glycine has been researched along with Mitochondrial Myopathies in 4 studies
Mitochondrial Myopathies: A group of muscle diseases associated with abnormal mitochondria function.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 3 (75.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Taylor, RW | 1 |
Schaefer, AM | 1 |
McFarland, R | 1 |
Maddison, P | 1 |
Turnbull, DM | 1 |
Karadimas, CL | 1 |
Salviati, L | 1 |
Sacconi, S | 1 |
Chronopoulou, P | 1 |
Shanske, S | 1 |
Bonilla, E | 1 |
De Vivo, DC | 1 |
DiMauro, S | 1 |
Müller, T | 1 |
Deschauer, M | 1 |
Neudecker, S | 1 |
Zierz, S | 1 |
Dumoulin, R | 1 |
Sagnol, I | 1 |
Ferlin, T | 1 |
Bozon, D | 1 |
Stepien, G | 1 |
Mousson, B | 1 |
1 trial available for glycine and Mitochondrial Myopathies
Article | Year |
---|---|
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA.
Topics: Adult; Alleles; Base Sequence; DNA Mutational Analysis; DNA, Mitochondrial; Female; Glycine; Humans; | 2002 |
3 other studies available for glycine and Mitochondrial Myopathies
Article | Year |
---|---|
A novel mitochondrial DNA tRNA(Ile) (A4267G) mutation in a sporadic patient with mitochondrial myopathy.
Topics: Adult; Alanine; Biopsy; DNA, Mitochondrial; Electron Transport Complex IV; Female; Germ-Line Mutatio | 2002 |
Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.
Topics: Adult; Alanine; Disease Progression; DNA Mutational Analysis; DNA, Mitochondrial; Family Health; Fem | 2005 |
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.
Topics: Adult; Cytochrome b Group; DNA, Mitochondrial; Electron Transport Complex III; Exercise Tolerance; F | 1996 |