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rdf:type |
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lifeskim:mentions |
umls-concept:C0001554,
umls-concept:C0008963,
umls-concept:C0011900,
umls-concept:C0015576,
umls-concept:C0239307,
umls-concept:C0332307,
umls-concept:C0796345,
umls-concept:C1264039,
umls-concept:C1273870,
umls-concept:C1336938,
umls-concept:C1521991,
umls-concept:C1710605,
umls-concept:C2603343
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pubmed:issue |
4
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pubmed:dateCreated |
2006-4-25
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pubmed:abstractText |
von Willebrand disease (VWD) type 1 is a congenital bleeding disorder caused by genetic defects in the von Willebrand factor (VWF) gene and characterized by a reduction of structurally normal VWF. The diagnosis of type 1 VWD is difficult because of clinical and laboratory variability. Furthermore, inconsistency of linkage between type 1 VWD and the VWF locus has been reported.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1538-7933
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pubmed:author |
pubmed-author:BatlleJJ,
pubmed-author:BuddeUU,
pubmed-author:CastamanGG,
pubmed-author:EikenboomJJ,
pubmed-author:FedericiA BAB,
pubmed-author:GoodeveAA,
pubmed-author:GoudemandJJ,
pubmed-author:HabaraYY,
pubmed-author:HilzHH,
pubmed-author:HolmbergLL,
pubmed-author:IngerslevJJ,
pubmed-author:LethagenSS,
pubmed-author:MazurierCC,
pubmed-author:MeyerDD,
pubmed-author:PasiJJ,
pubmed-author:PeakeII,
pubmed-author:PutterHH,
pubmed-author:RodeghieroFF,
pubmed-author:SchneppenheimRR,
pubmed-author:Van MarionVV,
pubmed-author:VorlovaZZ
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pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
774-82
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:16634746-Adolescent,
pubmed-meshheading:16634746-Adult,
pubmed-meshheading:16634746-Aged,
pubmed-meshheading:16634746-Blood Coagulation,
pubmed-meshheading:16634746-Child,
pubmed-meshheading:16634746-Child, Preschool,
pubmed-meshheading:16634746-Europe,
pubmed-meshheading:16634746-Family Health,
pubmed-meshheading:16634746-Female,
pubmed-meshheading:16634746-Genes, Dominant,
pubmed-meshheading:16634746-Genetic Linkage,
pubmed-meshheading:16634746-Humans,
pubmed-meshheading:16634746-Infant,
pubmed-meshheading:16634746-Male,
pubmed-meshheading:16634746-Middle Aged,
pubmed-meshheading:16634746-Odds Ratio,
pubmed-meshheading:16634746-Pedigree,
pubmed-meshheading:16634746-Risk Factors,
pubmed-meshheading:16634746-von Willebrand Diseases,
pubmed-meshheading:16634746-von Willebrand Factor
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pubmed:year |
2006
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pubmed:articleTitle |
Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD.
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pubmed:affiliation |
Department of Hematology, Hemostasis and Thrombosis Research Center, Leiden University Medical Center, Leiden, the Netherlands. h.c.j.eikenboom@lumc.nl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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