21103682

Source:http://linkedlifedata.com/resource/pubmed/id/21103682

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0028860, umls-concept:C0684224, umls-concept:C0868928
pubmed:issue	2
pubmed:dateCreated	2010-11-24
pubmed:abstractText	Lowe Syndrome, or Oculocerebrorenal Dystrophy (OCRL), has a recessive inheritance linked to X chromosome. It presents cataracts and glaucoma, delay in neuropsychomotor development, cognitive deficits, and renal Fanconi syndrome.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/21103682
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9426946
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	2175-8239
pubmed:author	pubmed-author:CarvalhaesJoão Tomás de AbreuJT, pubmed-author:FernandesFernanda Alves ThomazFA, pubmed-author:GenzaniCamila PenteadoCP, pubmed-author:MaiaMarta Liliane de AlmeidaML, pubmed-author:de AndradeMaria CristinaMC, pubmed-author:do ValMaria Luiza Dautro MoreiraML
pubmed:issnType	Electronic
pubmed:volume	32
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	216-22
pubmed:dateRevised	2011-9-12
pubmed:meshHeading	pubmed-meshheading:21103682-Child, pubmed-meshheading:21103682-Child, Preschool, pubmed-meshheading:21103682-Humans, pubmed-meshheading:21103682-Infant, pubmed-meshheading:21103682-Male, pubmed-meshheading:21103682-Oculocerebrorenal Syndrome
pubmed:articleTitle	Lowe syndrome: report of five cases.
pubmed:affiliation	Division of Pediatric Nephrology, Departament of Pediatrics, UNIFESPEPM- Universidade Federal de São Paulo- SP- Brazil, Division of Pediatric Nephrology, Hospital Infantil Darcy Vargas, São Paulo, SP, Brazil.
pubmed:publicationType	Journal Article