glycine has been researched along with MELAS in 4 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "The MELAS has been related to mutation A3243G in most cases, but some other mitochondrial DNA mutations were described in the background of this syndrome as well." | 1.37 | A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome. ( Gál, A; Lukács, T; Molnár, MJ; Reményi, V; Semjén, J; Valikovics, A; Vastagh, I, 2011) |
| "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 | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ikawa, M | 1 |
| Arakawa, K | 1 |
| Hamano, T | 1 |
| Nagata, M | 1 |
| Nakamoto, Y | 1 |
| Kuriyama, M | 1 |
| Koga, Y | 1 |
| Yoneda, M | 1 |
| Vastagh, I | 1 |
| Gál, A | 1 |
| Reményi, V | 1 |
| Semjén, J | 1 |
| Lukács, T | 1 |
| Valikovics, A | 1 |
| Molnár, MJ | 1 |
| Latvala, T | 1 |
| Mustonen, E | 1 |
| Uusitalo, R | 1 |
| Majamaa, K | 1 |
| Sparaco, M | 1 |
| Simonati, A | 1 |
| Cavallaro, T | 1 |
| Bartolomei, L | 1 |
| Grauso, M | 1 |
| Piscioli, F | 1 |
| Morelli, L | 1 |
| Rizzuto, N | 1 |
4 other studies available for glycine and MELAS
| Article | Year |
|---|---|
Evaluation of systemic redox states in patients carrying the MELAS A3243G mutation in mitochondrial DNA.
Topics: Adolescent; Adult; Alanine; Antioxidants; DNA, Mitochondrial; Female; Glycine; Humans; Hydrogen Pero | 2012 |
A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
Topics: Acidosis, Lactic; Adult; Alanine; Brain Ischemia; DNA, Mitochondrial; Glycine; Humans; Male; MELAS S | 2011 |
Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.
Topics: Adult; Aged; Alanine; DNA, Mitochondrial; Eye Diseases; Female; Glycine; Humans; Male; MELAS Syndrom | 2002 |
MELAS: clinical phenotype and morphological brain abnormalities.
Topics: Adenosine Triphosphatases; Adult; Alanine; Brain; Carboxylic Ester Hydrolases; Child; DNA, Mitochond | 2003 |