Literature DB >> 4370236

Olivopontocerebellar degeneration. Clinical and ultrastructural abnormalities.

D M Landis, R N Rosenberg, S C Landis, L Schut, W L Nyhan.   

Abstract

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Year:  1974        PMID： 4370236     DOI： 10.1001/archneur.1974.00490410043003

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  11 in total

1.  Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia.

Authors:  V Pietrini; M Godani; S Calzetti; A Negrotti; B Castellotti; M C Riggio; C Toffoli
Journal:  Ital J Neurol Sci       Date:  1998-12

2.  Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.

Authors:  S J Kish; L Schut; J Simmons; J Gilbert; L J Chang; M Rebbetoy
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-04       Impact factor: 10.154

3.  Neurochemical and genetic bases of psychopathology: future directions.

Authors:  S Matthysse; M Kling
Journal:  Behav Genet       Date:  1982-02       Impact factor: 2.805

4.  Krabbe's disease with giant lamellar bodies in Purkinje cells.

Authors:  J Hirato; Y Nakazato; A Sasaki; A Hikima; S Shimizu; H Yamanouchi
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

5.  Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Authors:  L P Ranum; L A Duvick; S S Rich; L J Schut; M Litt; H T Orr
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

6.  Purkinje cell ataxin-1 modulates climbing fiber synaptic input in developing and adult mouse cerebellum.

Authors:  Blake A Ebner; Melissa A Ingram; Justin A Barnes; Lisa A Duvick; Jill L Frisch; H Brent Clark; Huda Y Zoghbi; Timothy J Ebner; Harry T Orr
Journal:  J Neurosci       Date:  2013-03-27       Impact factor: 6.167

7.  Scanning electron microscopy studies of erythrocytes in spinocerebellar degeneration.

Authors:  Y Yasuda; I Akiguchi; H Shio; M Kameyama
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-03       Impact factor: 10.154

8.  Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

Authors:  S S Rich; P Wilkie; L Schut; G Vance; H T Orr
Journal:  Am J Hum Genet       Date:  1987-10       Impact factor: 11.025

9.  Clinical study of large kindreds with autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) of late onset.

Authors:  M Spadaro; P Giunti; G B Colazza; F Naso; F Bianco; C Morocutti
Journal:  Ital J Neurol Sci       Date:  1993-01

Review 10.  Inherited syndrome of infantile olivopontocerebellar atrophy, micronodular cirrhosis, and renal tubular microcysts: review of the literature and a report of an additional case.

Authors:  Y Chang; J L Twiss; D S Horoupian; S A Caldwell; K M Johnston
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088
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