The hereditary spinocerebellar ataxias in Japan
โ Scribed by Sasaki, H.; Yabe, I.; Tashiro, K.
- Book ID
- 119984372
- Publisher
- S. Karger AG
- Year
- 2003
- Tongue
- French
- Weight
- 138 KB
- Volume
- 100
- Category
- Article
- ISSN
- 1424-8581
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We read the article by van Gaalen et al. 1 with great interest. These authors reviewed the frequency and main type of movement disorders found in each form of spinocerebellar ataxia (SCA). They also reported unusual movement disorders and noncerebellar manifestations, such as stiff-person syndrome,
## Abstract Autosomal dominant spinocerebellar ataxias (SCAs) can present with a large variety of noncerebellar symptoms, including movement disorders. In fact, movement disorders are frequent in many of the various SCA subtypes, and they can be the presenting, dominant, or even isolated disease fe