Autosomal dominant cerebellar ataxias: a systematic review of clinical features-Reference-Cited by-同舟云学术

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Autosomal dominant cerebellar ataxias: a systematic review of clinical features

Published:2014-02-12 Issue:4 Volume:21 Page:607-615
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Rossi M.¹,Perez-Lloret S.²³,Doldan L.⁴,Cerquetti D.¹,Balej J.¹,Millar Vernetti P.¹,Hawkes M.⁴,Cammarota A.¹,Merello M.¹³

Affiliation:

1. Movement Disorders Section; Department of Neuroscience; Raul Carrea Institute for Neurological Research (FLENI); Buenos Aires Argentina

2. Clinical Pharmacology and Epidemiology Laboratory; Pontifical Catholic University of Argentina; Buenos Aires Argentina

3. Argentine National Scientific and Technological Research Council (CONICET); Buenos Aires Argentina

4. Department of Neurology; Raul Carrea Institute for Neurological Research; Buenos Aires Argentina

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.12350/fullpdf

Reference20 articles.

1. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis;Schöls;Lancet Neurol,2004

2. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Durr;Lancet Neurol,2010

3. The ever expanding spinocerebellar ataxias. Editorial;Matilla-Dueñas;Cerebellum,2012

4. Yet another spinocerebellar ataxia - will it ever end?;Paulson;Lancet Neurol,2002

5. Genetics of the dominant ataxias;Verbeek;Semin Neurol,2011

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