Literature DB >> 5571047

A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families).

N H Wadia, R K Swami.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5571047     DOI： 10.1093/brain/94.2.359

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  34 in total

1.  Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles.

Authors:  José Miguel Laffita-Mesa; Luis C Velázquez-Pérez; Nieves Santos Falcón; Tania Cruz-Mariño; Yanetza González Zaldívar; Yaimee Vázquez Mojena; Dennis Almaguer-Gotay; Luis Enrique Almaguer Mederos; Roberto Rodríguez Labrada
Journal:  Eur J Hum Genet       Date:  2011-09-21       Impact factor: 4.246

2.  Oculomotor disorders in Huntington's chorea.

Authors:  G Avanzini; F Girotti; T Caraceni; R Spreafico
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-07       Impact factor: 10.154

3.  Blink-related momentary activation of the default mode network while viewing videos.

Authors:  Tamami Nakano; Makoto Kato; Yusuke Morito; Seishi Itoi; Shigeru Kitazawa
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-24       Impact factor: 11.205

4.  A nonlinear generalization of the Savitzky-Golay filter and the quantitative analysis of saccades.

Authors:  Weiwei Dai; Ivan Selesnick; John-Ross Rizzo; Janet Rucker; Todd Hudson
Journal:  J Vis       Date:  2017-08-01       Impact factor: 2.240

5.  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

6.  Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias.

Authors:  Renu Kumari; Deepak Kumar; Samir K Brahmachari; Achal K Srivastava; Mohammed Faruq; Mitali Mukerji
Journal:  J Genet       Date:  2018-07       Impact factor: 1.166

Review 7.  Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives.

Authors:  J J Magaña; L Velázquez-Pérez; B Cisneros
Journal:  Mol Neurobiol       Date:  2012-09-21       Impact factor: 5.590

8.  Intermittent horizontal saccade failure ('ocular motor apraxia') in children.

Authors:  C M Harris; F Shawkat; I Russell-Eggitt; J Wilson; D Taylor
Journal:  Br J Ophthalmol       Date:  1996-02       Impact factor: 4.638

9.  Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

Authors:  I Lopes-Cendes; E Andermann; E Attig; F Cendes; S Bosch; M Wagner; F Gerstenbrand; F Andermann; G A Rouleau
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

10.  A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.

Authors:  A T Moore; D S Taylor
Journal:  Br J Ophthalmol       Date:  1984-06       Impact factor: 4.638
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