citrulline and Encephalomyopathies, Mitochondrial
citrulline has been researched along with Encephalomyopathies, Mitochondrial in 1 studies
Research
Studies (1)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Birk, OS; Ferreira, CR; Manor, E; Staretz-Chacham, O; Wormser, O | 1 |
Other Studies
1 other study(ies) available for citrulline and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
TMEM70 deficiency: Novel mutation and hypercitrullinemia during metabolic decompensation.
Topics: Child, Preschool; Citrulline; Electron Transport; Female; Frameshift Mutation; Humans; Hyperammonemia; Infant, Newborn; Male; Membrane Proteins; Mitochondrial Encephalomyopathies; Mitochondrial Proteins; Pedigree | 2019 |