ammonium hydroxide has been researched along with Genetic Predisposition in 6 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Excerpt | Relevance | Reference |
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"This study was aimed at identifying genetic and non-genetic risk factors for valproic acid (VPA)-induced hyperammonaemia in Chinese paediatric patients with epilepsy." | 7.88 | Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy. ( Li, X; Zhang, T; Zhao, L; Zhu, X, 2018) |
"Valproic acid, which is widely used to treat various types of epilepsy, may cause severe hyperammonemia." | 7.80 | 4217C>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) |
"This study was aimed at identifying genetic and non-genetic risk factors for valproic acid (VPA)-induced hyperammonaemia in Chinese paediatric patients with epilepsy." | 3.88 | Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy. ( Li, X; Zhang, T; Zhao, L; Zhu, X, 2018) |
"Valproic acid, which is widely used to treat various types of epilepsy, may cause severe hyperammonemia." | 3.80 | 4217C>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) |
"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." | 2.45 | Gut ammonia production and its modulation. ( Galán, JJ; Jover, M; Romero-Gómez, M; Ruiz, A, 2009) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Bein, K | 1 |
Ganguly, K | 1 |
Martin, TM | 1 |
Concel, VJ | 1 |
Brant, KA | 1 |
Di, YPP | 1 |
Upadhyay, S | 1 |
Fabisiak, JP | 1 |
Vuga, LJ | 1 |
Kaminski, N | 1 |
Kostem, E | 1 |
Eskin, E | 1 |
Prows, DR | 1 |
Jang, AS | 1 |
Leikauf, GD | 1 |
Wei, YL | 1 |
Tian, Q | 1 |
Zhao, XX | 1 |
Qiu, GZ | 1 |
Xu, Y | 1 |
Zhu, X | 1 |
Li, X | 1 |
Zhang, T | 1 |
Zhao, L | 1 |
Inoue, K | 1 |
Suzuki, E | 1 |
Takahashi, T | 1 |
Yamamoto, Y | 1 |
Yazawa, R | 1 |
Takahashi, Y | 1 |
Imai, K | 1 |
Miyakawa, K | 1 |
Inoue, Y | 1 |
Tsuji, D | 1 |
Hayashi, H | 1 |
Itoh, K | 1 |
Mitchell, S | 1 |
Ellingson, C | 1 |
Coyne, T | 1 |
Hall, L | 1 |
Neill, M | 1 |
Christian, N | 1 |
Higham, C | 1 |
Dobrowolski, SF | 1 |
Tuchman, M | 1 |
Summar, M | 1 |
Romero-Gómez, M | 1 |
Jover, M | 1 |
Galán, JJ | 1 |
Ruiz, A | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Longitudinal Study of Urea Cycle Disorders[NCT00237315] | 1,009 participants (Anticipated) | Observational | 2006-02-28 | Recruiting | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
1 review available for ammonium hydroxide and Genetic Predisposition
Article | Year |
---|---|
Gut ammonia production and its modulation.
Topics: Ammonia; Animals; Genetic Predisposition to Disease; Glutaminase; Glutamine; Hepatic Encephalopathy; | 2009 |
5 other studies available for ammonium hydroxide and Genetic Predisposition
Article | Year |
---|---|
Genetic determinants of ammonia-induced acute lung injury in mice.
Topics: Acute Lung Injury; Ammonia; Animals; Female; Gene Expression Regulation; Genetic Markers; Genetic Pr | 2021 |
Association between MFN2 gene polymorphisms and the risk and prognosis of acute liver failure: a case-control study in a Chinese population.
Topics: Adult; Ammonia; Asian People; Case-Control Studies; China; Female; Gene Frequency; Genetic Predispos | 2017 |
Risk Factors for Valproic Acid-induced Hyperammonaemia in Chinese Paediatric Patients with Epilepsy.
Topics: Age Factors; Ammonia; Anticonvulsants; Aspartate Aminotransferases; Chemical and Drug Induced Liver | 2018 |
4217C>A polymorphism in carbamoyl-phosphate synthase 1 gene may not associate with hyperammonemia development during valproic acid-based therapy.
Topics: Alleles; Amino-Acid N-Acetyltransferase; Ammonia; Anticonvulsants; Asian People; Biomarkers, Pharmac | 2014 |
Genetic variation in the urea cycle: a model resource for investigating key candidate genes for common diseases.
Topics: Ammonia; Arginase; Argininosuccinate Lyase; Argininosuccinate Synthase; Argininosuccinic Aciduria; C | 2009 |