574589

Source:http://linkedlifedata.com/resource/pubmed/id/574589

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011848, umls-concept:C0011849, umls-concept:C0029124, umls-concept:C0341628, umls-concept:C0858925
pubmed:issue	6
pubmed:dateCreated	1980-2-26
pubmed:abstractText	The DIDMOAD syndrome is a combination of diabetes mellitus, diabetes insipidus, optic atrophy and labyrinthine deafness. The inheritance is autosomalrecessive. Diagnostic and therapeutic possibilities are discussed on the basis of a further case of this pathogenetically not yet clarified disease pattern. Early detection of this syndrome in juvenile diabetics is important for long-term prognosis and genetic family advice.
pubmed:language	ger
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0326144
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0300-8630
pubmed:author	pubmed-author:GladtkeEE, pubmed-author:IjaiyaKK, pubmed-author:PuynUU, pubmed-author:RothBB
pubmed:issnType	Print
pubmed:volume	191
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	572-7
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:574589-Child, pubmed-meshheading:574589-Diabetes Complications, pubmed-meshheading:574589-Diabetes Insipidus, pubmed-meshheading:574589-Diabetes Mellitus, pubmed-meshheading:574589-Female, pubmed-meshheading:574589-Genetic Counseling, pubmed-meshheading:574589-Hearing Disorders, pubmed-meshheading:574589-Humans, pubmed-meshheading:574589-Optic Atrophy, pubmed-meshheading:574589-Syndrome
pubmed:year	1979
pubmed:articleTitle	[Diabetes insipidus, diabetes mellitus, optic atrophy and labyrinthine deafness: the DIDMOAD-syndrome (author's transl)].
pubmed:publicationType	Journal Article, English Abstract, Case Reports