Literature DB >> 1022769

Autosomal dominant spinocerebellar ataxia with slow eye movements-a common hereditary ataxia in Western India.

R S Wadia, R B Amin, U P Divate, P G Divate, G S Sainani, H V Sardesai.   

Abstract

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Year:  1976        PMID： 1022769

Source DB:  PubMed          Journal:  J Assoc Physicians India        ISSN： 0004-5772


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  2 in total

1.  Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia.

Authors:  K Bürk; M Fetter; M Skalej; F Laccone; G Stevanin; J Dichgans; T Klockgether
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-06       Impact factor: 10.154

2.  Clinical profile and genetic correlation of patients with spinocerebellar ataxia: A study from a tertiary care centre in Eastern India.

Authors:  Debabrata Pulai; Deb Shankar Guin; Kalyan B Bhattacharyya; Goutam Ganguly; Anindita Joardar; Sarnava Roy; Atanu Biswas; Alak Pandit; Arijit Roy; Asit Kumar Senapati
Journal:  Ann Indian Acad Neurol       Date:  2014-10       Impact factor: 1.383
  2 in total

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