ammonium hydroxide has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 4 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mitochondrial ornithine transporter deficiency, or HHH syndrome, is a metabolic disorder resulting in various neurologic symptoms, including mental retardation, spastic paraparesis with pyramidal signs, cerebellar ataxia, and episodic disturbance of consciousness or coma caused by hyperammonemia." | 3.71 | A novel mutation, P126R, in a Japanese patient with HHH syndrome. ( Hayakawa, C; Kanazawa, N; Miyamoto, T; Tsujino, S, 2002) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kumar, A | 1 |
| Bellar, A | 1 |
| Mishra, S | 1 |
| Sekar, J | 1 |
| Welch, N | 1 |
| Dasarathy, S | 1 |
| Mouadil, A | 1 |
| Debout, C | 1 |
| Read, MH | 1 |
| Morello, R | 1 |
| Allouche, S | 1 |
| Chapon, F | 1 |
| Tarnopolsky, M | 1 |
| Stevens, L | 1 |
| MacDonald, JR | 1 |
| Rodriguez, C | 1 |
| Mahoney, D | 1 |
| Rush, J | 1 |
| Maguire, J | 1 |
| Miyamoto, T | 1 |
| Kanazawa, N | 1 |
| Hayakawa, C | 1 |
| Tsujino, S | 1 |
4 other studies available for ammonium hydroxide and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
L-Isoleucine reverses hyperammonemia-induced myotube mitochondrial dysfunction and post-mitotic senescence.
Topics: Amino Acids, Branched-Chain; Ammonia; Animals; Humans; Hyperammonemia; Induced Pluripotent Stem Cell | 2024 |
Blood metabolite data in response to maximal exercise in healthy subjects.
Topics: Adult; Ammonia; Biomarkers; Energy Metabolism; Exercise; Exercise Test; Exercise Tolerance; Female; | 2012 |
Diagnostic utility of a modified forearm ischemic exercise test and technical issues relevant to exercise testing.
Topics: Adult; Ammonia; Catheterization, Peripheral; Eating; Exercise Test; Forearm; Glycogen Storage Diseas | 2003 |
A novel mutation, P126R, in a Japanese patient with HHH syndrome.
Topics: Adolescent; Ammonia; Base Sequence; Brain Diseases; Carrier Proteins; Cysts; DNA Primers; Exons; Gen | 2002 |