taurine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Spinocerebellar ataxia type 1 (SCA1) is a hereditary, progressive and fatal movement disorder that primarily affects the cerebellum." | 1.39 | Non-invasive detection of neurochemical changes prior to overt pathology in a mouse model of spinocerebellar ataxia type 1. ( Brent Clark, H; Eberly, LE; Emir, UE; Öz, G; Vollmers, ML, 2013) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Emir, UE | 1 |
| Brent Clark, H | 1 |
| Vollmers, ML | 1 |
| Eberly, LE | 1 |
| Öz, G | 1 |
| Kaemmerer, WF | 1 |
| Rodrigues, CM | 1 |
| Steer, CJ | 1 |
| Low, WC | 1 |
2 other studies available for taurine and Autosomal Dominant Cerebellar Ataxia, Type II
| Article | Year |
|---|---|
Non-invasive detection of neurochemical changes prior to overt pathology in a mouse model of spinocerebellar ataxia type 1.
Topics: Animals; Ataxin-1; Ataxins; Cerebellum; Choline; Disease Models, Animal; Disease Progression; Gene K | 2013 |
Creatine-supplemented diet extends Purkinje cell survival in spinocerebellar ataxia type 1 transgenic mice but does not prevent the ataxic phenotype.
Topics: Animals; Ataxin-1; Ataxins; Bile Acids and Salts; Cell Count; Cell Survival; Cerebellum; Creatine; D | 2001 |