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Article

Advances in the genetics and treatment of von Willebrand disease.

Current opinion in pediatrics - 1 Feb 2002

Federici Augusto B, Mannucci Pier Mannuccio

Abstract excerpt

von Willebrand disease (VWD) is a bleeding disorder caused by quantitative (type 1 and 3) or qualitative (type 2) defects of von Willebrand factor (VWF). The mechanisms of most inherited VWD types have been recently elucidated by genetic and molecular diagnosis, but the phenotypic tests based on measurements of plasma and platelet VWF, the ability of VWF to interact with its platelet receptor, and the analysis of...

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Source

Identifiers

PMID: 11880730
DOI: 10.1097/00008480-200202000-00005

Genes

VWF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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