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Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings

✍ Scribed by Heike Jacobi; Till-Karsten Hauser; Paola Giunti; Christoph Globas; Peter Bauer; Tanja Schmitz-Hübsch; László Baliko; Alessandro Filla; Caterina Mariotti; Maria Rakowicz; Perine Charles; Pascale Ribai; Sandra Szymanski; Jon Infante; Bart P. C. van de Warrenburg; Alexandra Dürr; Dagmar Timmann; Sylvia Boesch; Roberto Fancellu; Rafal Rola; Chantal Depondt; Ludger Schöls; Elzbieta Zdzienicka; Jun-Suk Kang; Susanne Ratzka; Berry Kremer; Dennis A. Stephenson; Béla Melegh; Massimo Pandolfo; Sophie Tezenas du Montcel; Johannes Borkert; Jörg B. Schulz; Thomas Klockgether

Book ID
113101458
Publisher
Springer-Verlag
Year
2011
Tongue
English
Weight
343 KB
Volume
11
Category
Article
ISSN
1473-4222

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Early symptoms in spinocerebellar ataxia
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✍ Christoph Globas; Sophie Tezenas du Montcel; Laslo Baliko; Syliva Boesch; Chanta 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB

## Abstract Onset of genetically determined neurodegenerative diseases is difficult to specify because of their insidious and slowly progressive nature. This is especially true for spinocerebellar ataxia (SCA) because of varying affection of many parts of the nervous system and huge variability of