Literature DB >> 13575796

[Clinical and genetic study of a family with progressive neuropathic muscular atrophy (Charcot-Marie amyotrophy)].

P STARK.   

Abstract

Entities:  

Keywords:  PROGRESSIVE MUSCULAR ATROPHY

Mesh：

Year:  1958        PMID： 13575796

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  5 in total

1.  [FAMILIAL SCAPULOPERONEAL MUSCULAR ATROPHY].

Authors:  H E KAESER
Journal:  Dtsch Z Nervenheilkd       Date:  1964-11-25

2.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1959-06       Impact factor: 11.025

3.  Segregation distortion in myotonic dystrophy.

Authors:  A C Magee; A E Hughes
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

4.  Neurogenic scapuloperoneal syndrome in childhood.

Authors:  R Mercelis; J Demeester; J J Martin
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-10       Impact factor: 10.154

5.  Presymptomatic diagnosis of myotonic dystrophy.

Authors:  H G Brunner; W Nillesen; B A van Oost; G Jansen; B Wieringa; H H Ropers; H J Smeets
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318
  5 in total

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