectroscopy."1.72Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome. ( Fukuyama, T; Hoshino, Y; Kaneko, T; Kodaira, M; Matsuno, A; Sekijima, Y; Takano, K; Yazaki, M, 2022)
"Hyperammonemia is a deleterious and inevitable consequence of liver failure."1.62Treatment of Hyperammonemia by Transplanting a Symbiotic Pair of Intestinal Microbes. ( Heo, HJ; Hong, ST; Kim, HJ; Kim, S; Lee, S; Liu, J; Rho, JR; Zhai, C, 2021)
" Glycerol phenylbutyrate (GPB) is safe and effective in reducing ammonia levels in patients with UCD above 2 months of age."1.62Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders. ( Ah Mew, N; Bannick, AA; Berry, SA; Canavan, C; Conway, RL; Diaz, GA; Hainline, B; Inbar-Feigenberg, M; Kok, T; Lichter-Konecki, U; Longo, N; McCandless, SE; Porter, MH; Schulze, A; Vescio, T; Zori, R, 2021)
"Hyperammonemia is one of the contributing factors of hepatic encephalopathy (HE)."1.56Comparative accuracy and precision of two commercial laboratory analyzers for the quantification of ammonia in cerebrospinal fluid. ( Bhatti, SFM; de Rooster, H; Devriendt, N; Meyer, E; Or, M; Paepe, D; Vallarino, N, 2020)
"Six of the 8 patients with cerebral edema had hyperammonemia related to ACLF, giving an incidence of 14% in this subset of patients."1.56Characteristics and outcomes of critically ill patients with severe hyperammonemia. ( Jacoby, KJ; Leatherman, JW; Prekker, ME; Singh, P, 2020)
"Hyperammonemia is a key contributing factor for cerebral edema in acute liver failure."1.56Correction and Control of Hyperammonemia in Acute Liver Failure: The Impact of Continuous Renal Replacement Timing, Intensity, and Duration. ( Bellomo, R; Fisher, C; Warrillow, S, 2020)
"Hepatic involvement in hereditary hemorrhagic telangiectasia (HHT) is common and can be associated with severe clinical consequences, including portal hypertension, cardiac failure, and encephalopathy."1.56Ammonia Predicts Hepatic Involvement and Pulmonary Hypertension in Patients With Hereditary Hemorrhagic Telangiectasia. ( Al-Samkari, H; Bloom, PP; Kuter, DJ; Luther, J; Mojtahed, A; Rodriguez-Lopez, J; Witkin, AS, 2020)
"5-FU-induced hyperammonaemic encephalopathy started 2 [1-4] days after 5-FU infusion onset."1.565-Fluorouracil-induced hyperammonaemic encephalopathy: A French national survey. ( Boige, V; Boilève, A; Chouchana, L; Ducreux, M; Gaboriau, L; Hillaire-Buys, D; Hollebecque, A; Jozwiak, M; Lillo-Le Louët, A; Malka, D; Thomas, L, 2020)
"Urea cycle disorders are congenital metabolism errors that affect ammonia elimination."1.56Perioperative management of children with urea cycle disorders. ( Del Río, C; Martín-Hernández, E; Quijada-Fraile, P; Rubio, P; Ruiz, A, 2020)
"Hyperammonemia was diagnosed in all cases during the evaluation of altered mental status, with 22% presenting with seizures."1.56A retrospective study of adult patients with noncirrhotic hyperammonemia. ( Baker, JJ; Barkoudah, E; Berry, GT; Khoury, CC; Krier, JB; Lin, AP; Mogensen, KM; Peake, RW; Sahai, I; Stergachis, AB; Sweetser, DA, 2020)
"Conclusion Rifaximin administration for hepatic encephalopathy improved the CONUT and ALBI scores."1.56Changes in the Body Composition and Nutritional Status after Long-term Rifaximin Therapy for Hyperammonemia in Japanese Patients with Hepatic Encephalopathy. ( Azumi, M; Endo, S; Honma, T; Imai, M; Ishikawa, T; Iwanaga, A; Nozawa, Y; Sano, T; Yoshida, T, 2020)
" They were also offered an increased dosage of stiripentol if treatment with carnitine improved the encephalopathy."1.56Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine. ( Andrade, DM; Marques, P; Sadoway, T; Selvarajah, A; Tabarestani, S; Zulfiqar Ali, Q, 2020)
"BACKGROUND Hyperammonemia has been reported in some critically ill patients with sepsis who do not have hepatic failure."1.56Prognosis of Patients with Sepsis and Non-Hepatic Hyperammonemia: A Cohort Study. ( Gao, Y; Ge, Z; Guo, S; Li, Y; Lu, X; Yu, S; Zhao, L; Zhu, H, 2020)
"Hyperammonemia is a common cause of metabolic encephalopathy, mainly related to hepatic cirrhosis."1.51Malnutrition-related hyperammonemic encephalopathy presenting with burst suppression: a case report. ( Fumeaux, T; Leidi, A; Pisaturo, M, 2019)
" One of the biggest problems of these compounds, however, is their very short bioavailability due to instant metabolism and rapid excretion."1.51Poly(ornithine)-based self-assembling drug for recovery of hyperammonemia and damage in acute liver injury. ( Ibayashi, Y; Lee, Y; Nagasaki, Y; Ngo, DN; Nishikawa, Y; Vong, LB, 2019)
"She was diagnosed with ornithine transcarbamylase deficiency (OTCD) by analyses of plasma amino acids, urinary orotic acid, and the OTC gene mutation."1.51Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency. ( Harada, M; Hiura, M; Honma, Y; Ishii, M; Koya, Y; Matsumoto, S; Senju, M; Shibata, M, 2019)
"Citrullinemia Type 1 (also known as classic citrullinemia) is a rare autosomal recessive urea cycle disorder due to reduced activity of argininosuccinate synthetase 1; characterized by hyperammonemia leading to neurological damage."1.51Citrullinemia Type 1: Behavioral Improvement with Late Liver Transplantation. ( Bagde, A; Bakshi, R; Janwadkar, A; Mirza, D; Nagral, A; Shirole, N; Vasanth, S; Yewale, V, 2019)
"To report a successfully treated hyperammonemia due to a portosystemic shunt in adult patient."1.51Acute hyperammonemic encephalopathy due to a portosystemic shunt in a non-cirrhotic adult patient. ( Ezquerro-Sáenz, S; Fuster-Cabré, M; Lapetra-Labé, AM; Medrano-Peña, J; Requena-Calleja, MÁ, 2019)
" Of the reported serious adverse events (AEs), which included 11 deaths, none was attributable to study medication."1.48Safety, tolerability, and pharmacokinetics of l-ornithine phenylacetate in patients with acute liver injury/failure and hyperammonemia. ( Bukofzer, S; Clasen, K; Durkalski, V; Fontana, RJ; Ganger, D; Gottfried, M; Hameed, B; Hanje, AJ; Koch, D; Lee, WM; Little, L; Ravis, WR; Sherker, A; Stravitz, RT; Subramanian, RM, 2018)
"Hyperammonemia is a common complication of a wide variety of both inherited and acquired liver diseases."1.48Enhancement of hepatic autophagy increases ureagenesis and protects against hyperammonemia. ( Allegri, G; Annunziata, P; Ballabio, A; Brunetti-Pierri, N; Häberle, J; Melck, D; Motta, A; Nusco, E; Paris, D; Pastore, N; Polishchuk, E; Soria, LR; Thöny, B, 2018)
"All neonates treated for hyperammonemia at a single children's hospital between 1992 and 2016 were identified."1.48Rapid resolution of hyperammonemia in neonates using extracorporeal membrane oxygenation as a platform to drive hemodialysis. ( Conroy, PC; Grubb, PH; Hamid, R; Hardison, D; Lovvorn, HN; Pietsch, JB; Robinson, JR, 2018)
"Hyperammonemia is a common finding in patients with methylmalonic acidemia."1.48Ammonia role in glial dysfunction in methylmalonic acidemia. ( Arend, J; Barbosa, S; do Nascimento, PS; Dos Santos, ARS; Fighera, MR; Furian, AF; Gabbi, P; Haupental, F; Nogueira, V; Oliveira, MS; Rodrigues, FS; Royes, LFF, 2018)
"To characterize seizures and evaluate the utility of continuous EEG recording during hyperammonemia due to inborn errors of metabolism."1.48The utility of EEG monitoring in neonates with hyperammonemia due to inborn errors of metabolism. ( Gaillard, WD; Gropman, AL; Massaro, A; Prust, M; Tsuchida, TN; Vezina, G; Wiwattanadittakul, N, 2018)
"We report five adult patients with frontal lobe epilepsy (FLE) who were treated with VPA and in whom a primary adverse effect was unstable gait and falls."1.46Gait instability in valproate-treated patients: Call to measure ammonia levels. ( Elger, CE; Kipervasser, S; Korczyn, AD; Nass, RD; Neufeld, MY; Quesada, CM, 2017)
"Muscle mass loss and hepatic encephalopathy (complex neuropsychiatric disorder) are serious complications of chronic liver disease (cirrhosis) which impact negatively on clinical outcome and quality of life and increase mortality."1.46The bile duct ligated rat: A relevant model to study muscle mass loss in cirrhosis. ( Bemeur, C; Bosoi, CR; Deutz, NE; Ochoa-Sanchez, R; Oliveira, MM; Rose, CF; Ten Have, GA; Tremblay, M, 2017)
"The pathogenesis of hepatic encephalopathy (HE) in cirrhosis is multifactorial and ammonia is thought to play a key role."1.46Ammonia mediates cortical hemichannel dysfunction in rodent models of chronic liver disease. ( Davies, N; De Chiara, F; Gourine, AV; Habtetion, A; Hadjihambi, A; Hosford, PS; Jalan, R; Karagiannis, A, 2017)
"Hyperammonemia is a consistent abnormality in cirrhosis that results in impaired skeletal muscle protein synthesis and breakdown (proteostasis)."1.46Ammonia lowering reverses sarcopenia of cirrhosis by restoring skeletal muscle proteostasis. ( Dasarathy, S; Davuluri, G; Deutz, NEP; Engelen, MPKJ; Kumar, A; Prayson, R; Silva, RNE; Ten Have, GAM, 2017)
"Hyperammonemia is a rare, often fatal complication after transplantation."1.43Hyperammonemia Syndrome After Lung Transplantation: A Single Center Experience. ( Bain, KB; Byers, DE; Chen, C; Hachem, RR; Iuppa, JA; Patterson, GA; Trulock, EP; Witt, CA; Yusen, RD, 2016)
" Rifaximin, a poorly absorbed antibiotic that targets gut flora, significantly improved symptoms of HE."1.43Development of an experimental rat model of hyperammonemic encephalopathy and evaluation of the effects of rifaximin. ( Fukui, N; Isobe, M; Okada, M; Saito, T; Suzuki, H; Tamaoki, S, 2016)
"Patients were grouped into generalized convulsive seizures (GCS), psychogenic nonepileptic seizures with convulsions (PNES-C), or focal seizures (FS) based on vEEG."1.43Postictal ammonia as a biomarker for electrographic convulsive seizures: A prospective study. ( Albadareen, R; Gronseth, G; Hammond, N; He, J; Landazuri, P; Uysal, U, 2016)
" Both biochemical and morphological studies clearly revealed that chrysin protects against cell injury induced by ammonia intoxication in a dose-response manner with respect to endogenous antioxidants and hypoammonemic effects."1.43Chrysin, a flavonoid attenuates histological changes of hyperammonemic rats: A dose dependent study. ( Ramakrishnan, A; Renuka, M; Vijayakumar, N, 2016)
"Diverse treatments exist for the treatment of hyperammonemia, but they have limited efficacy, adverse effects and elevated cost."1.42Delivery of glutamine synthetase gene by baculovirus vectors: a proof of concept for the treatment of acute hyperammonemia. ( Montiel-Martínez, AG; Muñoz-Fuentes, RM; Palomares, LA; Pastor, AR; Torres-Vega, MA; Vargas-Jerónimo, RY; Zamorano-Carrillo, A, 2015)
"Hyperammonemia is less severe in arginase 1 deficiency compared with other urea cycle defects."1.42Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy. ( Cantero, G; Cantero-Nieto, G; Cederbaum, SD; Chan, E; Hu, C; Lipshutz, GS; Park, H; Tai, DS; Yudkoff, M, 2015)
"The cause of hyperammonemia is urinary retention obstruction."1.42Hyperammonemia in Urinary Tract Infections. ( Fukui, M; Kato, K; Kenzaka, T; Kitao, A; Kosami, K; Minami, K; Okayama, M; Yahata, S, 2015)
"A total of 135 patients with liver cirrhosis and HE had serum ammonia levels measured on admission."1.40Ammonia levels and the severity of hepatic encephalopathy. ( Khokhar, N; Qureshi, MO; Shafqat, F, 2014)
"We report a case of reversible hepatic myelopathy."1.40[Reversible hepatic myelopathy: a case report]. ( Fukada, K; Hazama, T; Hirozawa, D; Hoshi, T; Sawada, J; Yaegaki, T, 2014)
"Glycine is an important ammoniagenic amino acid, which is increased in acute liver failure (ALF)."1.40L-Ornithine phenylacetate reduces ammonia in pigs with acute liver failure through phenylacetylglycine formation: a novel ammonia-lowering pathway. ( Fuskevåg, OM; Jalan, R; Kristiansen, RG; Mæhre, H; Revhaug, A; Rose, CF; Ytrebø, LM, 2014)
"In adults, hyperammonemia is generally associated with hepatic dysfunction or as a complication of urinary diversions when infected or obstructed."1.39Simultaneous double hemodialysis for the control of refractory hyperammonemia. ( Brucculeri, M; Gabbard, W; Jooma, N; Masson, J, 2013)
"Hyperammonemia is a major etiological toxic factor in the development of hepatic encephalopathy."1.39Brain alanine formation as an ammonia-scavenging pathway during hyperammonemia: effects of glutamine synthetase inhibition in rats and astrocyte-neuron co-cultures. ( Bak, LK; Dadsetan, S; Keiding, S; Kukolj, E; Ott, P; Schousboe, A; Sørensen, M; Vilstrup, H; Waagepetersen, HS, 2013)
"Carglumic acid was well tolerated with no side effects noted."1.39Use of carglumic acid in the treatment of hyperammonaemia during metabolic decompensation of patients with propionic acidaemia. ( Abacan, M; Boneh, A, 2013)
"Hyperammonemia is a metabolic derangement that can be potentially fatal."1.39A rare case of hyperammonemia complication of high-protein parenteral nutrition. ( Bhat, Z; Cadnapaphorncai, P; Kahlon, R; Pillai, U; Sondheimer, J, 2013)
"The BDL rats developed chronic liver failure and exhibited a decreased discrimination index for short term memory (STM) when compared to the control group."1.39Impairment of short term memory in rats with hepatic encephalopathy due to bile duct ligation. ( Escobar, TD; Forgiarini, LF; Hammes, TO; Keiding, S; Leke, R; Meyer, FS; Oliveira, DL; Schousboe, A; Silveira, TR, 2013)
"Specific treatments of hyperammonemia are rarely used in liver failure when compared with urea cycle defect even though use of ammonia scavengers may help to decrease ammonemia."1.38Threshold for toxicity from hyperammonemia in critically ill children. ( Alvarez, F; Cousineau, J; Ducruet, T; Jouvet, P; Lambert, M; Mitchell, G; Nelson, J; Ozanne, B; Phan, V, 2012)
"We analyzed the presence of mild cognitive impairment (CI) by using the PHES battery of psychometric tests and measured the levels of ammonia and of the inflammatory cytokines IL-6 and IL-18 in blood of patients with different types of liver or dermatological diseases resulting in different grades of hyperammonemia and/or inflammation."1.38Contribution of hyperammonemia and inflammatory factors to cognitive impairment in minimal hepatic encephalopathy. ( Cassinello, N; Civera, M; Felipo, V; Garcia-Torres, ML; Jordá, E; Martinez-Valls, J; Molina, I; Montesinos, E; Montoliu, C; Olmo, JA; Ortega, J; Serra, MA; Urios, A; Wassel, A, 2012)
"Hyperammonemia was significantly related to patient variables that had a poor outcome (R=0."1.38Prognostic value of venous blood ammonia in patients with out-of-hospital cardiac arrest. ( Kasai, A; Kikushima, K; Mastsuzaki, M; Matsuzaki, M; Nagao, K; Soga, T; Tachibana, E; Watanabe, K; Yagi, T, 2012)
"Patients admitted to the hospital with acute liver failure (ALF) and high arterial levels of ammonia are more likely to have complications and poor outcomes than patients with lower levels of ammonia."1.38Persistent hyperammonemia is associated with complications and poor outcomes in patients with acute liver failure. ( Acharya, SK; Khanal, S; Kumar, R; Panda, SK; Prakash, S; Sharma, H, 2012)
"Although hyperammonemia was suspected as the cause of the patient's mental changes, there was no evidence of chronic liver disease."1.38Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency. ( Choi, DE; Lee, KW; Na, KR; Shin, YT, 2012)
"Hyperammonemia is considered to be the main cause of decreased levels of the branched-chain amino acids (BCAA), valine, leucine, and isoleucine, in liver cirrhosis."1.37Acute hyperammonemia activates branched-chain amino acid catabolism and decreases their extracellular concentrations: different sensitivity of red and white muscle. ( Holecek, M; Kandar, R; Kovarik, M; Sispera, L, 2011)
"The standard treatment protocol for acute lymphoblastic leukemia (ALL) and non-Hodgkin lymphoma (NHL) in childhood includes intravenous therapy with asparaginase (Asp), which may cause hyperammonemia."1.37Transient hyperammonemia due to L-asparaginase therapy in children with acute lymphoblastic leukemia or non-Hodgkin lymphoma. ( Beblo, S; Bierbach, U; Jörck, C; Kiess, W; Mütze, U; Weigel, JF, 2011)
" The study consisted of three experiments: The first was a dose-finding study of four different dosing regimens of magnesium sulfate (MgSO4) in healthy rats."1.37Hypermagnesemia does not prevent intracranial hypertension and aggravates cerebral hyperperfusion in a rat model of acute hyperammonemia. ( Bernal, W; Bjerring, PN; Eefsen, M; Larsen, FS; Wendon, J, 2011)
"The aetiology of minimal hepatic encephalopathy (mHE) remains unclear."1.37Absence of neuropsychological impairment in hyperammonaemia in healthy young adults; possible synergism in development of hepatic encephalopathy (HE) symptoms? ( Castle, PC; Smeeton, NJ; Watt, PW; Wilkinson, DJ, 2011)
"Transient hyperammonemia is associated with postictal confusion."1.37Transient hyperammonemia associated with postictal state in generalized convulsion. ( Lee, CW; Lin, TJ; Liu, KT; Yang, SC; Yeh, IJ, 2011)
"The pathophysiology of cerebral edema in ALF is incompletely understood."1.37Ammonia-induced brain swelling and neurotoxicity in an organotypic slice model. ( Back, A; Bai, T; Brorson, JR; Chiranand, P; Frank, JI; Goldenberg, FD; Tupper, KY, 2011)
"Hyperammonemia was detected in 8 patients treated with valproic acid."1.36Serum biotinidase activity in children treated with valproic acid and carbamazepine. ( Castiñeiras-Ramos, DE; Castro-Gago, M; Díaz-Mayo, I; Eirís-Puñal, J; Gómez-Lado, C, 2010)
"Newborns with inborn errors of metabolism often present with hyperammonaemic coma, requiring prompt diagnosis and specific medical therapy, nutritional support and efficient toxin removal."1.36Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism. ( Arbeiter, AK; Bonzel, KE; Büscher, R; Dohna-Schwake, C; Hanssler, L; Hoyer, PF; Kranz, B; Neudorf, U; Wingen, AM, 2010)
"In acute hepatic encephalopathy, MR imaging abnormalities have been described in the PVWM, thalami, and corticospinal tracts."1.36Acute hepatic encephalopathy: diffusion-weighted and fluid-attenuated inversion recovery findings, and correlation with plasma ammonia level and clinical outcome. ( Brace, JR; Lohman, BD; McKinney, AM; Sarikaya, B; Singewald, T; Spanbauer, J; Uhlmann, E, 2010)
"To develop a reliable surgical model of acute hepatic failure and hyperammonemia in rats that avoids porto-systemic shunt and bile duct ligation, applicable to hepatic encephalopathy research."1.36A new experimental model for acute hepatic failure in rats. ( Bellodi-Privato, M; D'Albuquerque, LA; Kubrusly, MS; Leite, KR; Machado, MC; Molan, NT; Teixeira, AR, 2010)
"Transient hyperammonemia was observed in the majority of generalized tonic-clonic seizure patients examined in this study but not in those with other causes of consciousness disturbance."1.36Postictal transient hyperammonemia as an indicator of seizure disorder. ( Lee, CW; Lin, TJ; Liu, KT; Su, CS; Yang, SC; Yeh, IJ, 2010)
"Hyperammonemia is encountered frequently in acutely ill children presenting for emergency care with altered levels of consciousness (ALOC)."1.36Hyperammonemia in the pediatric emergency care setting. ( Dabnon, M; Fouad, HM; Galal, NM; Saied, A, 2010)
"Hyperammonemia is a main contributor to brain herniation and mortality in acute liver failure (ALF)."1.35Acute liver failure-induced death of rats is delayed or prevented by blocking NMDA receptors in brain. ( Agusti, A; Boix, J; Cauli, O; Felipo, V; Piedrafita, B; Rodrigo, R, 2008)
"He developed hyperammonaemic coma (ammonia >400 μmol/L; normal <90 μmol/L) on postnatal day 35."1.35Amino acids in CSF and plasma in hyperammonaemic coma due to arginase1 deficiency. ( Eichinger-Öttl, U; Ertl, C; Haberlandt, E; Häberle, J; Heinz-Erian, P; Karall, D; Rostásy, K; Scholl-Bürgi, S; Sigl, SB, 2008)
"Cotreatment with morin prevented the elevation of liver marker enzymes induced by ammonium chloride."1.35Morin a flavonoid exerts antioxidant potential in chronic hyperammonemic rats: a biochemical and histopathological study. ( Subash, S; Subramanian, P, 2009)
"However, the efficacy of CsA to protect cytotoxic brain edema in ALF is problematic because it poorly crosses the blood-brain barrier, which is relatively intact in ALF."1.35Inhibitors of the mitochondrial permeability transition reduce ammonia-induced cell swelling in cultured astrocytes. ( Norenberg, MD; Rama Rao, KV; Reddy, PV, 2009)
"Although hyperammonemia is also known to induce convulsion, biochemical analysis immediately after GC is not useful for diagnosing hyperammonemia-induced convulsion."1.35Hyperammonemia is associated with generalized convulsion. ( Nishi, K; Sakamoto, T; Yanagawa, Y, 2008)
"LPS induced cytotoxic brain swelling and maintained anatomical integrity of the blood-brain barrier."1.34Endotoxemia produces coma and brain swelling in bile duct ligated rats. ( Brooks, HF; Davies, C; Davies, NA; Harry, D; Hodges, SJ; Jalan, R; Mani, AR; Moore, KP; Shawcross, DL; Stadlbauer, V; Williams, R; Wright, G; Zou, Z; Zwingmann, C, 2007)
"Hyperammonemia is responsible for most neurological alterations in patients with hepatic encephalopathy by mechanisms that remain unclear."1.33Chronic exposure to ammonia induces isoform-selective alterations in the intracellular distribution and NMDA receptor-mediated translocation of protein kinase C in cerebellar neurons in culture. ( Burgal, M; Costa, LG; Felipo, V; Giordano, G; Montoliu, C; Sanchez-Perez, AM, 2005)
"Myo-inositol levels were strongly decreased already at 3h after treatment with NH4Cl; other intracellular osmolytes, such as hypotaurine and choline-containing compounds were also decreased, along with a concomitant increase of both the total concentration and the amount of newly synthesized glutamine, alanine, and glutathione."1.33Ammonia toxicity under hyponatremic conditions in astrocytes: de novo synthesis of amino acids for the osmoregulatory response. ( Leibfritz, D; Zwingmann, C, 2005)
"Because hyperammonemia is thought to contribute to the pathogenesis of hepatic encephalopathy, we examined the effects of ammonia on ATP levels, neuronal morphology, and synaptic function in rat hippocampal slices."1.33Ammonia-mediated LTP inhibition: effects of NMDA receptor antagonists and L-carnitine. ( Funatsu, M; Izumi, M; Izumi, Y; Matsukawa, M; Zorumski, CF, 2005)
"Subclinical hepatic encephalopathy (SHE) were detected 55 in 47."1.33[The effects of Helicobacter pylori infection on hyperammonaemia and hepatic encephalopathy in cirrhotic patients]. ( Cai, JT; Chen, T; Lü, B; Si, JM; Wang, LJ, 2006)
"However, hyperammonemia-induced convulsions were inhibited by GABA in a dose-dependent manner."1.32Inhibition of acute hyperammonemia-induced convulsions by systemically administered gamma aminobutyric acid in rats. ( Paul, V, 2003)
"Hyperammonemia was induced by oral administration of an amino-acid (aa) solution mimicking hemoglobin composition."1.32Systemic inflammatory response exacerbates the neuropsychological effects of induced hyperammonemia in cirrhosis. ( Davies, NA; Jalan, R; Shawcross, DL; Williams, R, 2004)
"The diagnosis of hereditary ornithine transcarbamylase deficiency was confirmed by liver biopsy in the immediate post-mortem period."1.31[Fulminant coma: think hyperammonemia and urea cycle disorders]. ( Augris, C; Benabdelmalek, F; Caramella, JP; Jouvet, P; Vauquelin, P, 2002)
"He roused from his coma, breathed spontaneously, and resumed bottle feeding."1.31Emergency treatment of neonatal hyperammonaemic coma with mild systemic hypothermia. ( Bridges, S; Evans, D; Leaf, A; Whitelaw, A, 2001)
"Currently, the diagnosis of ASL deficiency is based on the measurement of urea cycle intermediates and amino acids by automated quantitative ion exchange chromatography in plasma and urine."1.31Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry. ( Bauer, MF; Bieger, I; Gempel, K; Gerbitz, KD; Hofmann, S; Pontz, BF; Stadler, S, 2001)
"A partial but significant inhibition of convulsions was found in these animals."1.31Evidence for an involvement of the ammonia-decreasing action of L-arginine in suppressing picrotoxin-induced convulsions in rats and its additive action with diazepam. ( Jayakumar, AR; Vanaja, P, 2001)

Research

Studies (486)

TimeframeStudies, this research(%)All Research%
pre-199026 (5.35)18.7374
1990's0 (0.00)18.2507
2000's125 (25.72)29.6817
2010's226 (46.50)24.3611
2020's109 (22.43)2.80

Authors

AuthorsStudies
Ribas, GS2
Lopes, FF2
Deon, M1
Vargas, CR2
Brusilow, WSA1
Mao, X1
Chen, H1
Lin, AZ1
Kim, S2
Burczynski, ME1
Na, E2
Halasz, G1
Sleeman, MW1
Murphy, AJ1
Okamoto, H2
Cheng, X2
Fisher, C2
Baldwin, I2
Fealy, N1
Naorungroj, T2
Bellomo, R3
Liu, J2
Zhai, C1
Rho, JR1
Lee, S1
Heo, HJ1
Kim, HJ2
Hong, ST3
Stanescu, S2
Belanger-Quintana, A3
Fernandez-Felix, BM1
Ruiz-Sala, P1
Del Valle, M1
Garcia, F1
Arrieta, F1
Martinez-Pardo, M2
Deutsch-Link, S1
Moon, AM1
Jiang, Y2
Barritt, AS1
Tapper, EB2
Fleming, D1
Cunningham, SA3
Patel, R4
Refardt, J1
den Hoed, CM1
Langendonk, J1
Zandee, WT1
Charehbili, A1
Feelders, RA1
de Herder, WW1
Brabander, T1
Hofland, J1
Kim, K1
Jung, SM1
Ames, EG1
Powell, C1
Engen, RM1
Weaver, DJ1
Mansuri, A1
Rheault, MN1
Sanderson, K1
Lichter-Konecki, U6
Daga, A1
Burrage, LC1
Ahmad, A1
Wenderfer, SE1
Luckritz, KE1
Starr, MC1
Cater, DT1
Wilson, AC1
Wallace, S1
Bennett, WE1
Hains, DS1
Komatsu, A1
Iida, I1
Nasu, Y1
Ito, G1
Harada, F1
Kishikawa, S1
Moss, SJ1
Maeda, T1
Terunuma, M1
Fakharbad, MJ1
Moshiri, M1
Ommati, MM2
Talebi, M1
Etemad, L1
Sørensen, M6
Walls, AB1
Dam, G3
Bak, LK5
Andersen, JV1
Ott, P10
Vilstrup, H12
Schousboe, A7
Macedo de Oliveira, M1
Monnet-Aimard, A1
Bosoi, CR6
Tremblay, M7
Rose, CF11
Chen, Y3
Chen, J1
Zhuang, X1
Chen, X1
Zeng, J1
Wang, R2
Miao, J1
Zhang, M2
Fan, Y1
Jiang, H1
Shao, J1
Li, M4
Arrieta Blanco, F1
Barrio-Carreras, D1
Bergua Martínez, A1
Cañedo Villarroya, E1
García-Silva, MT1
Lama More, R1
Martín-Hernández, E2
López, AM1
Morales-Conejo, M1
Pedrón-Giner, C1
Quijada-Fraile, P2
Casanova, MM1
Fukui, K1
Takahashi, T3
Matsunari, H1
Uchikura, A1
Watanabe, M1
Nagashima, H1
Ishihara, N1
Kakuma, T1
Watanabe, Y2
Yamashita, Y1
Yoshino, M1
Nakamura, H1
Takada, K1
Murase, K1
Ikeda, H1
Iyama, S1
Manabe, T1
Kobune, M1
Tranah, TH1
Ballester, MP1
Carbonell-Asins, JA1
Ampuero, J1
Alexandrino, G1
Caracostea, A1
Sánchez-Torrijos, Y1
Thomsen, KL3
Kerbert, AJC1
Capilla-Lozano, M1
Romero-Gómez, M3
Escudero-García, D1
Montoliu, C4
Jalan, R19
Shawcross, DL7
Vakrinou, A1
Murphy, E2
Sisodiya, SM1
Vivekananda, U1
Balestrini, S1
Szczygieł-Pilut, EE1
Zajączkowska-Dutkiewicz, A1
Pilut, D1
Dutkiewicz, J1
Buddington, RK1
Buddington, KK1
Howard, SC1
Soria, LR5
Makris, G1
D'Alessio, AM1
De Angelis, A2
Boffa, I1
Pravata, VM1
Rüfenacht, V1
Attanasio, S2
Nusco, E2
Arena, P1
Ferenbach, AT1
Paris, D2
Cuomo, P1
Motta, A2
Nitzahn, M3
Lipshutz, GS6
Martínez-Pizarro, A1
Richard, E1
Desviat, LR1
Häberle, J16
van Aalten, DMF1
Brunetti-Pierri, N7
Sitta, A2
de Moura Coelho, D1
Faverzani, JL1
Dos Reis, BG1
Wajner, M2
Kann, AE1
Ba-Ali, S1
Seidelin, JB1
Larsen, FS6
Hamann, S1
Bjerring, PN4
Claeys, W1
Van Hoecke, L1
Geerts, A1
Van Vlierberghe, H1
Lefere, S1
Van Imschoot, G1
Van Wonterghem, E1
Ghesquière, B1
Vandenbroucke, RE1
Van Steenkiste, C1
Mikkelsen, ACD2
Aagaard, NK4
Granados-Fuentes, D1
Cho, K1
Patti, GJ1
Costa, R1
Herzog, ED1
Montagnese, S2
Yamamoto, S2
Yamashita, S1
Kakiuchi, T1
Kurogi, K1
Nishi, TM1
Tago, M1
Yamashita, SI1
Kim, J5
Cho, YS3
Chun, BJ3
Moon, JM3
Kim, DK3
Lee, BK3
Lee, DH4
Ryu, SJ3
Jung, E3
Hosseini, H3
Shafie, M3
Shakiba, A3
Ghayyem, H3
Mayeli, M3
Hassani, M3
Aghamollaii, V3
Zhou, Y4
Dou, X1
Zhang, C1
He, R1
Ding, Y2
Pan, X1
Xu, J1
Pan, L1
Wang, C1
Qiu, J1
Huang, X1
Yan, C1
Mao, M1
Aitkenhead, H1
Nasr, M1
Ahmed-Farid, OAH1
Ahmed, RF1
Schiavo, A1
Maldonado, C2
Vázquez, M2
Fagiolino, P2
Trocóniz, IF1
Ibarra, M2
Lu, K1
Redant, S2
Warrillow, S2
Honoré, PM2
Yoshida, H2
Iwata, Y1
Fuchigami, T1
Katagiri, J1
Cheon, SY1
Kim, MY1
Kim, EJ1
Kam, EH1
Cho, I1
Koo, BN1
Kim, SY1
Eriksen, PL1
Djernes, L1
Rabbany, JM1
Fitzgerald, K1
Bowman, J1
Dong, F1
Neeki, MM1
Choi, J1
Kim, JH1
Shakerdi, L1
Ryan, A1
Zhu, R1
Liu, L2
Zhang, G2
Dong, J1
Ren, Z1
Li, Z1
Lee, A1
Eldem, I1
Altintas, B1
Nguyen, H1
Willis, D1
Langley, R1
Shinawi, M1
Koda, Y1
Shashni, B1
Takeda, N1
Zhang, X1
Tanaka, N1
Nishikawa, Y4
Nagasaki, Y2
Sanz, JH1
McCarter, R1
Abdelmohcine, A1
Amine, SE1
Warda, K1
Baz, SE1
Khanouchi, M1
El-Mansoury, B1
Agnaou, M1
Smimih, K1
Zouhairi, N1
Chatoui, H1
Draoui, A1
Saad, F1
Ahmed, EM1
Ferssiwi, A1
Bitar, A1
Jayakumar, AR4
Fdil, N1
Hiba, OE1
Liu, XF1
Lu, JJ1
Li, Y3
Yang, XY1
Qiang, JW1
Kwack, DW1
Kim, DW1
Ceschia, G1
Parolin, M1
Longo, G1
Ronco, C1
Vidal, E1
Gallin, M1
Damaj, L1
Gandemer, V1
Bendavid, C1
Moreau, C1
Kumar, A3
Bellar, A1
Mishra, S1
Sekar, J1
Welch, N2
Dasarathy, S5
Leidi, A1
Pisaturo, M1
Fumeaux, T1
Vong, LB1
Ibayashi, Y1
Lee, Y2
Ngo, DN1
Truong, B2
Allegri, G3
Liu, XB1
Burke, KE1
Zhu, X3
Cederbaum, SD3
Martini, PGV1
Senzolo, M1
Zarantonello, L1
Formentin, C1
Orlando, C1
Beltrame, R1
Vuerich, A1
Angeli, P1
Burra, P1
Arora, S1
Srivastava, MVP1
Singh, MB1
Goyal, V1
Gupta, N1
Prabhakar, A1
Aggarwal, B1
Agarwal, A1
Vishnu, VY1
Saunders, JM1
González-Maeso, J1
Bajaj, JS2
Pliego Cosano, R1
Moreno Rosauro, JM1
Clavero Olmos, M1
Devriendt, N1
Or, M1
Meyer, E1
Paepe, D1
Vallarino, N1
Bhatti, SFM1
de Rooster, H1
Matoori, S4
Bao, Y1
Schmidt, A1
Fischer, EJ1
Ochoa-Sanchez, R3
Oliveira, MM3
Leroux, JC4
Spada, M1
Porta, F1
Righi, D1
Gazzera, C1
Tandoi, F1
Ferrero, I1
Fagioli, F1
Sanchez, MBH1
Calvo, PL1
Biamino, E1
Bruno, S1
Gunetti, M1
Contursi, C1
Lauritano, C1
Conio, A1
Amoroso, A1
Salizzoni, M1
Silengo, L1
Camussi, G1
Romagnoli, R1
Katayama, K1
Cormack, BE1
Harding, JE1
Crowther, CA1
Lynn, A1
Nair, A1
Hewson, M1
Meyer, M1
Broadbent, R1
Webster, D1
Glamuzina, E1
Ryder, B1
Bloomfield, FH1
Jacoby, KJ1
Singh, P2
Prekker, ME1
Leatherman, JW1
Bloom, PP1
Rodriguez-Lopez, J1
Witkin, AS1
Al-Samkari, H1
Kuter, DJ1
Mojtahed, A1
Luther, J1
Snehavardhan, P1
Lal, BB1
Sood, V1
Khanna, R1
Alam, S1
Boilève, A1
Thomas, L1
Lillo-Le Louët, A1
Gaboriau, L1
Chouchana, L1
Ducreux, M1
Malka, D1
Boige, V1
Hollebecque, A1
Hillaire-Buys, D1
Jozwiak, M1
Sepehrinezhad, A1
Zarifkar, A1
Namvar, G1
Shahbazi, A1
Williams, R6
Brandt, A1
Agarwal, N1
Giri, D1
Yung, Z1
Didi, M1
Senniappan, S1
Del Río, C1
Ruiz, A2
Rubio, P1
Madigan, T1
Block, DR2
Carey, WA1
Kaemingk, BD1
Veltman, TR1
Tsai, CJ1
Gomez-Ospina, N1
Kanan, MW1
Chu, G1
Peng, MZ1
Li, XZ1
Mei, HF1
Sheng, HY1
Yin, X1
Jiang, MY1
Cai, YN1
Su, L1
Lin, YT1
Shao, YX1
Miramontes, E1
Mozdziak, P1
Petitte, JN1
Kulus, M1
Wieczorkiewicz, M1
Kempisty, B1
Stergachis, AB1
Mogensen, KM1
Khoury, CC1
Lin, AP1
Peake, RW1
Baker, JJ1
Barkoudah, E1
Sahai, I1
Sweetser, DA1
Berry, GT3
Krier, JB1
Shah, PA1
Cho, J1
Albitar, HAH1
Pajot, G1
Liu, M1
Ravi, K1
Eid, T1
Hassel, B1
Danbolt, NC1
Forster, V2
Agostoni, V2
Bettschart-Wolfensberger, R1
Bektas, RN1
Thöny, B3
Kabbaj, M2
Drews, L1
Zimmermann, M1
Westhoff, P1
Brilhaus, D1
Poss, RE1
Bergmann, L1
Wiek, C1
Brenneisen, P1
Piekorz, RP1
Mettler-Altmann, T1
Weber, APM1
Reichert, AS1
Marques, PT1
Zulfiqar Ali, Q2
Selvarajah, A2
Faghfoury, H1
Wennberg, RA1
Andrade, DM2
Ozaki, Y1
Imamaki, H1
Ikeda, A1
Oura, M1
Nakagawa, S2
Funakoshi, T2
Kataoka, S1
Horimatsu, T2
Yonezawa, A2
Matsubara, T2
Yanagita, M2
Muto, M2
Watanabe, N1
Nilsson, CH1
Svensson, MB1
Säve, SJ1
Van Meervenne, SA1
Kenneson, A1
Singh, RH2
Ishikawa, T1
Endo, S1
Imai, M1
Azumi, M1
Nozawa, Y1
Sano, T1
Iwanaga, A1
Honma, T1
Yoshida, T1
Marques, P1
Tabarestani, S1
Sadoway, T1
Cavino, K1
Sung, B1
Su, Q1
Gromada, J1
Yan, T1
Li, F1
Xiong, W1
Wu, B1
Xiao, F1
He, B1
Jia, Y1
Yanase, F1
Eastwood, GM1
Zhao, L2
Gao, Y1
Guo, S1
Lu, X1
Yu, S1
Ge, Z1
Zhu, H1
Clément, MA1
Bémeur, C3
Longo, N5
Diaz, GA3
Schulze, A3
Inbar-Feigenberg, M1
Conway, RL1
Bannick, AA1
McCandless, SE3
Zori, R2
Hainline, B1
Ah Mew, N2
Canavan, C1
Vescio, T1
Kok, T1
Porter, MH1
Berry, SA4
Aamann, L2
Jones, H1
Mookerjee, RP2
Hamilton-Dutoit, S1
Frystyk, J1
Zhou, Q1
Song, JN1
Chen, XZ1
Zhang, XZ1
Sun, Y1
Santos, AC1
Land, MGP1
Lima, EC1
Sato, T1
Ishii, T1
Kato, M1
Oyanagi, T1
Nakatsuka, S1
Kuroda, T1
Hasegawa, T1
Kido, J1
Matsumoto, S2
Nakajima, Y1
Wada, Y1
Mochizuki, N1
Murayama, K2
Lee, T1
Mochizuki, H1
Horikawa, R1
Kasahara, M1
Nakamura, K2
Butterworth, RF7
Smith, KM1
Britton, JW1
Hocker, SE1
Toledano, M1
Marino, RT1
Sidlak, AM1
Cutler, NS1
Sadowski, BW1
MacGregor, DA1
Solipuram, V1
Baretti, M1
Kim, AY1
Chen, LX1
Fahrner, JA1
Gunay-Aygun, M1
Peng, XP1
Hardenbergh, D1
Ferguson, A1
Griffith, P1
Wang, Y3
Brancati, M1
Gopalakrishna, H1
Kato, T1
Shubert, C1
Laheru, D1
Yarchoan, M1
Cerrella Cano, C1
Junquera Alonso, E1
Terroba Alonso, M1
Cano Calderero, FX1
Seoane Blanco, L1
Armesto González, EM1
Adamek, M1
Teitge, F1
Baumann, I1
Jung-Schroers, V1
El Rahman, SA1
Paley, R1
Piackova, V1
Gela, D1
Kocour, M1
Rakers, S1
Bergmann, SM1
Ganter, M1
Steinhagen, D1
Vinegrad, N1
Staretz-Chacham, O1
Barski, L1
Bartal, C1
Grazioli, A1
Podell, JE1
Iacono, A1
Krupnik, AS1
Madathil, RJ1
Shah, SR1
Hoshino, Y1
Kodaira, M1
Matsuno, A1
Kaneko, T1
Fukuyama, T1
Takano, K2
Yazaki, M2
Sekijima, Y1
Kipervasser, S1
Elger, CE1
Korczyn, AD1
Nass, RD1
Quesada, CM1
Neufeld, MY1
Galland, F1
Negri, E1
Da Ré, C1
Fróes, F1
Strapazzon, L1
Guerra, MC1
Tortorelli, LS1
Gonçalves, CA1
Leite, MC1
Pozdeev, VI1
Lang, E1
Görg, B3
Bidmon, HJ3
Shinde, PV1
Kircheis, G1
Herebian, D1
Pfeffer, K1
Lang, F1
Häussinger, D3
Lang, KS1
Lang, PA1
Díaz-Fontenla, F1
Castillo-Pradillo, M1
Díaz-Gómez, A1
Ibañez-Samaniego, L1
Gancedo, P1
Guzmán-de-Villoria, JA1
Fernández-García, P1
Bañares-Cañizares, R1
García-Martínez, R1
Mendes, NF1
Mariotti, FFN1
de Andrade, JS1
de Barros Viana, M1
Céspedes, IC1
Nagaoka, MR1
Le Sueur-Maluf, L1
Meyburg, J1
Opladen, T1
Spiekerkötter, U1
Schlune, A1
Schenk, JP1
Schmidt, J1
Weitz, J1
Okun, J1
Bürger, F1
Omran, TB1
Abdoh, G1
Al Rifai, H1
Monavari, A2
Konstantopoulou, V1
Kölker, S1
Yudkoff, M3
Hoffmann, GF1
Stravitz, RT1
Gottfried, M1
Durkalski, V1
Fontana, RJ1
Hanje, AJ1
Koch, D1
Hameed, B1
Ganger, D1
Subramanian, RM1
Bukofzer, S1
Ravis, WR1
Clasen, K1
Sherker, A1
Little, L1
Lee, WM1
Ivanovski, I1
Ješić, M1
Ivanovski, A1
Garavelli, L1
Ivanovski, P1
Weiss, N2
Tripon, S1
Lodey, M1
Guiller, E1
Junot, H1
Monneret, D1
Mayaux, J1
Brisson, H1
Mallet, M2
Rudler, M2
Imbert-Bismut, F1
Thabut, D2
Dabrowska, K1
Skowronska, K1
Popek, M1
Obara-Michlewska, M1
Albrecht, J6
Zielinska, M2
Melck, D1
Pastore, N1
Annunziata, P2
Polishchuk, E1
Ballabio, A1
Montes-Cortés, DH1
Novelo-Del Valle, JL1
Olivares-Corichi, IM1
Rosas-Barrientos, JV1
Jara, LJ1
Cruz-Domínguez, MP1
Celik, M1
Akdeniz, O1
Ozgun, N1
Lkhagva, E1
Chung, HJ2
Wilnai, Y1
Blumenfeld, YJ1
Cusmano, K1
Hintz, SR1
Alcorn, D1
Benitz, WE1
Berquist, WE1
Bernstein, JA1
Castillo, RO1
Concepcion, W1
Cowan, TM1
Cox, KL1
Lyell, DJ1
Esquivel, CO1
Homeyer, M1
Hudgins, L1
Hurwitz, M1
Palma, JP1
Schelley, S1
Akula, VP1
Summar, ML2
Enns, GM2
Kongsuphon, N1
Soukavanitch, M1
Teeraaumpornpunt, N1
Konmun, J1
Ativitavas, T1
Ngamphaiboon, N1
Robinson, JR1
Conroy, PC1
Hardison, D1
Hamid, R1
Grubb, PH1
Pietsch, JB1
Lovvorn, HN1
Speas, AL1
Lyles, SE1
Wirth, KA1
Fahey, CE1
Kow, K1
Lejeune, AT1
Milner, RJ1
Mew, NA1
Hediger, N1
Landolt, MA1
Diez-Fernandez, C2
Huemer, M1
Giacalone, G1
Eggenschwiler, S1
Lussi, M1
De Gottardi, A1
Zamboni, N1
Hayasaka, K1
Numakura, C1
Yamakawa, M1
Mitsui, T1
Watanabe, H1
Haga, H1
Ohira, H1
Ochiai, Y1
Tahara, T1
Nakahara, T1
Yamashiki, N1
Nakayama, T2
Kon, T1
Mitsubuchi, H1
Jin, YY1
Li, X1
Zhang, T1
Khoja, S2
Hermann, K1
Borzone, R1
Willis, B1
Rudd, M1
Palmer, DJ2
Ng, P2
Gabbi, P2
Nogueira, V1
Haupental, F1
Rodrigues, FS2
do Nascimento, PS1
Barbosa, S1
Arend, J1
Furian, AF2
Oliveira, MS2
Dos Santos, ARS1
Royes, LFF1
Fighera, MR2
Gökceoğlu, AU1
Taşar, MA1
Yalaki, Z1
Güneş, A1
Bakır, A1
Holeček, M4
Vodeničarovová, M1
Ferreira, RT1
Gonçalves, SC1
Pedrosa, ML1
Silva, ME1
Bassini, A1
Coelho, WS1
de Magalhães-Neto, AM1
Prado, ES1
Cameron, LC1
Li, C1
Zhang, Q1
Qian, Y1
Crossland, H1
Smith, K1
Atherton, PJ1
Wilkinson, DJ2
Wiwattanadittakul, N1
Prust, M1
Gaillard, WD1
Massaro, A1
Vezina, G1
Tsuchida, TN1
Gropman, AL2
Kim, JY1
Cho, H1
Camilleri, L1
Oliveira, M1
Bennett, EE1
Hummel, K1
Smith, AG1
Martinelli, D1
Goffredo, BM1
Falvella, FS1
Marano, M1
Koya, Y1
Shibata, M1
Senju, M1
Honma, Y1
Hiura, M1
Ishii, M1
Harada, M1
Chakrapani, A3
Kurtz, CB1
Millet, YA1
Puurunen, MK1
Perreault, M1
Charbonneau, MR1
Isabella, VM1
Kotula, JW1
Antipov, E1
Dagon, Y1
Denney, WS1
Wagner, DA1
West, KA1
Degar, AJ1
Brennan, AM1
Miller, PF1
Deplazes, S1
Rimann, N1
Causton, B1
Scherer, T1
Leff, JW1
Klimovskaia, A1
Fingerhut, R1
Krijt, J1
Kožich, V1
Nuoffer, JM2
Grisch-Chan, HM1
Giva, S1
Finnegan, J1
Ihidero, P1
Maguire, G1
Power, B1
Knerr, I1
Brossier, D1
Goyer, I1
Ziani, L1
Marquis, C1
Mitchell, G2
Ozanne, B2
Jouvet, P3
Item, CB1
Schanzer, A1
Metz, T1
Greber-Platzer, S1
Lischka, J1
Janwadkar, A1
Shirole, N1
Nagral, A1
Bakshi, R1
Vasanth, S1
Bagde, A1
Yewale, V1
Mirza, D1
Qvartskhava, N2
Jin, CJ1
Buschmann, T1
Albrecht, U1
Bode, JG1
Monhasery, N1
Oenarto, J1
Saheki, T3
Moriyama, M2
Kuroda, E1
Funahashi, A1
Yasuda, I1
Setogawa, Y1
Gao, Q1
Ushikai, M1
Furuie, S1
Yamamura, KI1
Nakamura, Y2
Eto, K1
Kadowaki, T1
Sinasac, DS2
Furukawa, T1
Horiuchi, M3
Tai, YH1
Kant, S1
Davuluri, G3
Alchirazi, KA1
Heit, C1
Gangadhariah, M1
Kim, A1
McMullen, MR1
Willard, B1
Luse, DS1
Nagy, LE1
Vasiliou, V1
Marini, AM1
Weiner, ID2
Wu, YH1
Chen, IC1
Lin, JY1
Dai, ZK1
van Straten, G1
van Dalen, D1
Mesu, SJ1
Rothuizen, J1
Teske, E1
Spee, B1
Favier, RP1
van Geijlswijk, IM1
Yamada, H1
Shishido, T1
Mukai, T1
Araki, M1
Naka, H1
Tokinobu, H1
Buyeverov, AO1
Bogomolov, PO1
Mayev, IV1
Matsievich, MV1
Uvarova, OV1
Taoro-González, L1
Cabrera-Pastor, A1
Sancho-Alonso, M1
Arenas, YM1
Meseguer-Estornell, F1
Balzano, T1
ElMlili, N1
Felipo, V9
Fuster-Cabré, M1
Ezquerro-Sáenz, S1
Requena-Calleja, MÁ1
Medrano-Peña, J1
Lapetra-Labé, AM1
Cai, Z1
Wu, F1
Lin, H1
Tan, M1
Beretta-Piccoli, X1
Mugisha, A1
Attou, R1
Kaefer, K1
De Bels, D1
Tolwani, A1
Kwon, M1
Alvarez, F2
Moreno Franco, P1
Patel, A1
Canabal, JM1
Haddad, TJ1
Erasmus, DB1
Mallea, JM1
Narula, T1
Brucculeri, M1
Gabbard, W1
Masson, J1
Jooma, N1
Raturi, S1
Venkatesh, IH1
Nagesh, NK1
Venkatagiri, P1
Dadsetan, S3
Kukolj, E1
Keiding, S6
Waagepetersen, HS4
Mehrotra, A1
Trigun, SK2
Apushkin, M1
Das, A1
Joseph, C1
Leung, EK1
Yeo, KT1
Baron, JM1
Baron, BW1
Slack, AJ1
Auzinger, G1
Willars, C1
Dew, T1
Musto, R1
Corsilli, D1
Sherwood, R1
Wendon, JA1
Bernal, W2
Abacan, M1
Boneh, A1
Rockey, DC1
Vierling, JM1
Mantry, P1
Ghabril, M1
Brown, RS1
Alexeeva, O1
Zupanets, IA1
Grinevich, V1
Baranovsky, A1
Dudar, L1
Fadieienko, G1
Kharchenko, N1
Klaryts'ka, I1
Morozov, V1
Grewal, P1
McCashland, T1
Reddy, KG1
Reddy, KR1
Syplyviy, V1
Bass, NM1
Dickinson, K1
Norris, C1
Coakley, D1
Mokhtarani, M3
Scharschmidt, BF3
Rivera-Espinosa, L1
Floriano-Sánchez, E1
Pedraza-Chaverrí, J1
Coballase-Urrutia, E1
Sampieri, AI1
Ortega-Cuellar, D1
Cárdenas-Rodríguez, N1
Carmona-Aparicio, L1
Yamane, K1
Shinohara, K1
Doi, K1
Inokuchi, R1
Hiruma, T1
Nakajima, S1
Noiri, E1
Yahagi, N1
Jones, PM1
Córdoba, J1
Ventura-Cots, M1
Noiret, L2
Baigent, S1
Kaneko, M1
Ogasawara, K1
Go, H1
Imamura, T2
Momoi, N1
Hosoya, M1
DU, K1
Luan, Z1
Qu, SQ1
Yang, H1
Yang, YX1
Wang, ZY1
Jin, HY1
Liu, WP1
Cooper, AJ3
Kuhara, T1
Jover-Cobos, M1
Khetan, V2
Tallis, S1
Caltana, LR1
Souto, PA1
Delfante, AE1
Lago, NR1
Brusco, A1
Perazzo, JC1
Pellicer Corbí, M1
Herranz Muñoz, C1
Baldominos Utrilla, G1
Fernández-Pacheco García-Valdecasas, M1
Viegas, CM1
Zanatta, Â1
Grings, M1
Hickmann, FH1
Monteiro, WO1
Soares, LE1
Leipnitz, G1
de Oliveira, FH1
Qureshi, MO1
Khokhar, N1
Shafqat, F2
Lee, HJ1
Halliday, N1
Bray, GP1
Hirozawa, D1
Fukada, K1
Yaegaki, T1
Hoshi, T1
Sawada, J1
Hazama, T1
Mondal, P1
Olmos, I1
Alvariza, S1
Guevara, N1
Magallanes, L1
Olano, I1
Wang, Q3
Yu, Z2
Li, D1
Jia, B1
Li, J1
Guan, K1
Kan, Q2
Inoue, K3
Suzuki, E2
Yamamoto, Y2
Yazawa, R1
Takahashi, Y2
Imai, K2
Miyakawa, K1
Inoue, Y2
Tsuji, D2
Hayashi, H2
Itoh, K2
Hadjihambi, A2
Kosenko, EA2
Tikhonova, LA1
Reddy, VP2
Aliev, G1
Kaminsky, YG2
Haack, N1
Dublin, P1
Rose, CR1
Hashim, IA1
Cuthbert, JA1
Tseng, YL1
Huang, CR1
Lin, CH1
Lu, YT1
Lu, CH1
Chen, NC1
Chang, CC1
Chang, WN1
Chuang, YC1
Kristiansen, RG2
Fuskevåg, OM1
Mæhre, H1
Revhaug, A2
Ytrebø, LM3
Torres-Vega, MA1
Vargas-Jerónimo, RY1
Montiel-Martínez, AG1
Muñoz-Fuentes, RM1
Zamorano-Carrillo, A1
Pastor, AR1
Palomares, LA1
Hu, C1
Tai, DS1
Park, H1
Cantero, G1
Cantero-Nieto, G1
Chan, E2
Lee, B3
Rhead, W2
Feigenbaum, A2
Le Mons, C2
Bartley, JA1
Nagamani, SC2
Berquist, W2
Gallagher, R1
Bartholomew, D1
Harding, CO2
Korson, MS1
Smith, W2
Cederbaum, S1
Wong, D1
Merritt, JL1
Vockley, J1
Vockley, G1
Kronn, D1
Summar, M2
Milikien, DA1
Marino, M2
Coakley, DF2
Walker, V3
Uygun, V1
Karasu, G1
Daloğlu, H1
Hazar, V1
Yeşilipek, A1
Jiang, ZG1
Patwardhan, VR1
Bharat, A1
Scott Budinger, GR1
Kreisel, D1
DeWet, CJ1
Gelman, AE1
Waites, K1
Crabb, D1
Xiao, L1
Bhorade, S1
Ambalavanan, N1
Dilling, DF1
Lowery, EM1
Astor, T1
Hachem, R1
Krupnick, AS1
DeCamp, MM1
Ison, MG1
Shen, TC1
Albenberg, L1
Bittinger, K1
Chehoud, C1
Chen, YY1
Judge, CA1
Chau, L1
Ni, J1
Sheng, M1
Lin, A1
Wilkins, BJ1
Buza, EL1
Lewis, JD1
Daikhin, Y1
Nissim, I1
Bushman, FD1
Wu, GD1
Guo, C1
Han, C1
Kenzaka, T1
Kato, K1
Kitao, A1
Kosami, K1
Minami, K1
Yahata, S1
Fukui, M1
Okayama, M1
Chen, C1
Bain, KB1
Iuppa, JA1
Yusen, RD1
Byers, DE1
Patterson, GA1
Trulock, EP1
Hachem, RR1
Witt, CA1
Ali, EZ1
Khalid, MK1
Yunus, ZM1
Yakob, Y1
Chin, CB1
Abd Latif, K1
Hock, NL1
Patel, VC1
White, H1
Støy, S1
Howells, JW1
Short, PA1
Nishimi, S1
Ishikawa, K1
Sasaki, M1
Furukawa, H1
Takada, A1
Chida, S1
Bartley, J1
Gallagher, RC2
Rowell, R1
Hirai, K1
McDaniel, J1
Hill, EA1
Moyer, M1
Runkana, A1
Prayson, R2
van Lunteren, E1
Ahn, JO1
Li, Q1
Lee, YH1
Han, SM1
Hwang, CY1
Youn, HY1
Chung, JY1
Iwasa, M1
Sugimoto, R1
Ishihara, T1
Sekoguchi-Fujikawa, N1
Yoshikawa, K1
Mifuji-Moroka, R1
Tanaka, H1
Kobayashi, Y1
Hasegawa, H1
Takei, Y1
Yap, S1
Leong, HY1
Abdul Aziz, F1
Hassim, H1
Sthaneshwar, P1
Teh, SH1
Abdullah, IS1
Ngu, LH1
Mohamed, Z1
Royes, LF1
Ribeiro, LR1
Della-Pace, ID1
de Oliveira Ferreira, AP1
da Silveira Junior, ME1
da Silva, LR1
Grisólia, AB1
Braga, DV1
Dobrachinski, F1
da Silva, AM1
Soares, FA1
Marchesan, S1
Tamaoki, S1
Suzuki, H1
Okada, M1
Fukui, N1
Isobe, M1
Saito, T1
Valayannopoulos, V1
Baruteau, J2
Delgado, MB1
Cano, A1
Couce, ML1
Del Toro, M1
Donati, MA3
Garcia-Cazorla, A1
Gil-Ortega, D1
Gomez-de Quero, P1
Guffon, N1
Hofstede, FC1
Kalkan-Ucar, S1
Coker, M1
Lama-More, R1
Martinez-Pardo Casanova, M1
Molina, A1
Pichard, S1
Papadia, F1
Rosello, P1
Plisson, C1
Le Mouhaer, J1
Laemmle, A1
Keogh, A1
Stricker, T1
Gautschi, M1
Baumgartner, MR1
Gupta, S1
Fenves, AZ1
Hootkins, R1
Albadareen, R1
Gronseth, G1
Landazuri, P1
He, J1
Hammond, N1
Uysal, U1
Yonai, R1
Sato, R1
Nasu, M1
Hertz, L3
Song, D1
Peng, L3
Senthilkumaran, S1
Karthikeyan, N1
Menezes, RG1
Thirumalaikolundusubramanian, P1
Açıkalın, A1
Dişel, NR1
Wang, W1
Gu, L2
Verkhratsky, A1
Kovács, DÁ1
Al Huurman, V1
Wojcicki, M1
Soonowala, D1
Baranski, A1
Renuka, M1
Vijayakumar, N1
Ramakrishnan, A1
Wang, X1
Karau, MJ1
Greenwood-Quaintance, KE1
Mandrekar, JN1
Guo, X1
Gao, L1
Lin, W1
Wu, Y1
Xing, B1
Xu, Z1
Choi, JJ1
Kim, HS1
Lee, KC1
Shin, Y1
Jo, YY1
Sato, K1
Arai, N1
Omori, A1
Hida, A1
Kimura, A1
Takeuchi, S1
Orton, DJ1
Gifford, JL1
Seiden-Long, I1
Khan, A1
de Koning, L1
Ten Have, GA2
Deutz, NE5
Rackayova, V1
Rangroo Thrane, V1
Vairappan, B1
Jamshidzadeh, A1
Heidari, R1
Abasvali, M1
Zarei, M1
Abdoli, N1
Khodaei, F1
Yeganeh, Y1
Jafari, F1
Zarei, A1
Latifpour, Z1
Mardani, E1
Azarpira, N1
Asadi, B1
Najibi, A1
De Chiara, F1
Hosford, PS1
Habtetion, A1
Karagiannis, A1
Davies, N1
Gourine, AV1
Schrettl, V1
Felgenhauer, N1
Rabe, C1
Fernando, M1
Eyer, F1
Silva, RNE1
Engelen, MPKJ1
Ten Have, GAM1
Deutz, NEP1
Miyamoto, S1
Matsubara, K1
Jameson, E1
Morris, AA4
Santra, S1
Vijay, S2
Kocadag, H1
Beesley, CE1
Grunewald, S2
Cleary, M1
Mundy, H1
Abulhoul, L1
Broomfield, A2
Lachmann, R1
Rahman, Y1
Robinson, PH2
MacPherson, L1
Foster, K1
Chong, WK1
Ridout, DA1
Bounford, KM1
Waddington, SN1
Mills, PB1
Gissen, P1
Davison, JE1
Moffatt-Bruce, SD1
Pesavento, T1
Von Viger, J1
Nunley, D1
Pope-Harman, A1
Martin, S1
Ross, P1
Herrera, DJ1
Moore, S1
Heap, S1
Preece, MA1
Griffiths, P1
Cauli, O2
Rodrigo, R2
Boix, J2
Piedrafita, B1
Agusti, A1
Wright, GA1
Stadlbauer, V2
Hodges, SJ3
Davies, NA5
Wheeler-Jones, C1
Pitsillides, AA1
Nicaise, C1
Prozzi, D1
Viaene, E1
Moreno, C1
Gustot, T1
Quertinmont, E1
Demetter, P1
Suain, V1
Goffin, P1
Devière, J1
Hols, P1
Andersson, AK1
Adermark, L1
Persson, M1
Westerlund, A1
Olsson, T1
Hansson, E1
Purdie, NG1
Trout, DR1
Cieslar, SR1
Madsen, TG1
Poppi, DP1
Cant, JP1
Ahmad, I1
Khan, AA1
Alam, A1
Dilshad, A1
Butt, AK1
Malik, K1
Sarwar, S1
Eefsen, M2
Hansen, BA1
Scholl-Bürgi, S1
Sigl, SB1
Haberlandt, E1
Rostásy, K1
Ertl, C1
Eichinger-Öttl, U1
Heinz-Erian, P1
Karall, D1
Jover, M1
Galán, JJ1
Olde Damink, SW8
Dejong, CH4
Rejniuk, VL5
Schafer, TV5
Ivnitsky, JJ5
Subash, S1
Subramanian, P1
DeWolfe, JL1
Knowlton, RC1
Beasley, MT1
Cofield, S1
Faught, E1
Limdi, NA1
Gau, CL1
Rosenblatt, RA1
Cerullo, V1
Lay, FD1
Dow, AC1
Livesay, J1
Grody, WW1
Ikewaki, J1
Ogata, M1
Kohno, K1
Kadota, J1
Reddy, PV1
Rama Rao, KV3
Norenberg, MD3
Hamed, SA1
Abdella, MM1
Castro-Gago, M1
Gómez-Lado, C1
Eirís-Puñal, J1
Díaz-Mayo, I1
Castiñeiras-Ramos, DE1
Stojanovic, VD1
Doronjski, AR1
Barisic, N1
Kovacevic, BB1
Pavlovic, VS1
Schwahn, BC1
Pieterse, L1
Bisset, WM1
Galloway, PG1
Filippi, L1
Gozzini, E1
Fiorini, P1
Malvagia, S1
la Marca, G1
Kaminsky, Y1
Kosenko, E1
Arbeiter, AK1
Kranz, B1
Wingen, AM1
Bonzel, KE1
Dohna-Schwake, C1
Hanssler, L1
Neudorf, U1
Hoyer, PF1
Büscher, R1
Yang, X2
Jiang, W2
Munk, OL1
Bender, D1
Yadav, SK2
Saksena, S1
Srivastava, A3
Saraswat, VA2
Thomas, MA2
Rathore, RK1
Gupta, RK2
Xue, Z1
Li, B1
Hu, X1
McKinney, AM1
Lohman, BD1
Sarikaya, B1
Uhlmann, E1
Spanbauer, J1
Singewald, T1
Brace, JR1
Kotani, Y1
Shiota, M1
Umemoto, M1
Tsuritani, M1
Hoshiai, H1
Westrope, C1
Morris, K1
Burford, D1
Morrison, G1
Teixeira, AR1
Machado, MC1
Kubrusly, MS1
Molan, NT1
Bellodi-Privato, M1
Leite, KR1
D'Albuquerque, LA1
Hilgier, W1
Wegrzynowicz, M3
Ruszkiewicz, J1
Oja, SS1
Saransaari, P1
Liu, KT2
Lee, CW2
Yang, SC2
Yeh, IJ2
Lin, TJ2
Su, CS1
Kandar, R1
Sispera, L1
Kovarik, M1
Jörck, C1
Kiess, W1
Weigel, JF1
Mütze, U1
Bierbach, U1
Beblo, S1
Wright, G4
LaBuzetta, JN1
Yao, JZ1
Bourque, DL1
Zivin, J1
Galal, NM1
Fouad, HM1
Saied, A1
Dabnon, M1
Aires, CC1
van Cruchten, A1
Ijlst, L1
de Almeida, IT1
Duran, M2
Wanders, RJ1
Silva, MF1
Kasapkara, CS1
Ezgu, FS1
Okur, I1
Tumer, L1
Biberoglu, G1
Hasanoglu, A1
Ivnitsky, YY1
Yachha, SK1
Mahmoud, AM1
Wendon, J1
Leke, R2
Nelson, J1
Cousineau, J1
Lambert, M1
Phan, V1
Ducruet, T1
Mpabanzi, L2
van den Broek, MA1
Visschers, RG1
van de Poll, MC1
Nadalin, S1
Saner, FH1
Malago, M1
Laish, I1
Ben Ari, Z1
Smeeton, NJ1
Castle, PC1
Watt, PW1
Kyong, YY1
Choi, KH1
Oh, YM1
Lee, KU1
Skowrońska, M1
Hung, TY1
Chen, CC1
Wang, TL1
Su, CF1
Wang, RF1
Urios, A1
Montesinos, E1
Molina, I1
Garcia-Torres, ML1
Civera, M1
Olmo, JA1
Ortega, J1
Martinez-Valls, J1
Serra, MA1
Cassinello, N1
Wassel, A1
Jordá, E1
Brunelli, L1
Campagna, R1
Airoldi, L1
Llansola, M2
Pastorelli, R1
Cudalbu, C2
Lanz, B1
Duarte, JM1
Morgenthaler, FD1
Pilloud, Y1
Mlynárik, V1
Gruetter, R1
Back, A1
Tupper, KY1
Bai, T1
Chiranand, P1
Goldenberg, FD1
Frank, JI1
Brorson, JR1
Blanco Vela, CI1
Poo Ramírez, JL1
Huynh, J1
Parent-Robitaille, C1
Kasai, A1
Nagao, K1
Kikushima, K1
Watanabe, K1
Tachibana, E1
Soga, T1
Matsuzaki, M1
Mastsuzaki, M1
Yagi, T1
Deutz, N1
Hayes, PC4
Kumar, R1
Sharma, H1
Prakash, S1
Panda, SK1
Khanal, S1
Acharya, SK1
Choi, DE1
Lee, KW1
Shin, YT1
Na, KR1
Pillai, U1
Kahlon, R1
Sondheimer, J1
Cadnapaphorncai, P1
Bhat, Z1
Hong, L1
Schutz, J1
Nance, M1
Medeiros, WM1
Carvalho, AC1
Peres, P1
De Luca, FA1
Gun, C1
Zhang, Y1
Landau, YE1
Miller, DT1
Marsden, D1
Kellogg, MD1
Yoon, YA1
Ki, CS1
Lee, SY1
Kim, JW1
Lee, YW1
Park, HD1
Braissant, O3
McLin, VA1
Oliveira, DL1
Forgiarini, LF1
Escobar, TD1
Hammes, TO1
Meyer, FS1
Silveira, TR1
Schaefer, TV1
Rejuniuk, VL1
Malakhovsky, VN2
Mardini, H1
Record, C1
McQueen, F1
Izumi, Y2
Svrakic, N1
O'Dell, K1
Zorumski, CF2
Calligaris, L1
Vidoni, A1
Bruno, I1
Vidoni, M1
Barbi, E1
Nagasaka, H2
Miida, T1
Yorifuji, T2
Hirano, K1
Inui, A1
Fujisawa, T1
Tsukahara, H1
Inomata, Y1
Veauvy, CM1
Walsh, PJ1
Pérez-Pinzón, MA1
Bachmann, C2
Augris, C1
Benabdelmalek, F1
Vauquelin, P1
Caramella, JP1
Paul, V1
Murphy, JV1
Li, XX1
Kobayashi, K3
Jalil, A1
Yoshida, G1
Boscá, L1
Hortelano, S1
Balata, S2
Ferguson, K1
Marshall, I2
Wardlaw, J2
García, MV2
López-Mediavilla, C2
Juanes de la Peña, MC2
Medina, JM2
Redhead, DN1
Hynd, P1
Jalan, RA1
Soeters, PB1
Zullo, A1
Hassan, C1
Morini, S1
García, MJ1
Wermuth, B1
Torres, J1
Pallarés, E1
Ugarte, M1
FRIEDLANDER, WJ1
POSER, CM1
PEARL, DC1
McDERMOTT, WV1
LABORIT, H1
OBRENOVITCH, L1
LEGUEN, P1
JOUANY, JM1
WILSON, WP1
TYOR, MP2
FONGI, EG1
HERRERO, H1
BIANCHINI, HM1
RIVADULLA, II1
OWEN, EE1
JOHNSON, JH1
STAHL, J1
ROHMER, F1
BOCKEL, R1
KURTZ, D1
IMLER, M1
AIMARD, G2
DUFFRENE, D2
MAILLET, P1
VILLAROS, J1
HAEFELY, W1
HUERLIMANN, A1
STAUB, H1
SCHWARZMANN, V1
BERTHAUX, N1
TSUKIYAMA, K1
MINE, R1
KOYAMA, M1
FUKUSHIMA, K1
FUKAO, R1
KITANI, T2
FASEL, J1
MAGNENAT, P2
RUSSELL, A1
LEVIN, B1
OBERHOLZER, VG1
SINCLAIR, L1
SOBERON, G1
FLORES, G1
ROSADO, A1
TORRES GALLARDO, J1
MORA, J1
MAGGIO, R1
ZANINI, P1
FACCHETTI, A1
BRETTE, R1
FRANCOIS, B1
CILLE, Y1
STARER, F1
COUCH, R1
DEUIL, R1
GODARD, F1
GENTILHOMME, C1
AUBERTIN, E1
AUBERTIN, J1
WONE, C1
COON, WW1
ZUIDEMA, GD1
KIRSH, MM1
WU, KH1
SHERMAN, B1
HOSHAL, V1
DUCHENE-MARULLAZ, P1
TALVARD, J1
VACHER, J1
RIGAMONTI, PP1
ZECCA, C1
MOLINAROLI, P1
PERRET, C1
MONTANI, S1
Monfort, P2
Muñoz, MD1
Minauchi, K1
Fujie, T1
Matsubara, N1
Kasahara, H1
Ogura, Y1
Tamura, M1
Yamane, Y1
Tanaka, M2
Taneichi, K1
Rajpoot, DK1
Gargus, JJ1
Kaku, T1
Shiba, M1
Yoshimasu, F1
Yamada, T1
Duseja, A1
Sachdev, A1
Dhiman, RK1
Chawla, YK1
Stanley, CA2
Villard, AM1
Boulat, O1
Henry, H1
Chow, SL1
Gandhi, V1
Krywawych, S1
Clayton, PT1
Leonard, JV3
Koch, HG2
Romero Gómez, M1
Bautista, JD1
Grande, L1
Ramos Guerrero, RM1
Sánchez Muñoz, D1
Mallet, L1
Babin, S1
Morais, JA1
McCall, M1
Bourgeois, JA1
Giordano, G1
Sanchez-Perez, AM1
Burgal, M1
Costa, LG1
Erceg, S1
Hernández-Viadel, M1
Panda, S1
Radhakrishnan, K1
Cordero, DR1
Baker, J1
Dorinzi, D1
Toffle, R1
Kala, G2
Zwingmann, C3
Leibfritz, D1
Ahboucha, S1
Araqi, F1
Layrargues, GP1
Alexander, B1
Smart, KA1
Segal, MB1
Preston, JE1
Clemmesen, O1
Yang, YL1
Sun, F1
Qian, N1
Song, JQ1
Wang, S1
Chang, XZ1
Yang, HY1
Wang, SQ1
Li, L1
Zhang, YH1
Bao, XH1
Qi, Y1
Qin, J1
Wu, XR1
Izumi, M1
Matsukawa, M1
Funatsu, M1
Klejman, A1
Szatmari, EM1
Mioduszewska, B1
Hetman, M1
Cleary, MA1
Dorland, L1
de Koning, TJ1
Poll-The, BT1
Mandell, R1
Shih, VE1
Berger, R1
Olpin, SE1
Besley, GT1
Ihara, K1
Miyako, K1
Ishimura, M1
Kuromaru, R1
Wang, HY1
Yasuda, K1
Hara, T1
Li, MX1
Kannan, Y1
Iijima, M1
Tsui, LC1
Mohr, M1
Rasmussen, P1
Drust, B1
Nielsen, B1
Nybo, L1
Rose, C2
Kubota, M1
Kurokawa, K1
Murakami, T1
Kanazawa, M1
Takatani, T1
Ogawa, A1
Ogawa, E1
Adachi, M1
Takayanagi, M1
Sen, S1
Hodges, S1
Nedredal, GI1
Pidoplichko, VI1
Dani, JA1
Lin, C1
Tusa, JK1
Wang, LJ1
Cai, JT1
Chen, T1
Lü, B1
Si, JM1
Talamo, G1
Cavallo, F1
Zangari, M1
Barlogie, B1
Lee, CK1
Pineda-Roman, M1
Kiwan, E1
Krishna, S1
Tricot, G1
Bunchman, TE1
Barletta, GM1
Winters, JW1
Gardner, JJ1
Crumb, TL1
McBryde, KD1
Reinehr, R1
Becker, S1
Selbach, O1
Haas, HL1
Schliess, F1
Hiroyama, M1
Aoyagi, T1
Fujiwara, Y1
Oshikawa, S1
Sanbe, A1
Endo, F1
Tanoue, A1
Brooks, HF1
Mani, AR1
Harry, D1
Zou, Z2
Davies, C1
Moore, KP1
Pedersen, HR1
Ring-Larsen, H1
Olsen, NV1
Rhead, WJ1
Brusilow, SW1
Hamosh, A1
Wong, YC1
Au, WL1
Xu, M1
Ye, J1
Lim, CC1
Velioğlu, SK1
Gazioğlu, S1
Cagnon, L1
Bodega, G1
Suárez, I1
Paniagua, C1
Vacas, E1
Fernández, B1
Pela, I1
Seracini, D1
Lavoratti, G1
Pasquini, E1
Materassi, M1
Clay, AS1
Hainline, BE1
Vaquero, J1
Yanagawa, Y1
Nishi, K1
Sakamoto, T1
Mangin, JM1
Gordish-Dressman, H1
Hoffman, EP1
Gallo, V1
Konopacka, A1
Reinyuk, VL1
Shefer, TV1
Malakhovskii, VN1
Ovsep'yan, RV2
Ivnitskii, YY1
Meinardi, MC1
van den Berg, GB1
Groenhuijzen, A1
Driessen, JT1
Maas, HA1
Wolfhagen, FH1
Jones, S1
Reed, CA1
Walter, JH1
Tremolizzo, L1
Galbussera, A1
Frigo, M1
Apale, P1
Capra, M1
Appollonio, I1
Ferrarese, C1
Bertrand, P1
Faro, A1
Cantwell, P1
Tzakis, A1
Sibson, NR1
Mason, GF1
Shen, J1
Cline, GW1
Herskovits, AZ1
Wall, JE1
Behar, KL1
Rothman, DL1
Shulman, RG1
Mathias, RS1
Kostiner, D1
Packman, S1
McEwan, P1
Simpson, D1
Kirk, JM1
Barr, DG1
McKenzie, KJ1
Barr, J1
Eshel, G1
Chen-Levy, Z1
Lahat, E1
Whitelaw, A1
Bridges, S1
Leaf, A1
Evans, D1
Seiler, N1
Stadler, S1
Gempel, K1
Bieger, I1
Pontz, BF1
Gerbitz, KD1
Bauer, MF1
Hofmann, S1
Kelly, A1
Ng, D1
Ferry, RJ1
Grimberg, A1
Koo-McCoy, S1
Thornton, PS1
Vanaja, P1
Irie, T1
Miyamoto, E1
Kitagawa, K1
Maruyama, Y1
Inagaki, C1
Otsuki, T1
Wada, H1
Nakazawa, N1
Taniwaki, M1
Kouguchi, K1
Ohkura, M1
Uehira, K1
Isoda, K1
Yata, K1
Sakaguchi, H1
Yawata, Y1
Ueki, A1
Yamada, O1
Vossler, DG1
Wilensky, AJ1
Cawthon, DF1
Kraemer, DL1
Ojemann, LM1
Caylor, LM1
Morgan, JD1
Laube, GF1
Superti-Furga, A1
Losa, M1
Büttiker, V1
Berger, C1
Neuhaus, TJ1
Chan, WK1
But, WM1
Law, CW1
Schwarz, S1
Georgiadis, D1
Schwab, S1
Gehlen, F1
Mayatepek, E1
Zoubaa, S1

Clinical Trials (10)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
[NCT04771104]9 participants (Actual)Interventional2017-01-01Completed
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of HPN-100 for Maintaining Remission in Subjects With Cirrhosis and Episodic Hepatic Encephalopathy[NCT00999167]Phase 2189 participants (Actual)Interventional2009-12-31Completed
Effect of Polyethylene Glycol Versus Lactulose on Hepatic Encephalopathy in Patients With Liver Cirrhosis; a Randomized Clinical Trial (PEGHE Trial)[NCT04436601]Phase 4102 participants (Anticipated)Interventional2020-03-09Recruiting
Plasma Free Amino Acids in Patients With Hepatic Encephalopathy and Its Impact on Disease Outcomes.[NCT03306498]100 participants (Anticipated)Observational2017-12-15Not yet recruiting
Efficacy of Intravenous 'L-ornithine L-aspartate' in Reversal of Overt Acute Hepatic Encephalopathy in Patients With Liver Cirrhosis: a Prospective, Randomized, Double-blind, Placebo Controlled Trial[NCT01722578]Phase 4200 participants (Actual)Interventional2013-12-31Completed
Brain Energy Metabolism in Patients With Acute Hepatic Encephalopathy Measured With PET[NCT00424957]18 participants (Anticipated)Observational2006-11-30Completed
Evaluation of the Therapeutic Effect of Rifaximin on Covert Hepatic Encephalopathy With Underlying Small Intestinal Bacterial Overgrowth and Gastrointestinal Dysmotility in Liver Cirrhosis Patients[NCT04244877]Phase 30 participants (Actual)Interventional2021-09-15Withdrawn (stopped due to Study was unable to recruit participants..)
A Phase 2a Study to Evaluate the Safety and Tolerability of OCR-002 (Ornithine Phenylacetate) in the Treatment of Patients With Acute Liver Failure/Severe Acute Liver Injury[NCT01548690]Phase 247 participants (Actual)Interventional2012-06-30Completed
A Phase 2, Open-Label, Switch-Over, Dose-Escalation Study of the Safety and Tolerability of HPN-100 Compared to Buphenyl® (Sodium Phenylbutyrate) in Patients With Urea Cycle Disorders[NCT00551200]Phase 214 participants (Actual)Interventional2007-10-31Completed
Efficacy of Vitamin E in Hyperinsulinism/Hyperammonemia Syndrome[NCT04984798]Phase 20 participants (Actual)Interventional2022-11-30Withdrawn (stopped due to No study activity took place. The IND was withdrawn with the FDA by the Sponsor Investigator because of insurmountable hurdles in moving proposed research forward)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Part B: Proportion of Subjects Who Exhibit an HE Episode, Defined as Either of the Following During the Treatment Phase: WH ≥2; WH Grade and Asterixis Grade Increase of 1 Each, if Baseline WH = 0

"An HE event was defined as occurrences of either a West Haven (WH) Grade ≥2 or a WH Grade 1 and asterixis grade increase of 1 (if baseline WH = 0).~The WH criteria are widely used for rating the severity of HE and are summarized below:~Grade 1: trivial lack of awareness, euphoria or anxiety, shortened attention span, impaired performance of addition Grade 2: lethargy or apathy, minimal disorientation for time or place, subtle personality change, inappropriate behavior, impaired performance of subtraction Grade 3: somnolence to semi-stupor but responsive to verbal stimuli, confusion, gross disorientation Grade 4: coma (unresponsive to verbal or noxious stimuli)~Asterixis was assessed after arm and forearm extension along with wrist dorsiflexion for 30 seconds and assigned a grade according to the following criteria:~Grade 1: rare flaps Grade 2: occasional irregular flaps Grade 3: frequent flaps Grade 4: continuous flaps" (NCT00999167)
Timeframe: Part B: 112 Days

Interventionparticipants (Number)
HPN-10019
Placebo32

Time to Meeting the Primary Endpoint

Secondary efficacy endpoint. The time to the first HE episode during the treatment period was calculated using the Kaplan-Meier method. Subjects who did not experience an HE episode were censored at the time of their last asterixis assessment. Subjects who had no post-randomization data for the primary endpoint were considered to have an HE episode at Day 1. (NCT00999167)
Timeframe: 112 Days

InterventionDays (Median)
HPN-100NA
PlaceboNA

Total Number of HE Events

Secondary efficacy endpoint. The total number of HE events during the treatment phase for subjects in the placebo and active arms. (NCT00999167)
Timeframe: 112 Days

InterventionHE event (Number)
HPN-10035
Placebo57

Change From Baseline in Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) Score

Changes from Baseline to Day 56 and the Final Visit were compared between treatment groups using an ANCOVA model for the total index RBANS score ). The index score is a sum of the scores for each of the 5 individual domains (immediate memory, visuospatial/constructional, language, attention). The minimum and maximum total index scores are 40 and 160, respectively; a higher score is better. (NCT00999167)
Timeframe: Day 56, Final Visit (D112)

,
Interventionunits on a scale (Least Squares Mean)
Change from Baseline to D56 (Total Score)Change from Baseline to Final Visit (Total Score)
HPN-100-0.5-10.7
Placebo3.2-9.7

Part A: The Rate of AEs and Tolerability of HPN-100

Part A: The rate of AEs and tolerability of 6 mL and 9 mL doses of HPN-100 were considered the primary safety endpoints for Part A. Safety assessments included adverse events, laboratory tests (including ammonia, hematology, coagulation, liver function and serum chemistry parameters), vital signs, physical and neurological examinations, and electrocardiograms. (NCT00999167)
Timeframe: Part A: 28 days

InterventionSubjects (Number)
Any AEGastrointestinal disordersMetabolism and nutrition disordersInfection and infestationsNervous system disordersBlood and lymphatic system disordersInjury, poisoning and procedural complicationsMusculoskeletal and connective tissue disordersPsychiatric disordersAny SAEDeath
HPN-100 BID119744222252

Change in Ammonia

To evaluate the effect of OCR-002 on ammonia levels in patients with acute liver failure/severe acute liver injury (NCT01548690)
Timeframe: Baseline and 72 Hours

InterventionPercent Change (Mean)
Maximum Dose Level 3.33 g/24h41.2
Maximum Dose Level 6.65 g/24h16.6
Maximum Dose Level 10 g/24h41.8
Maximum Dose Level 20g/24h38.4

Measurement of OCR-002 Plasma Concentration

To evaluate the steady state pharmacokinetic and pharmacodynamic profile of OCR-002 in patients with impaired and intact renal function using urinary phenylacetylglutamine (PAGN) as a surrogate marker (NCT01548690)
Timeframe: 24 Hours after last infusion

Interventionmicrograms per millileter (Mean)
Maximum Dose Level 3.33 g/24h65.6
Maximum Dose Level 6.65 g/24h32.2
Maximum Dose Level 10 g/24h33.4
Maximum Dose Level 20g/24h104.9

Neurological Function Measured by the Orientation Log (O-log)

The orientation log focuses on orientation to place, time, and circumstance. There are 10 items on the orientation log, which are scored 0-3. A spontaneous correct response is awarded 3 points. A spontaneous response that is lacking or incorrect, but a correct response is provided following a logical cue is awarded 2 points. A score of 1 is given if spontaneous and cued responses are lacking or incorrect, but a correct response is provided in a recognition format. A score of 0 is given if the spontaneous, cued, or recognition format does not generate a correct answer. Scores from the 10 items are summed and the final score ranges from 0 to 30. (NCT01548690)
Timeframe: 30 Days

Interventionunits on a scale (Mean)
Maximum Dose Level 3.33 g/24h23.8
Maximum Dose Level 6.65 g/24h24.0
Maximum Dose Level 10 g/24h24.0
Maximum Dose Level 20g/24h24.0

Neurological Function Measured by the West Haven Criteria (WHC) for Hepatic Encephalopathy

The West Haven Criteria (WHC) for Hepatic Encephalopathy measures the severity of encephalopathy and patient's level of consciousness. The scale ranges from 0 to 4; a minimum score of 0 represents a better outcome, and a maximum total score of 4 represents a worse outcome. A score of 0 corresponds to normal consciousness and behavior and normal neurological examination. A score of 1 corresponds to mild lack of awareness, shortened attention span, and impaired addition or subtraction; mild asterixis or tremor. A score of 2 corresponds to lethargy, disorientated or inappropriate behavior, obvious asterixis; slurred speech. A score of 3 corresponds to somnolent but arousable, gross disorientation or bizarre behavior, muscle rigidity and clonus; hyperreflexia. A score of 4 corresponds to coma and decerebrate posturing. (NCT01548690)
Timeframe: 120 hours from start of infusion

Interventionunits on a scale (Mean)
Maximum Dose Level 3.33 g/24h2.4
Maximum Dose Level 6.65 g/24h3.2
Maximum Dose Level 10 g/24h1.6
Maximum Dose Level 20g/24h1.8

Number of Participants That do Not Tolerate the Administered Dose and Had Grade 3 or 4 Treatment Emergent Adverse Events as a Measure of Safety and Tolerability

To evaluate the safety and tolerability of OCR-002 in patients with acute liver failure/severe acute liver injury (NCT01548690)
Timeframe: 30 Days

InterventionParticipants (Count of Participants)
Maximum Dose Level 3.33 g/24h0
Maximum Dose Level 6.65 g/24h0
Maximum Dose Level 10 g/24h0
Maximum Dose Level 20g/24h0

Number of Subjects Experienced Adverse Events

(NCT00551200)
Timeframe: during the period on 100% Buphenyl (up to 4 weeks) or HPN-100 (up to 10 weeks)

Interventionparticipants (Number)
Buphenyl7
HPN-1005

Number of Subjects Experienced Serious Adverse Events

(NCT00551200)
Timeframe: during the period subjects on 100% Buphenyl (up to 4 weeks) or HPN-100 (up to 10 weeks)

Interventionparticipants (Number)
Buphenyl1
HPN-1000

Drug Preference for HPN-100 or Buphenyl® (as Assessed by Global Preference Question)

(NCT00551200)
Timeframe: End of Study

Interventionparticipants (Number)
prefer Buphenylprefer HPN-100
Buphenyl to HPN-10019

Pharmacokinetics (Plasma and Urine PK Parameters of Study Drugs and Their Metabolites)

measured AUC0-24 (Area under the curve from time 0 (pre-dose) to 24 hours) for each metabolite in plasma. Data were collected at 30 minutes and 1, 2, 4, 5, 6, 8, 10, 12, and 24 hours post-first dose. (NCT00551200)
Timeframe: At steady state (1 week) on each medication (Buphenyl® alone, HPN-100 alone)

,
Interventionμg*h/mL (Mean)
AUC0-24 PBA (phenylbutyrate) in plasmaAUC0-24 PAA (phenylacetate) in plasmaAUC0-24 PAGN (phenylacetylglutamine) in plasma
HPN-100 Steady State5405751098
NaPBA Steady State7405961133

Venous Ammonia Levels at the Peak and Mean TNUAC Time-normalized Area Under the Curve)

Data were collected at pre-first dose and at 30 minutes and 1, 2, 4, 5, 6, 8, 10, 12, and 24 hours post first dose. (NCT00551200)
Timeframe: At steady state (1 week) on each medication (Buphenyl® alone, HPN-100 alone), and at steady state (1 week) after each dose escalation

,
Interventionμmol/L (Mean)
in peakin TNAUC (time-normalized area under the curve)
HPN-100 Steady State56.326.5
NaPBA Steady State79.138.4

Reviews

99 reviews available for ammonium hydroxide and Hyperammonemia

ArticleYear
Hyperammonemia in Inherited Metabolic Diseases.
    Cellular and molecular neurobiology, 2022, Volume: 42, Issue:8

    Topics: Ammonia; Fatty Acids; Humans; Hyperammonemia; Infant, Newborn; Metabolic Diseases; Urea

2022
Serum Ammonia in Cirrhosis: Clinical Impact of Hyperammonemia, Utility of Testing, and National Testing Trends.
    Clinical therapeutics, 2022, Volume: 44, Issue:3

    Topics: Adult; Ammonia; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Cirrhosis; Sarcopenia

2022
A review of basic to clinical studies of the association between hyperammonemia, methamphetamine.
    Naunyn-Schmiedeberg's archives of pharmacology, 2022, Volume: 395, Issue:8

    Topics: Ammonia; Animals; Central Nervous System Stimulants; Glutamic Acid; Hyperammonemia; Methamphetamine

2022
Recommendations for the Diagnosis and Therapeutic Management of Hyperammonaemia in Paediatric and Adult Patients.
    Nutrients, 2022, Jul-02, Volume: 14, Issue:13

    Topics: Adult; Aged; Ammonia; Child; Humans; Hyperammonemia; Liver Diseases; Prognosis; Renal Dialysis

2022
Risk factors and outcome of hyperammonaemia in people with epilepsy.
    Journal of neurology, 2022, Volume: 269, Issue:12

    Topics: Adult; Ammonia; Epilepsy; Humans; Hyperammonemia; Observational Studies as Topic; Oxcarbazepine; Ris

2022
Hyperammonemia in a pregnant woman with citrullinemia type I: a case report and literature review.
    BMC pregnancy and childbirth, 2022, Dec-19, Volume: 22, Issue:1

    Topics: Adult; Amino Acids; Ammonia; Citrullinemia; Female; Humans; Hyperammonemia; Pregnancy; Pregnant Wome

2022
Cellular Pathogenesis of Hepatic Encephalopathy: An Update.
    Biomolecules, 2023, 02-19, Volume: 13, Issue:2

    Topics: Ammonia; Autophagy; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Failure

2023
Ammonia and nutritional therapy in the critically ill: when to worry, when to test and how to treat?
    Current opinion in clinical nutrition and metabolic care, 2023, 03-01, Volume: 26, Issue:2

    Topics: Ammonia; Critical Illness; Humans; Hyperammonemia; Nutrition Therapy; Nutritional Support

2023
Drug-induced hyperammonaemia.
    Journal of clinical pathology, 2023, Volume: 76, Issue:8

    Topics: Ammonia; Brain; Child; Humans; Hyperammonemia; Valproic Acid

2023
Risk factors of hyperammonemia in epilepsy patients with valproic acid therapy.
    Clinical neurology and neurosurgery, 2023, Volume: 233

    Topics: Adult; Ammonia; Anticonvulsants; Epilepsy; Humans; Hyperammonemia; Risk Factors; Topiramate; Valproi

2023
Expanding the Spectrum of Extracorporeal Strategies in Small Infants with Hyperammonemia.
    Blood purification, 2023, Volume: 52, Issue:9-10

    Topics: Acute Kidney Injury; Adolescent; Ammonia; Child; Child, Preschool; Continuous Renal Replacement Ther

2023
[Molecular basis of hyperammonemia secondary to asparaginase: from therapeutic efficacity to toxicity].
    Annales de biologie clinique, 2023, 10-20, Volume: 81, Issue:4

    Topics: Ammonia; Antineoplastic Agents; Asparaginase; Humans; Hyperammonemia; Precursor Cell Lymphoblastic L

2023
Zinc and protein metabolism in chronic liver diseases.
    Nutrition research (New York, N.Y.), 2020, Volume: 74

    Topics: Amino Acids, Branched-Chain; Ammonia; Chronic Disease; Dietary Supplements; Humans; Hyperammonemia;

2020
Astrocyte swelling in hepatic encephalopathy: molecular perspective of cytotoxic edema.
    Metabolic brain disease, 2020, Volume: 35, Issue:4

    Topics: Ammonia; Astrocytes; Brain; Brain Edema; Cell Size; Hepatic Encephalopathy; Humans; Hyperammonemia;

2020
Skeletal Muscle and the Effects of Ammonia Toxicity in Fish, Mammalian, and Avian Species: A Comparative Review Based on Molecular Research.
    International journal of molecular sciences, 2020, Jun-30, Volume: 21, Issue:13

    Topics: Ammonia; Animals; Birds; Fishes; Hyperammonemia; Liver Cirrhosis; Mammals; Muscle Development; Muscl

2020
Novel aspects of glutamine synthetase in ammonia homeostasis.
    Neurochemistry international, 2020, Volume: 140

    Topics: Ammonia; Animals; Brain; Brain Diseases; Glutamate-Ammonia Ligase; Glutamic Acid; Glutamine; Homeost

2020
Presentation and management of N-acetylglutamate synthase deficiency: a review of the literature.
    Orphanet journal of rare diseases, 2020, 10-09, Volume: 15, Issue:1

    Topics: Amino-Acid N-Acetyltransferase; Ammonia; Humans; Hyperammonemia; Infant, Newborn; Urea Cycle Disorde

2020
Primary hyperammonaemia: Current diagnostic and therapeutic strategies.
    Journal of mother and child, 2020, Oct-02, Volume: 24, Issue:2

    Topics: Ammonia; Early Diagnosis; Female; Humans; Hyperammonemia; Infant; Infant, Newborn; Male; Renal Dialy

2020
Extracorporeal Ammonia Clearance for Hyperammonemia in Critically Ill Patients: A Scoping Review.
    Blood purification, 2021, Volume: 50, Issue:4-5

    Topics: Ammonia; Continuous Renal Replacement Therapy; Critical Illness; Humans; Hyperammonemia; Peritoneal

2021
Ammonia Removal by Metabolic Scavengers for the Prevention and Treatment of Hepatic Encephalopathy in Cirrhosis.
    Drugs in R&D, 2021, Volume: 21, Issue:2

    Topics: Ammonia; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Cirrhosis

2021
Nonhepatic hyperammonemic encephalopathy complications following bariatric surgery: a case report and review of the literature.
    Journal of medical case reports, 2021, Jul-20, Volume: 15, Issue:1

    Topics: Adult; Ammonia; Bariatric Surgery; Female; Humans; Hyperammonemia; Obesity; Urea Cycle Disorders, In

2021
Roles of Glutamate and Glutamine Transport in Ammonia Neurotoxicity: State of the Art and Question Marks.
    Endocrine, metabolic & immune disorders drug targets, 2018, Volume: 18, Issue:4

    Topics: Amino Acid Transport System X-AG; Amino Acid Transport Systems; Amino Acid Transport Systems, Neutra

2018
The Pharmabiotic Approach to Treat Hyperammonemia.
    Nutrients, 2018, Jan-28, Volume: 10, Issue:2

    Topics: Ammonia; Animals; Clinical Trials, Phase II as Topic; Clinical Trials, Phase III as Topic; Disease M

2018
Inborn Errors of Metabolism with Hyperammonemia: Urea Cycle Defects and Related Disorders.
    Pediatric clinics of North America, 2018, Volume: 65, Issue:2

    Topics: Ammonia; Emergency Treatment; Humans; Hyperammonemia; Infant; Infant, Newborn; Urea; Urea Cycle Diso

2018
The impact of ammonia levels and dialysis on outcome in 202 patients with neonatal onset urea cycle disorders.
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:4

    Topics: Age of Onset; Ammonia; Humans; Hyperammonemia; Infant, Newborn; Renal Dialysis; Treatment Outcome; U

2018
Why and when to measure ammonemia in cirrhosis?
    Clinics and research in hepatology and gastroenterology, 2018, Volume: 42, Issue:6

    Topics: Ammonia; Diagnosis, Differential; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Cirrhosis; L

2018
Blood Ammonia as a Possible Etiological Agent for Alzheimer's Disease.
    Nutrients, 2018, May-04, Volume: 10, Issue:5

    Topics: Alzheimer Disease; Ammonia; Amyloid beta-Peptides; Diet, Mediterranean; Humans; Hyperammonemia; Lact

2018
Lesson of the month 1: Sodium valproate-induced encephalopathy.
    Clinical medicine (London, England), 2018, Volume: 18, Issue:5

    Topics: Aged; Ammonia; Anticonvulsants; Brain Diseases; Carnitine; Consciousness Disorders; Epilepsy; Humans

2018
Hyperammonaemia in classic organic acidaemias: a review of the literature and two case histories.
    Orphanet journal of rare diseases, 2018, 12-06, Volume: 13, Issue:1

    Topics: Ammonia; Glucose; Glutamates; Humans; Hyperammonemia; Propionic Acidemia

2018
Ammonia and autophagy: An emerging relationship with implications for disorders with hyperammonemia.
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:6

    Topics: Ammonia; Animals; Autophagy; Glutamate-Ammonia Ligase; Glutamine; Homeostasis; Humans; Hyperammonemi

2019
Comprehensive characterization of ureagenesis in the spf
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:6

    Topics: Age Factors; Aging; Ammonia; Animals; Disease Models, Animal; Humans; Hyperammonemia; Liver; Male; M

2019
[Valproic acid-induced hyperammonemic encephalopathy in a patient receiving valproic acid monotherapy].
    Rinsho shinkeigaku = Clinical neurology, 2019, May-28, Volume: 59, Issue:5

    Topics: Aged; Ammonia; Anticonvulsants; Biomarkers; Cardiomyopathies; Carnitine; Consciousness Disorders; Ep

2019
L-Ornithine L-Aspartate for the Treatment of Sarcopenia in Chronic Liver Disease: The Taming of a Vicious Cycle.
    Canadian journal of gastroenterology & hepatology, 2019, Volume: 2019

    Topics: Ammonia; Dipeptides; End Stage Liver Disease; Humans; Hyperammonemia; Liver; Sarcopenia; Treatment O

2019
Hyperammonemia, the Last Indication of High-Volume Hemodiafiltration in Adult and Children: A Structured Review.
    Blood purification, 2019, Volume: 48, Issue:4

    Topics: Adult; Ammonia; Child; Hemodiafiltration; Humans; Hyperammonemia; Prognosis

2019
Clinical and biochemical aspects of primary and secondary hyperammonemic disorders.
    Archives of biochemistry and biophysics, 2013, Aug-15, Volume: 536, Issue:2

    Topics: Amino-Acid N-Acetyltransferase; Ammonia; Animals; Glutamate-Ammonia Ligase; Humans; Hyperammonemia;

2013
Contributions of microdialysis to new alternative therapeutics for hepatic encephalopathy.
    International journal of molecular sciences, 2013, Aug-05, Volume: 14, Issue:8

    Topics: Ammonia; Animals; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver; Liver Cirrhosis; Microdialy

2013
Evidence of a vicious cycle in glutamine synthesis and breakdown in pathogenesis of hepatic encephalopathy-therapeutic perspectives.
    Metabolic brain disease, 2014, Volume: 29, Issue:1

    Topics: Amino Acids, Branched-Chain; Ammonia; Brain; Critical Illness; Drug Interactions; Enterocytes; Gluta

2014
α-Ketoglutaramate: an overlooked metabolite of glutamine and a biomarker for hepatic encephalopathy and inborn errors of the urea cycle.
    Metabolic brain disease, 2014, Volume: 29, Issue:4

    Topics: Amidohydrolases; Aminohydrolases; Ammonia; Animals; Biomarkers; Carbon; Glutamine; Hepatic Encephalo

2014
Treatment of hyperammonemia in liver failure.
    Current opinion in clinical nutrition and metabolic care, 2014, Volume: 17, Issue:1

    Topics: Ammonia; Brain; Glycerol; Hepatic Encephalopathy; Humans; Hyperammonemia; Lactulose; Phenylbutyrates

2014
Cerebral effects of ammonia in liver disease: current hypotheses.
    Metabolic brain disease, 2014, Volume: 29, Issue:4

    Topics: Ammonia; Animals; Astrocytes; Blood-Brain Barrier; Brain Edema; Diffusion; Energy Metabolism; gamma-

2014
Measurement and interpretation of plasma ammonia.
    British journal of hospital medicine (London, England : 2005), 2014, Volume: 75, Issue:3

    Topics: Ammonia; Chronic Disease; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Diseases

2014
Pharmacotherapy for hyperammonemia.
    Expert opinion on pharmacotherapy, 2014, Volume: 15, Issue:12

    Topics: Ammonia; Animals; Gastrointestinal Agents; Hepatic Encephalopathy; Humans; Hyperammonemia; Lactulose

2014
Ammonia and amino acid profiles in liver cirrhosis: effects of variables leading to hepatic encephalopathy.
    Nutrition (Burbank, Los Angeles County, Calif.), 2015, Volume: 31, Issue:1

    Topics: Amino Acids, Aromatic; Amino Acids, Branched-Chain; Ammonia; Brain; Dietary Proteins; Glutamine; Hep

2015
Ammonia metabolism and hyperammonemic disorders.
    Advances in clinical chemistry, 2014, Volume: 67

    Topics: Ammonia; Animals; Arginine; Biological Transport; Brain; Cell Membrane; Humans; Hyperammonemia; Hype

2014
Refining the ammonia hypothesis: a physiology-driven approach to the treatment of hepatic encephalopathy.
    Mayo Clinic proceedings, 2015, Volume: 90, Issue:5

    Topics: Ammonia; Clinical Protocols; Hepatic Encephalopathy; Humans; Hyperammonemia

2015
Recent advances in the treatment of hyperammonemia.
    Advanced drug delivery reviews, 2015, Aug-01, Volume: 90

    Topics: Ammonia; Animals; Humans; Hyperammonemia; Inactivation, Metabolic

2015
Clinical science workshop: targeting the gut-liver-brain axis.
    Metabolic brain disease, 2016, Volume: 31, Issue:6

    Topics: Ammonia; Animals; Anti-Inflammatory Agents; Brain; Drug Delivery Systems; Education; Gastrointestina

2016
The Importance of Clinical Context When Interpreting Serum Ammonia Levels: A Teachable Moment.
    JAMA internal medicine, 2015, Volume: 175, Issue:12

    Topics: Adult; Ammonia; Diagnosis, Differential; Fatty Liver; Humans; Hyperammonemia; Male

2015
Roles of renal ammonia metabolism other than in acid-base homeostasis.
    Pediatric nephrology (Berlin, Germany), 2017, Volume: 32, Issue:6

    Topics: Acid-Base Equilibrium; Ammonia; Humans; Hyperammonemia; Hypokalemia; Kidney Tubules, Collecting; Kid

2017
The Role of RRT in Hyperammonemic Patients.
    Clinical journal of the American Society of Nephrology : CJASN, 2016, 10-07, Volume: 11, Issue:10

    Topics: Adult; Ammonia; Brain Diseases; Humans; Hyperammonemia; Infant, Newborn; Renal Replacement Therapy

2016
Multifactorial Effects on Different Types of Brain Cells Contribute to Ammonia Toxicity.
    Neurochemical research, 2017, Volume: 42, Issue:3

    Topics: Ammonia; Animals; Astrocytes; Brain; Cyclic GMP; Energy Metabolism; Glutamine; Hepatic Encephalopath

2017
Current state of knowledge of hepatic encephalopathy (part I): newer treatment strategies for hyperammonemia in liver failure.
    Metabolic brain disease, 2016, Volume: 31, Issue:6

    Topics: Ammonia; Animals; Glutamate-Ammonia Ligase; Health Knowledge, Attitudes, Practice; Hepatic Encephalo

2016
Ammonia toxicity: from head to toe?
    Metabolic brain disease, 2017, Volume: 32, Issue:2

    Topics: Ammonia; Animals; Brain; Brain Chemistry; Hepatic Encephalopathy; Humans; Hyperammonemia; Muscle, Sk

2017
The brain in acute liver failure. A tortuous path from hyperammonemia to cerebral edema.
    Metabolic brain disease, 2009, Volume: 24, Issue:1

    Topics: Ammonia; Animals; Brain; Brain Edema; Hepatic Encephalopathy; Humans; Hyperammonemia; Intracranial H

2009
Gut ammonia production and its modulation.
    Metabolic brain disease, 2009, Volume: 24, Issue:1

    Topics: Ammonia; Animals; Genetic Predisposition to Disease; Glutaminase; Glutamine; Hepatic Encephalopathy;

2009
Interorgan ammonia trafficking in liver disease.
    Metabolic brain disease, 2009, Volume: 24, Issue:1

    Topics: Amino Acids; Ammonia; Animals; Brain; Glutamine; Humans; Hyperammonemia; Intestinal Mucosa; Intestin

2009
Identifying the direct effects of ammonia on the brain.
    Metabolic brain disease, 2009, Volume: 24, Issue:1

    Topics: Adenosine Triphosphatases; Ammonia; Animals; Brain; Cation Transport Proteins; Cell Membrane; Hepati

2009
Ammonia toxicity and its prevention in inherited defects of the urea cycle.
    Diabetes, obesity & metabolism, 2009, Volume: 11, Issue:9

    Topics: Adult; Ammonia; Animals; Arginine; Genetic Therapy; Humans; Hyperammonemia; Ornithine Carbamoyltrans

2009
Interorgan ammonia metabolism in liver failure: the basis of current and future therapies.
    Liver international : official journal of the International Association for the Study of the Liver, 2011, Volume: 31, Issue:2

    Topics: Adipose Tissue; Amino Acids; Ammonia; Arginine; Brain; Dipeptides; Glutamate-Ammonia Ligase; Glutami

2011
Adult nonhepatic hyperammonemia: a case report and differential diagnosis.
    The American journal of medicine, 2010, Volume: 123, Issue:10

    Topics: Ammonia; Diagnosis, Differential; Humans; Hyperammonemia; Liver Diseases; Male; Metabolism, Inborn E

2010
Clinical practice: the management of hyperammonemia.
    European journal of pediatrics, 2011, Volume: 170, Issue:1

    Topics: Amino Acids; Ammonia; Child; Diagnosis, Differential; Humans; Hyperammonemia; Practice Guidelines as

2011
Noncirrhotic hyperammonaemic encephalopathy.
    Liver international : official journal of the International Association for the Study of the Liver, 2011, Volume: 31, Issue:9

    Topics: Adult; Ammonia; Biomarkers; Brain Diseases, Metabolic; Early Diagnosis; Humans; Hyperammonemia; Live

2011
Alterations of blood brain barrier function in hyperammonemia: an overview.
    Neurotoxicity research, 2012, Volume: 21, Issue:2

    Topics: Amino Acids; Ammonia; Animals; Biological Transport; Blood-Brain Barrier; Brain; Brain Edema; Humans

2012
Severe hyperammonaemia in adults not explained by liver disease.
    Annals of clinical biochemistry, 2012, Volume: 49, Issue:Pt 3

    Topics: Adult; Amino Acids; Ammonia; Biological Transport; Blood-Brain Barrier; Brain; Glutamine; Humans; Hy

2012
Ammonia-lowering strategies for the treatment of hepatic encephalopathy.
    Clinical pharmacology and therapeutics, 2012, Volume: 92, Issue:3

    Topics: Ammonia; Brain; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver

2012
Possible treatment of end-stage hyperammonemic encephalopathy by inhibition of glutamine synthetase.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Ammonia; Animals; Brain; Enzyme Inhibitors; Glutamate-Ammonia Ligase; Hepatic Encephalopathy; Homeos

2013
Changes in cerebral oxidative metabolism in patients with acute liver failure.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Amino Acids; Ammonia; Animals; Brain; Brain Chemistry; Humans; Hyperammonemia; Lactic Acid; Liver Fa

2013
Ammonia toxicity to the brain.
    Journal of inherited metabolic disease, 2013, Volume: 36, Issue:4

    Topics: Ammonia; Animals; Brain; Brain Neoplasms; Humans; Hyperammonemia; Neuroprotective Agents

2013
Pathogenesis of hepatic encephalopathy: lessons from nitrogen challenges in man.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Amino Acids; Ammonia; Animals; Colon; Glutamine; Hepatic Encephalopathy; Humans; Hyperammonemia; Nit

2013
Valproate-induced hyperammonaemia superimposed upon severe neuropsychiatric lupus: a case report and review of the literature.
    Clinical rheumatology, 2013, Volume: 32, Issue:3

    Topics: Ammonia; Antimanic Agents; Fatal Outcome; Female; Humans; Hyperammonemia; Lupus Vasculitis, Central

2013
Branched-chain amino acids and muscle ammonia detoxification in cirrhosis.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Amino Acids, Branched-Chain; Ammonia; Animals; Humans; Hyperammonemia; Liver Cirrhosis; Liver Diseas

2013
Role of branched chain amino acids in cerebral ammonia homeostasis related to hepatic encephalopathy.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Amino Acids, Branched-Chain; Ammonia; Animals; Citric Acid Cycle; Energy Metabolism; Hepatic Encepha

2013
Neurobiology of ammonia.
    Progress in neurobiology, 2002, Volume: 67, Issue:4

    Topics: Ammonia; Brain; Humans; Hyperammonemia

2002
Mechanisms of hyperammonemia.
    Clinical chemistry and laboratory medicine, 2002, Volume: 40, Issue:7

    Topics: Amino Acids; Ammonia; Animals; Brain; Hepatic Encephalopathy; Humans; Hyperammonemia

2002
Hepatic encephalopathy and Helicobacter pylori: a critical reappraisal.
    Journal of clinical gastroenterology, 2003, Volume: 37, Issue:2

    Topics: Ammonia; Animals; Case-Control Studies; Gastric Juice; Helicobacter pylori; Hepatic Encephalopathy;

2003
[Hepatic encephalopathy].
    Nihon rinsho. Japanese journal of clinical medicine, 2004, Volume: 62 Suppl

    Topics: Ammonia; Biomarkers; Dementia; Diagnosis, Differential; Electroencephalography; Hepatic Encephalopat

2004
[Chronic portal-systemic encephalopathy].
    Nihon rinsho. Japanese journal of clinical medicine, 2004, Volume: 62 Suppl

    Topics: Ammonia; Biomarkers; Chronic Disease; Dementia; Diagnosis, Differential; Diagnostic Imaging; Hepatic

2004
Helicobacter pylori and hepatic encephalopathy.
    Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2003, Volume: 22 Suppl 2

    Topics: Ammonia; Gastric Juice; Helicobacter Infections; Helicobacter pylori; Hepatic Encephalopathy; Humans

2003
Hyperinsulinism/hyperammonemia syndrome: insights into the regulatory role of glutamate dehydrogenase in ammonia metabolism.
    Molecular genetics and metabolism, 2004, Volume: 81 Suppl 1

    Topics: Adolescent; Ammonia; Animals; Female; Glutamate Dehydrogenase; Humans; Hyperammonemia; Hyperinsulini

2004
Ammonia toxicity to the brain and creatine.
    Molecular genetics and metabolism, 2004, Volume: 81 Suppl 1

    Topics: Ammonia; Animals; Brain Chemistry; Creatine; Culture Media, Serum-Free; Glutamic Acid; Hyperammonemi

2004
[New concepts in the physiopathology of hepatic encephalopathy and therapeutic prospects].
    Gastroenterologia y hepatologia, 2004, Volume: 27 Suppl 1

    Topics: Ammonia; Brain; Brain Edema; Dipeptides; Flumazenil; Glutaminase; Glutamine; Hepatic Encephalopathy;

2004
[Hyperammonemia: causes, diagnosis and therapy. 2. Symptoms and therapy].
    Deutsche medizinische Wochenschrift (1946), 2004, Jun-18, Volume: 129, Issue:25-26

    Topics: Ammonia; Anticonvulsants; Aspirin; Diagnosis, Differential; Diuretics; Humans; Hyperammonemia; Progn

2004
Ammonia neurotoxicity and the mitochondrial permeability transition.
    Journal of bioenergetics and biomembranes, 2004, Volume: 36, Issue:4

    Topics: Ammonia; Animals; Apoptosis; Astrocytes; Cell Membrane; Cell Membrane Permeability; Hepatic Encephal

2004
Cerebral metabolic disturbances in the brain during acute liver failure: from hyperammonemia to energy failure and proteolysis.
    Neurochemistry international, 2005, Volume: 47, Issue:1-2

    Topics: Ammonia; Animals; Astrocytes; Cerebral Cortex; Citric Acid Cycle; Hepatic Encephalopathy; Humans; Hy

2005
Endogenous neuro-protectants in ammonia toxicity in the central nervous system: facts and hypotheses.
    Metabolic brain disease, 2005, Volume: 20, Issue:4

    Topics: Ammonia; Animals; Antidotes; Excitatory Amino Acid Antagonists; Glutathione; Humans; Hyperammonemia;

2005
Effect of ammonia on astrocytic glutamate uptake/release mechanisms.
    Journal of neurochemistry, 2006, Volume: 97 Suppl 1

    Topics: Ammonia; Animals; Astrocytes; Brain; Calcium; Cell Size; Cells, Cultured; Excitatory Amino Acid Tran

2006
[Disturbances in ammonia metabolism in hepatic failure].
    Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 2007, May-31, Volume: 127, Issue:11

    Topics: Ammonia; Animals; Brain; Hepatic Encephalopathy; Humans; Hyperammonemia; Intestinal Mucosa; Kidney;

2007
The anaplerotic flux and ammonia detoxification in hepatic encephalopathy.
    Metabolic brain disease, 2007, Volume: 22, Issue:3-4

    Topics: Ammonia; Animals; Astrocytes; Brain; Citric Acid Cycle; Energy Metabolism; Glucose; Glutamine; Hepat

2007
Hyperammonemia-induced toxicity for the developing central nervous system.
    Brain research reviews, 2007, Volume: 56, Issue:1

    Topics: Ammonia; Animals; Brain; Brain Diseases, Metabolic, Inborn; Cerebral Palsy; Child; Energy Metabolism

2007
Energy metabolism in brain cells: effects of elevated ammonia concentrations.
    Metabolic brain disease, 2007, Volume: 22, Issue:3-4

    Topics: Ammonia; Animals; Astrocytes; Brain; Citric Acid Cycle; Energy Metabolism; Glucose; Glutamic Acid; G

2007
Hyperammonemia in the ICU.
    Chest, 2007, Volume: 132, Issue:4

    Topics: Acute Disease; Algorithms; Ammonia; Astrocytes; Brain; Brain Edema; Cerebral Hemorrhage; Critical Ca

2007
Nutritional management of patients with urea cycle disorders.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:6

    Topics: Adolescent; Adult; Ammonia; Child; Child, Preschool; Diet Therapy; Enzymes; Female; Humans; Hyperamm

2007
Neurological implications of urea cycle disorders.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:6

    Topics: Ammonia; Brain; Cognition; Enzymes; Female; Humans; Hyperammonemia; Magnetic Resonance Imaging; Male

2007
Mechanisms of brain edema in acute liver failure and impact of novel therapeutic interventions.
    Neurological research, 2007, Volume: 29, Issue:7

    Topics: Ammonia; Animals; Brain; Brain Diseases, Metabolic; Brain Edema; Energy Metabolism; Glutamine; Hepat

2007
Hyperammonemia in urea cycle disorders: role of the nephrologist.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2001, Volume: 37, Issue:5

    Topics: Algorithms; Ammonia; Brain Diseases, Metabolic; Child, Preschool; Coma; Developmental Disabilities;

2001
Ornithine aminotransferase, a potential target for the treatment of hyperammonemias.
    Current drug targets, 2000, Volume: 1, Issue:2

    Topics: Ammonia; Animals; Biogenic Polyamines; Brain; Chorioretinitis; Enzyme Inhibitors; Humans; Hyperammon

2000
Glutamate transporter and receptor function in disorders of ammonia metabolism.
    Mental retardation and developmental disabilities research reviews, 2001, Volume: 7, Issue:4

    Topics: Adenosine Triphosphate; Amino Acid Transport System X-AG; Ammonia; Apoptosis; Astrocytes; Binding Si

2001
Role of glutamine in cerebral nitrogen metabolism and ammonia neurotoxicity.
    Mental retardation and developmental disabilities research reviews, 2001, Volume: 7, Issue:4

    Topics: Ammonia; Astrocytes; Brain; Cerebrovascular Circulation; Glutamic Acid; Glutamine; Humans; Hyperammo

2001
Urea cycle disorders.
    Seminars in neonatology : SN, 2002, Volume: 7, Issue:1

    Topics: Ammonia; Diagnosis, Differential; Emergency Treatment; Humans; Hyperammonemia; Infant, Newborn; Pren

2002

Trials

25 trials available for ammonium hydroxide and Hyperammonemia

ArticleYear
The effect of induced hyperammonaemia on sleep and melanopsin-mediated pupillary light response in patients with liver cirrhosis: A single-blinded randomized crossover trial.
    PloS one, 2022, Volume: 17, Issue:9

    Topics: Amino Acids; Ammonia; Circadian Rhythm; Cross-Over Studies; Glucose; Humans; Hyperammonemia; Liver C

2022
Clearance and production of ammonia quantified in humans by constant ammonia infusion - the effects of cirrhosis and ammonia-targeting treatments.
    Journal of hepatology, 2023, Volume: 79, Issue:2

    Topics: Ammonia; Hepatic Encephalopathy; Humans; Hyperammonemia; Lactulose; Liver Cirrhosis; Male; Phenylbut

2023
Intrahepatic Administration of Human Liver Stem Cells in Infants with Inherited Neonatal-Onset Hyperammonemia: A Phase I Study.
    Stem cell reviews and reports, 2020, Volume: 16, Issue:1

    Topics: Age of Onset; Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinic Aciduria; Cell Differe

2020
Plasma ammonia concentrations in extremely low birthweight infants in the first week after birth: secondary analysis from the ProVIDe randomized clinical trial.
    Pediatric research, 2020, Volume: 88, Issue:2

    Topics: Ammonia; Birth Weight; Data Interpretation, Statistical; Female; Gestational Age; Humans; Hyperammon

2020
Efficacy and Safety of Sodium Benzoate in The Management of Hyperammonemia in Decompensated Chronic Liver Disease of the Childhood-A Double-blind Randomized Controlled Trial.
    Journal of pediatric gastroenterology and nutrition, 2020, Volume: 70, Issue:2

    Topics: Ammonia; Child; Double-Blind Method; Hepatic Encephalopathy; Humans; Hyperammonemia; Prospective Stu

2020
Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders.
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:1

    Topics: Ammonia; Biomarkers; Cell Transplantation; Europe; Female; Humans; Hyperammonemia; Infant; Infant, N

2018
Impact of intestinal mannitol on hyperammonemia, oxidative stress and severity of hepatic encephalopathy in the ED.
    The American journal of emergency medicine, 2018, Volume: 36, Issue:9

    Topics: Adult; Ammonia; Biomarkers; Diuretics, Osmotic; Drug Administration Routes; End Stage Liver Disease;

2018
Optimal Prescriptions of Continuous Renal Replacement Therapy in Neonates with Hyperammonemia.
    Blood purification, 2019, Volume: 47, Issue:1-3

    Topics: Ammonia; Asian People; Female; Humans; Hyperammonemia; Infant, Newborn; Infant, Newborn, Diseases; M

2019
An engineered
    Science translational medicine, 2019, 01-16, Volume: 11, Issue:475

    Topics: Ammonia; Animals; Arginine; Biosynthetic Pathways; Disease Models, Animal; Escherichia coli; Feces;

2019
Efficacy of orally administered sodium benzoate and sodium phenylbutyrate in dogs with congenital portosystemic shunts.
    Journal of veterinary internal medicine, 2019, Volume: 33, Issue:3

    Topics: Ammonia; Animals; Bile Acids and Salts; Cross-Over Studies; Dogs; Double-Blind Method; Female; Hyper

2019
Randomized, double-blind, controlled study of glycerol phenylbutyrate in hepatic encephalopathy.
    Hepatology (Baltimore, Md.), 2014, Volume: 59, Issue:3

    Topics: Adult; Aged; Ammonia; Double-Blind Method; Female; Glutamine; Glycerol; Hepatic Encephalopathy; Huma

2014
Randomized, double-blind, controlled study of glycerol phenylbutyrate in hepatic encephalopathy.
    Hepatology (Baltimore, Md.), 2014, Volume: 59, Issue:3

    Topics: Adult; Aged; Ammonia; Double-Blind Method; Female; Glutamine; Glycerol; Hepatic Encephalopathy; Huma

2014
Randomized, double-blind, controlled study of glycerol phenylbutyrate in hepatic encephalopathy.
    Hepatology (Baltimore, Md.), 2014, Volume: 59, Issue:3

    Topics: Adult; Aged; Ammonia; Double-Blind Method; Female; Glutamine; Glycerol; Hepatic Encephalopathy; Huma

2014
Randomized, double-blind, controlled study of glycerol phenylbutyrate in hepatic encephalopathy.
    Hepatology (Baltimore, Md.), 2014, Volume: 59, Issue:3

    Topics: Adult; Aged; Ammonia; Double-Blind Method; Female; Glutamine; Glycerol; Hepatic Encephalopathy; Huma

2014
Glutamine and hyperammonemic crises in patients with urea cycle disorders.
    Molecular genetics and metabolism, 2016, Volume: 117, Issue:1

    Topics: Adolescent; Adult; Ammonia; Biomarkers; Child; Child, Preschool; Fasting; Female; Glutamine; Glycero

2016
Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study.
    Orphanet journal of rare diseases, 2016, Mar-31, Volume: 11

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Glutamates; Humans; Hyperammonemia; Infant, N

2016
Ammonia impairs neutrophil phagocytic function in liver disease.
    Hepatology (Baltimore, Md.), 2008, Volume: 48, Issue:4

    Topics: Amino Acids; Ammonia; Animals; Cell Survival; Cells, Cultured; Disease Models, Animal; Double-Blind

2008
L-ornithine-L-aspartate infusion efficacy in hepatic encephalopathy.
    Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2008, Volume: 18, Issue:11

    Topics: Adult; Aged; Ammonia; Cognition; Dipeptides; Female; Health Status Indicators; Hepatic Encephalopath

2008
Hyperammonemia following intravenous valproate loading.
    Epilepsy research, 2009, Volume: 85, Issue:1

    Topics: Adult; Aged; Ammonia; Analysis of Variance; Anticonvulsants; Bilirubin; Dose-Response Relationship,

2009
The risk of asymptomatic hyperammonemia in children with idiopathic epilepsy treated with valproate: relationship to blood carnitine status.
    Epilepsy research, 2009, Volume: 86, Issue:1

    Topics: Adolescent; Ammonia; Anticonvulsants; Carnitine; Child; Epilepsy; Female; Humans; Hyperammonemia; Ma

2009
Overnight glucose infusion suppresses renal ammoniagenesis and reduces hyperammonaemia induced by a simulated bleed in cirrhotic patients.
    Alimentary pharmacology & therapeutics, 2012, Volume: 35, Issue:8

    Topics: Aged; Amino Acids; Ammonia; Cross-Over Studies; Fasting; Female; Gastrointestinal Hemorrhage; Glucag

2012
The dysfunction of ammonia in heart failure increases with an increase in the intensity of resistance exercise, even with the use of appropriate drug therapy.
    European journal of preventive cardiology, 2014, Volume: 21, Issue:2

    Topics: Adult; Ammonia; Biomarkers; Brazil; Cardiovascular Agents; Cross-Over Studies; Heart Failure; Humans

2014
Induced hyperammonemia alters neuropsychology, brain MR spectroscopy and magnetization transfer in cirrhosis.
    Hepatology (Baltimore, Md.), 2003, Volume: 37, Issue:4

    Topics: Amino Acids; Ammonia; Body Water; Brain; Female; Glutamine; Hemoglobins; Humans; Hyperammonemia; Mag

2003
Low myo-inositol and high glutamine levels in brain are associated with neuropsychological deterioration after induced hyperammonemia.
    American journal of physiology. Gastrointestinal and liver physiology, 2004, Volume: 287, Issue:3

    Topics: Adult; Aged; Amino Acids; Ammonia; Basal Ganglia; Brain Chemistry; Choline; Creatinine; Female; Glut

2004
Environmental heat stress, hyperammonemia and nucleotide metabolism during intermittent exercise.
    European journal of applied physiology, 2006, Volume: 97, Issue:1

    Topics: Adult; Ammonia; Environment, Controlled; Exercise; Heat Stress Disorders; Heat-Shock Response; Human

2006
Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency.
    European journal of pediatrics, 2006, Volume: 165, Issue:9

    Topics: Age of Onset; Amino Acids; Ammonia; Analysis of Variance; Arginine; Biomarkers; Blood Proteins; Body

2006
Role of ammonia and inflammation in minimal hepatic encephalopathy.
    Metabolic brain disease, 2007, Volume: 22, Issue:1

    Topics: Adult; Aged; Amino Acids; Ammonia; Biomarkers; C-Reactive Protein; Female; Hepatic Encephalopathy; H

2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.
    The New England journal of medicine, 2007, May-31, Volume: 356, Issue:22

    Topics: Adolescent; Adult; Age Factors; Age of Onset; Amino Acid Metabolism, Inborn Errors; Ammonia; Carbamo

2007

Other Studies

362 other studies available for ammonium hydroxide and Hyperammonemia

ArticleYear
Saul Brusilow: Understanding and treating diseases of ammonia toxicity.
    Analytical biochemistry, 2022, 01-01, Volume: 636

    Topics: Ammonia; Animals; Hepatic Encephalopathy; History, 20th Century; History, 21st Century; Humans; Hype

2022
Glutaminase 2 knockdown reduces hyperammonemia and associated lethality of urea cycle disorder mouse model.
    Journal of inherited metabolic disease, 2022, Volume: 45, Issue:3

    Topics: Ammonia; Animals; Disease Models, Animal; Glutaminase; Glutamine; Humans; Hyperammonemia; Liver; Mic

2022
Ammonia Clearance with Different Continuous Renal Replacement Therapy Techniques in Patients with Liver Failure.
    Blood purification, 2022, Volume: 51, Issue:10

    Topics: Acute Kidney Injury; Adult; Ammonia; Continuous Renal Replacement Therapy; Creatinine; Humans; Hyper

2022
Treatment of Hyperammonemia by Transplanting a Symbiotic Pair of Intestinal Microbes.
    Frontiers in cellular and infection microbiology, 2021, Volume: 11

    Topics: Ammonia; Animals; Hyperammonemia; Limosilactobacillus reuteri; Mice; Probiotics

2021
Interorgan amino acid interchange in propionic acidemia: the missing key to understanding its physiopathology.
    Amino acids, 2022, Volume: 54, Issue:5

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Glutamine; Humans; Hyperammonem

2022
Contribution of Uremia to
    Microbiology spectrum, 2022, 02-23, Volume: 10, Issue:1

    Topics: Ammonia; Animals; Humans; Hyperammonemia; Immunocompromised Host; Lung; Lung Transplantation; Mice;

2022
Prognostic significance of hyperammonemia in neuroendocrine neoplasm patients with liver metastases.
    Endocrine-related cancer, 2022, 03-24, Volume: 29, Issue:5

    Topics: Ammonia; Brain Diseases; Hepatic Insufficiency; Humans; Hyperammonemia; Liver Neoplasms; Neuroendocr

2022
Desflurane and remifentanil anesthesia in a child with citrin deficiency: A case report.
    Medicine, 2022, Mar-04, Volume: 101, Issue:9

    Topics: Ammonia; Anesthesia, General; Arginine; Blepharoplasty; Calcium-Binding Proteins; Child, Preschool;

2022
Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism.
    The Journal of pediatrics, 2022, Volume: 246

    Topics: Ammonia; Child; Humans; Hyperammonemia; Infant, Newborn; Metabolism, Inborn Errors; Renal Replacemen

2022
Association Between Continuous Kidney Replacement Therapy Clearance and Outcome in Pediatric Patients With Hyperammonemia Not Due to Inborn Error of Metabolism.
    Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies, 2022, 07-01, Volume: 23, Issue:7

    Topics: Adult; Ammonia; Brain Edema; Child; Continuous Renal Replacement Therapy; Humans; Hyperammonemia; Re

2022
Ammonia induces amyloidogenesis in astrocytes by promoting amyloid precursor protein translocation into the endoplasmic reticulum.
    The Journal of biological chemistry, 2022, Volume: 298, Issue:5

    Topics: Alzheimer Disease; Ammonia; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Amyloid Precursor

2022
Low cerebral energy metabolism in hepatic encephalopathy reflects low neuronal energy demand. Role of ammonia-induced increased GABAergic tone.
    Analytical biochemistry, 2022, 10-01, Volume: 654

    Topics: Ammonia; Brain; Energy Metabolism; Glutamine; Hepatic Encephalopathy; Humans; Hyperammonemia; Neuron

2022
Sex is associated with differences in oxidative stress and susceptibility to severe hepatic encephalopathy in bile-duct ligated rats.
    Journal of neurochemistry, 2022, Volume: 162, Issue:4

    Topics: Allopurinol; Ammonia; Animals; Bile; Disease Models, Animal; Female; Hepatic Encephalopathy; Hyperam

2022
Risk factors of elevated blood ammonia level in epilepsy patients treated with lamotrigine.
    Medicine, 2022, Jul-01, Volume: 101, Issue:26

    Topics: Ammonia; Anticonvulsants; Epilepsy; Humans; Hyperammonemia; Lamotrigine; Risk Factors; Seizures; Tri

2022
Establishment of hyperammonemia mode in yellow catfish and the mitigation of exogenous L-ornithine-L-aspartate.
    Developmental and comparative immunology, 2022, Volume: 135

    Topics: Ammonia; Animals; Catfishes; Dipeptides; Hyperammonemia; Sodium Chloride

2022
Moving towards a novel therapeutic strategy for hyperammonemia that targets glutamine metabolism.
    Journal of inherited metabolic disease, 2022, Volume: 45, Issue:6

    Topics: Ammonia; Animals; Fibroblasts; Glutamate Dehydrogenase; Glutamine; Hyperammonemia; Mice; Ornithine;

2022
Multiple Myeloma with Hyperammonemia Treated with Novel Agents: A Case Series of Three Patients.
    Internal medicine (Tokyo, Japan), 2023, Mar-01, Volume: 62, Issue:5

    Topics: Ammonia; Consciousness Disorders; Humans; Hyperammonemia; Multiple Myeloma

2023
Plasma ammonia levels predict hospitalisation with liver-related complications and mortality in clinically stable outpatients with cirrhosis.
    Journal of hepatology, 2022, Volume: 77, Issue:6

    Topics: Ammonia; Esophageal and Gastric Varices; Gastrointestinal Hemorrhage; Hepatic Encephalopathy; Hospit

2022
HYPERAMMONAEMIA AND COGNITIVE IMPAIRMENT IN EPILEPSY PATIENTS TREATED WITH VALPROIC ACID - PRELIMINARY STUDY.
    Wiadomosci lekarskie (Warsaw, Poland : 1960), 2022, Volume: 75, Issue:6

    Topics: Ammonia; Anticonvulsants; Cognitive Dysfunction; Dementia; Epilepsy; Female; Humans; Hyperammonemia;

2022
Multiple Asparaginase Infusions Cause Increasingly Severe Acute Hyperammonemia.
    Medical sciences (Basel, Switzerland), 2022, 08-12, Volume: 10, Issue:3

    Topics: Ammonia; Animals; Antineoplastic Agents; Asparaginase; Hyperammonemia; Precursor Cell Lymphoblastic

2022
O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis.
    Nature communications, 2022, 09-05, Volume: 13, Issue:1

    Topics: Acetylglucosamine; Ammonia; Animals; Biocatalysis; Carbamoyl-Phosphate Synthase (Ammonia); Disease M

2022
Clinical findings of patients with hyperammonemia affected by urea cycle disorders with hepatic encephalopathy.
    International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience, 2022, Volume: 82, Issue:8

    Topics: Ammonia; Hepatic Encephalopathy; Humans; Hyperammonemia; Ornithine Carbamoyltransferase Deficiency D

2022
A mouse model of hepatic encephalopathy: bile duct ligation induces brain ammonia overload, glial cell activation and neuroinflammation.
    Scientific reports, 2022, 10-20, Volume: 12, Issue:1

    Topics: Ammonia; Animals; Bile Acids and Salts; Bile Ducts; Brain; Choline; Disease Models, Animal; Glutamin

2022
Hypokalaemia - an active contributor to hepatic encephalopathy?
    Metabolic brain disease, 2023, Volume: 38, Issue:5

    Topics: Ammonia; Hepatic Encephalopathy; Humans; Hyperammonemia; Hypokalemia; Liver Cirrhosis; Potassium

2023
Hyperammonaemia disrupts daily rhythms reversibly by elevating glutamate in the central circadian pacemaker.
    Liver international : official journal of the International Association for the Study of the Liver, 2023, Volume: 43, Issue:3

    Topics: Ammonia; Animals; Circadian Rhythm; Excitatory Amino Acid Antagonists; Glutamic Acid; Hyperammonemia

2023
Late-Onset Ornithine Transcarbamylase Deficiency Complicated with Extremely High Serum Ammonia Level: Prompt Induction of Hemodialysis as the Key to Successful Treatment.
    The American journal of case reports, 2022, Nov-15, Volume: 23

    Topics: Adult; Ammonia; Child; Humans; Hyperammonemia; Infant; Male; Ornithine Carbamoyltransferase; Ornithi

2022
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
The trend of ammonia levels in patients with glufosinate ammonium poisoning with respect to neurotoxicity.
    Naunyn-Schmiedeberg's archives of pharmacology, 2023, Volume: 396, Issue:3

    Topics: Aminobutyrates; Ammonia; Herbicides; Humans; Hyperammonemia; Neurotoxicity Syndromes

2023
Valproic acid-induced hyperammonemia in neuropsychiatric disorders: a 2-year clinical survey.
    Psychopharmacology, 2023, Volume: 240, Issue:1

    Topics: Ammonia; Anticonvulsants; Epilepsy; Humans; Hyperammonemia; Risperidone; Valproic Acid

2023
Valproic acid-induced hyperammonemia in neuropsychiatric disorders: a 2-year clinical survey.
    Psychopharmacology, 2023, Volume: 240, Issue:1

    Topics: Ammonia; Anticonvulsants; Epilepsy; Humans; Hyperammonemia; Risperidone; Valproic Acid

2023
Valproic acid-induced hyperammonemia in neuropsychiatric disorders: a 2-year clinical survey.
    Psychopharmacology, 2023, Volume: 240, Issue:1

    Topics: Ammonia; Anticonvulsants; Epilepsy; Humans; Hyperammonemia; Risperidone; Valproic Acid

2023
Valproic acid-induced hyperammonemia in neuropsychiatric disorders: a 2-year clinical survey.
    Psychopharmacology, 2023, Volume: 240, Issue:1

    Topics: Ammonia; Anticonvulsants; Epilepsy; Humans; Hyperammonemia; Risperidone; Valproic Acid

2023
Hyperammonemia in a septic patient with Ureaplasma parvum arthritis: a case report.
    BMC infectious diseases, 2022, Dec-22, Volume: 22, Issue:1

    Topics: Aged; Ammonia; Anti-Bacterial Agents; Arthritis, Infectious; Humans; Hyperammonemia; Male; Ureaplasm

2022
UK National audit of the measurement of ammonia.
    Annals of clinical biochemistry, 2023, Volume: 60, Issue:2

    Topics: Ammonia; Humans; Hyperammonemia; Laboratories; Surveys and Questionnaires; United Kingdom

2023
Curcumin-resveratrol nano-formulation counteracting hyperammonemia in rats.
    Metabolic brain disease, 2023, Volume: 38, Issue:4

    Topics: Ammonia; Animals; Child; Curcumin; Dietary Proteins; Humans; Hyperammonemia; Male; Rats; Resveratrol

2023
Quantitative systems pharmacology Model to characterize valproic acid-induced hyperammonemia and the effect of L-carnitine supplementation.
    European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 2023, Apr-01, Volume: 183

    Topics: Ammonia; Anticonvulsants; Carnitine; Dietary Supplements; Drug Overdose; Drug-Related Side Effects a

2023
Acute onset of ornithine transcarbamylase deficiency after total anomalous pulmonary venous connection repair to a 2-day-old neonate.
    Cardiology in the young, 2023, Volume: 33, Issue:9

    Topics: Ammonia; Humans; Hyperammonemia; Infant, Newborn; Male; Ornithine Carbamoyltransferase Deficiency Di

2023
Hyperammonemia induces microglial NLRP3 inflammasome activation via mitochondrial oxidative stress in hepatic encephalopathy.
    Biomedical journal, 2023, Volume: 46, Issue:5

    Topics: Ammonia; Animals; Hepatic Encephalopathy; Hyperammonemia; Inflammasomes; Lipopolysaccharides; Mice;

2023
Methamphetamine-induced encephalopathy in the absence of hyperammonemia.
    BMC psychiatry, 2023, 04-20, Volume: 23, Issue:1

    Topics: Ammonia; Brain Diseases; Chemical and Drug Induced Liver Injury; Drug-Related Side Effects and Adver

2023
Feline hyperammonemia associated with functional cobalamin deficiency: A case report.
    The Canadian veterinary journal = La revue veterinaire canadienne, 2023, Volume: 64, Issue:5

    Topics: Amino Acids; Ammonia; Animals; Cat Diseases; Cats; Female; Hyperammonemia; Methylmalonic Acid; Urea;

2023
[Expert consensus on the diagnosis and treatment of neonatal hyperammonemia].
    Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2023, May-15, Volume: 25, Issue:5

    Topics: Ammonia; China; Consensus; Humans; Hyperammonemia; Infant, Newborn

2023
The pathogenesis of gut microbiota in hepatic encephalopathy by the gut-liver-brain axis.
    Bioscience reports, 2023, 06-28, Volume: 43, Issue:6

    Topics: Ammonia; Brain; Fibrosis; Gastrointestinal Microbiome; Hepatic Encephalopathy; Humans; Hyperammonemi

2023
Treatment and outcomes of symptomatic hyperammonemia following asparaginase therapy in children with acute lymphoblastic leukemia.
    Molecular genetics and metabolism, 2023, Volume: 139, Issue:3

    Topics: Ammonia; Antineoplastic Agents; Asparaginase; Child; Glutamine; Humans; Hyperammonemia; Phenylbutyra

2023
An orally deliverable ornithine-based self-assembling polymer nanomedicine ameliorates hyperammonemia in acetaminophen-induced acute liver injury.
    Acta biomaterialia, 2023, 09-15, Volume: 168

    Topics: Acetaminophen; Ammonia; Animals; Hyperammonemia; Liver; Mice; Nanomedicine; Ornithine; Polyethylene

2023
Relationship between longitudinal changes in neuropsychological outcome and disease biomarkers in urea cycle disorders.
    Pediatric research, 2023, Volume: 94, Issue:6

    Topics: Ammonia; Biomarkers; Glutamine; Humans; Hyperammonemia; Longitudinal Studies; Neuropsychological Tes

2023
Hyperammonemia induced gut microbiota dysbiosis and motor coordination disturbances in mice: new insight into gut‑brain axis involvement in hepatic encephalopathy.
    Acta neurobiologiae experimentalis, 2023, Volume: 83, Issue:2

    Topics: Ammonia; Animals; Brain-Gut Axis; Dysbiosis; Gastrointestinal Microbiome; Hepatic Encephalopathy; Hy

2023
The interaction of ammonia and manganese in abnormal metabolism of minimal hepatic encephalopathy: A comparison metabolomics study.
    PloS one, 2023, Volume: 18, Issue:8

    Topics: Alanine; Ammonia; Animals; Arginine; Brain; Citrulline; gamma-Aminobutyric Acid; Glutamic Acid; Glut

2023
L-Isoleucine reverses hyperammonemia-induced myotube mitochondrial dysfunction and post-mitotic senescence.
    The Journal of nutritional biochemistry, 2024, Volume: 123

    Topics: Amino Acids, Branched-Chain; Ammonia; Animals; Humans; Hyperammonemia; Induced Pluripotent Stem Cell

2024
Malnutrition-related hyperammonemic encephalopathy presenting with burst suppression: a case report.
    Journal of medical case reports, 2019, Aug-10, Volume: 13, Issue:1

    Topics: Aged, 80 and over; Ammonia; Brain Diseases; Coma; Electroencephalography; Humans; Hyperammonemia; Ma

2019
Poly(ornithine)-based self-assembling drug for recovery of hyperammonemia and damage in acute liver injury.
    Journal of controlled release : official journal of the Controlled Release Society, 2019, 09-28, Volume: 310

    Topics: Acetaminophen; Ammonia; Animals; Cattle; Cell Survival; Chemical and Drug Induced Liver Injury; Chon

2019
Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency.
    Proceedings of the National Academy of Sciences of the United States of America, 2019, 10-15, Volume: 116, Issue:42

    Topics: Ammonia; Animals; Arginase; Arginine; Codon; Disease Models, Animal; Glutamine; Hyperammonemia; Hype

2019
Predictive value of induced hyperammonaemia and neuropsychiatric profiling in relation to the occurrence of post-TIPS hepatic encephalopathy.
    Metabolic brain disease, 2019, Volume: 34, Issue:6

    Topics: Aged; Amino Acids; Ammonia; Female; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Cirrhosis;

2019
Adult onset type II citrullinemia--a great masquerader.
    QJM : monthly journal of the Association of Physicians, 2020, Jan-01, Volume: 113, Issue:1

    Topics: Ammonia; Brain Diseases; Citrullinemia; Humans; Hyperammonemia; Liver Transplantation; Magnetic Reso

2020
The Toll of Hyperammonemia on the Brain.
    Cellular and molecular gastroenterology and hepatology, 2019, Volume: 8, Issue:4

    Topics: Ammonia; Brain; Brain Edema; Humans; Hyperammonemia; Macrophages; T-Lymphocytes; Toll-Like Receptor

2019
Valproicacid-induced hyperammonemic encephalopathy in the emergency department.
    Emergencias : revista de la Sociedad Espanola de Medicina de Emergencias, 2019, Volume: 31, Issue:5

    Topics: Ammonia; Anticonvulsants; Brain Diseases, Metabolic; Female; Humans; Hyperammonemia; Middle Aged; Re

2019
Comparative accuracy and precision of two commercial laboratory analyzers for the quantification of ammonia in cerebrospinal fluid.
    Veterinary clinical pathology, 2020, Volume: 49, Issue:1

    Topics: Ammonia; Animals; Blood Chemical Analysis; Hepatic Encephalopathy; Horse Diseases; Horses; Hyperammo

2020
An Investigation of PS-b-PEO Polymersomes for the Oral Treatment and Diagnosis of Hyperammonemia.
    Small (Weinheim an der Bergstrasse, Germany), 2019, Volume: 15, Issue:50

    Topics: Administration, Oral; Ammonia; Animals; Bile Ducts; Body Fluids; Hydrogels; Hyperammonemia; Ligation

2019
Characteristics and outcomes of critically ill patients with severe hyperammonemia.
    Journal of critical care, 2020, Volume: 56

    Topics: Acute-On-Chronic Liver Failure; Adult; Ammonia; Brain Edema; Critical Illness; Female; Humans; Hyper

2020
Correction and Control of Hyperammonemia in Acute Liver Failure: The Impact of Continuous Renal Replacement Timing, Intensity, and Duration.
    Critical care medicine, 2020, Volume: 48, Issue:2

    Topics: Adult; Age Factors; Ammonia; APACHE; Body Weight; Continuous Renal Replacement Therapy; Female; Huma

2020
Ammonia Predicts Hepatic Involvement and Pulmonary Hypertension in Patients With Hereditary Hemorrhagic Telangiectasia.
    Clinical and translational gastroenterology, 2020, Volume: 11, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Alanine Transaminase; Alkaline Phosphatase; Ammonia; Arteriovenous M

2020
5-Fluorouracil-induced hyperammonaemic encephalopathy: A French national survey.
    European journal of cancer (Oxford, England : 1990), 2020, Volume: 129

    Topics: Aged; Ammonia; Antimetabolites, Antineoplastic; Brain Diseases; Citric Acid Cycle; Dose-Response Rel

2020
Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution.
    Journal of pediatric endocrinology & metabolism : JPEM, 2020, May-26, Volume: 33, Issue:5

    Topics: Ammonia; Blood Glucose; Child; Child, Preschool; Diazoxide; Female; Glutamate Dehydrogenase; Humans;

2020
Perioperative management of children with urea cycle disorders.
    Paediatric anaesthesia, 2020, Volume: 30, Issue:7

    Topics: Ammonia; Anesthesia, General; Child; Humans; Hyperammonemia; Prognosis; Urea Cycle Disorders, Inborn

2020
Proposed Plasma Ammonia Reference Intervals in a Reference Group of Hospitalized Term and Preterm Neonates.
    The journal of applied laboratory medicine, 2020, 03-01, Volume: 5, Issue:2

    Topics: Ammonia; Biomarkers; Case-Control Studies; Female; Gestational Age; Humans; Hyperammonemia; Hyperbil

2020
Point-of-Care Analysis of Blood Ammonia with a Gas-Phase Sensor.
    ACS sensors, 2020, 08-28, Volume: 5, Issue:8

    Topics: Adult; Ammonia; Child; Humans; Hyperammonemia; Point-of-Care Systems

2020
Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency.
    Clinical biochemistry, 2020, Volume: 84

    Topics: Adolescent; Adult; Ammonia; Arginine; Child; Child, Preschool; China; Creatine; Female; Humans; Hype

2020
A retrospective study of adult patients with noncirrhotic hyperammonemia.
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:6

    Topics: Adult; Age of Onset; Aged; Ammonia; Female; Humans; Hyperammonemia; Male; Middle Aged; Retrospective

2020
Hyperammonemic Encephalopathy Exacerbated by Parenteral Nutrition in Fibrolamellar Hepatocellular Carcinoma.
    The American journal of medicine, 2020, Volume: 133, Issue:12

    Topics: Adult; Ammonia; Brain Diseases; Carcinoma, Hepatocellular; Female; Gastrointestinal Agents; Humans;

2020
Preclinical evaluation of liposome-supported peritoneal dialysis for the treatment of hyperammonemic crises.
    Journal of controlled release : official journal of the Controlled Release Society, 2020, 12-10, Volume: 328

    Topics: Ammonia; Animals; Ascitic Fluid; Hyperammonemia; Liposomes; Peritoneal Dialysis; Rats; Swine; Swine,

2020
Ammonia inhibits energy metabolism in astrocytes in a rapid and glutamate dehydrogenase 2-dependent manner.
    Disease models & mechanisms, 2020, 11-04, Volume: 13, Issue:10

    Topics: Amination; Amino Acids; Ammonia; Astrocytes; Cell Line, Tumor; Cell Respiration; Citric Acid Cycle;

2020
Hyperammonemic Encephalopathy Associated with Perampanel: Case Report and Discussion.
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2021, Volume: 48, Issue:3

    Topics: Ammonia; Brain Diseases; Humans; Hyperammonemia; Neurotoxicity Syndromes; Nitriles; Pyridones

2021
Successful management of hyperammonemia with hemodialysis on day 2 during 5-fluorouracil treatment in a patient with gastric cancer: a case report with 5-fluorouracil metabolite analyses.
    Cancer chemotherapy and pharmacology, 2020, Volume: 86, Issue:5

    Topics: Aged, 80 and over; Ammonia; Antimetabolites, Antineoplastic; beta-Alanine; Drug Administration Sched

2020
Transient hyperammonaemia following epileptic seizures in cats.
    Journal of feline medicine and surgery, 2021, Volume: 23, Issue:6

    Topics: Ammonia; Animals; Cat Diseases; Cats; Epilepsy; Hyperammonemia; Retrospective Studies; Seizures

2021
Changes in the Body Composition and Nutritional Status after Long-term Rifaximin Therapy for Hyperammonemia in Japanese Patients with Hepatic Encephalopathy.
    Internal medicine (Tokyo, Japan), 2020, Volume: 59, Issue:20

    Topics: Aged; Ammonia; Bilirubin; Body Composition; Carcinoma, Hepatocellular; Female; Hepatic Encephalopath

2020
Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine.
    Epilepsia, 2020, Volume: 61, Issue:11

    Topics: Adult; Ammonia; Anticonvulsants; Carnitine; Cohort Studies; Dioxolanes; Epilepsies, Myoclonic; Femal

2020
Glucagon Receptor Inhibition Reduces Hyperammonemia and Lethality in Male Mice with Urea Cycle Disorder.
    Endocrinology, 2021, 01-01, Volume: 162, Issue:1

    Topics: Amino Acids; Ammonia; Animals; Antibodies, Monoclonal; Body Weight; Gene Expression Regulation; Glut

2021
Nootkatone improves anxiety- and depression-like behavior by targeting hyperammonemia-induced oxidative stress in D-galactosamine model of liver injury.
    Environmental toxicology, 2021, Volume: 36, Issue:4

    Topics: Ammonia; Animals; Antidepressive Agents; Antioxidants; Anxiety; Behavior, Animal; Brain; Cell Surviv

2021
Prognosis of Patients with Sepsis and Non-Hepatic Hyperammonemia: A Cohort Study.
    Medical science monitor : international medical journal of experimental and clinical research, 2020, Dec-29, Volume: 26

    Topics: Aged; Ammonia; APACHE; Area Under Curve; Brain Diseases; Cohort Studies; Critical Illness; Escherich

2020
Bile-duct ligation renders the brain susceptible to hypotension-induced neuronal degeneration: Implications of ammonia.
    Journal of neurochemistry, 2021, Volume: 157, Issue:3

    Topics: Ammonia; Animals; Antigens, Nuclear; Anxiety; Apoptosis; Behavior, Animal; Bile Ducts; Caspase 3; Ce

2021
Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders.
    Molecular genetics and metabolism, 2021, Volume: 132, Issue:1

    Topics: Age of Onset; Ammonia; Child, Preschool; Female; Glycerol; Humans; Hyperammonemia; Infant; Infant, N

2021
Potassium deficiency decreases the capacity for urea synthesis and markedly increases ammonia in rats.
    American journal of physiology. Gastrointestinal and liver physiology, 2021, 04-01, Volume: 320, Issue:4

    Topics: Ammonia; Animals; Disease Models, Animal; Female; Gene Expression Regulation, Enzymologic; Hyperammo

2021
Analysis of clinical prognosis in patients with non-hepatic hyperammonemia.
    Medicine, 2021, Jan-22, Volume: 100, Issue:3

    Topics: Age Factors; Aged; Ammonia; Critical Illness; Female; Humans; Hyperammonemia; Male; Middle Aged; Nom

2021
Ammonia level as a proxy of asparaginase inactivation in children: A strategy for classification of infusion reactions.
    Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners, 2022, Volume: 28, Issue:3

    Topics: Ammonia; Antineoplastic Agents; Asparaginase; Child; Drug Hypersensitivity; Humans; Hyperammonemia;

2022
Oral sodium phenylbutyrate for hyperammonemia associated with congenital portosystemic shunt: a case report.
    Journal of pediatric endocrinology & metabolism : JPEM, 2021, Mar-26, Volume: 34, Issue:3

    Topics: Administration, Oral; Amino Acids, Branched-Chain; Ammonia; Humans; Hyperammonemia; Infant; Male; Ph

2021
Long-term outcome of urea cycle disorders: Report from a nationwide study in Japan.
    Journal of inherited metabolic disease, 2021, Volume: 44, Issue:4

    Topics: Adolescent; Adult; Ammonia; Child; Child, Preschool; Female; Humans; Hyperammonemia; Japan; Liver Tr

2021
Hyperammonemia in Patients With Status Epilepticus Treated With or Without Valproic Acid.
    The neurologist, 2021, May-05, Volume: 26, Issue:3

    Topics: Adult; Ammonia; Anticonvulsants; Humans; Hyperammonemia; Status Epilepticus; Valproic Acid

2021
Hyperammonemia in acetaminophen toxicity.
    Clinical toxicology (Philadelphia, Pa.), 2022, Volume: 60, Issue:1

    Topics: Acetaminophen; Ammonia; Animals; Hepatic Encephalopathy; Humans; Hyperammonemia; Retrospective Studi

2022
Use of Lactulose to Treat Hyperammonemia in ICU Patients Without Chronic Liver Disease or Significant Hepatocellular Injury.
    Journal of intensive care medicine, 2022, Volume: 37, Issue:5

    Topics: Adult; Ammonia; Carcinoma, Hepatocellular; Humans; Hyperammonemia; Intensive Care Units; Lactulose;

2022
Surgical Debulking for Refractory Hyperammonemic Encephalopathy in Fibrolamellar Hepatocellular Carcinoma.
    Hepatology (Baltimore, Md.), 2021, Volume: 74, Issue:5

    Topics: Adult; Ammonia; Carcinoma, Hepatocellular; Cytoreduction Surgical Procedures; Hepatic Encephalopathy

2021
Capecitabine-induced hyperammonemic encephalopathy.
    Revista espanola de enfermedades digestivas, 2022, Volume: 114, Issue:1

    Topics: Adenocarcinoma; Aged; Ammonia; Brain Diseases; Capecitabine; Humans; Hyperammonemia; Male; Pancreati

2022
Koi sleepy disease as a pathophysiological and immunological consequence of a branchial infection of common carp with carp edema virus.
    Virulence, 2021, Volume: 12, Issue:1

    Topics: Ammonia; Animals; Carps; Edema; Fish Diseases; Hyperammonemia; Hyponatremia; Poxviridae; Poxviridae

2021
Treatment of hyperammonemia using in-line renal replacement and hyperosmolar therapies within an extracorporeal membrane oxygenation circuit.
    Perfusion, 2023, Volume: 38, Issue:1

    Topics: Ammonia; Brain Edema; Extracorporeal Membrane Oxygenation; Hemofiltration; Humans; Hyperammonemia; R

2023
Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome.
    Internal medicine (Tokyo, Japan), 2022, Feb-15, Volume: 61, Issue:4

    Topics: Ammonia; Child; Humans; Hyperammonemia; Leukoencephalopathies; Male; Middle Aged; Ornithine; Urea Cy

2022
Gait instability in valproate-treated patients: Call to measure ammonia levels.
    Acta neurologica Scandinavica, 2017, Volume: 136, Issue:5

    Topics: Accidental Falls; Adult; Ammonia; Anticonvulsants; Disease Progression; Epilepsy, Frontal Lobe; Fema

2017
Hyperammonemia compromises glutamate metabolism and reduces BDNF in the rat hippocampus.
    Neurotoxicology, 2017, Volume: 62

    Topics: Ammonia; Animals; Animals, Newborn; Astrocytes; Brain-Derived Neurotrophic Factor; Cells, Cultured;

2017
TNFα induced up-regulation of Na
    Scientific reports, 2017, 08-11, Volume: 7, Issue:1

    Topics: Ammonia; Animals; Brain; Hyperammonemia; Liver; Mice; Mice, Knockout; Receptors, Tumor Necrosis Fact

2017
Refractory hepatic encephalopathy in a patient with hypothyroidism: Another element in ammonia metabolism.
    World journal of gastroenterology, 2017, Jul-28, Volume: 23, Issue:28

    Topics: Adrenergic beta-Antagonists; Alcoholism; Ammonia; Antithyroid Agents; Brain; Carbimazole; Diagnosis,

2017
Lactulose decreases neuronal activation and attenuates motor behavioral deficits in hyperammonemic rats.
    Metabolic brain disease, 2017, Volume: 32, Issue:6

    Topics: Ammonia; Animals; Aquaporin 4; Aspartate Aminotransferases; Behavior, Animal; Bilirubin; Creatinine;

2017
Safety, tolerability, and pharmacokinetics of l-ornithine phenylacetate in patients with acute liver injury/failure and hyperammonemia.
    Hepatology (Baltimore, Md.), 2018, Volume: 67, Issue:3

    Topics: Acetates; Adolescent; Adult; Aged; Ammonia; Female; Glutamine; Humans; Hyperammonemia; Kidney Functi

2018
Metabolically based liver damage pathophysiology in patients with urea cycle disorders - A new hypothesis.
    World journal of gastroenterology, 2017, Nov-28, Volume: 23, Issue:44

    Topics: Ammonia; Central Nervous System; Citrullinemia; Enterobacter; Fatal Outcome; Hepatocytes; Humans; Hy

2017
Treating hepatic encephalopathy in cirrhotic patients admitted to ICU with sodium phenylbutyrate: a preliminary study.
    Fundamental & clinical pharmacology, 2018, Volume: 32, Issue:2

    Topics: Aged; Ammonia; Biomarkers; Case-Control Studies; Female; Hepatic Encephalopathy; Hospital Mortality;

2018
Enhancement of hepatic autophagy increases ureagenesis and protects against hyperammonemia.
    Proceedings of the National Academy of Sciences of the United States of America, 2018, 01-09, Volume: 115, Issue:2

    Topics: Ammonia; Animals; Autophagy; Humans; Hyperammonemia; Liver; Male; Mechanistic Target of Rapamycin Co

2018
Efficacy of peritoneal dialysis in neonates presenting with hyperammonaemia due to urea cycle defects and organic acidaemia.
    Nephrology (Carlton, Vic.), 2019, Volume: 24, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Humans; Hyperammonemia; Infant, Newborn; Male

2019
Prenatal treatment of ornithine transcarbamylase deficiency.
    Molecular genetics and metabolism, 2018, Volume: 123, Issue:3

    Topics: Ammonia; Drug Combinations; Female; Glutamine; Humans; Hyperammonemia; Infant, Newborn; Male; Mutati

2018
Multi-Targeted Tyrosine Kinase Inhibitor-Induced Hyperammonemic Encephalopathy: a Report of Two Cases Using Pazopanib, Sunitinib, and Regorafenib.
    Journal of gastrointestinal cancer, 2019, Volume: 50, Issue:3

    Topics: Aged; Ammonia; Anti-Bacterial Agents; Anticonvulsants; Antineoplastic Combined Chemotherapy Protocol

2019
Rapid resolution of hyperammonemia in neonates using extracorporeal membrane oxygenation as a platform to drive hemodialysis.
    Journal of perinatology : official journal of the California Perinatal Association, 2018, Volume: 38, Issue:6

    Topics: Ammonia; Cohort Studies; Extracorporeal Membrane Oxygenation; Female; Hospitals, Pediatric; Humans;

2018
Plasma ammonia concentration after L-asparaginase therapy in 27 dogs with high-grade lymphoma or leukemia.
    Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001), 2018, Volume: 28, Issue:2

    Topics: Ammonia; Animals; Antineoplastic Agents; Asparaginase; Case-Control Studies; Dogs; Female; Humans; H

2018
Liposome-supported peritoneal dialysis in the treatment of severe hyperammonemia: An investigation on potential interactions.
    Journal of controlled release : official journal of the Controlled Release Society, 2018, 05-28, Volume: 278

    Topics: Acute-On-Chronic Liver Failure; Adrenergic beta-Antagonists; Ammonia; Animals; Anti-Bacterial Agents

2018
Medium-chain triglycerides supplement therapy with a low-carbohydrate formula can supply energy and enhance ammonia detoxification in the hepatocytes of patients with adult-onset type II citrullinemia.
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:5

    Topics: Aged; Ammonia; Argininosuccinate Synthase; Carbohydrates; Citrullinemia; Dietary Supplements; Fatty

2018
Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy.
    Basic & clinical pharmacology & toxicology, 2018, Volume: 123, Issue:5

    Topics: Age Factors; Ammonia; Anticonvulsants; Aspartate Aminotransferases; Chemical and Drug Induced Liver

2018
Conditional disruption of hepatic carbamoyl phosphate synthetase 1 in mice results in hyperammonemia without orotic aciduria and can be corrected by liver-directed gene therapy.
    Molecular genetics and metabolism, 2018, Volume: 124, Issue:4

    Topics: Ammonia; Animals; Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Deficiency

2018
Ammonia role in glial dysfunction in methylmalonic acidemia.
    Toxicology letters, 2018, Oct-01, Volume: 295

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Ammonium Chloride; Animals; Behavior, Animal; Brain;

2018
An infant with hypercalcemia and hyperammonia: inborn error of metabolism or not? Answers.
    Pediatric nephrology (Berlin, Germany), 2019, Volume: 34, Issue:2

    Topics: Acidosis, Renal Tubular; Administration, Oral; Ammonia; Diagnosis, Differential; Exome Sequencing; F

2019
Targeting autophagy for therapy of hyperammonemia.
    Autophagy, 2018, Volume: 14, Issue:7

    Topics: Ammonia; Autophagy; Humans; Hyperammonemia; Liver; Urea

2018
Effects of branched-chain amino acids on muscles under hyperammonemic conditions.
    Journal of physiology and biochemistry, 2018, Volume: 74, Issue:4

    Topics: Amino Acids, Branched-Chain; Ammonia; Animals; Carbon Radioisotopes; Citric Acid Cycle; Glutamine; H

2018
Keto analogues and amino acid supplementation and its effects on ammonaemia during extenuating endurance exercise in ketogenic diet-fed rats.
    The British journal of nutrition, 2018, Volume: 120, Issue:7

    Topics: Amino Acids; Ammonia; Animals; Diet; Diet, Ketogenic; Dietary Supplements; Hyperammonemia; Keto Acid

2018
Effect of dietary alanyl-glutamine dipeptide against chronic ammonia stress induced hyperammonemia in the juvenile yellow catfish (Pelteobagrus fulvidraco).
    Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 2018, Volume: 213

    Topics: Ammonia; Animal Nutritional Physiological Phenomena; Animals; Antioxidants; Aquaculture; Catfishes;

2018
The metabolic and molecular mechanisms of hyperammonaemia- and hyperethanolaemia-induced protein catabolism in skeletal muscle cells.
    Journal of cellular physiology, 2018, Volume: 233, Issue:12

    Topics: Ammonia; Animals; Cell Line; Cell Survival; DNA; Ethanol; Hyperammonemia; Mice; Muscle Cells; Muscle

2018
The utility of EEG monitoring in neonates with hyperammonemia due to inborn errors of metabolism.
    Molecular genetics and metabolism, 2018, Volume: 125, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria

2018
Progressive resistance training prevents loss of muscle mass and strength in bile duct-ligated rats.
    Liver international : official journal of the International Association for the Study of the Liver, 2019, Volume: 39, Issue:4

    Topics: Ammonia; Animals; Bile Ducts; Body Composition; Disease Models, Animal; Hepatic Encephalopathy; Hype

2019
Acute Presentation and Management of the Encephalopathic Child With an Undiagnosed Inborn Error of Metabolism.
    The Journal of emergency medicine, 2019, Volume: 56, Issue:1

    Topics: Ammonia; Brain Diseases; Child; Delayed Diagnosis; Delirium; Emergency Service, Hospital; Humans; Hy

2019
Acute hyperammonemia in children under deferasirox treatment: cutting the Gordian knot.
    Clinical toxicology (Philadelphia, Pa.), 2019, Volume: 57, Issue:5

    Topics: Acute Disease; Adolescent; Age Factors; Ammonia; Biomarkers; Child, Preschool; Deferasirox; Female;

2019
Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency.
    Internal medicine (Tokyo, Japan), 2019, Apr-01, Volume: 58, Issue:7

    Topics: Adolescent; Amino Acids; Ammonia; Arginine; Coma; Female; Humans; Hyperammonemia; Male; Middle Aged;

2019
Hyperammonaemia in Neonates and Young Children: Potential Metabolic Causes, Diagnostic Approaches and Clinical Consequences
    Irish medical journal, 2019, 01-15, Volume: 112, Issue:1

    Topics: Ammonia; Arginine; Biomarkers; Brain Diseases, Metabolic, Inborn; Carnitine; Critical Illness; Diet,

2019
Hepatic glutamine synthetase augmentation enhances ammonia detoxification.
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:6

    Topics: Ammonia; Animals; Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Deficiency

2019
Influence of implementing a protocol for an intravenously administered ammonia scavenger on the management of acute hyperammonemia in a pediatric intensive care unit.
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:1

    Topics: Acute Disease; Ammonia; Canada; Child; Child, Preschool; Female; Humans; Hyperammonemia; Infant; Inf

2019
Demethylation of the hypoxia induction factor 1 binding site of GPX3 at excess blood ammonia in propionic acidemia.
    Clinical biochemistry, 2019, Volume: 66

    Topics: Ammonia; Binding Sites; Demethylation; DNA Methylation; Glutathione Peroxidase; Humans; Hyperammonem

2019
Citrullinemia Type 1: Behavioral Improvement with Late Liver Transplantation.
    Indian journal of pediatrics, 2019, Volume: 86, Issue:7

    Topics: Amino Acids; Ammonia; Argininosuccinate Synthase; Child; Citrullinemia; Exons; Heterozygote; Humans;

2019
Taurine transporter (TauT) deficiency impairs ammonia detoxification in mouse liver.
    Proceedings of the National Academy of Sciences of the United States of America, 2019, 03-26, Volume: 116, Issue:13

    Topics: Ammonia; Animals; Deficiency Diseases; Disease Models, Animal; GABA Plasma Membrane Transport Protei

2019
Pivotal role of inter-organ aspartate metabolism for treatment of mitochondrial aspartate-glutamate carrier 2 (citrin) deficiency, based on the mouse model.
    Scientific reports, 2019, 03-12, Volume: 9, Issue:1

    Topics: Amino Acids; Ammonia; Ammonium Chloride; Animals; Aspartic Acid; Citrulline; Citrullinemia; Disease

2019
Ethanol sensitizes skeletal muscle to ammonia-induced molecular perturbations.
    The Journal of biological chemistry, 2019, 05-03, Volume: 294, Issue:18

    Topics: Ammonia; Animals; Cell Line; Ethanol; Hepatocytes; Humans; Hyperammonemia; Membrane Transport Protei

2019
Hyperammonemic encephalopathy in a pediatric patient with Salmonella enteritis and after Roux-en-Y surgery.
    The Kaohsiung journal of medical sciences, 2019, Volume: 35, Issue:3

    Topics: Ammonia; Anastomosis, Roux-en-Y; Brain Diseases; Child; Enteritis; Humans; Hyperammonemia; Infant; S

2019
Possibilities of therapeutic correction of hyperammonemia and minimal hepatic encephalopathy in patients with chronic hepatitis C at the pre-cirrhotic stage.
    Terapevticheskii arkhiv, 2019, Mar-18, Volume: 91, Issue:2

    Topics: Adult; Ammonia; Case-Control Studies; Dipeptides; Hepatic Encephalopathy; Hepatitis C, Chronic; Huma

2019
Differential role of interleukin-1β in neuroinflammation-induced impairment of spatial and nonspatial memory in hyperammonemic rats.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019, Volume: 33, Issue:9

    Topics: Ammonia; Animal Feed; Animals; Cerebral Cortex; Gene Expression Regulation; Hippocampus; Hyperammone

2019
Acute hyperammonemic encephalopathy due to a portosystemic shunt in a non-cirrhotic adult patient.
    Journal of critical care, 2019, Volume: 53

    Topics: Aged; Ammonia; Diagnosis, Differential; Embolization, Therapeutic; Hepatic Encephalopathy; Humans; H

2019
Ammonia induces calpain-dependent cleavage of CRMP-2 during neurite degeneration in primary cultured neurons.
    Aging, 2019, 07-06, Volume: 11, Issue:13

    Topics: Ammonia; Animals; Calcium; Calpain; Hyperammonemia; Intercellular Signaling Peptides and Proteins; N

2019
Extracorporeal Liver Support for the Treatment of Hyperammonemia After Lung Transplantation.
    Transplantation, 2020, Volume: 104, Issue:3

    Topics: Ammonia; Brain Diseases, Metabolic; Female; Hemofiltration; Humans; Hyperammonemia; Lung Transplanta

2020
Simultaneous double hemodialysis for the control of refractory hyperammonemia.
    The International journal of artificial organs, 2013, Volume: 36, Issue:2

    Topics: Aged; Ammonia; Antineoplastic Combined Chemotherapy Protocols; Biomarkers; Dexamethasone; Encephalit

2013
Hepatic encephalopathy: an enigma from patient to enzyme and back.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Ammonia; Animals; Hepatic Encephalopathy; Humans; Hyperammonemia; Nitrogen

2013
Use of continuous hemodiafiltration for the treatment of a neonate with hyperammonemia secondary to argininosuccinate lyase (ASAL) deficiency.
    Indian journal of pediatrics, 2013, Volume: 80, Issue:9

    Topics: Ammonia; Arginine; Argininosuccinate Lyase; Argininosuccinic Aciduria; Breast Feeding; Combined Moda

2013
Brain alanine formation as an ammonia-scavenging pathway during hyperammonemia: effects of glutamine synthetase inhibition in rats and astrocyte-neuron co-cultures.
    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2013, Volume: 33, Issue:8

    Topics: Alanine; Amino Acids; Ammonia; Animals; Astrocytes; Brain Chemistry; Chromatography, High Pressure L

2013
Moderate grade hyperammonemia activates lactate dehydrogenase-4 and 6-phosphofructo-2-kinase to support increased lactate turnover in the brain slices.
    Molecular and cellular biochemistry, 2013, Volume: 381, Issue:1-2

    Topics: Ammonia; Animals; Brain; Enzyme Activation; Female; Hyperammonemia; Isoenzymes; L-Lactate Dehydrogen

2013
Reducing the risk of hyperammonemia from transfusion of stored red blood cells.
    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis, 2013, Volume: 49, Issue:3

    Topics: Ammonia; Blood Preservation; Erythrocyte Transfusion; Erythrocytes; Humans; Hyperammonemia

2013
Ammonia clearance with haemofiltration in adults with liver disease.
    Liver international : official journal of the International Association for the Study of the Liver, 2014, Volume: 34, Issue:1

    Topics: Adult; Ammonia; Female; Hemodiafiltration; Humans; Hyperammonemia; Liver Failure; Male; Middle Aged;

2014
Use of carglumic acid in the treatment of hyperammonaemia during metabolic decompensation of patients with propionic acidaemia.
    Molecular genetics and metabolism, 2013, Volume: 109, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Carnitine; Child, Preschool; Female; Glutamates; Huma

2013
Hyperammonemia in idiopathic epileptic seizure.
    The American journal of emergency medicine, 2013, Volume: 31, Issue:10

    Topics: Acid-Base Imbalance; Adult; Ammonia; Emergency Service, Hospital; Epilepsy; Female; Humans; Hydrogen

2013
Altered mental status in a teenager.
    Clinical chemistry, 2013, Volume: 59, Issue:10

    Topics: Adolescent; Ammonia; Child; Confusion; Diagnosis, Differential; Humans; Hyperammonemia; Male; Ornith

2013
Drug-induced removal of nitrogen derivatives in urine: a new concept whose time has come.
    Hepatology (Baltimore, Md.), 2014, Volume: 59, Issue:3

    Topics: Ammonia; Female; Glycerol; Hepatic Encephalopathy; Humans; Hyperammonemia; Male; Phenylbutyrates

2014
Arterial ammonia levels in cirrhosis are determined by systemic and hepatic hemodynamics, and by organ function: a quantitative modelling study.
    Liver international : official journal of the International Association for the Study of the Liver, 2014, Volume: 34, Issue:6

    Topics: Ammonia; Biomarkers; Computer Simulation; Hemodynamics; Humans; Hyperammonemia; Liver Circulation; L

2014
Continuous hemodialysis therapy for an extremely low-birthweight infant with hyperammonemia.
    Pediatrics international : official journal of the Japan Pediatric Society, 2013, Volume: 55, Issue:5

    Topics: Ammonia; Fatal Outcome; Follow-Up Studies; Humans; Hyperammonemia; Infant, Extremely Low Birth Weigh

2013
[Clinical effect of stem cell transplantation via hepatic artery in the treatment of type II hyperammonemia: a report on 6 cases].
    Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2013, Volume: 15, Issue:11

    Topics: AC133 Antigen; Ammonia; Antigens, CD; Arginine; Citrulline; Female; Glycoproteins; Hepatic Artery; H

2013
Changes in CNS cells in hyperammonemic portal hypertensive rats.
    Journal of neurochemistry, 2014, Volume: 128, Issue:3

    Topics: Alzheimer Disease; Ammonia; Animals; Antigens, Nuclear; Arterial Pressure; Astrocytes; ATP Binding C

2014
[Partial deficiency of ornithine transcarbamylase. A case report].
    Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria, 2014, Jan-01, Volume: 38, Issue:1

    Topics: Aged; Ammonia; Female; Humans; Hyperammonemia; Ornithine Carbamoyltransferase Deficiency Disease

2014
Disruption of redox homeostasis and brain damage caused in vivo by methylmalonic acid and ammonia in cerebral cortex and striatum of developing rats.
    Free radical research, 2014, Volume: 48, Issue:6

    Topics: Ammonia; Animals; Antioxidants; Catalase; Cerebral Cortex; Corpus Striatum; Fluoresceins; Glutathion

2014
Ammonia levels and the severity of hepatic encephalopathy.
    Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2014, Volume: 24, Issue:3

    Topics: Adult; Ammonia; Female; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver Cirrhosis; Male; Middl

2014
[Reversible hepatic myelopathy: a case report].
    Rinsho shinkeigaku = Clinical neurology, 2014, Volume: 54, Issue:3

    Topics: Administration, Oral; Adult; Ammonia; Biomarkers; Evoked Potentials, Somatosensory; Female; Gastroin

2014
Pannexin1 as a novel cerebral target in pathogenesis of hepatic encephalopathy.
    Metabolic brain disease, 2014, Volume: 29, Issue:4

    Topics: Ammonia; Brain; Connexins; Energy Metabolism; Glutamic Acid; Heart Arrest; Hepatic Encephalopathy; H

2014
Hyperammonemia associated with valproic acid concentrations.
    BioMed research international, 2014, Volume: 2014

    Topics: Adolescent; Adult; Ammonia; Bipolar Disorder; Carnitine; Child; Dietary Supplements; Dose-Response R

2014
Ammonia-induced energy disorders interfere with bilirubin metabolism in hepatocytes.
    Archives of biochemistry and biophysics, 2014, Volume: 555-556

    Topics: Ammonia; Ammonium Chloride; Apoptosis; Bilirubin; Cell Survival; Citric Acid Cycle; Energy Metabolis

2014
4217C>A polymorphism in carbamoyl-phosphate synthase 1 gene may not associate with hyperammonemia development during valproic acid-based therapy.
    Epilepsy research, 2014, Volume: 108, Issue:6

    Topics: Alleles; Amino-Acid N-Acetyltransferase; Ammonia; Anticonvulsants; Asian People; Biomarkers, Pharmac

2014
Differential up-regulation of ammonia detoxifying enzymes in cerebral cortex, cerebellum, hippocampus, striatum and liver in hyperammonemia.
    CNS & neurological disorders drug targets, 2014, Volume: 13, Issue:6

    Topics: Alanine Transaminase; Ammonia; AMP Deaminase; Animals; Aspartate Aminotransferases; Brain; Disease M

2014
Dysbalance of astrocyte calcium under hyperammonemic conditions.
    PloS one, 2014, Volume: 9, Issue:8

    Topics: Ammonia; Animals; Astrocytes; Calcium; Cerebellum; Glutamate-Ammonia Ligase; Hepatic Encephalopathy;

2014
Elevated ammonia concentrations: potential for pre-analytical and analytical contributing factors.
    Clinical biochemistry, 2014, Volume: 47, Issue:16-17

    Topics: Ammonia; Humans; Hyperammonemia; Specimen Handling

2014
Risk factors of hyperammonemia in patients with epilepsy under valproic acid therapy.
    Medicine, 2014, Volume: 93, Issue:11

    Topics: Adolescent; Adult; Age Factors; Aged; Aged, 80 and over; Ammonia; Anticonvulsants; Antipsychotic Age

2014
L-Ornithine phenylacetate reduces ammonia in pigs with acute liver failure through phenylacetylglycine formation: a novel ammonia-lowering pathway.
    American journal of physiology. Gastrointestinal and liver physiology, 2014, Nov-15, Volume: 307, Issue:10

    Topics: Ammonia; Animals; Biomarkers; Brain; Disease Models, Animal; Female; Glycine; Hyperammonemia; Kidney

2014
Delivery of glutamine synthetase gene by baculovirus vectors: a proof of concept for the treatment of acute hyperammonemia.
    Gene therapy, 2015, Volume: 22, Issue:1

    Topics: Ammonia; Animals; Baculoviridae; Genetic Therapy; Genetic Vectors; Glutamate-Ammonia Ligase; Hyperam

2015
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy.
    Gene therapy, 2015, Volume: 22, Issue:2

    Topics: Ammonia; Animals; Arginase; Dependovirus; Disease Models, Animal; Genetic Therapy; Hyperammonemia; H

2015
Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2015, Volume: 17, Issue:7

    Topics: Adolescent; Adult; Ammonia; Child; Child, Preschool; Female; Glutamine; Humans; Hyperammonemia; Infa

2015
Idiopathic hyperammonemia after hematopoietic stem cell transplantation: A case report.
    Pediatric transplantation, 2015, Volume: 19, Issue:4

    Topics: Ammonia; Brain Edema; Child; Fanconi Anemia; Fatal Outcome; Febrile Neutropenia; Female; Hematopoiet

2015
Disseminated Ureaplasma infection as a cause of fatal hyperammonemia in humans.
    Science translational medicine, 2015, Apr-22, Volume: 7, Issue:284

    Topics: Adult; Ammonia; Carbon Dioxide; Cohort Studies; Drug Resistance, Bacterial; Female; Humans; Hyperamm

2015
Engineering the gut microbiota to treat hyperammonemia.
    The Journal of clinical investigation, 2015, Jul-01, Volume: 125, Issue:7

    Topics: Ammonia; Animals; Bacteria; Bacterial Proteins; Bioengineering; Biological Therapy; Chemical and Dru

2015
[Specific expression of CPS-II in hyperammonemia-injured liver cells].
    Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology, 2015, Volume: 23, Issue:5

    Topics: Ammonia; Apoptosis; Hepatocytes; Humans; Hyperammonemia; Liver; Real-Time Polymerase Chain Reaction;

2015
Hyperammonemia in Urinary Tract Infections.
    PloS one, 2015, Volume: 10, Issue:8

    Topics: Aged; Aged, 80 and over; Ammonia; Anti-Infective Agents; Female; Humans; Hyperammonemia; Male; Middl

2015
Hyperammonemia Syndrome After Lung Transplantation: A Single Center Experience.
    Transplantation, 2016, Volume: 100, Issue:3

    Topics: Aged; Ammonia; Arginine; Biomarkers; Carnitine; Combined Modality Therapy; Decontamination; Female;

2016
Carbamoylphosphate synthetase 1 (CPS1) deficiency: clinical, biochemical, and molecular characterization in Malaysian patients.
    European journal of pediatrics, 2016, Volume: 175, Issue:3

    Topics: Ammonia; Asian People; Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Defici

2016
Ability of a novel system for neonatal extracorporeal renal replacement therapy with an ultra-small volume circuit to remove solutes in vitro.
    Pediatric nephrology (Berlin, Germany), 2016, Volume: 31, Issue:3

    Topics: Acute Kidney Injury; Ammonia; Automation; Biomarkers; Blood Urea Nitrogen; Creatinine; Dialysis Solu

2016
Influence of glutamine synthetase gene polymorphisms on the development of hyperammonemia during valproic acid-based therapy.
    Seizure, 2015, Volume: 33

    Topics: Adolescent; Ammonia; Anticonvulsants; Child; Child, Preschool; Epilepsy; Female; Genotype; Glutamate

2015
Hyperammonemia results in reduced muscle function independent of muscle mass.
    American journal of physiology. Gastrointestinal and liver physiology, 2016, Feb-01, Volume: 310, Issue:3

    Topics: Aged; Ammonia; Animals; Electric Stimulation; Female; Hand Strength; Humans; Hyperammonemia; Liver C

2016
Hyperammonemic hepatic encephalopathy management through L-ornithin-L-aspartate administration in dogs.
    Journal of veterinary science, 2016, Sep-30, Volume: 17, Issue:3

    Topics: Ammonia; Animals; Dipeptides; Dog Diseases; Dogs; Female; Hepatic Encephalopathy; Hyperammonemia; Ma

2016
Usefulness of Levocarnitine and/or Branched-Chain Amino Acids during Invasive Treatment for Hepatocellular Carcinoma.
    Journal of nutritional science and vitaminology, 2015, Volume: 61, Issue:6

    Topics: Ablation Techniques; Aged; Aged, 80 and over; Albumins; Amino Acids, Branched-Chain; Ammonia; Carcin

2015
N-Carbamylglutamate Is an Effective Treatment for Acute Neonatal Hyperammonaemia in a Patient with Methylmalonic Aciduria.
    Neonatology, 2016, Volume: 109, Issue:4

    Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Ammonia; Glutamates; Humans; Hyperammone

2016
A neuronal disruption in redox homeostasis elicited by ammonia alters the glycine/glutamate (GABA) cycle and contributes to MMA-induced excitability.
    Amino acids, 2016, Volume: 48, Issue:6

    Topics: Ammonia; Animals; Cerebral Cortex; Cytokines; Electroencephalography; Glutamic Acid; Glycine; Homeos

2016
Development of an experimental rat model of hyperammonemic encephalopathy and evaluation of the effects of rifaximin.
    European journal of pharmacology, 2016, May-15, Volume: 779

    Topics: Ammonia; Animals; Behavior, Animal; Brain; Coma; Disease Models, Animal; Hepatic Encephalopathy; Hyp

2016
Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD).
    PloS one, 2016, Volume: 11, Issue:4

    Topics: Adolescent; Adult; Ammonia; Child; Female; Humans; Hyperammonemia; Liver; Liver Failure, Acute; Long

2016
Postictal ammonia as a biomarker for electrographic convulsive seizures: A prospective study.
    Epilepsia, 2016, Volume: 57, Issue:8

    Topics: Adult; Ammonia; Biomarkers; Cohort Studies; Electroencephalography; Female; Humans; Hyperammonemia;

2016
Cerebral edema induced by hyperammonemia: a case report.
    The American journal of emergency medicine, 2016, Volume: 34, Issue:12

    Topics: Aged; Ammonia; Brain Edema; Coma; Female; Hemodiafiltration; Humans; Hyperammonemia

2016
Hyperammonemia: clinical, therapeutic, and educational aspects.
    The American journal of emergency medicine, 2016, Volume: 34, Issue:9

    Topics: Ammonia; Humans; Hyperammonemia

2016
A rare cause of postpartum coma: isolated hyperammonemia due to urea cycle disorder.
    The American journal of emergency medicine, 2016, Volume: 34, Issue:9

    Topics: Ammonia; Coma; Female; Humans; Hyperammonemia; Ornithine Carbamoyltransferase Deficiency Disease; Po

2016
Ammonium Increases TRPC1 Expression Via Cav-1/PTEN/AKT/GSK3β Pathway.
    Neurochemical research, 2017, Volume: 42, Issue:3

    Topics: Ammonia; Animals; Astrocytes; Caveolin 1; Cell Membrane; Cells, Cultured; Female; Glycogen Synthase

2017
Excessively Long Duodenum of the Pancreatic Graft Segment as a Rare Cause of Hyperammonemia After Simultaneous Pancreas-Kidney Transplant.
    Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2018, Volume: 16, Issue:4

    Topics: Adult; Ammonia; Anastomosis, Surgical; Anemia, Iron-Deficiency; Biomarkers; Diabetes Mellitus, Type

2018
Chrysin, a flavonoid attenuates histological changes of hyperammonemic rats: A dose dependent study.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2016, Volume: 82

    Topics: Ammonia; Animals; Bilirubin; Biomarkers; Body Weight; Brain; Creatinine; Dose-Response Relationship,

2016
Ureaplasma urealyticum Causes Hyperammonemia in an Experimental Immunocompromised Murine Model.
    PloS one, 2016, Volume: 11, Issue:8

    Topics: Ammonia; Animals; Disease Models, Animal; Hyperammonemia; Immunocompromised Host; Immunosuppressive

2016
Hyperammonemia induced by prophylactic administration of antiepileptic drugs during the perioperative period of craniotomy.
    Clinica chimica acta; international journal of clinical chemistry, 2016, Nov-01, Volume: 462

    Topics: Ammonia; Anticonvulsants; Chemoprevention; Craniotomy; Epilepsy; Female; Humans; Hyperammonemia; Mal

2016
Anesthetic experience of an adult male with citrullinemia type II: a case report.
    BMC anesthesiology, 2016, 10-11, Volume: 16, Issue:1

    Topics: Ammonia; Anesthesia, Spinal; Brain Diseases; Citrullinemia; Humans; Hyperammonemia; Male; Middle Age

2016
Hyperammonaemia and associated factors in unprovoked convulsive seizures: A cross-sectional study.
    Seizure, 2016, Volume: 43

    Topics: Adult; Aged; Ammonia; Cross-Sectional Studies; Female; Humans; Hyperammonemia; Male; Middle Aged; Mu

2016
Critically High Plasma Ammonia in an Adolescent Girl.
    Clinical chemistry, 2016, Volume: 62, Issue:12

    Topics: Ammonia; Arginine; Child; Clinical Chemistry Tests; Diagnostic Errors; Fatigue; Female; Fever; Heada

2016
The bile duct ligated rat: A relevant model to study muscle mass loss in cirrhosis.
    Metabolic brain disease, 2017, Volume: 32, Issue:2

    Topics: Ammonia; Animals; Base Composition; Bile Ducts; Disease Models, Animal; Eating; Hepatic Encephalopat

2017
Taurine treatment preserves brain and liver mitochondrial function in a rat model of fulminant hepatic failure and hyperammonemia.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2017, Volume: 86

    Topics: Adenosine Triphosphate; Ammonia; Animals; Brain; Hepatic Encephalopathy; Hyperammonemia; Liver; Live

2017
Ammonia mediates cortical hemichannel dysfunction in rodent models of chronic liver disease.
    Hepatology (Baltimore, Md.), 2017, Volume: 65, Issue:4

    Topics: Ammonia; Analysis of Variance; Animals; Bile Ducts; Biomarkers; Blotting, Western; Cerebral Cortex;

2017
L-Arginine in the treatment of valproate overdose - five clinical cases.
    Clinical toxicology (Philadelphia, Pa.), 2017, Volume: 55, Issue:4

    Topics: Acyl Coenzyme A; Adult; Amino-Acid N-Acetyltransferase; Ammonia; Arginine; Carnitine; Coma; Drug Ove

2017
Ammonia lowering reverses sarcopenia of cirrhosis by restoring skeletal muscle proteostasis.
    Hepatology (Baltimore, Md.), 2017, Volume: 65, Issue:6

    Topics: Ammonia; Analysis of Variance; Animals; Autophagy; Disease Models, Animal; Homeostasis; Hyperammonem

2017
Accumulation of alpha-fluoro-beta-alanine and fluoro mono acetate in a patient with 5-fluorouracil-associated hyperammonemia.
    Cancer chemotherapy and pharmacology, 2017, Volume: 79, Issue:3

    Topics: Aged; Ammonia; Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; beta

2017
Expanding the phenotype in argininosuccinic aciduria: need for new therapies.
    Journal of inherited metabolic disease, 2017, Volume: 40, Issue:3

    Topics: Adolescent; Adult; Ammonia; Argininosuccinic Acid; Argininosuccinic Aciduria; Child; Child, Preschoo

2017
Successful management of immunosuppression in a patient with severe hyperammonemia after lung transplantation.
    The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2008, Volume: 27, Issue:7

    Topics: Ammonia; Humans; Hyperammonemia; Immunosuppressive Agents; Lung Transplantation; Male; Middle Aged

2008
Can plasma ammonia be measured in patients with acute liver disease?
    Annals of clinical biochemistry, 2008, Volume: 45, Issue:Pt 4

    Topics: Alanine Transaminase; Ammonia; Artifacts; Humans; Hyperammonemia; Liver Diseases; Sensitivity and Sp

2008
Acute liver failure-induced death of rats is delayed or prevented by blocking NMDA receptors in brain.
    American journal of physiology. Gastrointestinal and liver physiology, 2008, Volume: 295, Issue:3

    Topics: Ammonia; Animals; Brain; Disease Models, Animal; Disease Progression; Dizocilpine Maleate; Excitator

2008
Control of acute, chronic, and constitutive hyperammonemia by wild-type and genetically engineered Lactobacillus plantarum in rodents.
    Hepatology (Baltimore, Md.), 2008, Volume: 48, Issue:4

    Topics: Acute Disease; Alanine; Ammonia; Animals; Carbon Tetrachloride; Chronic Disease; Disease Models, Ani

2008
Lactate contributes to ammonia-mediated astroglial dysfunction during hyperammonemia.
    Neurochemical research, 2009, Volume: 34, Issue:3

    Topics: Actin Cytoskeleton; Ammonia; Ammonium Chloride; Animals; Astrocytes; Calcium; Cell Size; Cells, Cult

2009
The effect of short-term hyperammonaemia on milk synthesis in dairy cows.
    The Journal of dairy research, 2009, Volume: 76, Issue:1

    Topics: Acetates; Amino Acids; Ammonia; Animals; Cattle; Cattle Diseases; Dairying; Eating; Female; Hyperamm

2009
Amino acids in CSF and plasma in hyperammonaemic coma due to arginase1 deficiency.
    Journal of inherited metabolic disease, 2008, Volume: 31 Suppl 2

    Topics: Adult; Amino Acids; Ammonia; Arginine; Biomarkers; Chromatography, Ion Exchange; Coma; Glutamine; Hu

2008
Ammonia potentiates the lethal effect of ethanol on rats.
    Bulletin of experimental biology and medicine, 2008, Volume: 145, Issue:6

    Topics: Ammonia; Animals; Central Nervous System Depressants; Drug Synergism; Ethanol; Hyperammonemia; Inhal

2008
Morin a flavonoid exerts antioxidant potential in chronic hyperammonemic rats: a biochemical and histopathological study.
    Molecular and cellular biochemistry, 2009, Volume: 327, Issue:1-2

    Topics: Ammonia; Animals; Antioxidants; Brain; Flavonoids; Hyperammonemia; Lipid Peroxidation; Liver; Male;

2009
Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vector.
    Molecular therapy : the journal of the American Society of Gene Therapy, 2009, Volume: 17, Issue:7

    Topics: Adenoviridae; Amino Acids; Ammonia; Animals; Animals, Newborn; Arginase; Genetic Therapy; Genetic Ve

2009
Development of hyperammonemic encephalopathy in patients with multiple myeloma may be associated with the appearance of peripheral blood myeloma cells.
    Leukemia & lymphoma, 2009, Volume: 50, Issue:4

    Topics: Aged; Ammonia; Brain Diseases, Metabolic; Female; Humans; Hyperammonemia; Male; Multiple Myeloma; Ne

2009
Inhibitors of the mitochondrial permeability transition reduce ammonia-induced cell swelling in cultured astrocytes.
    Journal of neuroscience research, 2009, Volume: 87, Issue:12

    Topics: Ammonia; Animals; Astrocytes; Blood-Brain Barrier; Brain; Brain Edema; Cell Size; Cells, Cultured; C

2009
Serum biotinidase activity in children treated with valproic acid and carbamazepine.
    Journal of child neurology, 2010, Volume: 25, Issue:1

    Topics: Alanine Transaminase; Ammonia; Anticonvulsants; Aspartate Aminotransferases; Biotinidase; Carbamazep

2010
A case of transient hyperammonemia in the newborn transient neonatal hyperammonemia.
    The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2010, Volume: 23, Issue:4

    Topics: Ammonia; Coma; Gestational Age; Hemodiafiltration; Humans; Hyperammonemia; Infant, Newborn; Infant,

2010
Biochemical efficacy of N-carbamylglutamate in neonatal severe hyperammonaemia due to propionic acidaemia.
    European journal of pediatrics, 2010, Volume: 169, Issue:1

    Topics: Ammonia; Dose-Response Relationship, Drug; Female; Follow-Up Studies; Glutamates; Humans; Hyperammon

2010
N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria.
    Neonatology, 2010, Volume: 97, Issue:3

    Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Ammonia; Emergency Medical Services; Female; Gl

2010
AMP deaminase and adenosine deaminase activities in liver and brain regions in acute ammonia intoxication and subacute toxic hepatitis.
    Brain research, 2010, Jan-22, Volume: 1311

    Topics: Acute Disease; Adenine Nucleotides; Adenosine Deaminase; Ammonia; AMP Deaminase; Animals; Brain; Car

2010
Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2010, Volume: 25, Issue:4

    Topics: Ammonia; Child; Female; Humans; Hyperammonemia; Infant; Infant, Newborn; Male; Metabolism, Inborn Er

2010
Portacaval anastomosis-induced hyperammonemia does not lead to oxidative stress.
    Metabolic brain disease, 2010, Volume: 25, Issue:1

    Topics: Aldehydes; Ammonia; Animals; Biomarkers; Blotting, Western; Brain; Disease Models, Animal; Frontal L

2010
Human (13)N-ammonia PET studies: the importance of measuring (13)N-ammonia metabolites in blood.
    Metabolic brain disease, 2010, Volume: 25, Issue:1

    Topics: Ammonia; Brain; Brain Chemistry; Chromatography, High Pressure Liquid; Hepatic Encephalopathy; Human

2010
Brain MR imaging and 1H-MR spectroscopy changes in patients with extrahepatic portal vein obstruction from early childhood to adulthood.
    AJNR. American journal of neuroradiology, 2010, Volume: 31, Issue:7

    Topics: Adolescent; Adult; Age Factors; Ammonia; Basal Ganglia; Child; Female; Hepatic Encephalopathy; Human

2010
Increased Na, K-ATPase alpha2 isoform gene expression by ammonia in astrocytes and in brain in vivo.
    Neurochemistry international, 2010, Volume: 57, Issue:4

    Topics: Ammonia; Animals; Astrocytes; Blotting, Western; Brain; Cell Membrane; Cells, Cultured; Dipeptides;

2010
Acute hepatic encephalopathy: diffusion-weighted and fluid-attenuated inversion recovery findings, and correlation with plasma ammonia level and clinical outcome.
    AJNR. American journal of neuroradiology, 2010, Volume: 31, Issue:8

    Topics: Acute Disease; Adolescent; Adult; Aged; Ammonia; Cerebellum; Cerebral Cortex; Child; Diffusion Magne

2010
Carbamyl phosphate synthetase deficiency and postpartum hyperammonemia.
    American journal of obstetrics and gynecology, 2010, Volume: 203, Issue:1

    Topics: Adult; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Female; Humans; Hyperammonemia; Postpartum P

2010
Continuous hemofiltration in the control of neonatal hyperammonemia: a 10-year experience.
    Pediatric nephrology (Berlin, Germany), 2010, Volume: 25, Issue:9

    Topics: Ammonia; Anticoagulants; England; Female; Hemodynamics; Hemofiltration; Humans; Hyperammonemia; Infa

2010
A new experimental model for acute hepatic failure in rats.
    Acta cirurgica brasileira, 2010, Volume: 25, Issue:3

    Topics: Ammonia; Animals; Bilirubin; Creatine; Disease Models, Animal; Hepatectomy; Hepatic Encephalopathy;

2010
Direct exposure to ammonia and hyperammonemia increase the extracellular accumulation and degradation of astroglia-derived glutathione in the rat prefrontal cortex.
    Toxicological sciences : an official journal of the Society of Toxicology, 2010, Volume: 117, Issue:1

    Topics: Ammonia; Animals; Astrocytes; Cell Line, Tumor; Extracellular Space; Glutathione; Hyperammonemia; Ma

2010
Postictal transient hyperammonemia as an indicator of seizure disorder.
    European neurology, 2010, Volume: 64, Issue:1

    Topics: Aged; Aged, 80 and over; Ammonia; Epilepsy; Female; Follow-Up Studies; Humans; Hyperammonemia; Male;

2010
Acute hyperammonemia activates branched-chain amino acid catabolism and decreases their extracellular concentrations: different sensitivity of red and white muscle.
    Amino acids, 2011, Volume: 40, Issue:2

    Topics: Acute Disease; Amino Acids, Branched-Chain; Ammonia; Animals; Disease Models, Animal; Extracellular

2011
Transient hyperammonemia due to L-asparaginase therapy in children with acute lymphoblastic leukemia or non-Hodgkin lymphoma.
    Pediatric hematology and oncology, 2011, Volume: 28, Issue:1

    Topics: Adolescent; Ammonia; Antineoplastic Agents; Asparaginase; Child; Female; Humans; Hyperammonemia; Lym

2011
Cyclophosphamide-induced leakage of gastrointestinal ammonia into the common bloodstream in rats.
    Drug and chemical toxicology, 2011, Volume: 34, Issue:1

    Topics: Ammonia; Animals; Antineoplastic Agents, Alkylating; Behavior, Animal; Cyclophosphamide; Dose-Respon

2011
Hyperammonemia in the pediatric emergency care setting.
    Pediatric emergency care, 2010, Volume: 26, Issue:12

    Topics: Ammonia; Brain Damage, Chronic; Child; Child, Preschool; Consciousness Disorders; Critical Illness;

2010
New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoA.
    Journal of hepatology, 2011, Volume: 55, Issue:2

    Topics: Acyl Coenzyme A; Amino-Acid N-Acetyltransferase; Ammonia; Animals; Anticonvulsants; Citrulline; Dise

2011
Activation of AMP deaminase and adenosine deaminase in the liver during ammonia poisoning and hepatitis.
    Bulletin of experimental biology and medicine, 2010, Volume: 150, Issue:1

    Topics: Adenosine Deaminase; Ammonia; AMP Deaminase; Analysis of Variance; Animals; Carbon Tetrachloride; He

2010
N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia.
    European journal of pediatrics, 2011, Volume: 170, Issue:6

    Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Ammonia; Glutamates; Humans; Hyperammonemia; In

2011
Ammonia redistribution from the gastrointestinal tract to general circulation after intraperitoneal injection of cyclophosphamide to rats.
    Bulletin of experimental biology and medicine, 2010, Volume: 150, Issue:2

    Topics: Alanine Transaminase; Ammonia; Animals; Aspartate Aminotransferases; Cyclophosphamide; Dose-Response

2010
Pro-inflammatory cytokines are raised in extrahepatic portal venous obstruction, with minimal hepatic encephalopathy.
    Journal of gastroenterology and hepatology, 2011, Volume: 26, Issue:6

    Topics: Adolescent; Adult; Ammonia; Brain; Brain Edema; Case-Control Studies; Child; Diffusion Tensor Imagin

2011
Influence of rutin on biochemical alterations in hyperammonemia in rats.
    Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie, 2012, Volume: 64, Issue:7-8

    Topics: Administration, Oral; Ammonia; Animals; Antioxidants; Body Weight; Brain; Disease Models, Animal; Hy

2012
Hypermagnesemia does not prevent intracranial hypertension and aggravates cerebral hyperperfusion in a rat model of acute hyperammonemia.
    Hepatology (Baltimore, Md.), 2011, Volume: 53, Issue:6

    Topics: Ammonia; Animals; Aquaporin 4; Blood Pressure; Brain; Cerebrovascular Circulation; Dose-Response Rel

2011
Inhibition of glutamine synthesis induces glutamate dehydrogenase-dependent ammonia fixation into alanine in co-cultures of astrocytes and neurons.
    Neurochemistry international, 2011, Volume: 59, Issue:4

    Topics: Alanine; Alanine Transaminase; Ammonia; Animals; Astrocytes; Cells, Cultured; Cerebral Cortex; Cocul

2011
Threshold for toxicity from hyperammonemia in critically ill children.
    Journal of hepatology, 2012, Volume: 56, Issue:1

    Topics: Ammonia; Brain Edema; Child; Child, Preschool; Critical Illness; Encephalocele; Female; Humans; Hype

2012
Urinary ammonia excretion increases acutely during living donor liver transplantation.
    Liver international : official journal of the International Association for the Study of the Liver, 2011, Volume: 31, Issue:8

    Topics: Adult; Aged; Ammonia; Biomarkers; Female; Germany; Hepatectomy; Hepatic Encephalopathy; Homeostasis;

2011
Absence of neuropsychological impairment in hyperammonaemia in healthy young adults; possible synergism in development of hepatic encephalopathy (HE) symptoms?
    Metabolic brain disease, 2011, Volume: 26, Issue:3

    Topics: Adult; Ammonia; Analysis of Variance; Cross-Over Studies; Double-Blind Method; Fatigue; Hepatic Ence

2011
"Hyperammonemia following glufosinate-containing herbicide poisoning: a potential marker of severe neurotoxicity" by Yan-Chido Mao et al., Clin Toxicol (Phila) 2011; 49:48-52.
    Clinical toxicology (Philadelphia, Pa.), 2011, Volume: 49, Issue:6

    Topics: Adult; Aged; Aminobutyrates; Ammonia; Biomarkers; Female; Herbicides; Humans; Hyperammonemia; Male;

2011
Transient hyperammonemia associated with postictal state in generalized convulsion.
    The Kaohsiung journal of medical sciences, 2011, Volume: 27, Issue:10

    Topics: Adult; Ammonia; Consciousness; Epilepsy, Post-Traumatic; Female; Humans; Hyperammonemia; Male; Middl

2011
Transient hyperammonemia in seizures: a prospective study.
    Epilepsia, 2011, Volume: 52, Issue:11

    Topics: Ammonia; Creatinine; Emergency Service, Hospital; Female; Humans; Hyperammonemia; Male; Middle Aged;

2011
Contribution of hyperammonemia and inflammatory factors to cognitive impairment in minimal hepatic encephalopathy.
    Metabolic brain disease, 2012, Volume: 27, Issue:1

    Topics: Adult; Aged; Ammonia; Cognitive Dysfunction; Fatty Liver; Female; Hepatic Encephalopathy; Humans; Hy

2012
Exploratory investigation on nitro- and phospho-proteome cerebellum changes in hyperammonemia and hepatic encephalopathy rat models.
    Metabolic brain disease, 2012, Volume: 27, Issue:1

    Topics: Ammonia; Animals; Cerebellum; Cognition; Disease Models, Animal; Hepatic Encephalopathy; Humans; Hyp

2012
How to use serum ammonia.
    Archives of disease in childhood. Education and practice edition, 2012, Volume: 97, Issue:2

    Topics: Ammonia; Child; Child, Preschool; Education, Medical, Continuing; Humans; Hyperammonemia; Infant; Me

2012
Cerebral glutamine metabolism under hyperammonemia determined in vivo by localized (1)H and (15)N NMR spectroscopy.
    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2012, Volume: 32, Issue:4

    Topics: Ammonia; Animals; Brain; Glutamate-Ammonia Ligase; Glutamic Acid; Glutamine; Hyperammonemia; Magneti

2012
Ammonia-induced brain swelling and neurotoxicity in an organotypic slice model.
    Neurological research, 2011, Volume: 33, Issue:10

    Topics: Ammonia; Animals; Animals, Newborn; Brain; Brain Edema; Disease Models, Animal; Hepatic Encephalopat

2011
Efficacy of oral L-ornithine L-aspartate in cirrhotic patients with hyperammonemic hepatic encephalopathy.
    Annals of hepatology, 2011, Volume: 10 Suppl 2

    Topics: Administration, Oral; Ammonia; Dipeptides; Glutamine; Hepatic Encephalopathy; Humans; Hyperammonemia

2011
Systemic oxidative stress is implicated in the pathogenesis of brain edema in rats with chronic liver failure.
    Free radical biology & medicine, 2012, Apr-01, Volume: 52, Issue:7

    Topics: Ammonia; Animals; Blood-Brain Barrier; Brain Edema; Disease Models, Animal; End Stage Liver Disease;

2012
Prognostic value of venous blood ammonia in patients with out-of-hospital cardiac arrest.
    Circulation journal : official journal of the Japanese Circulation Society, 2012, Volume: 76, Issue:4

    Topics: Aged; Ammonia; Biomarkers; Chi-Square Distribution; Confidence Intervals; Emergency Medical Services

2012
Persistent hyperammonemia is associated with complications and poor outcomes in patients with acute liver failure.
    Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2012, Volume: 10, Issue:8

    Topics: Adolescent; Adult; Aged; Ammonia; Blood Chemical Analysis; Brain Edema; Child; Communicable Diseases

2012
Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency.
    Journal of Korean medical science, 2012, Volume: 27, Issue:5

    Topics: Age of Onset; Ammonia; Arginine; Citrulline; Humans; Hyperammonemia; Male; Middle Aged; Ornithine; O

2012
A rare case of hyperammonemia complication of high-protein parenteral nutrition.
    JPEN. Journal of parenteral and enteral nutrition, 2013, Volume: 37, Issue:1

    Topics: Adult; Ammonia; Brain Edema; Dietary Proteins; Fatal Outcome; Humans; Hyperammonemia; Male; Parenter

2013
A case of valproate-induced encephalopathy.
    The Australian and New Zealand journal of psychiatry, 2012, Volume: 46, Issue:12

    Topics: Ammonia; Antimanic Agents; Brain Diseases, Metabolic; Female; Humans; Hyperammonemia; Middle Aged; P

2012
Recurrent unexplained hyperammonemia in an adolescent with arginase deficiency.
    Clinical biochemistry, 2012, Volume: 45, Issue:18

    Topics: Adolescent; Ammonia; Child; Hospitalization; Humans; Hyperammonemia; Hyperargininemia; Male; Recurre

2012
SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation.
    Annals of clinical and laboratory science, 2012,Fall, Volume: 42, Issue:4

    Topics: Ammonia; Base Sequence; Cardiomyopathies; Carnitine; Humans; Hyperammonemia; Infant, Newborn; Lactic

2012
Interorgan metabolism of ornithine phenylacetate (OP)--a novel strategy for treatment of hyperammonemia.
    Biochemical pharmacology, 2013, Jan-01, Volume: 85, Issue:1

    Topics: Acetates; Ammonia; Animals; Arteries; Bile Ducts; Drug Interactions; Female; Glutamine; Hyperammonem

2013
Impairment of short term memory in rats with hepatic encephalopathy due to bile duct ligation.
    Metabolic brain disease, 2013, Volume: 28, Issue:2

    Topics: Ammonia; Animals; Bile Ducts; End Stage Liver Disease; Hepatic Encephalopathy; Hyperammonemia; Ligat

2013
Aggravation of cyclophosphamide-induced acute neurological disorders under conditions of artificial acidification of chyme in rats.
    Bulletin of experimental biology and medicine, 2012, Volume: 153, Issue:6

    Topics: Acute Disease; Administration, Oral; Ammonia; Animals; Boric Acids; Cyclophosphamide; Gastric Juice;

2012
Ammonia inhibits long-term potentiation via neurosteroid synthesis in hippocampal pyramidal neurons.
    Neuroscience, 2013, Mar-13, Volume: 233

    Topics: Adaptation, Physiological; Ammonia; Animals; CA1 Region, Hippocampal; Cognition; gamma-Aminobutyric

2013
Efficacy of clonidine in hyperammonemia induced hyperexcitability syndrome.
    Paediatric anaesthesia, 2013, Volume: 23, Issue:2

    Topics: Adrenergic alpha-Agonists; Ammonia; Brain Chemistry; Clonidine; Glucose; Glutamic Acid; Humans; Hype

2013
Metabolic improvements in intrahepatic porto-systemic venous shunt presenting various metabolic abnormalities by 4-phenylacetate.
    Clinica chimica acta; international journal of clinical chemistry, 2013, Apr-18, Volume: 419

    Topics: Administration, Intravenous; Adolescent; Ammonia; Child; Female; Hepatic Veins; Humans; Hyperammonem

2013
Comparison of the effects of ammonia on brain mitochondrial function in rats and gulf toadfish.
    American journal of physiology. Regulatory, integrative and comparative physiology, 2002, Volume: 283, Issue:3

    Topics: Ammonia; Animals; Antimycin A; Batrachoidiformes; Brain; Cyanides; Electron Transport; Glutamine; He

2002
[Fulminant coma: think hyperammonemia and urea cycle disorders].
    Annales francaises d'anesthesie et de reanimation, 2002, Volume: 21, Issue:10

    Topics: Adolescent; Ammonia; Coma; Family; Fatal Outcome; Humans; Hyperammonemia; Male; Ornithine Carbamoylt

2002
Inhibition of acute hyperammonemia-induced convulsions by systemically administered gamma aminobutyric acid in rats.
    Pharmacology, biochemistry, and behavior, 2003, Volume: 74, Issue:3

    Topics: Ammonia; Animals; Brain; Dose-Response Relationship, Drug; gamma-Aminobutyric Acid; Hyperammonemia;

2003
Valproate-induced hyperammonemic encephalopathy.
    Epilepsia, 2003, Volume: 44, Issue:2

    Topics: Ammonia; Anticonvulsants; Basal Ganglia Diseases; Brain Diseases, Metabolic; Diagnosis, Differential

2003
Hyperammonemia in carnitine-deficient adult JVS mice used by starvation.
    Metabolic brain disease, 2002, Volume: 17, Issue:4

    Topics: Aging; Amino Acids; Ammonia; Animals; Animals, Newborn; Carbamoyl-Phosphate Synthase (Ammonia); Carn

2002
Ammonia prevents glutamate-induced but not low K(+)-induced apoptosis in cerebellar neurons in culture.
    Neuroscience, 2003, Volume: 117, Issue:4

    Topics: Ammonia; Animals; Animals, Newborn; Apoptosis; Calcium; Calcium Signaling; Caspase 3; Caspases; Cell

2003
Tolerance of neonatal rat brain to acute hyperammonemia.
    Brain research, 2003, May-23, Volume: 973, Issue:1

    Topics: Acute Disease; Adenosine Triphosphate; Age Factors; Ammonia; Animals; Animals, Newborn; Brain; Femal

2003
The kidney plays a major role in the hyperammonemia seen after simulated or actual GI bleeding in patients with cirrhosis.
    Hepatology (Baltimore, Md.), 2003, Volume: 37, Issue:6

    Topics: Adult; Ammonia; Blood Circulation; Female; Gastrointestinal Hemorrhage; Humans; Hyperammonemia; Kidn

2003
Hyperammonaemia as a cause of psychosis in an adolescent.
    European journal of pediatrics, 2003, Volume: 162, Issue:11

    Topics: Adolescent; Ammonia; Follow-Up Studies; Glutamates; Humans; Hyperammonemia; Male; Psychotic Disorder

2003
Electroencephalographic changes in hyperammonemia.
    Electroencephalography and clinical neurophysiology, 1956, Volume: 8, Issue:3

    Topics: Ammonia; Blood; Electroencephalography; Humans; Hyperammonemia

1956
Electroencephalographic changes and hyperammonemia.
    Electroencephalography and clinical neurophysiology, 1958, Volume: 10, Issue:1

    Topics: Ammonia; Electroencephalography; Humans; Hyperammonemia

1958
A vulnerable and rate-limiting step in urea synthesis in patients with hyperammoniaemia.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1958, Volume: 97, Issue:2

    Topics: Amino Acids; Ammonia; Humans; Hyperammonemia; Urea

1958
[Effects of potassium & magnesium salts of DL-aspartic acid on the hyperammoniemia of experimental hemorrhagic shock].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1958, Volume: 152, Issue:6

    Topics: Ammonia; Aspartic Acid; Humans; Hyperammonemia; Magnesium; Potassium; Potassium Compounds; Salts; Sh

1958
Electroencephalographic observations during experimental hyperammonemia.
    Neurology, 1958, Volume: 8, Issue:12

    Topics: Ammonia; Blood-Brain Barrier; Electroencephalography; Humans; Hyperammonemia

1958
[Glutamate of arginine as medication of hyperammoniemia in grave hepatic insufficiency].
    El Dia medico, 1960, Sep-29, Volume: 32

    Topics: Ammonia; Arginine; Glutamates; Glutamic Acid; Hepatic Insufficiency; Humans; Hyperammonemia; Liver D

1960
The effect of induced hyperammonemia on renal ammonia metabolism.
    The Journal of clinical investigation, 1961, Volume: 40

    Topics: Ammonia; Humans; Hyperammonemia; Kidney

1961
[Electroencephalographic studies in the course of induced hyperammoniemia due to ingestion of ammoniacal salts and by protein ingestion in cirrhotics].
    La Presse medicale, 1959, Nov-07, Volume: 67

    Topics: Ammonia; Eating; Electroencephalography; Hyperammonemia; Liver Cirrhosis; Salts

1959
[Arginase and experimental hyperammoniemia. I. Effect of arginase on hyperammoniemia induced in the rat by amino acid solutions].
    La Presse medicale, 1962, May-19, Volume: 70

    Topics: Amidohydrolases; Amino Acids; Ammonia; Animals; Arginase; Hyperammonemia; Rats

1962
[Arginase and experimental hyperammoniemia. II. Action of arginase on experimental portacaval encephalopathy in the dog].
    La Presse medicale, 1962, May-19, Volume: 70

    Topics: Amidohydrolases; Ammonia; Animals; Arginase; Brain; Brain Diseases; Dogs; Hepatic Encephalopathy; Hu

1962
[On the pathophysiology of ammonia metabolism. Importance of the bacterial urease effect in the intestinal tract for hyperammoniemia in portacaval shunt].
    Medizinische Klinik, 1962, Apr-27, Volume: 57

    Topics: Ammonia; Gastrointestinal Tract; Humans; Hyperammonemia; Intestines; Portacaval Shunt, Surgical; Ure

1962
[Hyperammoniemia induced by glutamine in cirrhotics. The renal origin of this hyperammoniemia].
    Revue francaise d'etudes cliniques et biologiques, 1962, Volume: 7

    Topics: Ammonia; Glutamine; Humans; Hyperammonemia; Kidney; Liver Cirrhosis

1962
Electromyographic studies on the flapping tremor, especially its relationship to hyperammonemia.
    Folia psychiatrica et neurologica japonica, 1961, Volume: 15

    Topics: Ammonia; Dyskinesias; Electromyography; Humans; Hyperammonemia; Liver Diseases; Tremor

1961
[The significance of hyperammoniemia].
    Praxis, 1963, Feb-28, Volume: 52

    Topics: Ammonia; Blood Chemical Analysis; Hyperammonemia

1963
Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea.
    Lancet (London, England), 1962, Oct-06, Volume: 2, Issue:7258

    Topics: Amino Acids; Ammonia; Hyperammonemia; Transferases; Urea

1962
[Hyperammonemia and hepatic insufficiency].
    Gaceta medica de Mexico, 1963, Volume: 93

    Topics: Ammonia; Blood Chemical Analysis; Chemical and Drug Induced Liver Injury; Hepatic Encephalopathy; He

1963
[Protective action of the potassium and magnesium salts of aspartic acid in hyperammonemia induced in animals (dogs) undergoing partial hepatectomy].
    Archivio italiano di chirurgia, 1961, Volume: 87

    Topics: Ammonia; Animals; Aspartic Acid; Dogs; Hepatectomy; Hyperammonemia; Magnesium; Potassium; Salts

1961
[The association of malic acid and arginine in the preventive treatment of hyperammonemia. Experimental study].
    La Presse medicale, 1963, Jan-12, Volume: 71

    Topics: Ammonia; Arginine; Humans; Hyperammonemia; Malates

1963
CEREBRAL ATROPHY IN HYPERAMMONAEMIA.
    Clinical radiology, 1963, Volume: 14

    Topics: Ammonia; Atrophy; Blood Chemical Analysis; Brain Diseases; Cerebral Ventriculography; Diagnostic Ima

1963
[ORAL TREATMENT OF HYPERAMMONIEMIA BY CALCIUM ALPHA-KETOGLUTARATE].
    La Presse medicale, 1964, Jan-04, Volume: 72

    Topics: Administration, Oral; Ammonia; Blood Chemical Analysis; Hepatic Encephalopathy; Humans; Hyperammonem

1964
[ON 3 CASES OF PORTACAVAL ANASTOMOSIS WELL ENDURED DESPITE A PROLONGED HYPERAMMONIEMIA].
    Toulouse medical, 1964, Volume: 65

    Topics: Ammonia; Blood Chemical Analysis; Hyperammonemia; Portacaval Shunt, Surgical

1964
THE PRODUCTION OF HYPERAMMONEMIA IN DOGS WITH ECK FISTULA. EFFECT OF WHOLE BLOOD, CASEIN AND CASEIN HYDROLYSATE.
    The Journal of surgical research, 1964, Volume: 4

    Topics: Ammonia; Animals; Blood; Blood Chemical Analysis; Blood Transfusion; Caseins; Dogs; Hyperammonemia;

1964
[VENOUS HYPERAMMONIEMIA INDUCED BY PENTETRAZOL AND STRYCHNINE. INFLUENCE OF A CURARIZING AGENT].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1964, Volume: 158

    Topics: Ammonia; Blood; Gallamine Triethiodide; Hyperammonemia; Pentylenetetrazole; Pharmacology; Rabbits; R

1964
[EXPERIMENTAL STUDY OF ACTION OF ARGININE GLUCOSE-L-PHOSPHATE ON HYPERAMMONIEMIA IN THE COURSE OF RESPIRATORY ACIDOSIS].
    Minerva anestesiologica, 1965, Volume: 31

    Topics: Acidosis; Acidosis, Respiratory; Ammonia; Animals; Arginine; Blood; Dogs; Glucose; Hexosephosphates;

1965
[HYPERAMMONIEMIA OF RESPIRATORY INSUFFICIENCY].
    Helvetica medica acta, 1964, Volume: 31

    Topics: Ammonia; Blood Chemical Analysis; Humans; Hyperammonemia; Pulmonary Valve Insufficiency; Respiratory

1964
[Autopsy findings of a case, a special type of hepatocerebral disease, with sustained hyperammonemia].
    Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica, 1962, Volume: 64

    Topics: Ammonia; Autopsy; Brain; Brain Diseases; Humans; Hyperammonemia; Liver Diseases

1962
Systemic inflammatory response exacerbates the neuropsychological effects of induced hyperammonemia in cirrhosis.
    Journal of hepatology, 2004, Volume: 40, Issue:2

    Topics: Amino Acids; Ammonia; C-Reactive Protein; Female; Hepatic Encephalopathy; Humans; Hyperammonemia; In

2004
Hyperammonemia impairs long-term potentiation in hippocampus by altering the modulation of cGMP-degrading phosphodiesterase by protein kinase G.
    Neurobiology of disease, 2004, Volume: 15, Issue:1

    Topics: 3',5'-Cyclic-GMP Phosphodiesterases; Ammonia; Animals; Cyclic GMP; Cyclic GMP-Dependent Protein Kina

2004
[Primary plasma cell leukemia (IgD-lambda) with hyperammonemia].
    Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 2004, Jan-10, Volume: 93, Issue:1

    Topics: Ammonia; Antineoplastic Combined Chemotherapy Protocols; Biomarkers, Tumor; Cyclophosphamide; Dexame

2004
Antioxidant defence of the neonatal rat brain against acute hyperammonemia.
    Brain research, 2004, Mar-19, Volume: 1001, Issue:1-2

    Topics: Ammonia; Animals; Animals, Newborn; Antioxidants; Brain; Catalase; Glutathione; Glutathione Disulfid

2004
Acute hemodialysis for hyperammonemia in small neonates.
    Pediatric nephrology (Berlin, Germany), 2004, Volume: 19, Issue:4

    Topics: Ammonia; Humans; Hyperammonemia; Infant, Newborn; Male; Renal Dialysis; Treatment Outcome

2004
The significance of a high plasma ammonia value.
    Archives of disease in childhood, 2004, Volume: 89, Issue:6

    Topics: Ammonia; Humans; Hyperammonemia; Specimen Handling

2004
[Hyperammonemia: pathogenesis, diagnosis and therapy].
    Deutsche medizinische Wochenschrift (1946), 2004, Jun-11, Volume: 129, Issue:24

    Topics: Acute Disease; Amino Acids; Ammonia; Chronic Disease; Humans; Hyperammonemia

2004
Valproic acid-induced hyperammonemia and thrombocytopenia in an elderly woman.
    The Annals of pharmacotherapy, 2004, Volume: 38, Issue:10

    Topics: Aged; Ammonia; Anticonvulsants; Female; Humans; Hyperammonemia; Platelet Count; Thrombocytopenia; Va

2004
Valproic acid-induced hyperammonemia: a case report.
    Journal of clinical psychopharmacology, 2004, Volume: 24, Issue:5

    Topics: Ammonia; Anticonvulsants; Blood Urea Nitrogen; Consciousness Disorders; Diagnosis, Differential; Dru

2004
Chronic exposure to ammonia induces isoform-selective alterations in the intracellular distribution and NMDA receptor-mediated translocation of protein kinase C in cerebellar neurons in culture.
    Journal of neurochemistry, 2005, Volume: 92, Issue:1

    Topics: Ammonia; Animals; Cells, Cultured; Cerebellum; Dose-Response Relationship, Drug; Hyperammonemia; Int

2005
Oral administration of sildenafil restores learning ability in rats with hyperammonemia and with portacaval shunts.
    Hepatology (Baltimore, Md.), 2005, Volume: 41, Issue:2

    Topics: Administration, Oral; Ammonia; Animals; Brain; Cyclic GMP; Extracellular Fluid; Glutamic Acid; Hyper

2005
Two cases of valproate-induced hyperammonemic encephalopathy without hepatic failure.
    The Journal of the Association of Physicians of India, 2004, Volume: 52

    Topics: Ammonia; Anticonvulsants; Child; Child, Preschool; Drug Therapy, Combination; Female; Fructose; Huma

2004
Ornithine transcarbamylase deficiency in pregnancy.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:2

    Topics: Adult; Ammonia; Female; Heterozygote; Humans; Hyperammonemia; Infant, Newborn; Male; Ornithine Carba

2005
Ammonia effects on pyruvate/lactate production in astrocytes--interaction with glutamate.
    Neurochemistry international, 2005, Volume: 47, Issue:1-2

    Topics: Ammonia; Animals; Animals, Newborn; Aspartic Acid; Astrocytes; Bucladesine; Cells, Cultured; Cerebra

2005
Ammonia toxicity under hyponatremic conditions in astrocytes: de novo synthesis of amino acids for the osmoregulatory response.
    Neurochemistry international, 2005, Volume: 47, Issue:1-2

    Topics: Alanine; Amino Acids; Ammonia; Ammonium Chloride; Animals; Animals, Newborn; Astrocytes; Brain Edema

2005
Role of oxidative stress in the ammonia-induced mitochondrial permeability transition in cultured astrocytes.
    Neurochemistry international, 2005, Volume: 47, Issue:1-2

    Topics: Ammonia; Ammonium Chloride; Animals; Animals, Newborn; Antioxidants; Astrocytes; Brain; Cell Membran

2005
Differential effects of ammonia on the benzodiazepine modulatory site on the GABA-A receptor complex of human brain.
    Neurochemistry international, 2005, Volume: 47, Issue:1-2

    Topics: Ammonia; Binding Sites; Binding, Competitive; Brain; Cell Membrane; Dose-Response Relationship, Drug

2005
Hyperammonaemia reduces intracellular 22Na (sodium) ion and extracellular 86Rb ion concentrations in the blood-brain barrier of the rat.
    Metabolic brain disease, 2005, Volume: 20, Issue:1

    Topics: Ammonia; Animals; Blood-Brain Barrier; Carbon Radioisotopes; Choroid Plexus; Diffusion; Disease Mode

2005
[Clinical and laboratory screening studies on urea cycle defects].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2005, Volume: 43, Issue:5

    Topics: Adolescent; Ammonia; Child; Child, Preschool; Female; Follow-Up Studies; Humans; Hyperammonemia; Inf

2005
Ammonia-mediated LTP inhibition: effects of NMDA receptor antagonists and L-carnitine.
    Neurobiology of disease, 2005, Volume: 20, Issue:2

    Topics: Adenosine Triphosphate; Ammonia; Animals; Carnitine; Cell Respiration; Dose-Response Relationship, D

2005
Mechanisms of ammonia-induced cell death in rat cortical neurons: roles of NMDA receptors and glutathione.
    Neurochemistry international, 2005, Volume: 47, Issue:1-2

    Topics: Ammonia; Ammonium Chloride; Animals; Animals, Newborn; Apoptosis; Cell Survival; Cells, Cultured; Ce

2005
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Diagnosis, Differential; Female

2005
A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl-phosphate synthetase-1 activity in liver: a pitfall in enzymatic diagnosis for hyperammonaemia.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:5

    Topics: Adolescent; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Diagnosis, Differential; DNA, Complemen

2005
Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice.
    Journal of hepatology, 2006, Volume: 44, Issue:5

    Topics: Amino Acids; Ammonia; Animals; Anticoagulants; Aspartic Acid; Calcium-Binding Proteins; Citric Acid;

2006
Fulminant hyperammonaemia induced by thiopental coma in rats.
    Toxicology, 2006, Jul-25, Volume: 224, Issue:3

    Topics: Acetates; Ammonia; Animals; Blood Urea Nitrogen; Coma; Defecation; Dose-Response Relationship, Drug;

2006
Interorgan ammonia, glutamate, and glutamine trafficking in pigs with acute liver failure.
    American journal of physiology. Gastrointestinal and liver physiology, 2006, Volume: 291, Issue:3

    Topics: Ammonia; Animals; Biological Transport, Active; Female; Glutamic Acid; Glutamine; Hyperammonemia; Ki

2006
Acid-sensitive ionic channels in midbrain dopamine neurons are sensitive to ammonium, which may contribute to hyperammonemia damage.
    Proceedings of the National Academy of Sciences of the United States of America, 2006, Jul-25, Volume: 103, Issue:30

    Topics: Acid Sensing Ion Channels; Ammonia; Animals; Arachnida; Central Nervous System; Dopamine; Dose-Respo

2006
Equimolar ammonia interference in potassium measurement on the Osmetech OPTI CCA: a reply.
    Clinical chemistry, 2006, Volume: 52, Issue:11

    Topics: Ammonia; Autoanalysis; Child; False Positive Reactions; Humans; Hyperammonemia; Infant, Newborn; Ion

2006
[The effects of Helicobacter pylori infection on hyperammonaemia and hepatic encephalopathy in cirrhotic patients].
    Zhonghua nei ke za zhi, 2006, Volume: 45, Issue:8

    Topics: Adult; Aged; Ammonia; Female; Helicobacter Infections; Helicobacter pylori; Hepatic Encephalopathy;

2006
Hyperammonemia and encephalopathy in patients with multiple myeloma.
    American journal of hematology, 2007, Volume: 82, Issue:5

    Topics: Ammonia; Brain; Brain Diseases, Metabolic; Humans; Hyperammonemia; Multiple Myeloma; Retrospective S

2007
Phenylacetate and benzoate clearance in a hyperammonemic infant on sequential hemodialysis and hemofiltration.
    Pediatric nephrology (Berlin, Germany), 2007, Volume: 22, Issue:7

    Topics: Ammonia; Hemofiltration; Humans; Hyperammonemia; Infant, Newborn; Phenylacetates; Renal Dialysis; So

2007
Hypoosmotic swelling and ammonia increase oxidative stress by NADPH oxidase in cultured astrocytes and vital brain slices.
    Glia, 2007, Volume: 55, Issue:7

    Topics: Ammonia; Animals; Animals, Newborn; Astrocytes; Brain; Brain Edema; Cells, Cultured; Enzyme Inhibito

2007
Hyperammonaemia in V1a vasopressin receptor knockout mice caused by the promoted proteolysis and reduced intrahepatic blood volume.
    The Journal of physiology, 2007, Jun-15, Volume: 581, Issue:Pt 3

    Topics: Amino Acids; Ammonia; Ammonium Chloride; Animals; Arginine Vasopressin; Blood Glucose; Blood Volume;

2007
L-Ornithine phenylacetate (OP): a novel treatment for hyperammonemia and hepatic encephalopathy.
    Medical hypotheses, 2007, Volume: 69, Issue:5

    Topics: Ammonia; Drug Therapy, Combination; Hepatic Encephalopathy; Humans; Hyperammonemia; Liver; Models, B

2007
Endotoxemia produces coma and brain swelling in bile duct ligated rats.
    Hepatology (Baltimore, Md.), 2007, Volume: 45, Issue:6

    Topics: Ammonia; Animals; Brain; Brain Edema; Capillaries; Cholestasis, Extrahepatic; Coma; Consciousness; C

2007
Hyperammonemia acts synergistically with lipopolysaccharide in inducing changes in cerebral hemodynamics in rats anaesthetised with pentobarbital.
    Journal of hepatology, 2007, Volume: 47, Issue:2

    Topics: Amiloride; Ammonia; Anesthesia; Animals; Blood Pressure; Brain; Cerebral Cortex; Cerebrovascular Cir

2007
Magnetic resonance spectroscopy in adult-onset citrullinemia: elevated glutamine levels in comatose patients.
    Archives of neurology, 2007, Volume: 64, Issue:7

    Topics: Adult; Ammonia; Biomarkers; Brain; Brain Mapping; Cerebral Cortex; Choline; Citrulline; Citrullinemi

2007
Non-convulsive status epilepticus secondary to valproic acid-induced hyperammonemic encephalopathy.
    Acta neurologica Scandinavica, 2007, Volume: 116, Issue:2

    Topics: Adult; Ammonia; Anticonvulsants; Brain; Electroencephalography; Hepatic Encephalopathy; Humans; Hype

2007
Effect of ammonia, glutamine, and serum on calcineurin, p38MAPK-diP, GADD153/CHOP10, and CNTF in primary rat astrocyte cultures.
    Brain research, 2007, Oct-17, Volume: 1175

    Topics: Ammonia; Animals; Astrocytes; Blood Proteins; Brain; Calcineurin; Cells, Cultured; Ciliary Neurotrop

2007
Peritoneal dialysis in neonates with inborn errors of metabolism: is it really out of date?
    Pediatric nephrology (Berlin, Germany), 2008, Volume: 23, Issue:1

    Topics: Ammonia; Female; Humans; Hyperammonemia; Infant, Newborn; Male; Metabolism, Inborn Errors; Peritonea

2008
Hyperammonemia is associated with generalized convulsion.
    Internal medicine (Tokyo, Japan), 2008, Volume: 47, Issue:1

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Ammonia; Child; Female; Humans; Hyperammonemia; Male; Mi

2008
Gene expression profiling of astrocytes from hyperammonemic mice reveals altered pathways for water and potassium homeostasis in vivo.
    Glia, 2008, Volume: 56, Issue:4

    Topics: Amino Acids; Ammonia; Animals; Aquaporin 4; Astrocytes; Connexin 43; Diet, Reducing; Disease Models,

2008
Ammonia inhibits the C-type natriuretic peptide-dependent cyclic GMP synthesis and calcium accumulation in a rat brain endothelial cell line.
    Neurochemistry international, 2008, Volume: 52, Issue:6

    Topics: Ammonia; Aniline Compounds; Animals; Binding Sites; Binding, Competitive; Calcium; Calcium Channel B

2008
Hyperammoniemia in rats with barbiturate coma.
    Bulletin of experimental biology and medicine, 2007, Volume: 143, Issue:3

    Topics: Ammonia; Animals; Coma; Female; Gastrointestinal Motility; Hyperammonemia; Rats; Thiopental

2007
Effect of atmospheric ammonia on mortality rate of rats with barbiturate intoxication.
    Bulletin of experimental biology and medicine, 2007, Volume: 143, Issue:6

    Topics: Acetates; Administration, Inhalation; Ammonia; Animals; Drug Synergism; Female; Hyperammonemia; Oxyg

2007
[Metabolic encephalopathy can be a potentially life-threatening complication from valproic acid].
    Nederlands tijdschrift voor geneeskunde, 2008, Feb-02, Volume: 152, Issue:5

    Topics: Aged, 80 and over; Ammonia; Brain Diseases, Metabolic; Consciousness Disorders; Diagnosis, Different

2008
N-carbamylglutamate for neonatal hyperammonaemia in propionic acidaemia.
    Journal of inherited metabolic disease, 2008, Volume: 31 Suppl 2

    Topics: Ammonia; Biomarkers; Female; Glutamates; Humans; Hyperammonemia; Infant, Newborn; Intubation, Gastro

2008
Rapidly cycling encephalopathy from an almost forgotten entity.
    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2008, Volume: 29, Issue:2

    Topics: Aged, 80 and over; Ammonia; Brain Diseases, Metabolic; Colon, Sigmoid; Consciousness Disorders; Diso

2008
Intravenous ribavirin and hyperammonemia in an immunocompromised patient infected with adenovirus.
    Pharmacotherapy, 2000, Volume: 20, Issue:10

    Topics: Adenoviridae Infections; Ammonia; Antiviral Agents; Child; Female; Humans; Hyperammonemia; Organ Tra

2000
In vivo (13)C NMR measurement of neurotransmitter glutamate cycling, anaplerosis and TCA cycle flux in rat brain during.
    Journal of neurochemistry, 2001, Volume: 76, Issue:4

    Topics: Acetates; Ammonia; Animals; Astrocytes; Blood Glucose; Brain; Brain Chemistry; Carbon Isotopes; Cere

2001
Short report: Hyperammonaemia in critically ill septic infants.
    Archives of disease in childhood, 2001, Volume: 84, Issue:6

    Topics: Ammonia; Critical Care; Critical Illness; Fatal Outcome; Female; Humans; Hyperammonemia; Hypoxia-Isc

2001
Heliox use in the treatment of acute hyperammonemia.
    Journal of child neurology, 2001, Volume: 16, Issue:6

    Topics: Administration, Inhalation; Ammonia; Animals; Disease Models, Animal; Drug Evaluation, Preclinical;

2001
Emergency treatment of neonatal hyperammonaemic coma with mild systemic hypothermia.
    Lancet (London, England), 2001, Jul-07, Volume: 358, Issue:9275

    Topics: Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Coma; Electroencephalography; Emergencies; Hemofilt

2001
Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry.
    Journal of inherited metabolic disease, 2001, Volume: 24, Issue:3

    Topics: Amino Acid Sequence; Amino Acids; Ammonia; Arginine; Argininosuccinate Lyase; Argininosuccinic Acid;

2001
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome.
    The Journal of clinical endocrinology and metabolism, 2001, Volume: 86, Issue:8

    Topics: Adolescent; Adult; Amino Acid Substitution; Ammonia; Blood Glucose; Child; Child, Preschool; Diazoxi

2001
Evidence for an involvement of the ammonia-decreasing action of L-arginine in suppressing picrotoxin-induced convulsions in rats and its additive action with diazepam.
    Neurological research, 2001, Volume: 23, Issue:6

    Topics: Ammonia; Animals; Arginine; Brain; Diazepam; Drug Interactions; Epilepsy; GABA Antagonists; GABA Mod

2001
An anxiolytic agent, dihydrohonokiol-B, inhibits ammonia-induced increases in the intracellular Cl(-) of cultured rat hippocampal neurons via GABA(c) receptors.
    Neuroscience letters, 2001, Oct-19, Volume: 312, Issue:2

    Topics: Ammonia; Ammonium Chloride; Animals; Anti-Anxiety Agents; Biphenyl Compounds; Chlorides; Dose-Respon

2001
Establishment of CD7+ human myeloma sister cell lines, KMS-21-PE and KMS-21-BM, carrying t(11;14) and t(8;14).
    Leukemia & lymphoma, 2001, Volume: 42, Issue:4

    Topics: Adult; Ammonia; Antigens, CD7; Bone Marrow Cells; Chromosomes, Human, Pair 11; Chromosomes, Human, P

2001
Serum and CSF glutamine levels in valproate-related hyperammonemic encephalopathy.
    Epilepsia, 2002, Volume: 43, Issue:2

    Topics: Adolescent; Adult; Ammonia; Anticonvulsants; Brain; Brain Diseases; Electroencephalography; Female;

2002
Hyperammonaemic encephalopathy in a 13-year-old boy.
    European journal of pediatrics, 2002, Volume: 161, Issue:3

    Topics: Adolescent; Ammonia; Amoxicillin; Brain Diseases; Coma; Corynebacterium diphtheriae; Humans; Hyperam

2002
Ammonia detoxification by continuous venovenous haemofiltration in an infant with urea cycle defect.
    Hong Kong medical journal = Xianggang yi xue za zhi, 2002, Volume: 8, Issue:3

    Topics: Ammonia; Carbamoyl-Phosphate Synthase I Deficiency Disease; Hemofiltration; Humans; Hyperammonemia;

2002
Fulminant progression of hyperammonaemic encephalopathy after treatment with valproate in a patient with ureterosigmoidostomy.
    Journal of neurology, neurosurgery, and psychiatry, 2002, Volume: 73, Issue:1

    Topics: Adult; Ammonia; Anastomosis, Surgical; Anticonvulsants; Brain Diseases, Metabolic; Colon, Sigmoid; F

2002