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...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier España
2011-01-01
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Series: | Neurología (English Edition) |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2173580811700323 |