Literature DB >> 3681339

Benign juvenile focal muscular atrophy of upper extremities--a familial case.

U Schlegel1, F Jerusalem, W Tackmann, A Cordt, Y Tsuda.   

Abstract

A 53-year-old man and his 18-year-old son, both suffering from benign focal muscular atrophy of upper extremities are described. To our knowledge this is the first familial case of this disease in Caucasians.

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Mesh：

Year:  1987        PMID： 3681339     DOI： 10.1016/0022-510x(87)90169-9

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


  5 in total

1.  Juvenile Muscular Atrophy of a Unilateral Upper Extremity (Hirayama Disease) in a Patient with CHARGE Syndrome.

Authors:  T Yagihashi; K Hatori; K Ishii; C Torii; S Momoshima; T Takahashi; K Kosaki
Journal:  Mol Syndromol       Date:  2010-06-30

2.  Multifocal motor neuropathy: clinical and electrophysiological findings.

Authors:  A Jaspert; D Claus; H Grehl; B Neundörfer
Journal:  J Neurol       Date:  1996-10       Impact factor: 4.849

Review 3.  [Hirayama disease in Germany: case reports and review of the literature].

Authors:  J-S Kang; S Jochem-Gawehn; H Laufs; A Ferbert; P Vieregge; U Ziemann
Journal:  Nervenarzt       Date:  2011-10       Impact factor: 1.214

4.  Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation study.

Authors:  Kai Boelmans; Jörn Kaufmann; Sophie Schmelzer; Stefan Vielhaber; Malte Kornhuber; Alexander Münchau; Stephan Zierz; Charly Gaul
Journal:  J Neurol       Date:  2012-09-25       Impact factor: 4.849

5.  Bilateral familial Hirayama disease in a father and daughter.

Authors:  Sanjay Pandey; Shruti Jain
Journal:  Ann Indian Acad Neurol       Date:  2016 Apr-Jun       Impact factor: 1.383
  5 in total

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