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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Spinocerebellar ataxia type 2: clinical features of a pedigree displaying prominent frontal-executive dysfunction.
TL;DR: In this paper, the authors studied 8 affected members of an Australian pedigree of northern Italian origin with SCA2 caused by spinocerebellar ataxia type II.
Journal ArticleDOI
The diagnostic value of saccades in movement disorder patients: a practical guide and review
TL;DR: The anatomy of horizontal and vertical saccades is explored, practical aspects of their examination are discussed, and how saccadic abnormalities in hyperkinetic and hypokinetic movement disorders aid in diagnosis are reviewed.
Journal ArticleDOI
Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India
Priyadarshi Basu,Biswanath Chattopadhyay,Prasanta K. Gangopadhaya,Subhas C. Mukherjee,Krishna K. Sinha,Shyamal Kumar Das,Susanta Roychoudhury,Partha P. Majumder,Nitai P. Bhattacharyya +8 more
TL;DR: In this paper, the authors identify various subtypes of spinocerebellar ataxias (SCAs) among 57 unrelated individuals clinically diagnosed as ataxia patients.
Journal ArticleDOI
The natural history of Machado-Joseph disease: An analysis of 138 personally examined cases
André Barbeau,Madeleine Roy,L. Cunha,A. N. de Vincente,Roger N. Rosenberg,William L. Nyhan,P. L. MacLeod,G. Chazot,L. B. Langston,David M. Dawson +9 more
TL;DR: The main components of the clinical presentation are delineated, it is concluded that the marked variability in clinical expressions does not negate the homogeneity of the disorder, and the natural history of this entity should be called, for historical reasons, “Machado-Joseph Disease”.
Journal ArticleDOI
Clinical features and natural history of spinocerebellar ataxia type 1
Hidenao Sasaki,T. Fukazawa,Yanagihara T,Takeshi Hamada,K. Shima,Akihisa Matsumoto,K. Hashimoto,N. Ito,Akemi Wakisaka,Kunio Tashiro +9 more
TL;DR: Although the phenotype of SCA1 overlaps with those of other dominant SCAs, some facets of the neurological events differ from either SCA2 with ataxia‐hyporeflexia‐slow saccade syndrome, or early‐onset Machado‐Joseph disease with dystonia‐bradykinesia‐spasticity syndrome.
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