Literature DB >> 5170970

Spinocerebellar ataxia with neural myatrophy.

H C Hopf, E Volles.   

Abstract

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Year:  1971        PMID： 5170970     DOI： 10.1055/s-0028-1091802

Source DB:  PubMed          Journal:  Neuropadiatrie        ISSN： 0028-3797


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  4 in total

1.  Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.

Authors:  A Gabreëls-Festen; S van Beersum; L Eshuis; E LeGuern; F Gabreëls; B van Engelen; E Mariman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-05       Impact factor: 10.154

2.  Electron-microscopic heterogeneity of onion-bulb neuropathies of the Déjerine-Sottas type. Two patients in one family with the variant described by Lyon (1969).

Authors:  E Joosten; F Gabreëls; A Gabrèèls-Festen; G Vrensen; J Korten; S Notermans
Journal:  Acta Neuropathol       Date:  1974-02-28       Impact factor: 17.088

3.  [An autopsy case of olivocerebellar and thalamic degeneration, diffuse sclerosis and hypertrophic neuropathy: infantile system degeneration? (author's transl)].

Authors:  M Oda; K Nagashima; Y Konishi
Journal:  J Neurol       Date:  1975-12-02       Impact factor: 4.849

4.  [Investigations of peripheral and central somatosensory pathways in peroneal muscular atrophy and Friedreich's heredoataxia (author's transl)].

Authors:  M Sauer
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1980
  4 in total

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