[Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].

Abstract

BACKGROUND AND PURPOSE Spinocerebellar ataxias type 1 (SCA1) and type 2 (SCA2) belong to neurodegenerative disorders of autosomal dominant inheritance, genetically and clinically heterogeneous, caused by the expansion of CAG trinucleotides. Trunk and limb ataxia, dysarthria, dysphagia, gaze palsy, sensory and motor axonal neuropathy are the dominant… (More)

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Cite this paper

@article{Rakowicz2005SpinocerebellarAT, title={[Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].}, author={Maria J Rakowicz and Elzbieta Zdzienicka and Renata Poniatowska and Elżbieta Waliniowska and Anna Sułek and Teresa Jakubowska and Krystyna Niedzielska and Rafał Rola and Aleksandra Wierzbicka and Dorota Hoffman-Zacharska and Czesław Głazowski and Tomasz Jakubczyk and Maria Niewiadomska and Jacek Zaremba}, journal={Neurologia i neurochirurgia polska}, year={2005}, volume={39 4}, pages={263-275} }