leucine has been researched along with Chronic Progressive External Ophthalmoplegia with Myopathy 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 | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Emma, F; Salviati, L | 1 |
| Ceuterick-De Groote, C; De Meirleir, L; Lissens, W; Meire, F; Seneca, S; Van Coster, R; Verhelst, H | 1 |
2 review(s) available for leucine and Chronic Progressive External Ophthalmoplegia with Myopathy
| Article | Year |
|---|---|
Mitochondrial cytopathies and the kidney.
Topics: DNA, Mitochondrial; Fanconi Syndrome; Humans; Kearns-Sayre Syndrome; Kidney Diseases; Leucine; Mitochondria; Mitochondrial Myopathies; Mutation; Oxidative Phosphorylation | 2017 |
A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.
Topics: Adult; Atrophy; Brain; DNA, Mitochondrial; Humans; Kearns-Sayre Syndrome; Leucine; Magnetic Resonance Imaging; Male; Mitochondria, Muscle; Muscle, Skeletal; Phenotype; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; RNA | 2001 |