Autonomic dysfunction in presymptomatic spinocerebellar ataxia type-2
✍ Scribed by J. Montes-Brown; A. Machado; M. Estévez; C. Carricarte; L. Velázquez-Pérez
- Book ID
- 109339259
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 104 KB
- Volume
- 125
- Category
- Article
- ISSN
- 0001-6314
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
when it was present in at least 5 of 10 trials. Tremor axes were determined by the directions of maximal tremor power assessed over 360°. There were 29 cases (mean age, 68.8 Ϯ 10.6 years). Fifteen (51.7%) had a tremor severity rating of 2 or 3 (moderate or severe tremor), 12 (41.4%) had a rating of
The inherited neurodegenerative disorders such as the spinocerebellar ataxias, Huntington's disease, dentatorubral-pallidoluysian atrophy, and spinal and bulbar muscular atrophy associated with CAG/polyglutamine repeat expansion have been reported to exhibit intranuclear inclusions (NIs) in neurons.