thiamine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II 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 |
|---|---|---|
| "Spinocerebellar ataxia type 2 is a genetic disorder characterised by the degeneration of the cerebellum, its connections and degeneration in brainstem areas." | 1.39 | Thiamine and spinocerebellar ataxia type 2. ( Colangeli, M; Costantini, A; Pala, MI; Savelli, S, 2013) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Costantini, A | 1 |
| Pala, MI | 1 |
| Colangeli, M | 1 |
| Savelli, S | 1 |
1 other study available for thiamine and Autosomal Dominant Cerebellar Ataxia, Type II
| Article | Year |
|---|---|
Thiamine and spinocerebellar ataxia type 2.
Topics: Fatigue; Humans; Male; Middle Aged; Spinocerebellar Ataxias; Thiamine; Vitamin B Complex | 2013 |