Journal ArticleDOI
A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)
N. H. Wadia,R. K. Swami +1 more
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This article is published in Brain.The article was published on 1971-01-01. It has received 166 citations till now. The article focuses on the topics: Spinocerebellar Degenerations.read more
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Journal ArticleDOI
Spinocerebellar ataxia 2 (SCA2).
TL;DR: This review aims to portray the particular profile of the SCA2 disease process and correlate it to the specific features of ataxin-2, a subcellular localization at the Golgi, the endoplasmic reticulum and the plasma membrane.
Journal ArticleDOI
Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba.
TL;DR: In this article, the authors describe 263 patients with autosomal dominant cerebellar ataxia from the Holguin province, Cuba, who were found to have a common ancestry.
Journal ArticleDOI
Vestibulo‐ocular function in patients with cerebellar atrophy
TL;DR: It is concluded that quantitative vestibulo-ocular tests can be useful in classifying the cerebellar atrophy syndromes.
Book ChapterDOI
Spinocerebellar Ataxia Type 2
TL;DR: The autosomal dominant cerebellar ataxias are a clinically, pathologically and genetically heterogeneous group of neurodegenerative disorders caused by degeneration of cerebellum and its afferent and efferent connections.
Journal ArticleDOI
The ocular motor system.
Robert H. Spector,B. Todd Troost +1 more
TL;DR: Recent advances in ocular motor neurophysiology are reviewed with emphasis on brainstem control of horizontal saccadic and pursuit eye movements and the role of the cerebellum and medial longitudinal fasciculus is discussed.
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