17986494

Source:http://linkedlifedata.com/resource/pubmed/id/17986494

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Predicate	Object
rdf:type	pubmed:Citation
pubmed:issue	1
pubmed:dateCreated	2008-1-2
pubmed:abstractText	Facioscapulohumeral dystrophy (FSHD) is the third most common inherited muscular dystrophy after Duchenne dystrophy and myotonic dystrophy. Over the last decade, major advances have occurred in the understanding of the genetics of this disorder. Despite these advances, the exact mechanisms that lead to atrophy and weakness secondary to the genetic defect are still not understood. The purposes of this article are to increase awareness of FSHD among clinicians; to provide an update regarding the genetics, clinical features, natural history, and current management of FSHD; and to discuss opportunities for research.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0022623
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0031-9023
pubmed:author	pubmed-author:KingWendy MWM, pubmed-author:PandyaShreeS, pubmed-author:TawilRabiR
pubmed:issnType	Print
pubmed:volume	88
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	105-13
pubmed:dateRevised	2009-11-11
pubmed:meshHeading	pubmed-meshheading:17986494-Humans, pubmed-meshheading:17986494-Muscular Dystrophy, Facioscapulohumeral
pubmed:year	2008
pubmed:articleTitle	Facioscapulohumeral dystrophy.
pubmed:affiliation	School of Medicine and Dentistry, University of Rochester, Rochester, NY 14627, USA. shree_pandya@urmc.rochester.edu
pubmed:publicationType	Journal Article, Review, Research Support, Non-U.S. Gov't