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Article

Rethinking the diagnosis of von Willebrand disease.

Thrombosis research - 1 Jan 2011

Favaloro Emmanuel J

Abstract excerpt

von Willebrand disease (VWD) is the most common inherited bleeding disorder and arises from deficiencies and/or defects in the plasma protein von Willebrand factor (VWF). VWD is classified into 6 different types, with type 1 identified as a (partial) quantitative deficiency of VWF, type 3 defined by a (virtual) total deficiency of VWF, and type 2 identifying four separate types (2A, 2B, 2M, 2N) characterised by...

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Identifiers

PMID: 21193108
DOI: 10.1016/S0049-3848(10)70149-3

Genes

VWF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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