Literature DB >> 13157969

[A new heredodegenerative group: heredofamilial myoscleroses].

A LOWENTHAL.   

Abstract

Keywords:  MUSCLES/diseases; SCLEROSIS

Mesh：

Year:  1954        PMID： 13157969

Source DB:  PubMed          Journal:  Acta Neurol Psychiatr Belg        ISSN： 0001-6284


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  3 in total

1.  [An unusual muscular affection manifested by extensive contractures; also a contribution on the differential diagnosis of primary muscle diseases].

Authors:  D SEITZ
Journal:  Dtsch Z Nervenheilkd       Date:  1958

Review 2.  The collagen VI-related myopathies Ullrich congenital muscular dystrophy and Bethlem myopathy.

Authors:  Carsten G Bönnemann
Journal:  Handb Clin Neurol       Date:  2011

3.  The syndrome of myosclerosis.

Authors:  W G Bradley; P Hudgson; D Gardner-Medwin; J N Walton
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-08       Impact factor: 10.154
  3 in total

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