Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias

Background: The spinocerebellar ataxias (SCA) are a group of genetic neurodegenerative diseases, clinically and pathologically heterogeneous, characterized by slowly progressive cerebellar ataxia. Objective: To identify the neural pathways affected neurophysiologically, correlate the findings with t...

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Bibliographic Details
Main Authors: S. Álvarez-Paradelo, A. García, J. Infante, J. Berciano
Format: Article
Language:English
Published: Elsevier España 2011-01-01
Series:Neurología (English Edition)
Online Access:http://www.sciencedirect.com/science/article/pii/S2173580811700323