𝔖 Bobbio Scriptorium
✦   LIBER   ✦

DO02 Spinocerebellar ataxia type 2 in a Turkish family

✍ Scribed by E. Dirik; U. Yiş; N. Başak; E. Soydan; O. Hüdaoğlu; F. Özgönül


Book ID
114359441
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
45 KB
Volume
11
Category
Article
ISSN
1090-3798

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Spinocerebellar ataxia types 2 and 3 seg
✍ Marcondes C. França Jr; Maria E. Calcagnotto; Jaderson C. Da Costa; Iscia Lopes- 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 49 KB

## Abstract Spinocerebellar ataxia (SCA) types 2 and 3 are autosomal‐dominant neurodegenerative disorders caused by mutations in two different genes. We identified mutations for __SCA2__ and __SCA3__ segregating simultaneously in a single Brazilian family. The index patient had __SCA2__, whereas he

Cervical dystonia in spinocerebellar ata
✍ Kateřina Zárubová; Evžen Růžička 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 59 KB

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