5115748

Source:http://linkedlifedata.com/resource/pubmed/id/5115748

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011164, umls-concept:C0205292, umls-concept:C0242697, umls-concept:C0270960, umls-concept:C0270962, umls-concept:C0332185, umls-concept:C0332281
pubmed:issue	10
pubmed:dateCreated	1972-1-10
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0405543
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Aspartate Aminotransferases, http://linkedlifedata.com/resource/pubmed/chemical/Creatine Kinase
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0025-6196
pubmed:author	pubmed-author:EngelA GAG, pubmed-author:GomezM RMR, pubmed-author:GrooverR VRV
pubmed:issnType	Print
pubmed:volume	46
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	666-81
pubmed:dateRevised	2007-10-29
pubmed:meshHeading	pubmed-meshheading:5115748-Adolescent, pubmed-meshheading:5115748-Aspartate Aminotransferases, pubmed-meshheading:5115748-Asthenia, pubmed-meshheading:5115748-Biopsy, pubmed-meshheading:5115748-Child, pubmed-meshheading:5115748-Child, Preschool, pubmed-meshheading:5115748-Creatine Kinase, pubmed-meshheading:5115748-Electromyography, pubmed-meshheading:5115748-Female, pubmed-meshheading:5115748-Histocytochemistry, pubmed-meshheading:5115748-Humans, pubmed-meshheading:5115748-Infant, pubmed-meshheading:5115748-Infant, Newborn, pubmed-meshheading:5115748-Male, pubmed-meshheading:5115748-Microscopy, Electron, pubmed-meshheading:5115748-Mitochondria, Muscle, pubmed-meshheading:5115748-Muscular Diseases, pubmed-meshheading:5115748-Myofibrils, pubmed-meshheading:5115748-Neuromuscular Junction, pubmed-meshheading:5115748-Peripheral Nerves
pubmed:year	1971
pubmed:articleTitle	Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.
pubmed:publicationType	Journal Article