21269740

Source:http://linkedlifedata.com/resource/pubmed/id/21269740

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001675, umls-concept:C0019202
pubmed:issue	6
pubmed:dateCreated	2011-5-23
pubmed:abstractText	Wilson's disease (WD) is an inherited disorder of copper metabolism, characterized by the accumulation of copper in the body due to defective biliary copper excretion by hepatocytes. We report a series of 19 patients with WD.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8101383
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1768-3122
pubmed:author	pubmed-author:BronowickiJ-PJP, pubmed-author:JacquierAA, pubmed-author:KaminskyPP, pubmed-author:Mercier-JacquierMM, pubmed-author:RaabeJ-JJJ
pubmed:copyrightInfo	Copyright © 2010 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.
pubmed:issnType	Electronic
pubmed:volume	32
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	341-6
pubmed:meshHeading	pubmed-meshheading:21269740-Adolescent, pubmed-meshheading:21269740-Adult, pubmed-meshheading:21269740-Aged, pubmed-meshheading:21269740-Child, pubmed-meshheading:21269740-Child, Preschool, pubmed-meshheading:21269740-Female, pubmed-meshheading:21269740-Hepatolenticular Degeneration, pubmed-meshheading:21269740-Humans, pubmed-meshheading:21269740-Male, pubmed-meshheading:21269740-Middle Aged, pubmed-meshheading:21269740-Retrospective Studies, pubmed-meshheading:21269740-Young Adult
pubmed:year	2011
pubmed:articleTitle	[Wilson's disease in an adult].
pubmed:affiliation	Service de médecine interne orientée vers les maladies orphelines et systémiques, hôpitaux de Brabois, CHU de Nancy, rue du Morvan, Vandœuvre, France.
pubmed:publicationType	Journal Article, English Abstract