Cutaneous Sympathetic Dysfunction in Patients with Machado–Joseph Disease
✍ Scribed by Yoshitaka Yamanaka, Masato Asahina, Yuichi Akaogi, Yoshikatsu Fujinuma, Akira Katagiri, Kazuaki Kanai, Satoshi Kuwabara
- Book ID
- 118825449
- Publisher
- Springer-Verlag
- Year
- 2012
- Tongue
- English
- Weight
- 194 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1473-4222
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## Abstract Machado‐Joseph disease (MJD) is an autosomal dominant spinocerebellar ataxia. Few studies have examined the neuropsychological and neurobehavioral profiles of patients with MJD. In this study, six individuals with MJD were given a battery of neuropsychological tests. Relative impairment
## Abstract Although ataxia is the most distressing manifestation of Machado‐Joseph disease (MJD), little is known about its natural history. Therefore, we prospectively followed a cohort of patients with MJD for 13 months to characterize the progression of ataxia and identify its contributory fact