Literature DB >> 13298385

[Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].

S THIEFFRY, M ARTHUIS, E BARGETON.   

Abstract

Entities:  

Keywords:  PROGRESSIVE MUSCULAR ATROPHY/pathology

Mesh：

Year:  1955        PMID： 13298385

Source DB:  PubMed          Journal:  Rev Neurol (Paris)        ISSN： 0035-3787            Impact factor:   2.607


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  6 in total

1.  Ultrastructural aspects of muscle and nerve in Werdnig-Hoffmann disease.

Authors:  H B Szliwowski; P Drochmans
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

2.  CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

Authors:  R M NORMAN; J M KAY
Journal:  Arch Dis Child       Date:  1965-06       Impact factor: 3.791

3.  Anterior horn cell disease associated with pontocerebellar hypoplasia in infants.

Authors:  F Goutières; J Aicardi; E Farkas
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-04       Impact factor: 10.154

4.  A new genetic variant of the spinal muscular atrophies in infancy.

Authors:  H Zellweger; E Hanhart; H J Schneider
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

5.  Progressive bulbar paralysis in childhood: a case report.

Authors:  G F Perticoni; T A Cantisani; H Fisher
Journal:  Ital J Neurol Sci       Date:  1983-04

Review 6.  The nosology of the spinal muscular atrophies.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318
  6 in total

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