ammonium hydroxide has been researched along with Mitochondrial Diseases in 4 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
| 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 Mitochondrial Diseases
| 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 |