glycine has been researched along with Encephalomyopathies, Mitochondrial in 3 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cerebral focal lesions in MELAS might have a metabolic nature and several pathogenetic mechanisms might be involved in the genesis of stroke-like episodes when there is a local increased ATP demand." | 1.32 | MELAS: clinical phenotype and morphological brain abnormalities. ( Bartolomei, L; Cavallaro, T; Grauso, M; Morelli, L; Piscioli, F; Rizzuto, N; Simonati, A; Sparaco, M, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sparaco, M | 1 |
| Simonati, A | 1 |
| Cavallaro, T | 1 |
| Bartolomei, L | 1 |
| Grauso, M | 1 |
| Piscioli, F | 1 |
| Morelli, L | 1 |
| Rizzuto, N | 1 |
| MartÃ, R | 1 |
| Verschuuren, JJ | 1 |
| Buchman, A | 1 |
| Hirano, I | 1 |
| Tadesse, S | 1 |
| van Kuilenburg, AB | 1 |
| van Gennip, AH | 1 |
| Poorthuis, BJ | 1 |
| Hirano, M | 1 |
| Fernandez-Moreira, D | 1 |
| Ugalde, C | 1 |
| Smeets, R | 1 |
| Rodenburg, RJ | 1 |
| Lopez-Laso, E | 1 |
| Ruiz-Falco, ML | 1 |
| Briones, P | 1 |
| Martin, MA | 1 |
| Smeitink, JA | 1 |
| Arenas, J | 1 |
3 other studies available for glycine and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
MELAS: clinical phenotype and morphological brain abnormalities.
Topics: Adenosine Triphosphatases; Adult; Alanine; Brain; Carboxylic Ester Hydrolases; Child; DNA, Mitochond | 2003 |
Late-onset MNGIE due to partial loss of thymidine phosphorylase activity.
Topics: Arginine; Chromatography, High Pressure Liquid; Conserved Sequence; Female; Glycine; Humans; Leucine | 2005 |
X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.
Topics: Animals; Arginine; DNA Mutational Analysis; Electron Transport Complex I; Electrophoresis, Gel, Two- | 2007 |