leucine has been researched along with Encephalomyopathies, Mitochondrial in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Buchman, A; Hirano, I; Hirano, M; MartÃ, R; Poorthuis, BJ; Tadesse, S; van Gennip, AH; van Kuilenburg, AB; Verschuuren, JJ | 1 |
| Koch, G; Mariman, E; Okhuijsen-Kroes, EJ; Sengers, RC; Smeitink, JA; Trijbels, JM; van den Heuvel, LP; Wendel, U | 1 |
1 review(s) available for leucine and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.
Topics: Acidosis, Lactic; Child, Preschool; Diagnosis, Differential; DNA, Mitochondrial; Failure to Thrive; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Infant, Premature, Diseases; Leucine; Male; MELAS Syndrome; Mitochondrial Encephalomyopathies; Muscle Hypotonia; Muscle, Skeletal; Mutation; Phenotype | 2001 |
1 other study(ies) available for leucine and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
Late-onset MNGIE due to partial loss of thymidine phosphorylase activity.
Topics: Arginine; Chromatography, High Pressure Liquid; Conserved Sequence; Female; Glycine; Humans; Leucine; Male; Middle Aged; Mitochondrial Encephalomyopathies; Polymorphism, Restriction Fragment Length; Thymidine Phosphorylase; Valine | 2005 |