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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Ataxia espinocerebelar do tipo 2: aspectos clínicos, qualidade de vida, depressão e ansiedade em cinco portadores de uma família
Fernanda de Oliveira Yamane,Lorrana Maria Costa Mantovani,Danillo Barbosa,Thiago Franco Nasser,Ana Paula Santos +4 more
TL;DR: O objetivo deste estudo foi descrever aspectos clinicos de cinco membros de uma mesma familia portadores de SCA2 e correlaciona-los com qualidade de vida, depressao e ansiedade e entre tempo de doenca e ICARS.
Alteraciones de los movimientos oculares sacádicos en las enfermedades poliglutamínicas Saccadic eye movements abnormalities in polyglutamine diseases
TL;DR: An updated review of saccadic abnormalities in polyglutamine diseases is presented, emphasizing in the usefulness of these features for diagnosis and disease biomarkers identifications.
Book ChapterDOI
Mathematical models and human disease.
TL;DR: A few examples of how clinical disorders have led to improvements in models and how these models could lead to neural prostheses for patients are shown.
Book ChapterDOI
Oculomotor Abnormalities in Cerebellar Degeneration
M. Fetter,J. Dichgans +1 more
TL;DR: Clinicians can at least try to attribute specific oculomotor subfunctions and related eye-movement abnormalities to distinct parts of the cerebellum, as well as anatomical tracing techniques, to cast some light on this dilemma.
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