14743650

Source:http://linkedlifedata.com/resource/pubmed/id/14743650

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011900, umls-concept:C0017398, umls-concept:C0026850, umls-concept:C0814812
pubmed:issue	4
pubmed:dateCreated	2004-1-27
pubmed:abstractText	A specific genetic diagnosis can be reached for most children with muscular dystrophy. Advanced diagnostics, including genetic testing and analysis of nonmuscle tissues, such as skin and blood, often allow the diagnosis to be reached using minimally invasive procedures. These diagnostic advances accompany improved understanding of pathophysiology and pave the way for specific and curative treatments.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8219232
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0733-8619
pubmed:author	pubmed-author:MathewsKatherine DKD
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	795-816
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:14743650-Diagnosis, Differential, pubmed-meshheading:14743650-Humans, pubmed-meshheading:14743650-Muscular Dystrophies
pubmed:year	2003
pubmed:articleTitle	Muscular dystrophy overview: genetics and diagnosis.
pubmed:affiliation	Department of Pediatrics, University of Iowa, 200 Hawkins Drive, Iowa City, IA 52240, USA. katherine-mathews@uiowa.edu
pubmed:publicationType	Journal Article, Review