Literature DB >> 888738

Clinical examination of patients with neuromuscular disease.

M H Brooke.   

Abstract

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Year:  1977        PMID： 888738

Source DB:  PubMed          Journal:  Adv Neurol        ISSN： 0091-3952


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  2 in total

1.  Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD).

Authors:  Rianne J M Goselink; Tim H A Schreuder; Karlien Mul; Nicol C Voermans; Maaike Pelsma; Imelda J M de Groot; Nens van Alfen; Bas Franck; Thomas Theelen; Richard J Lemmers; Jean K Mah; Silvère M van der Maarel; Baziel G van Engelen; Corrie E Erasmus
Journal:  BMC Neurol       Date:  2016-08-17       Impact factor: 2.474

2.  Sporadic DUX4 expression in FSHD myocytes is associated with incomplete repression by the PRC2 complex and gain of H3K9 acetylation on the contracted D4Z4 allele.

Authors:  Premi Haynes; Karol Bomsztyk; Daniel G Miller
Journal:  Epigenetics Chromatin       Date:  2018-08-20       Impact factor: 4.954
  2 in total

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