Clinical and Neurophysiological Profile of Four German Families with Spinocerebellar Ataxia Type 14-Reference-Cited by-同舟云学术

Clinical and Neurophysiological Profile of Four German Families with Spinocerebellar Ataxia Type 14

Published:2013-09-13 Issue:1 Volume:13 Page:89-96
ISSN:1473-4222
Container-title:The Cerebellum
language:en
Short-container-title:Cerebellum

Author:

Ganos Christos,Zittel Simone,Minnerop Martina,Schunke Odette,Heinbokel Christina,Gerloff Christian,Zühlke Christine,Bauer Peter,Klockgether Thomas,Münchau Alexander,Bäumer Tobias

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s12311-013-0522-7.pdf

Reference45 articles.

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2. Klockgether T. Update on degenerative ataxias. Curr Opin Neurol. 2011;24:339–45.

3. van Gaalen J, Giunti P, van de Warrenburg BP. Movement disorders in spinocerebellar ataxias. Mov Disord. 2011;26:792–800.

4. Chen DH, Brkanac Z, Verlinde CL, et al. Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia. Am J Hum Genet. 2003;72:839–49.

5. Chen DH, Cimino PJ, Ranum LP, et al. The clinical and genetic spectrum of spinocerebellar ataxia 14. Neurology. 2005;64:1258–60.

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