18581092

Source:http://linkedlifedata.com/resource/pubmed/id/18581092

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007328, umls-concept:C0009566, umls-concept:C0012929, umls-concept:C0022646, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0035331, umls-concept:C0342289, umls-concept:C0733755
pubmed:issue	9
pubmed:dateCreated	2008-8-6
pubmed:abstractText	We assessed the prevalence and determinants of retinal and renal complications in patients with maternally inherited diabetes and deafness (MIDD).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0006777
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial, http://linkedlifedata.com/resource/pubmed/chemical/Hemoglobin A, Glycosylated
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0012-186X
pubmed:author	pubmed-author:BauduceauBB, pubmed-author:Bellanné-ChantelotCC, pubmed-author:BertilGG, pubmed-author:BlickleJ-FJF, pubmed-author:BouhanickBB, pubmed-author:Cahen-VarsauxJJ, pubmed-author:CasanovaSS, pubmed-author:CharpentierGG, pubmed-author:ChedinPP, pubmed-author:Dubois-LaforgueDD, pubmed-author:DupuyOO, pubmed-author:GEDIAM (Mitochondrial Diabetes French Study Group), pubmed-author:GinHH, pubmed-author:GrimaldiAA, pubmed-author:GuerciBB, pubmed-author:GuillausseauP JPJ, pubmed-author:KaloustianEE, pubmed-author:Laloi-MichelinMM, pubmed-author:Lecleire-ColletAA, pubmed-author:LorenziniFF, pubmed-author:MassinPP, pubmed-author:MeasTT, pubmed-author:MuratAA, pubmed-author:NarbonneHH, pubmed-author:OlivierFF, pubmed-author:Paquis-FlucklingerVV, pubmed-author:TimsitJJ, pubmed-author:VialettesBB, pubmed-author:VincenotMM, pubmed-author:VirallyMM
pubmed:issnType	Print
pubmed:volume	51
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1664-70
pubmed:meshHeading	pubmed-meshheading:18581092-Blood Pressure, pubmed-meshheading:18581092-DNA, Mitochondrial, pubmed-meshheading:18581092-Diabetes Mellitus, Type 1, pubmed-meshheading:18581092-Diabetes Mellitus, Type 2, pubmed-meshheading:18581092-Diabetic Angiopathies, pubmed-meshheading:18581092-Diabetic Nephropathies, pubmed-meshheading:18581092-Diabetic Retinopathy, pubmed-meshheading:18581092-Female, pubmed-meshheading:18581092-Glomerular Filtration Rate, pubmed-meshheading:18581092-Hemoglobin A, Glycosylated, pubmed-meshheading:18581092-Humans, pubmed-meshheading:18581092-Kidney Diseases, pubmed-meshheading:18581092-Mitochondrial Diseases, pubmed-meshheading:18581092-Mutation, pubmed-meshheading:18581092-Phenotype, pubmed-meshheading:18581092-Retinal Diseases
pubmed:year	2008
pubmed:articleTitle	Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study.
pubmed:affiliation	APHP, Department of Ophthalmology, Lariboisiere Hospital, University Paris 7 Denis-Diderot, Paris, France.
pubmed:publicationType	Journal Article