12908758

Source:http://linkedlifedata.com/resource/pubmed/id/12908758

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0332307, umls-concept:C0751336
pubmed:issue	4
pubmed:dateCreated	2003-8-11
pubmed:abstractText	Miyoshi myopathy is an autosomal recessive muscular dystrophy. It is characterized by distal muscle involvement, especially the gastrocnemius and soleus. The disease starts with weakness and atrophy of the calves.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8214420
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Creatine Kinase
pubmed:status	MEDLINE
pubmed:issn	0722-5091
pubmed:author	pubmed-author:AtasoyH THT, pubmed-author:CoskunOO, pubmed-author:EmreUU, pubmed-author:ErlamRR, pubmed-author:InanL ELE, pubmed-author:YildizHH
pubmed:issnType	Print
pubmed:volume	22
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	204-8
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:12908758-Adult, pubmed-meshheading:12908758-Biopsy, pubmed-meshheading:12908758-Creatine Kinase, pubmed-meshheading:12908758-Electromyography, pubmed-meshheading:12908758-Female, pubmed-meshheading:12908758-Humans, pubmed-meshheading:12908758-Leg, pubmed-meshheading:12908758-Male, pubmed-meshheading:12908758-Muscle, Skeletal, pubmed-meshheading:12908758-Muscular Dystrophies, pubmed-meshheading:12908758-Siblings
pubmed:articleTitle	Distal muscular dystrophy of the Miyoshi type.
pubmed:affiliation	Department of Neurology, Ministry of Health, Ankara Research Hospital, Ankara, Turkey.
pubmed:publicationType	Journal Article