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Article

Advances in the diagnosis and management of type 1 von Willebrand disease.

Expert review of hematology - 1 Feb 2011

Castaman Giancarlo, Rodeghiero Francesco

Abstract excerpt

Von Willebrand disease (VWD) is an autosomally inherited bleeding disorder caused by a deficiency and/or abnormality of von Willebrand factor (VWF). VWF is a multimeric adhesive protein that plays an important role in primary hemostasis by promoting platelet adhesion to the subendothelium at sites of vascular injury and platelet-platelet interactions at high-shear rate conditions. Furthermore, VWF is the carrier...

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Identifiers

PMID: 21322782
DOI: 10.1586/ehm.11.1

Genes

VWF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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