Transcranial sonography in spinocerebellar ataxia type 2
✍ Scribed by M. Mijajlović; N. Dragašević; E. Stefanova; I. Petrović; M. Svetel; V. S. Kostić
- Book ID
- 106094001
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 512 KB
- Volume
- 255
- Category
- Article
- ISSN
- 0340-5354
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.
## Abstract Spinocerebellar ataxias are heterogeneous disorders with overlapping clinical features. Spinocerebellar ataxia‐6 is a dominantly inherited condition characterized by relatively pure ataxia with a paucity of other manifestations including extrapyramidal findings. We report on two patient