ammonium hydroxide has been researched along with Fatty Liver with Encephalopathy in 115 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The pathogenesis of Reye's syndrome encephalopathy was analyzed in terms of uniform criteria designed to clarify and assist evaluation of the leading hypotheses." | 2.36 | Encephalopathy of Reye's syndrome: a review of pathogenetic hypotheses. ( DeLong, GR; Glick, TH, 1982) |
| "Reye Syndrome is an acute encephalopathy with increased liver enzymes and blood ammonia, without jaundice." | 1.72 | What are the clues for an inherited metabolic disorder in Reye syndrome? A single Centre study of 58 children. ( Angoulvant, F; Arnoux, JB; Brassier, A; de Lonlay, P; Debray, D; Girard, M; Goetz, V; Heilbronner, C; Lacaille, F; Oualha, M; Pelosi, M; Renolleau, S; Salvador, E; Schiff, M; Yang, DD, 2022) |
| "Compared with rats with untreated Reye's syndrome, 1 h pretreatment by low dose resveratrol (10 mg/kg by oral gavage) resulted in marked amelioration in liver functions in the form of significant decrease in serum transaminases (AST, ALT) and plasma ammonia levels, shortening of prothrombin time, and increase in serum albumin levels." | 1.40 | Resveratrol protects against experimental induced Reye's syndrome by prohibition of oxidative stress and restoration of complex I activity. ( Abdin, A; Sarhan, N, 2014) |
| "Reye's syndrome is an acute illness characterized by hepatic encephalopathy and fatty degeneration of the liver." | 1.38 | [21-year-old woman with Reye's syndrome after influenza]. ( Böhm, M; Kaplan, BT; Link, A, 2012) |
| "Because Reye's syndrome is now very rare, any infant or child suspected of having this disorder should undergo extensive investigation to rule out the treatable inborn metabolic disorders that can mimic Reye's syndrome." | 1.30 | Reye's syndrome in the United States from 1981 through 1997. ( Belay, ED; Bresee, JS; Holman, RC; Khan, AS; Schonberger, LB; Shahriari, A, 1999) |
| "Ibuprofen treatment, either solely or in combination with influenza infection, did not produce significant change in the plasma levels of aspartate or ornithine aminotransferase activities." | 1.28 | Interactions of ibuprofen with influenza infection and hyperammonemia in an animal model of Reye's syndrome. ( Deshmukh, DR; Mukhopadhyay, A; Sarnaik, AP, 1992) |
| "Hyperlysinemia was observed with neonatal propionic and methylmalonic acidurias." | 1.28 | [Hyperlysinemia and hyperammonemia]. ( Bardet, J; Kamoun, P; Parvy, P; Rabier, D, 1991) |
| "At this time, Reye's syndrome was suspected because of the acute change of consciousness and the presence of hyperammonemia." | 1.28 | A case of ornithine transcarbamylase deficiency with acute and late onset simulating Reye's syndrome in an adult male. ( Mizoguchi, K; Ogata, M; Onizuka, S; Sukehiro, K; Watanabe, J; Yoshida, I; Yoshino, M, 1990) |
| "5 of these patients developed toxic encephalopathy with hyperammonemia induced by VPA." | 1.27 | Treatment of epileptic patients with valproic acid does not modify plasma and urine short-chain-fatty acids. ( Arnetoli, G; Boncinelli, L; Campostrini, R; Paganini, M; Zaccara, G; Zappoli, R, 1983) |
| "In Europe Reye's syndrome is a rather rare but often fatal disease affecting children and teenagers." | 1.27 | [Reye syndrome--a status review of current concepts of its pathogenesis]. ( Plauth, M, 1984) |
| "The ferret model resembled Reye's syndrome in developing increased levels of individual and total serum free fatty acids, liver triacylglycerol and total lipids." | 1.27 | Free fatty acids in an animal model of Reye's syndrome. ( Deshmukh, DR; Deshmukh, GD; Radin, NS; Shope, TC, 1983) |
| "Reye's syndrome is a serious childhood disorder that develops following influenza infections and is characterized in part by an encephalopathy, hyperammonemia and elevated serum transaminases." | 1.27 | Arginine deficiency, hyperammonemia and Reye's syndrome in ferrets. ( Deshmukh, DR; Thomas, PE, 1985) |
| "Carnitine status was evaluated in 8 patients with partial ornithine transcarbamylase (OTC) deficiency and 19 patients with secondary carnitine deficiency, who were used as positive references." | 1.27 | Hyperammonemia related to carnitine metabolism with particular emphasis on ornithine transcarbamylase deficiency. ( Matsuda, I; Ohtani, Y; Ohyanagi, K; Yamamoto, S, 1987) |
| "Patients with Reye's syndrome (RS) whose degree of severity was classified as stage 0 (alert and awake) were compared with patients with a severity classification of stage 1 or greater." | 1.27 | Reye's syndrome. An epidemiologic analysis of mild disease. ( Campbell, RJ; Hall, LJ; Halpin, TJ; Holtzhauer, FJ, 1986) |
| "One theory of the etiology of Reye's syndrome is that environmental toxins predispose the child to react abnormally to virus infection." | 1.27 | Biochemical and morphological characteristics of a mouse model of Reye's syndrome induced by the interaction of influenza B virus and a chemical emulsifier. ( Crocker, JF; Digout, SC; Lee, SH; Malatjalian, DA; Renton, KW; Rozee, KR, 1986) |
| "Urine from 12 patients with Reye syndrome was examined by gas-liquid chromatography for identification of organic acids." | 1.27 | Urinary dicarboxylic acids in Reye syndrome. ( Tonsgard, JH, 1985) |
| "A 14-year-old girl in whom Reye syndrome developed during aspirin therapy for an inflammatory disorder proven to be systemic lupus erythematosus is reported." | 1.27 | Reye syndrome associated with aspirin therapy for systemic lupus erythematosus. ( Bale, JF; Corbett, AJ; Flanders, DJ; Hansen, JR; McCray, PB, 1985) |
| "Thus, many of the abnormalities seen in Reye's syndrome were seen in this model; however, there were no hepatic enzyme changes despite altered mitochondrial morphology and no evidence of cerebral edema despite a florid encephalopathy." | 1.27 | Investigation of an animal model of a Reye-like syndrome caused by Margosa oil. ( Arcinue, EL; Mitchell, RA; Schwartz, PH; Sinniah, D, 1985) |
| "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) |
| "Recent studies of Reye syndrome (RS) patients have suggested aspirin treatment as a possible factor in the etiology of this often fatal childhood disorder." | 1.26 | Interactions of aspirin and other potential etiologic factors in an animal model of Reye syndrome. ( Deshmukh, DR; Maassab, HF; Mason, M, 1982) |
| "Ammonia metabolism in Reye syndrome was studied by quantitative analysis of the time course of hyperammonemia and the urinary excretion of ammonia, urea, and total nitrogen." | 1.26 | Ammonia metabolism in Reye syndrome and the effect of citrulline. ( DeLong, GR; Glick, TH, 1982) |
| "The EEGs of 7 children with Reye's syndrome (fatty liver and encephalopathy) were continuously recorded on magnetic tape for times ranging from 12 to 80 h." | 1.26 | Computerized evaluation of electroencephalographic changes accompanying exchange transfusion in Reye's syndrome. ( Ackmann, JJ; Barr, RE; Casper, JT; Harrington, GJ; Lewis, JD; Varma, RR, 1977) |
| "Since Reye's syndrome is associated with hyperammonemia, we measured the urea-cycle enzymes in hepatic tissue of 13 patients." | 1.26 | Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome. ( Bove, K; Brown, H; Brown, T; Hug, G; Lansky, L; Lloyd-Still, J; Partin, JC; Ryan, M; Scheve, A; Schubert, WK, 1976) |
| "Increased HVA in Reye syndrome may reflect cerebral ischemia and release of vasoactive amines (particularly dopamine) into the brain and cerebrospinal fluid (CSF)." | 1.26 | Reye syndrome: monoamine metabolites in ventricular fluid. ( Bowers, MB; Cohen, DJ; Shaywitz, BA; Venes, J, 1979) |
| "Eight patients with Reye's syndrome were followed through the course of their disease with serial measurements of serum concentrations of ammonia, short-chain organic acids, and amino acids." | 1.26 | Biochemical correlates of illness and recovery in Reye's syndrome. ( Holm, J; Kulovich, S; Nyhan, WL; Sweetman, L; Trauner, D, 1977) |
| "A patient with Reye syndrome was studied throughout the course of the illness with continuous EEG monitoring, and these patterns were correlated with serial determinations of serum ammonia and short-chain fatty acid concentrations." | 1.26 | EEG correlations with biochemical abnormalities in Reye syndrome. ( Stockard, JJ; Sweetman, L; Trauner, DA, 1977) |
| "In the epidemiologic setting of influenza B outbreaks, children who have the acute onset of noninflammatory encephalopathy associated with elevated serum transaminase levels, hypoprothrombinemia, and elevated blood ammonia levels should be considered to have Reye's syndrome." | 1.26 | Diagnostic criteria for influenza B-associated Reye's syndrome: clinical vs. pathologic criteria. ( Bregman, D; Corey, L; Gregg, MB; Rubin, RJ, 1977) |
| "Among survivors of Reye's syndrome, 30% of those who developed either decerebrate posturing or seizures during hospitalization had serious neurologic sequelae upon discharge." | 1.26 | Reye's syndrome: clinical progression and evaluation of therapy. ( Corey, L; Hattwick, MA; Rubin, RJ, 1977) |
| "The hyperammonemia of Reye's syndrome apparently results from excess waste nitrogen that overwhelms the ability of reduced ornithine transcarbamylase (and occasionally carbamyl phosphate synthetase) to detoxify the ammonia load." | 1.26 | Urea-cycle enzyme deficiencies and an increased nitrogen load producing hyperammonemia in Reye's syndrome. ( DeLong, GR; Snodgrass, PJ, 1976) |
| "This is a further example of Reye's syndrome with only minimal fatty infiltration of the liver." | 1.26 | Reye's syndrome without fatty liver. ( De Meyer, R; Gosseye, S; Maldague, P, 1976) |
| "Although frequently unrecognized, Reye's syndrome is a significant cause of serious illness and death in children." | 1.25 | Reye's syndrome. ( Hosfield, WB; Hutton, JT; Levy, BS, 1975) |
| "Sixteen patients with Reye's syndrome were seen over a 3-year period and treated with conservative management with an overall mortality of 31%." | 1.25 | Anticerebral oedema therapy in Reye's syndrome. ( Bresnan, MJ; Lombroso, CT; Lovejoy, FH; Smith, AL, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 99 (86.09) | 18.7374 |
| 1990's | 12 (10.43) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (2.61) | 24.3611 |
| 2020's | 1 (0.87) | 2.80 |
| Authors | Studies |
|---|---|
| Goetz, V | 1 |
| Yang, DD | 1 |
| Lacaille, F | 1 |
| Pelosi, M | 1 |
| Angoulvant, F | 1 |
| Brassier, A | 1 |
| Arnoux, JB | 1 |
| Schiff, M | 1 |
| Heilbronner, C | 1 |
| Salvador, E | 1 |
| Debray, D | 1 |
| Oualha, M | 1 |
| Renolleau, S | 1 |
| Girard, M | 1 |
| de Lonlay, P | 1 |
| Abdin, A | 1 |
| Sarhan, N | 1 |
| Brannelly, NT | 1 |
| Hamilton-Shield, JP | 1 |
| Killard, AJ | 1 |
| Link, A | 1 |
| Kaplan, BT | 1 |
| Böhm, M | 1 |
| Brown, RE | 1 |
| Forman, DT | 1 |
| Holt, JT | 1 |
| Arvan, DA | 1 |
| Mayer, TK | 1 |
| D'Eufemia, P | 1 |
| Corrado, G | 1 |
| Sabetta, G | 1 |
| Castro, M | 1 |
| Martino, F | 1 |
| Cantani, A | 1 |
| Ruberto, U | 1 |
| Meier, FA | 1 |
| Baron, JA | 1 |
| Greenberg, ER | 1 |
| Visek, WJ | 3 |
| Yoshida, I | 3 |
| Yamashita, F | 2 |
| Sugimoto, T | 2 |
| Nishida, N | 2 |
| Yasuhara, A | 1 |
| Ono, A | 1 |
| Sakane, Y | 1 |
| Matsumura, T | 1 |
| Zaccara, G | 1 |
| Boncinelli, L | 1 |
| Paganini, M | 1 |
| Campostrini, R | 1 |
| Arnetoli, G | 1 |
| Zappoli, R | 1 |
| Powell-Jackson, PR | 1 |
| Tredger, JM | 1 |
| Williams, R | 1 |
| Rarey, KE | 1 |
| Rush, NL | 1 |
| Davis, JA | 1 |
| Deshmukh, DR | 7 |
| Plauth, M | 1 |
| Heubi, JE | 1 |
| Daugherty, CC | 1 |
| Partin, JS | 2 |
| Partin, JC | 3 |
| Schubert, WK | 2 |
| Deshmukh, GD | 1 |
| Shope, TC | 1 |
| Radin, NS | 1 |
| Awrich, P | 1 |
| Madge, GE | 1 |
| Wolf, B | 1 |
| Tomaszewski, L | 1 |
| Crocker, JF | 3 |
| Van Gennip, AH | 1 |
| Van Bree-Blom, EJ | 1 |
| Grift, J | 1 |
| DeBree, PK | 1 |
| Wadman, SK | 1 |
| Shaywitz, BA | 4 |
| Rothstein, P | 1 |
| Venes, JL | 3 |
| Chaves-Carballo, E | 1 |
| Ellefson, RD | 1 |
| Maassab, HF | 2 |
| Mason, M | 3 |
| DeLong, GR | 3 |
| Glick, TH | 3 |
| Rasenack, U | 1 |
| Tonsgard, JH | 2 |
| Huttenlocher, PR | 1 |
| Thisted, RA | 1 |
| Rittenhouse, JW | 1 |
| Baublis, JV | 2 |
| Kao, W | 1 |
| Trauner, DA | 3 |
| Kang, ES | 1 |
| Schwenzer, KS | 1 |
| Wall, HP | 1 |
| Jabbour, JT | 1 |
| Shade, R | 1 |
| Crofton, JT | 1 |
| Share, L | 1 |
| Fitzgerald, JF | 2 |
| Clark, JH | 2 |
| Angelides, AG | 1 |
| Wyllie, R | 1 |
| Stumpf, DA | 1 |
| Parks, JK | 1 |
| Cox, KL | 1 |
| Cannon, RA | 1 |
| McArthur, BS | 1 |
| Arcinue, EL | 3 |
| Schultz, GE | 1 |
| Yokoi, T | 1 |
| Honke, K | 1 |
| Funabashi, T | 1 |
| Hayashi, R | 1 |
| Suzuki, Y | 1 |
| Taniguchi, N | 1 |
| Hosoya, M | 1 |
| Saheki, T | 1 |
| Boutros, AR | 1 |
| Esfandiari, S | 1 |
| Orlowski, JP | 1 |
| Smith, JS | 1 |
| Treem, WR | 1 |
| Badizadegan, K | 1 |
| Perez-Atayde, AR | 1 |
| Bik-Multanowski, M | 1 |
| Belay, ED | 1 |
| Bresee, JS | 1 |
| Holman, RC | 1 |
| Khan, AS | 1 |
| Shahriari, A | 1 |
| Schonberger, LB | 1 |
| Forget, PP | 1 |
| van Oosterhout, M | 1 |
| Bakker, JA | 1 |
| Wermuth, B | 1 |
| Vles, JS | 1 |
| Spaapen, LJ | 1 |
| Barr, RE | 1 |
| Ackmann, JJ | 1 |
| Harrington, GJ | 1 |
| Varma, RR | 2 |
| Lewis, JD | 1 |
| Casper, JT | 2 |
| Applegarth, DA | 1 |
| MacLeod, PM | 1 |
| Toone, JR | 1 |
| Kirby, LT | 1 |
| MacLean, JR | 1 |
| Mamer, OA | 1 |
| Montgomery, JA | 1 |
| Brown, T | 2 |
| Hug, G | 2 |
| Lansky, L | 2 |
| Bove, K | 1 |
| Scheve, A | 1 |
| Ryan, M | 1 |
| Brown, H | 2 |
| Lloyd-Still, J | 1 |
| Glasgow, AM | 5 |
| Chase, HP | 3 |
| Spencer, DD | 1 |
| De Vivo, DC | 1 |
| Haller, JS | 1 |
| Venes, J | 1 |
| Cohen, DJ | 1 |
| Bowers, MB | 1 |
| Trauner, D | 1 |
| Sweetman, L | 3 |
| Holm, J | 1 |
| Kulovich, S | 1 |
| Nyhan, WL | 2 |
| Smith, VS | 1 |
| Mikesell, D | 1 |
| Stoker, JA | 1 |
| Thaler, MM | 3 |
| Aicardi, J | 1 |
| Diebler, C | 1 |
| Devivo, DC | 1 |
| Keating, JP | 1 |
| Stockard, JJ | 1 |
| Leventhal, JM | 1 |
| Kramer, MS | 1 |
| Yamada, T | 1 |
| Young, S | 1 |
| Kimura, J | 1 |
| Corey, L | 2 |
| Rubin, RJ | 2 |
| Bregman, D | 1 |
| Gregg, MB | 1 |
| Hattwick, MA | 1 |
| Chesney, RW | 1 |
| McPherson, E | 1 |
| Hall, D | 1 |
| Segar, WE | 1 |
| Hutton, JT | 1 |
| Levy, BS | 1 |
| Hosfield, WB | 1 |
| Tang, TT | 2 |
| Siegesmund, KA | 2 |
| Sedmak, GV | 1 |
| McCreadie, SR | 2 |
| Shannon, DC | 1 |
| De Long, R | 1 |
| Bercu, B | 1 |
| Glick, T | 1 |
| Herrin, JT | 1 |
| Moylan, FM | 1 |
| Todres, ID | 1 |
| Lovejoy, FH | 2 |
| Bresnan, MJ | 2 |
| Lombroso, CT | 1 |
| Smith, AL | 3 |
| Sunakorn, P | 1 |
| Snodgrass, PJ | 1 |
| Gosseye, S | 1 |
| De Meyer, R | 1 |
| Maldague, P | 1 |
| Ernst, T | 1 |
| Ross, BD | 1 |
| Flores, R | 1 |
| Murphy, MG | 1 |
| Jollimore, C | 1 |
| Her, H | 1 |
| Mukhopadhyay, A | 1 |
| Sarnaik, AP | 2 |
| Rabier, D | 1 |
| Parvy, P | 1 |
| Bardet, J | 1 |
| Kamoun, P | 1 |
| Woo, M | 1 |
| Araki, A | 1 |
| Murakami, K | 1 |
| Kobayashi, Y | 1 |
| Mizoguchi, K | 1 |
| Sukehiro, K | 1 |
| Ogata, M | 1 |
| Onizuka, S | 1 |
| Watanabe, J | 1 |
| Yoshino, M | 2 |
| Chi, CS | 1 |
| Law, KL | 1 |
| Wong, TT | 1 |
| Su, GY | 1 |
| Lin, N | 1 |
| Hart, MA | 1 |
| Swisher, JA | 1 |
| Caspers, ML | 1 |
| Gomirato, G | 1 |
| Giaretto, G | 1 |
| Bonomi, A | 1 |
| Rossi, E | 1 |
| Rovere, A | 1 |
| Radeschi, G | 1 |
| Crosato, M | 1 |
| Thomas, PE | 1 |
| Matsuda, I | 2 |
| Ohtani, Y | 2 |
| Ninomiya, N | 1 |
| Walter, JH | 1 |
| Clayton, PT | 1 |
| Leonard, JV | 1 |
| Békési, A | 1 |
| Kerepesi, T | 1 |
| Szombathy, G | 1 |
| Karsai, T | 1 |
| Kopieczna-Grzebieniak, E | 1 |
| Tarnawski, R | 1 |
| Toborek, M | 1 |
| Jakubowska, D | 1 |
| Ohyanagi, K | 1 |
| Yamamoto, S | 1 |
| Shoemaker, JD | 1 |
| Granot, E | 1 |
| Matoth, I | 1 |
| Lotan, C | 1 |
| Shvil, Y | 1 |
| Lijovetzky, G | 1 |
| Yatziv, S | 1 |
| Holtzhauer, FJ | 1 |
| Campbell, RJ | 1 |
| Hall, LJ | 1 |
| Halpin, TJ | 1 |
| Meites, S | 1 |
| Bubis, S | 1 |
| Kimura, A | 1 |
| Ono, E | 1 |
| Matsuishi, T | 1 |
| Yamamoto, M | 1 |
| Hashimoto, T | 1 |
| Shinka, T | 1 |
| Kuhara, T | 1 |
| Renton, KW | 1 |
| Lee, SH | 1 |
| Rozee, KR | 1 |
| Digout, SC | 1 |
| Malatjalian, DA | 1 |
| Yoder, MC | 1 |
| Egler, JM | 1 |
| Yudkoff, M | 1 |
| Chatten, J | 1 |
| Douglas, SD | 1 |
| Polin, RA | 1 |
| Nagamori, K | 1 |
| Hansen, JR | 1 |
| McCray, PB | 1 |
| Bale, JF | 1 |
| Corbett, AJ | 1 |
| Flanders, DJ | 1 |
| Drewes, LR | 1 |
| Leino, RL | 1 |
| Mitchell, RA | 2 |
| Ram, ML | 1 |
| Sinniah, D | 1 |
| Schwartz, PH | 1 |
| Hoogenraad, NJ | 1 |
| Boswell, M | 1 |
| Lazoff, S | 1 |
| Renschler, A | 1 |
| Samaha, FJ | 1 |
| Blau, E | 1 |
| Berardinelli, JL | 1 |
| Dhiensiri, K | 1 |
| Good, TA | 1 |
| Dorrington, AJ | 1 |
| Wood, JN | 1 |
| Victor, DI | 1 |
| Adams, PC | 1 |
16 reviews available for ammonium hydroxide and Fatty Liver with Encephalopathy
| Article | Year |
|---|---|
The Measurement of Ammonia in Human Breath and its Potential in Clinical Diagnostics.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Breath Tests; Humans; Hyperinsulinism; Hypoglycemia; | 2016 |
The biochemistry of Reye's syndrome.
Topics: Abdomen; Acid-Base Imbalance; Adipose Tissue; Alanine Transaminase; Amino Acids; Ammonia; Aspartate | 1982 |
[Congenital deficiency of ornithine transcarbamylase. Description of 2 clinical cases].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Diagnosis, Differential; Female; Humans; Infant; Infa | 1983 |
Reye's syndrome. A review from the forensic viewpoint.
Topics: Aflatoxins; Ammonia; Child; Coroners and Medical Examiners; Forensic Medicine; Humans; Infant; Insec | 1983 |
An update of concepts of essential amino acids.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Ammonia; Animals; Arginine; Atrophy; C | 1984 |
[Etiological mechanism of Reye's syndrome--from the viewpoint of metabolic disorders].
Topics: Ammonia; Animals; Aspirin; Child; Child, Preschool; Fatty Acids; Female; Humans; Infant; Male; Mitoc | 1984 |
Hepatotoxicity to sodium valproate: a review.
Topics: Adolescent; Adult; Ammonia; Animals; Chemical and Drug Induced Liver Injury; Child; Child, Preschool | 1984 |
[Reye's syndrome].
Topics: Aflatoxins; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Child; Humans; Hypoglycins; Leucine; Mi | 1982 |
Reye's syndrome.
Topics: Aflatoxins; Ammonia; Animals; Biopsy; Chickenpox; Child; Child, Preschool; Diagnosis, Differential; | 1982 |
Encephalopathy of Reye's syndrome: a review of pathogenetic hypotheses.
Topics: Acidosis; Ammonia; Animals; Brain; Citrulline; Fatty Acids, Nonesterified; Glucose; Humans; Insulin; | 1982 |
Inherited and acquired syndromes of hyperammonemia and encephalopathy in children.
Topics: Ammonia; Child; Hepatic Encephalopathy; Humans; Liver Diseases; Metabolism, Inborn Errors; Reye Synd | 1994 |
[Inherited hyperammonemia].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Consciousness Disorders; Diagnosis, Differential; Hum | 1998 |
Metabolic mechanisms in Reye syndrome. End of a Mystery?
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Aspirin; Brain Diseases; Carbamoyl-Phosphate Synthase | 1976 |
[Reye's syndrome].
Topics: Ammonia; Fatty Liver; Humans; Hypoglycemia; Liver; Metabolism, Inborn Errors; Mitochondria, Liver; R | 1976 |
Reye's syndrome.
Topics: Ammonia; Blood Coagulation Disorders; Brain; Brain Diseases; Child; Clinical Enzyme Tests; Electroen | 1976 |
Orotic acid, arginine, and hepatotoxicity.
Topics: Adult; Alcoholism; Ammonia; Animals; Arginine; Dietary Fats; Dietary Proteins; Ethanol; Fasting; Fer | 1986 |
99 other studies available for ammonium hydroxide and Fatty Liver with Encephalopathy
| Article | Year |
|---|---|
What are the clues for an inherited metabolic disorder in Reye syndrome? A single Centre study of 58 children.
Topics: Acidosis; Ammonia; Child; Child, Preschool; Humans; Metabolic Diseases; Retrospective Studies; Reye | 2022 |
Resveratrol protects against experimental induced Reye's syndrome by prohibition of oxidative stress and restoration of complex I activity.
Topics: Ammonia; Animals; Antioxidants; Electron Transport Complex I; Fatty Acids, Monounsaturated; Malondia | 2014 |
[21-year-old woman with Reye's syndrome after influenza].
Topics: Ammonia; Anti-Inflammatory Agents, Non-Steroidal; Aspirin; Brain Edema; Diagnosis, Differential; Ele | 2012 |
Masking by enzyme inhibitor of raised serum glutamate dehydrogenase activity in Reye's syndrome.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Clinical Enzyme Tests; Dialysis; F | 1983 |
Reye-like syndrome associated with valproic acid.
Topics: Adolescent; Ammonia; Biopsy; Female; Humans; Liver; Liver Function Tests; Reye Syndrome; Status Epil | 1983 |
Treatment of epileptic patients with valproic acid does not modify plasma and urine short-chain-fatty acids.
Topics: Adolescent; Adult; Ammonia; Brain Diseases; Butyrates; Epilepsy; Fatty Acids; Female; Hemiterpenes; | 1983 |
Altered auditory brainstem evoked responses in the ferret model for Reye's syndrome.
Topics: Ammonia; Animals; Aspirin; Audiometry; Audiometry, Evoked Response; Brain Stem; Disease Models, Anim | 1984 |
[Reye syndrome--a status review of current concepts of its pathogenesis].
Topics: Aflatoxins; Ammonia; Aspirin; Carbamoyl-Phosphate Synthase (Ammonia); Child; Fatty Acids, Nonesterif | 1984 |
Grade I Reye's syndrome--outcome and predictors of progression to deeper coma grades.
Topics: Ammonia; Child; Female; Hepatic Encephalopathy; Humans; Liver; Male; Prognosis; Prothrombin Time; Re | 1984 |
Free fatty acids in an animal model of Reye's syndrome.
Topics: Ammonia; Animals; Aspirin; Carnivora; Diet; Disease Models, Animal; Fatty Acids, Nonesterified; Ferr | 1983 |
Fatty liver and kidney syndrome in chickens as an animal model for Reye's syndrome.
Topics: Ammonia; Animals; Blood Glucose; Carbon-Carbon Ligases; Carboxy-Lyases; Chickens; Disease Models, An | 1983 |
Urinary purines and pyrimidines in patients with hyperammonemia of various origins.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria | 1980 |
Monitoring and management of increased intracranial pressure in Reye syndrome: results in 29 children.
Topics: Adolescent; Ammonia; Barbiturates; Child; Child, Preschool; Female; Humans; Infant; Intracranial Pre | 1980 |
Tissue lipids in hyperammonemic encephalopathies of childhood.
Topics: Adipose Tissue; Adolescent; Ammonia; Brain; Brain Diseases, Metabolic; Child; Child, Preschool; Chol | 1980 |
Interactions of aspirin and other potential etiologic factors in an animal model of Reye syndrome.
Topics: Ammonia; Animals; Arginine; Aspartate Aminotransferases; Aspirin; Diet; Disease Models, Animal; Ferr | 1982 |
[Reye syndrome: clinical course and therapy].
Topics: Ammonia; Glucose; Insulin; Reye Syndrome | 1982 |
Lactic acidemia in Reye's syndrome.
Topics: Acidosis; Ammonia; Blood Glucose; Coma; Humans; Lactates; Pyruvate Carboxylase; Pyruvate Dehydrogena | 1982 |
Ammonia metabolism in Reye syndrome and the effect of citrulline.
Topics: Ammonia; Child; Citrulline; Humans; Male; Metabolic Clearance Rate; Nitrogen; Reye Syndrome; Urea | 1982 |
Serum ornithine carbamyl transferase activities in Reye's syndrome.
Topics: Alanine Transaminase; Ammonia; Aspartate Aminotransferases; Child; Humans; Liver; Ornithine Carbamoy | 1982 |
Serum enzyme alterations in arginine-deficient, influenza-infected ferrets: a potential animal model of Reye's syndrome.
Topics: Ammonia; Animals; Arginine; Aspartate Aminotransferases; Disease Models, Animal; Ferrets; Humans; In | 1982 |
Reye's syndrome.
Topics: Adolescent; Ammonia; Child; Child, Preschool; Diagnosis, Differential; Fatty Acids; Humans; Infant; | 1982 |
Urea, altered renal function, and vasopressin in Reye-Johnson syndrome.
Topics: Amino Acids; Ammonia; Blood Urea Nitrogen; Child; Electrolytes; Humans; Kidney Diseases; Reye Syndro | 1982 |
The prognostic significance of peak ammonia levels in Reye syndrome.
Topics: Adolescent; Adult; Ammonia; Child; Child, Preschool; Female; Humans; Infant; Male; Prognosis; Reye S | 1982 |
Urea cycle regulation: I. Coupling of ornithine metabolism to mitochondrial oxidative phosphorylation.
Topics: Adenosine Triphosphate; Ammonia; Animals; Citric Acid Cycle; Citrulline; Glutamate Dehydrogenase; Ke | 1980 |
Recurrent Reye's syndrome without liver lipid deposition.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child, Preschool; Diagnosis, Differential; Female; Hu | 1981 |
Total alpha-amino acid nitrogen quantification as prognosticator in Reye's syndrome.
Topics: Amino Acids; Ammonia; Humans; Nitrogen; Prognosis; Reye Syndrome | 1981 |
Partial ornithine transcarbamylase deficiency simulating Reye syndrome.
Topics: Ammonia; Diagnosis, Differential; Humans; Hydrogen-Ion Concentration; Infant; Liver; Male; Ornithine | 1981 |
Reye syndrome: a predictably curable disease.
Topics: Adolescent; Adult; Ammonia; Barbiturates; Child; Child, Preschool; Diuretics, Osmotic; Hemodynamics; | 1980 |
Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance.
Topics: Adolescent; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Preschool; Diagnosis, Dif | 1997 |
Reye's syndrome in the United States from 1981 through 1997.
Topics: Adolescent; Age Factors; Ammonia; Child; Child, Preschool; Female; Humans; Incidence; Infant; Male; | 1999 |
Partial N-acetyl-glutamate synthetase deficiency masquerading as a valproic acid-induced Reye-like syndrome.
Topics: Ammonia; Child, Preschool; Glutamate Synthase; Humans; Liver Function Tests; Male; Reye Syndrome; Va | 1999 |
Computerized evaluation of electroencephalographic changes accompanying exchange transfusion in Reye's syndrome.
Topics: Adolescent; Ammonia; Animals; Aspartate Aminotransferases; Chick Embryo; Child; Child, Preschool; Co | 1977 |
Organic acids and Reye's syndrome.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Diagnosis, Di | 1979 |
Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome.
Topics: Age Factors; Ammonia; Brain Diseases; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Preschoo | 1976 |
Exchange transfusion to remove ammonia.
Topics: Adult; Age Factors; Ammonia; Brain Diseases; Child; Evaluation Studies as Topic; Exchange Transfusio | 1975 |
Management of severe cerebral edema in the metabolic encephalopathy of Reye-Johnson syndrome.
Topics: Adolescent; Ammonia; Brain Edema; Cerebrospinal Fluid; Child; Child, Preschool; Female; Humans; Infa | 1978 |
Reye syndrome: a metabolic response to an acute mitochondrial insult?
Topics: Acute Disease; Adolescent; Adult; Ammonia; Brain Edema; Child; Coma; Diagnosis, Differential; Female | 1978 |
Recent developments in etiology and therapy of Reye syndrome.
Topics: Ammonia; Child, Preschool; Exchange Transfusion, Whole Blood; Fatty Acids, Nonesterified; Glutamates | 1978 |
Reye syndrome: monoamine metabolites in ventricular fluid.
Topics: Adolescent; Ammonia; Brain Edema; Child; Child, Preschool; Dopamine; Female; Homovanillic Acid; Huma | 1979 |
Biochemical correlates of illness and recovery in Reye's syndrome.
Topics: Amino Acids; Ammonia; Child; Child, Preschool; Exchange Transfusion, Whole Blood; Fatty Acids, Volat | 1977 |
The use of lactulose syrup for the control of hyperammonemia in Reye's syndrome: report of case.
Topics: Ammonia; Child; Disaccharides; Humans; Lactulose; Male; Reye Syndrome | 1978 |
EEG correlations with biochemical abnormalities in Reye syndrome.
Topics: Ammonia; Blood Glucose; Butyrates; Electroencephalography; Female; Humans; Infant; Propionates; Reye | 1977 |
Prolonged continuous monitoring of intracranial pressure in severe Reye's syndrome.
Topics: Ammonia; Brain Edema; Child, Preschool; Dexamethasone; Exchange Transfusion, Whole Blood; Female; Gl | 1977 |
Significance of positive spike burst in Reye syndrome.
Topics: Acoustic Stimulation; Adolescent; Alkaline Phosphatase; Ammonia; Aspartate Aminotransferases; Child; | 1977 |
Potential hazard of therapy for Reye's syndrome with urea cycle intermediates.
Topics: Ammonia; Humans; Ornithine; Orotic Acid; Reye Syndrome; Urea | 1977 |
Diagnostic criteria for influenza B-associated Reye's syndrome: clinical vs. pathologic criteria.
Topics: Acid-Base Imbalance; Ammonia; Aspirin; Humans; Hypoglycemia; Influenza, Human; Liver Function Tests; | 1977 |
Reye's syndrome: clinical progression and evaluation of therapy.
Topics: Ammonia; Child; Coma; Evaluation Studies as Topic; Exchange Transfusion, Whole Blood; Hospitalizatio | 1977 |
Effect of propionic acid on fatty acid oxidation and ureagenesis.
Topics: Ammonia; Animals; Carbon Dioxide; Fatty Acids; Fatty Liver; Fibroblasts; Liver; Methylmalonic Acid; | 1976 |
Letter: Severe mixed metabolic and respiratory alkalosis in Reye syndrome.
Topics: Alkalosis; Alkalosis, Respiratory; Ammonia; Bicarbonates; Brain Diseases; Carbon Dioxide; Child, Pre | 1976 |
Reye's syndrome.
Topics: Adolescent; Ammonia; Antiemetics; Bilirubin; Blood Glucose; Brain Diseases; Child; Child, Preschool; | 1975 |
Production of the features of Reye's syndrome in rats with 4-pentenoic acid.
Topics: Ammonia; Animals; Aspartate Aminotransferases; Brain Diseases; Fasting; Fatty Acids, Nonesterified; | 1975 |
Short-chain organic acidemia and Reye's syndrome.
Topics: Adolescent; Ammonia; Blood Glucose; Blood Urea Nitrogen; Brain Diseases; Butyrates; Child; Child, Pr | 1975 |
Reye syndrome. A correlated electron-microscopic, viral, and biochemical observation.
Topics: Adolescent; Ammonia; Antibodies, Viral; Antibody Formation; Autopsy; Biopsy, Needle; Brain Diseases; | 1975 |
Pathogenesis of Reye's syndrome: A working hypothesis.
Topics: Ammonia; Arginine; Brain Diseases; Child; Humans; Ornithine; Reye Syndrome | 1975 |
Studies on the pathophysiology of encephalopathy in Reye's syndrome; Hyperammonemia in Reye's syndrome.
Topics: Acid-Base Imbalance; Ammonia; Brain; Brain Diseases; Child; Humans; Hyperventilation; Lactates; Reye | 1975 |
Anticerebral oedema therapy in Reye's syndrome.
Topics: Adolescent; Ammonia; Brain Diseases; Brain Edema; Child; Dexamethasone; Female; Glycerol; Humans; In | 1975 |
Cerebrospinal fluid glutamine in Reye's syndrome.
Topics: Ammonia; Brain Diseases; Child; Child, Preschool; Glutamine; Hepatic Encephalopathy; Humans; Infant; | 1975 |
Urea-cycle enzyme deficiencies and an increased nitrogen load producing hyperammonemia in Reye's syndrome.
Topics: Adolescent; Adult; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Brain Diseases; C | 1976 |
Editorial: Ammonia disposal in Reye's syndrome.
Topics: Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Brain Diseases; Carbamoyl-Phosphate | 1976 |
Reye's syndrome without fatty liver.
Topics: Ammonia; Brain Diseases; Child, Preschool; Humans; Liver; Male; Reye Syndrome | 1976 |
Cerebral MRS in infant with suspected Reye's syndrome.
Topics: Ammonia; Brain Chemistry; Humans; Infant; Magnetic Resonance Spectroscopy; Male; Reye Syndrome | 1992 |
Beta-oxidation of [1-14C]palmitic acid by mouse astrocytes in primary culture: effects of agents implicated in the encephalopathy of Reye's syndrome.
Topics: Ammonia; Animals; Animals, Newborn; Astrocytes; Body Water; Cells, Cultured; Child; Child, Preschool | 1992 |
Interactions of ibuprofen with influenza infection and hyperammonemia in an animal model of Reye's syndrome.
Topics: Alanine Transaminase; Ammonia; Animals; Arginine; Aspartate Aminotransferases; Diet; Disease Models, | 1992 |
[Hyperlysinemia and hyperammonemia].
Topics: Ammonia; Female; Humans; Infant, Newborn; Lysine; Male; Metabolism, Inborn Errors; Retrospective Stu | 1991 |
The effect of L-carnitine supplementation in 4 pentenoic acid treated rats.
Topics: Ammonia; Animals; Blood Glucose; Carnitine; Disease Models, Animal; Fatty Acids, Monounsaturated; Fa | 1990 |
A case of ornithine transcarbamylase deficiency with acute and late onset simulating Reye's syndrome in an adult male.
Topics: Adolescent; Ammonia; Humans; Male; Ornithine Carbamoyltransferase Deficiency Disease; Reye Syndrome | 1990 |
Continuous monitoring of intracranial pressure in Reye's syndrome--5 years experience.
Topics: Ammonia; Child, Preschool; Female; Humans; Infant; Intracranial Pressure; Male; Monitoring, Physiolo | 1990 |
Alterations in plasma amino acids and hepatic enzymes in the 4-pentenoic acid model of Reye's syndrome.
Topics: Amino Acids; Ammonia; Animals; Disease Models, Animal; Fatty Acids, Monounsaturated; Glutamate Dehyd | 1989 |
[Remarks on a clinical case of partial carbamyl phosphate synthetase deficiency].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); D | 1989 |
Arginine deficiency, hyperammonemia and Reye's syndrome in ferrets.
Topics: Ammonia; Animals; Animals, Laboratory; Arginine; Carnivora; Disease Models, Animal; Ferrets; Influen | 1985 |
Renal handling of carnitine in children with carnitine deficiency and hyperammonemia associated with valproate therapy.
Topics: Ammonia; Carnitine; Epilepsy; Humans; Infant; Intellectual Disability; Kidney; Metabolic Clearance R | 1986 |
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Genetic Carrier Screening; Humans; Hypoglycem | 1986 |
[Reye's syndrome: management of hyperammonemia by essential amino acid-ketoacid substitution].
Topics: Amino Acids, Essential; Ammonia; Blood Urea Nitrogen; Fluid Therapy; Humans; Infant; Keto Acids; Mal | 1988 |
[Hyperammonemias of childhood. III. Acquired diseases].
Topics: Ammonia; Carnitine; Diagnosis, Differential; Erythroblastosis, Fetal; Humans; Infant, Newborn; Reye | 1988 |
Hyperammonemia related to carnitine metabolism with particular emphasis on ornithine transcarbamylase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Benzoates; Benzoic Acid; Carnitine; Child; Dietary Pr | 1987 |
Partial carbamyl phosphate synthetase deficiency, simulating Reye's syndrome, in a 9-year-old girl.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Diagnosis, Differential; Female; Humans; Reye | 1986 |
Reye's syndrome. An epidemiologic analysis of mild disease.
Topics: Acetaminophen; Ammonia; Aspirin; Bilirubin; Female; Humans; Male; Reye Syndrome | 1986 |
Diagnostic quality of laboratory tests as evaluated by graphic comparison of "first test" data, with Reye's syndrome "workup" assays as a model.
Topics: Alanine Transaminase; Ammonia; Aspartate Aminotransferases; Blood Chemical Analysis; Blood Glucose; | 1987 |
Acute encephalopathy with hyperammonemia and dicarboxylic aciduria during calcium hopantenate therapy: a patient report.
Topics: Acute Disease; Ammonia; Brain Diseases; Child, Preschool; Female; gamma-Aminobutyric Acid; Humans; P | 1986 |
Arginine and disease states.
Topics: Ammonia; Animals; Arginine; Blood Glucose; Humans; Insulin; Lipid Metabolism; Liver Diseases; Male; | 1985 |
Biochemical and morphological characteristics of a mouse model of Reye's syndrome induced by the interaction of influenza B virus and a chemical emulsifier.
Topics: Ammonia; Animals; Animals, Suckling; Disease Models, Animal; Emulsions; Female; Influenza B virus; L | 1986 |
Metabolic and mitochondrial morphological changes that mimic Reye syndrome after endotoxin administration to rats.
Topics: Alanine Transaminase; Ammonia; Animals; Aspartate Aminotransferases; Blood Glucose; Disease Models, | 1985 |
Confirmation of serum salicylate levels in Reye's syndrome: a comparison between the Natelson colorimetric method and high performance liquid chromatography.
Topics: Ammonia; Aspirin; Child; Chromatography, High Pressure Liquid; Colorimetry; Humans; Reye Syndrome; S | 1985 |
Urinary dicarboxylic acids in Reye syndrome.
Topics: Ammonia; Child; Chromatography, Gas; Creatinine; Dicarboxylic Acids; Humans; Ketone Bodies; Lactates | 1985 |
Reye syndrome associated with aspirin therapy for systemic lupus erythematosus.
Topics: Adolescent; Ammonia; Aspartate Aminotransferases; Aspirin; Biopsy, Needle; Electroencephalography; F | 1985 |
Neuron-specific mitochondrial degeneration induced by hyperammonemia and octanoic acidemia.
Topics: Ammonia; Animals; Brain; Caprylates; Disease Models, Animal; Dogs; In Vitro Techniques; Mitochondria | 1985 |
Prognosis and diagnosis of Reye syndrome by discriminant analysis.
Topics: Ammonia; Bilirubin; Blood Chemical Analysis; Child; Diagnosis, Differential; Factor Analysis, Statis | 1985 |
Investigation of an animal model of a Reye-like syndrome caused by Margosa oil.
Topics: Alanine Transaminase; Ammonia; Animals; Aspartate Aminotransferases; Blood Glucose; Brain Edema; Dis | 1985 |
Editorial: Encephalopathy and fatty degeneration of viscera.
Topics: Age Factors; Ammonia; Arginine; Brain Diseases; Chickenpox; Child; Fatty Liver; Humans; Influenza, H | 1974 |
Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency.
Topics: Ammonia; Brain Diseases; Child; Fatty Liver; Female; Hepatic Encephalopathy; Humans; Kinetics; Liver | 1974 |
Letter: Reye's syndrome.
Topics: Ammonia; Brain Diseases; Child; Female; Humans; Liver; Liver Function Tests; Male; Ornithine Carbamo | 1974 |
Letter: Carbamyl phosphate synthetase and ornithine transcarbamylase in liver of Reye's syndrome.
Topics: Ammonia; Brain Diseases; Child; Humans; Liver; Ornithine Carbamoyltransferase; Phosphotransferases; | 1974 |
Letter: Clinical staging in Reye syndrome.
Topics: Adolescent; Ammonia; Blood Glucose; Brain Diseases; Child; Child, Preschool; Humans; Infant; Male; P | 1974 |
Lean Reye syndrome.
Topics: Adult; Age Factors; Alanine Transaminase; Ammonia; Aspartate Aminotransferases; Brain Diseases; Diag | 1973 |
Reye's syndrome:clinical diagnosis and treatment with peritoneal dialysis.
Topics: Acid-Base Equilibrium; Adolescent; Alanine Transaminase; Ammonia; Arginine; Aspartate Aminotransfera | 1974 |
Improved assay for spinal fluid glutamine, and values for children with Reye's syndrome.
Topics: Ammonia; Brain Diseases; Deamination; Fatty Liver; Glutaminase; Glutamine; Humans; Methods; Reye Syn | 1974 |
Reye's syndrome: clinical delineation and evaluation.
Topics: Adolescent; Ammonia; Brain Diseases; Child; Child, Preschool; Dexamethasone; Exchange Transfusion, W | 1974 |
Clinical staging in Reye syndrome.
Topics: Adolescent; Ammonia; Blood Glucose; Brain Diseases; Brain Edema; Cerebrospinal Fluid Proteins; Child | 1974 |
Letter: Citrulline for Reye's syndrome.
Topics: Ammonia; Brain Diseases; Citrulline; Fatty Liver; Reye Syndrome | 1974 |