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Article

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

Neurologia (Barcelona, Spain) - 1 Apr 2011

Álvarez-Paradelo S, García A, Infante J, Berciano J

Abstract excerpt

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 the size of CAG expansion and determine the contribution of neurophysiological studies in the differential diagnosis...

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PMID: 21163215
DOI: 10.1016/j.nrl.2010.09.012

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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