Neurophysiological features in spinocerebellar ataxia type 2: Prospects for novel biomarkers

Author:

Velázquez-Pérez Luis,Rodríguez-Labrada Roberto,González-Garcés Yasmany,Vázquez-Mojena Yaimeé,Pérez-Rodríguez Roberto,Ziemann Ulf

Funder

Alexander von Humboldt-Stiftung

Publisher

Elsevier BV

Subject

Physiology (medical),Neurology (clinical),Neurology,Sensory Systems

Reference106 articles.

1. Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3;Abele;Brain,1997

2. Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3;Abele;J Neurol,2001

3. Association between spinocerebellar ataxias caused by glutamine expansion and psychiatric and neuropsychological signals – a literature review;Almeida-Silva;Am J Neurodegener Dis,2013

4. Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population;Alonso;Mov Disord,2007

5. The multiple faces of spinocerebellar ataxia type 2;Antenora;Ann Clin Transl Neurol,2017

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