Literature DB >> 14845356

[Spinal amyotrophia in children (Werdnig-Hoffmann paralysis) as hereditary degeneration].

J RADERMECKER.   

Abstract

Entities:  

Keywords:  ATROPHY, MUSCULAR

Mesh：

Year:  1951        PMID： 14845356

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


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  7 in total

1.  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

2.  [On the morphology, nosological position and pathogenesis of Oppenheim's myotonia congenita and Werdnig-Hoffmann's infantile spinal progressive muscular atrophy].

Authors:  G GEILER; G GEILER
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1962

3.  Cerebellar hypoplasia in Werdnig-Hoffmann disease.

Authors:  R M NORMAN
Journal:  Arch Dis Child       Date:  1961-02       Impact factor: 3.791

4.  Animal model of human disease. Infantile spinal muscular atrophy, Werdnig-Hoffman disease. Animal model: Hereditary neuronal abiotrophy in Swedish Lapland dogs.

Authors:  E Sandefeldt; J F Cummings; A de Lahunta; G Björck; L P Krook
Journal:  Am J Pathol       Date:  1976-03       Impact factor: 4.307

5.  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

6.  Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?

Authors:  J Towfighi; R S Young; R M Ward
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

7.  Pathological involvement of primary sensory neurons in Werdnig-Hoffmann disease.

Authors:  S Carpenter; G Karpati; S Rothman; G Watters; F Andermann
Journal:  Acta Neuropathol       Date:  1978-05-24       Impact factor: 17.088
  7 in total

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