ammonium hydroxide has been researched along with Acquired Metabolic Diseases, Brain in 52 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Urea cycle disorders are inborn errors of metabolism that, in rare cases, can present for the first time in adulthood." | 1.42 | Urea cycle disorders: a life-threatening yet treatable cause of metabolic encephalopathy in adults. ( Blair, NF; Cremer, PD; Tchan, MC, 2015) |
| "Finally, ornithine transcarbamylase deficiency was diagnosed by DNA analysis." | 1.34 | Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy. ( Chan, GC; Kwong, NS; Lam, CW; Lau, KY; Li, SK; Low, LC; Mak, CM; Poon, GW; Siu, TS; Tam, S; Tang, NL; Wong, KY, 2007) |
| "Ornithine transcarbamylase deficiency is an X linked disorder and the most common inherited cause of hyperammonaemia." | 1.30 | Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency. ( Kohlschütter, A; Oechsner, M; Steen, C; Stürenburg, HJ, 1998) |
| "Ornithine transcarbamylase deficiency is an X-linked recessive disorder of urea biosynthesis characterized by recurrent, often fatal, hyperammonemic encephalopathy in affected males; carrier females are usually asymptomatic." | 1.29 | Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy. ( Blaser, S; Clarke, JT; Pridmore, CL, 1995) |
| "Acute hepatic failure is associated with many biochemical abnormalities in plasma and brain." | 1.29 | Metabolic abnormalities and grade of encephalopathy in acute hepatic failure. ( DeJoseph, MR; Hawkins, RA; Mans, AM, 1994) |
| "Eleven patients had Reye's syndrome, three had acute "toxic" encephalopathy (without fatty liver), two had glycogen storage disease type 1, and one had congenital hyperammonemia type 2." | 1.26 | Tissue lipids in hyperammonemic encephalopathies of childhood. ( Chaves-Carballo, E; Ellefson, RD, 1980) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (25.00) | 18.7374 |
| 1990's | 14 (26.92) | 18.2507 |
| 2000's | 16 (30.77) | 29.6817 |
| 2010's | 8 (15.38) | 24.3611 |
| 2020's | 1 (1.92) | 2.80 |
| Authors | Studies |
|---|---|
| Pliego Cosano, R | 1 |
| Moreno Rosauro, JM | 1 |
| Clavero Olmos, M | 1 |
| Kwon, M | 1 |
| Alvarez, F | 1 |
| Moreno Franco, P | 1 |
| Patel, A | 1 |
| Canabal, JM | 1 |
| Haddad, TJ | 1 |
| Erasmus, DB | 1 |
| Mallea, JM | 1 |
| Narula, T | 1 |
| Blair, NF | 1 |
| Cremer, PD | 1 |
| Tchan, MC | 1 |
| Singh, S | 1 |
| Suresh, S | 1 |
| McClave, SA | 1 |
| Cave, M | 1 |
| Chou, HF | 1 |
| Yang, RC | 1 |
| Chen, CY | 1 |
| Jong, YJ | 1 |
| Ikewaki, J | 1 |
| Ogata, M | 1 |
| Imamura, T | 1 |
| Kohno, K | 1 |
| Nakayama, T | 1 |
| Kadota, J | 1 |
| Bøhmer, T | 1 |
| Bøen, A | 1 |
| Høymork, SC | 1 |
| Sudour, H | 1 |
| Schmitt, C | 1 |
| Contet, A | 1 |
| Chastagner, P | 1 |
| Feillet, F | 1 |
| Laish, I | 1 |
| Ben Ari, Z | 1 |
| Divers, TJ | 1 |
| Hong, L | 1 |
| Schutz, J | 1 |
| Nance, M | 1 |
| Murphy, JV | 1 |
| Day, B | 1 |
| Talamo, G | 1 |
| Cavallo, F | 1 |
| Zangari, M | 1 |
| Barlogie, B | 1 |
| Lee, CK | 1 |
| Pineda-Roman, M | 1 |
| Kiwan, E | 1 |
| Krishna, S | 1 |
| Tricot, G | 1 |
| Shenoy, C | 1 |
| Mak, CM | 1 |
| Siu, TS | 1 |
| Lam, CW | 1 |
| Chan, GC | 1 |
| Poon, GW | 1 |
| Wong, KY | 1 |
| Low, LC | 1 |
| Tang, NL | 1 |
| Li, SK | 1 |
| Lau, KY | 1 |
| Kwong, NS | 1 |
| Tam, S | 1 |
| Vaquero, J | 1 |
| Butterworth, RF | 2 |
| Meinardi, MC | 1 |
| van den Berg, GB | 1 |
| Groenhuijzen, A | 1 |
| Driessen, JT | 1 |
| Maas, HA | 1 |
| Wolfhagen, FH | 1 |
| Tremolizzo, L | 1 |
| Galbussera, A | 1 |
| Frigo, M | 1 |
| Apale, P | 1 |
| Capra, M | 1 |
| Appollonio, I | 1 |
| Ferrarese, C | 1 |
| Call, G | 1 |
| Seay, AR | 1 |
| Sherry, R | 1 |
| Qureshi, IA | 1 |
| Prensky, AL | 1 |
| Takayanagi, M | 1 |
| Ohtake, A | 1 |
| Ogura, N | 1 |
| Nakajima, H | 1 |
| Hoshino, M | 1 |
| Kendall, BE | 1 |
| Kingsley, DP | 1 |
| Leonard, JV | 2 |
| Lingam, S | 1 |
| Oberholzer, VG | 1 |
| Deshmukh, DR | 1 |
| Shope, TC | 1 |
| Chaves-Carballo, E | 1 |
| Ellefson, RD | 1 |
| Pridmore, CL | 1 |
| Clarke, JT | 1 |
| Blaser, S | 1 |
| Baganz, MD | 1 |
| Dross, PE | 1 |
| Mans, AM | 1 |
| DeJoseph, MR | 1 |
| Hawkins, RA | 1 |
| Liaw, CC | 1 |
| Liaw, SJ | 1 |
| Wang, CH | 1 |
| Chiu, MC | 1 |
| Huang, JS | 1 |
| Niwa, J | 1 |
| Taguchi, E | 1 |
| Takeda, A | 1 |
| Imamura, K | 1 |
| Washimi, S | 1 |
| Mabuchi, C | 1 |
| Ishiguro, Y | 1 |
| Iwasaki, A | 1 |
| Nishimura, E | 1 |
| Das, A | 1 |
| Henderson, D | 1 |
| Oechsner, M | 1 |
| Steen, C | 1 |
| Stürenburg, HJ | 1 |
| Kohlschütter, A | 1 |
| Bortone, E | 1 |
| Bettoni, L | 1 |
| Buzio, S | 1 |
| Giorgi, C | 1 |
| Melli, G | 1 |
| Mineo, F | 1 |
| Mancia, D | 1 |
| Martland, T | 1 |
| Mbamali, AC | 1 |
| Rittey, C | 1 |
| Tanner, S | 1 |
| Bonham, JR | 1 |
| Griffiths, PD | 1 |
| Brunquell, P | 1 |
| Tezcan, K | 1 |
| DiMario, FJ | 1 |
| Hasel, KM | 1 |
| Summers, BA | 1 |
| De Lahunta, A | 1 |
| Kuze, N | 1 |
| Nishizaka, Y | 1 |
| Okamoto, K | 1 |
| Wakayama, T | 1 |
| Imanaka, M | 1 |
| Kubo, Y | 1 |
| Oda, Y | 1 |
| Amitani, R | 1 |
| Kifune, A | 1 |
| Kubota, F | 1 |
| Shibata, N | 1 |
| Akata, T | 1 |
| Kikuchi, S | 1 |
| Mathias, RS | 1 |
| Kostiner, D | 1 |
| Packman, S | 1 |
| Shinkai, M | 1 |
| Ohhama, Y | 1 |
| Nishi, T | 1 |
| Yamamoto, H | 1 |
| Fujita, S | 1 |
| Take, H | 1 |
| Adachi, M | 1 |
| Tachibana, K | 1 |
| Aida, N | 1 |
| Kato, K | 1 |
| Tanaka, Y | 1 |
| Takemiya, S | 1 |
| Schwarz, S | 1 |
| Georgiadis, D | 1 |
| Schwab, S | 1 |
| Gehlen, F | 1 |
| Mayatepek, E | 1 |
| Zoubaa, S | 1 |
| Maestracci, P | 1 |
| Grimaud, D | 1 |
| Kahler, JP | 1 |
| Goldsmith, LA | 1 |
| Gjedde, A | 1 |
| Lockwood, AH | 1 |
| Duffy, TE | 1 |
| Plum, F | 1 |
| Goldstein, B | 1 |
| Brown, MR | 1 |
| Hulbert, WC | 1 |
| Rabinowitz, R | 1 |
| Rutledge, SL | 1 |
| Havens, PL | 1 |
| Haymond, MW | 1 |
| McLean, RH | 1 |
| Kan, JS | 1 |
| Brusilow, SW | 1 |
| Mizock, BA | 1 |
| Sabelli, HC | 1 |
| Dubin, A | 1 |
| Javaid, JI | 1 |
| Poulos, A | 1 |
| Rackow, EC | 1 |
| Surtees, R | 1 |
| Cascino, GD | 1 |
| Jensen, JM | 1 |
| Nelson, LA | 1 |
| Schutta, HS | 1 |
| Sharp, RA | 1 |
| Lang, CC | 1 |
| Gilchrist, JM | 1 |
| Coleman, RA | 1 |
7 reviews available for ammonium hydroxide and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Treating Every Needle in the Haystack: Hyperammonemic Encephalopathy and Severe Malnutrition After Bariatric Surgery-A Case Report and Review of the Literature.
Topics: Adult; Ammonia; Brain Diseases, Metabolic; Diagnostic Errors; Female; Fibrosis; Gastric Bypass; Huma | 2015 |
Noncirrhotic hyperammonaemic encephalopathy.
Topics: Adult; Ammonia; Biomarkers; Brain Diseases, Metabolic; Early Diagnosis; Humans; Hyperammonemia; Live | 2011 |
Metabolic causes of encephalopathy in horses.
Topics: Ammonia; Animals; Blood Glucose; Brain Diseases, Metabolic; Diagnosis, Differential; Horse Diseases; | 2011 |
Mechanisms of brain edema in acute liver failure and impact of novel therapeutic interventions.
Topics: Ammonia; Animals; Brain; Brain Diseases, Metabolic; Brain Edema; Energy Metabolism; Glutamine; Hepat | 2007 |
Hyperammonemia in urea cycle disorders: role of the nephrologist.
Topics: Algorithms; Ammonia; Brain Diseases, Metabolic; Child, Preschool; Coma; Developmental Disabilities; | 2001 |
Glutamate transporter and receptor function in disorders of ammonia metabolism.
Topics: Adenosine Triphosphate; Amino Acid Transport System X-AG; Ammonia; Apoptosis; Astrocytes; Binding Si | 2001 |
Acute metabolic encephalopathy: a review of causes, mechanisms and treatment.
Topics: Acute Disease; Ammonia; Brain Diseases, Metabolic; Diagnosis, Differential; Glucose; Humans; Hypogly | 1989 |
45 other studies available for ammonium hydroxide and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Valproicacid-induced hyperammonemic encephalopathy in the emergency department.
Topics: Ammonia; Anticonvulsants; Brain Diseases, Metabolic; Female; Humans; Hyperammonemia; Middle Aged; Re | 2019 |
Extracorporeal Liver Support for the Treatment of Hyperammonemia After Lung Transplantation.
Topics: Ammonia; Brain Diseases, Metabolic; Female; Hemofiltration; Humans; Hyperammonemia; Lung Transplanta | 2020 |
Urea cycle disorders: a life-threatening yet treatable cause of metabolic encephalopathy in adults.
Topics: Adult; Ammonia; Arginine; Brain Diseases, Metabolic; Diet, Protein-Restricted; Fat Emulsions, Intrav | 2015 |
Valproate-induced hyperammonemic encephalopathy.
Topics: Adolescent; Ammonia; Brain Diseases, Metabolic; Female; Humans; Seizures; Valproic Acid | 2008 |
Development of hyperammonemic encephalopathy in patients with multiple myeloma may be associated with the appearance of peripheral blood myeloma cells.
Topics: Aged; Ammonia; Brain Diseases, Metabolic; Female; Humans; Hyperammonemia; Male; Multiple Myeloma; Ne | 2009 |
Valproate-induced hyperammonemic encephalopathy, rapidly improved by i.v. carnitine and glucose/thiamine.
Topics: Aged; Ammonia; Anticonvulsants; Brain Diseases, Metabolic; Carnitine; Dose-Response Relationship, Dr | 2010 |
Acute metabolic encephalopathy in two patients treated with asparaginase and ondasetron.
Topics: Adolescent; Ammonia; Asparaginase; Brain Diseases, Metabolic; Humans; Male; Precursor Cell Lymphobla | 2011 |
A case of valproate-induced encephalopathy.
Topics: Ammonia; Antimanic Agents; Brain Diseases, Metabolic; Female; Humans; Hyperammonemia; Middle Aged; P | 2012 |
Valproate-induced hyperammonemic encephalopathy.
Topics: Ammonia; Anticonvulsants; Basal Ganglia Diseases; Brain Diseases, Metabolic; Diagnosis, Differential | 2003 |
Spike-wave stupor in a patient with metabolic encephalopathy.
Topics: Ammonia; Anticonvulsants; Brain Diseases, Metabolic; Coma; Diagnosis, Differential; Diazepam; Electr | 2007 |
Hyperammonemia and encephalopathy in patients with multiple myeloma.
Topics: Ammonia; Brain; Brain Diseases, Metabolic; Humans; Hyperammonemia; Multiple Myeloma; Retrospective S | 2007 |
Hyperammonaemic encephalopathy in plasma cell leukaemia.
Topics: Aged; Ammonia; Brain Diseases, Metabolic; Diagnosis, Differential; Humans; Leukemia, Plasma Cell; Ma | 2007 |
Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy.
Topics: Ammonia; Brain Diseases, Metabolic; Child, Preschool; DNA Mutational Analysis; Glutamine; Humans; Ma | 2007 |
[Metabolic encephalopathy can be a potentially life-threatening complication from valproic acid].
Topics: Aged, 80 and over; Ammonia; Brain Diseases, Metabolic; Consciousness Disorders; Diagnosis, Different | 2008 |
Rapidly cycling encephalopathy from an almost forgotten entity.
Topics: Aged, 80 and over; Ammonia; Brain Diseases, Metabolic; Colon, Sigmoid; Consciousness Disorders; Diso | 2008 |
Clinical features of carbamyl phosphate synthetase-I deficiency in an adult.
Topics: Adult; Ammonia; Brain; Brain Diseases, Metabolic; Carbamoyl-Phosphate Synthase (Ammonia); Electroenc | 1984 |
Time--a fourth dimension for encephalopathies.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Brain Diseases, Metabolic; Child; Cognition; Humans; | 1984 |
A female case of ornithine transcarbamylase deficiency with marked computed tomographic abnormalities of the brain.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Brain Diseases, Metabolic; Child, Preschool; F | 1984 |
Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Atrophy; Brain; Brain Diseases, Metaboli | 1983 |
Arginine requirement and ammonia toxicity in ferrets.
Topics: Ammonia; Animals; Arginine; Brain Diseases, Metabolic; Carnivora; Ferrets; Male; Nutritional Require | 1983 |
Tissue lipids in hyperammonemic encephalopathies of childhood.
Topics: Adipose Tissue; Adolescent; Ammonia; Brain; Brain Diseases, Metabolic; Child; Child, Preschool; Chol | 1980 |
Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Brain Damage, Chronic; Brain Disea | 1995 |
Valproic acid-induced hyperammonemic encephalopathy: MR appearance.
Topics: Adult; Ammonia; Atrophy; Brain Diseases, Metabolic; Cerebral Cortex; Diagnosis, Differential; Epilep | 1994 |
Metabolic abnormalities and grade of encephalopathy in acute hepatic failure.
Topics: Ammonia; Animals; Arginine; Aspartic Acid; Blood Glucose; Blood-Brain Barrier; Brain Chemistry; Brai | 1994 |
Transient hyperammonemia related to chemotherapy with continuous infusion of high-dose 5-fluorouracil.
Topics: Adult; Aged; Ammonia; Antineoplastic Combined Chemotherapy Protocols; Brain Diseases, Metabolic; Dos | 1993 |
[A case of ileo-vesical fistula with recurrent metabolic encephalopathy].
Topics: Acidosis; Aged; Ammonia; Brain Diseases, Metabolic; Female; Humans; Ileal Diseases; Intestinal Fistu | 1995 |
Hyperammonemic encephalopathy in a four-year-old child with prune belly syndrome.
Topics: Ammonia; Brain Diseases, Metabolic; Child, Preschool; Humans; Male; Proteus Infections; Proteus mira | 1996 |
Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Anticonvulsants; Brain Diseases, Metaboli | 1998 |
Triphasic waves associated with acute naproxen overdose: a case report.
Topics: Acidosis, Lactic; Adult; Ammonia; Anti-Inflammatory Agents, Non-Steroidal; Brain Diseases, Metabolic | 1998 |
Ornithine transcarbamylase deficiency: a case report.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Brain Diseases, Metabolic; Fatal Outcome; Fema | 1998 |
Electroencephalographic findings in ornithine transcarbamylase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Brain Diseases, Metabolic; Cerebral Cortex; Electroen | 1999 |
Encephalopathy with idiopathic hyperammonaemia and Alzheimer type II astrocytes in equidae.
Topics: Alzheimer Disease; Ammonia; Animals; Astrocytes; Brain Diseases, Metabolic; Fatal Outcome; Female; H | 1999 |
[Empyema thoracis accompanied by hyperammonemic encephalopathy].
Topics: Ammonia; Bacteroides Infections; Brain Diseases, Metabolic; Empyema; Humans; Male; Middle Aged | 2000 |
Valproic acid-induced hyperammonemic encephalopathy with triphasic waves.
Topics: Amino Acids; Ammonia; Brain Diseases, Metabolic; Electroencephalography; Humans; Male; Middle Aged; | 2000 |
Congenital absence of the portal vein and role of liver transplantation in children.
Topics: Adolescent; Ammonia; Brain Diseases, Metabolic; Female; Galactose; Humans; Infant; Liver Transplanta | 2001 |
Fulminant progression of hyperammonaemic encephalopathy after treatment with valproate in a patient with ureterosigmoidostomy.
Topics: Adult; Ammonia; Anastomosis, Surgical; Anticonvulsants; Brain Diseases, Metabolic; Colon, Sigmoid; F | 2002 |
[Acute hepatocellular insufficiency or severe jaundice].
Topics: Acute Disease; Ammonia; Brain Diseases, Metabolic; Chemical and Drug Induced Liver Injury; Citric Ac | 1976 |
Extractable hair protein in Menkes syndrome.
Topics: Ammonia; Brain Diseases, Metabolic; Hair; Humans; Menkes Kinky Hair Syndrome; Proteins; Solubility | 1978 |
Cerebral blood flow and metabolism in chronically hyperammonemic rats: effect of an acute ammonia challenge.
Topics: Ammonia; Animals; Brain; Brain Diseases, Metabolic; Cerebrovascular Circulation; Glutamates; Glutami | 1978 |
Hyperammonemic encephalopathy secondary to diphtheroid urinary tract infection in a patient with prune belly syndrome.
Topics: Ammonia; Brain Diseases, Metabolic; Child; Corynebacterium; Corynebacterium Infections; Diagnosis, D | 1991 |
Neonatal hemodialysis: effective therapy for the encephalopathy of inborn errors of metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Ammonia; Argininosuccinate Syntha | 1990 |
Septic encephalopathy. Evidence for altered phenylalanine metabolism and comparison with hepatic encephalopathy.
Topics: Ammonia; Bacterial Infections; Brain Diseases, Metabolic; Glutamine; Hepatic Encephalopathy; Humans; | 1990 |
Periodic hyperammonemic encephalopathy associated with a ureterosigmoidostomy.
Topics: Adult; Ammonia; Brain Diseases, Metabolic; Colon, Sigmoid; Electroencephalography; Female; Humans; I | 1989 |
Hyperammonaemic encephalopathy in chronic myelomonocytic leukaemia.
Topics: Ammonia; Brain Diseases, Metabolic; Chronic Disease; Humans; Leukemia, Myeloid; Male; Middle Aged; T | 1987 |
Ornithine transcarbamylase deficiency: adult onset of severe symptoms.
Topics: Adult; Ammonia; Brain Diseases, Metabolic; Female; Hemiplegia; Heterozygote; Humans; Mental Disorder | 1987 |