Lynch and Sima [I] point out that glial cytoplasmic inclusions (GCIs
No association betweenFMR1premutations and multiple system atrophy
β Scribed by Ichiro Yabe; Hiroyuki Soma; Asako Takei; Naoto Fujik; Hidenao Sasaki
- Publisher
- Springer
- Year
- 2004
- Tongue
- English
- Weight
- 139 KB
- Volume
- 251
- Category
- Article
- ISSN
- 0340-5354
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π SIMILAR VOLUMES
Multiple system atrophy (MSA) is a sporadic neurodegenerative disorder that usually manifests in the early sixth decade of life and progresses relentlessly with a mean survival of 9 years. Clinically, MSA is dominated by autonomic/urogenital failure, which may be associated with either levodopa (L-d
## Abstract We here report survival in patients with multiple system atrophy (MSA) in a large, prospectively studied group of patients with MSA. Eightyβfive of 100 patients were known to have died. Three patients were rediagnosed as having PD. Twentyβfour patients came to autopsy, which showed MSA