thiamine has been researched along with Luft Disease in 1 studies
thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We studied two siblings with a mitochondrial myopathy, familial thiamine deficiency, and an A3243G mutation of the mitochondrial DNA (mtDNA)." | 7.70 | Mitochondrial myopathy and familial thiamine deficiency. ( Higuchi, I; Naito, E; Nakagawa, M; Oizumi, K; Osame, M; Sato, Y, 2000) |
| "We studied two siblings with a mitochondrial myopathy, familial thiamine deficiency, and an A3243G mutation of the mitochondrial DNA (mtDNA)." | 3.70 | Mitochondrial myopathy and familial thiamine deficiency. ( Higuchi, I; Naito, E; Nakagawa, M; Oizumi, K; Osame, M; Sato, Y, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sato, Y | 1 |
| Nakagawa, M | 1 |
| Higuchi, I | 1 |
| Osame, M | 1 |
| Naito, E | 1 |
| Oizumi, K | 1 |
1 other study available for thiamine and Luft Disease
| Article | Year |
|---|---|
Mitochondrial myopathy and familial thiamine deficiency.
Topics: Adult; Atrophy; DNA, Mitochondrial; Electrocardiography; Female; Hemodynamics; Humans; Mitochondria, | 2000 |