Literature DB >> 13897523

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

G GEILER, G GEILER.   

Abstract

Entities:  

Keywords:  MUSCULAR ATROPHY/pathology; MYOTONIA CONGENITA/pathology

Mesh：

Year:  1962        PMID： 13897523

Source DB:  PubMed          Journal:  Virchows Arch Pathol Anat Physiol Klin Med        ISSN： 0376-0081


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  6 in total

1.  Arthrogryposis multiplex due to congenital muscular dystrophy.

Authors:  B Q BANKER; M VICTOR; R D ADAMS
Journal:  Brain       Date:  1957-09       Impact factor: 13.501

2.  [Arthrogrypotic myodystrophia fetalis deformans].

Authors:  W BUCHHOLZ
Journal:  Zentralbl Allg Pathol       Date:  1956-10-30

3.  Amyotonia congenita; a report of three cases with a review of the literature.

Authors:  J A EPSTEIN
Journal:  J Mt Sinai Hosp N Y       Date:  1949 Sep-Oct

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

Authors:  J RADERMECKER
Journal:  Rev Neurol (Paris)       Date:  1951-01       Impact factor: 2.607

5.  Contributions to the symptomatology of amyotonia congenita (infantile spinal muscular atrophy).

Authors:  G WOHLFART
Journal:  Acta Med Scand       Date:  1946

6.  [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children].

Authors:  S BRANDT
Journal:  Nord Med       Date:  1950-09-15
  6 in total

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