The Molecular Basis of Von Willebrand Disease

Luciano Baronciani; Pier Mannuccio Mannucci

doi:10.1002/9781444318531.ch19

The Molecular Basis of Von Willebrand Disease

Luciano Baronciani, Pier Mannuccio Mannucci

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Original language	English
Title of host publication	Molecular Hematology: Third Edition
Publisher	Wiley-Blackwell
Pages	233-245
Number of pages	13
ISBN (Print)	9781405182317
DOIs	https://doi.org/10.1002/9781444318531.ch19
Publication status	Published - Mar 10 2010

Keywords

Gene encoding VWF-mapped on chromosome 12
Molecular basis of von Willebrand disease
Transfusional therapy with plasma products containing FVIII and VWF-treatment of choice
Type 2 VWD-approximately 20% of all VWD cases
Type 3 VWD, autosomal recessive severe disorder-and nearly complete absence of VWF
Von Willebrand disease (VWD)-common inherited bleeding disorder
Von Willebrand disease and its classification
Von Willebrand factor in primary hemostasis
VWD and deficiency or multimeric plasma glycoprotein dysfunction of von Willebrand factor (VWF)
VWF multimer synthesis and subcellular localization of post-translational modification events

ASJC Scopus subject areas

Medicine(all)

Access to Document

10.1002/9781444318531.ch19

Cite this

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title = "The Molecular Basis of Von Willebrand Disease",

keywords = "Gene encoding VWF-mapped on chromosome 12, Molecular basis of von Willebrand disease, Transfusional therapy with plasma products containing FVIII and VWF-treatment of choice, Type 2 VWD-approximately 20% of all VWD cases, Type 3 VWD, autosomal recessive severe disorder-and nearly complete absence of VWF, Von Willebrand disease (VWD)-common inherited bleeding disorder, Von Willebrand disease and its classification, Von Willebrand factor in primary hemostasis, VWD and deficiency or multimeric plasma glycoprotein dysfunction of von Willebrand factor (VWF), VWF multimer synthesis and subcellular localization of post-translational modification events",

author = "Luciano Baronciani and Mannucci, {Pier Mannuccio}",

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KW - Molecular basis of von Willebrand disease

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KW - Type 2 VWD-approximately 20% of all VWD cases

KW - Type 3 VWD, autosomal recessive severe disorder-and nearly complete absence of VWF

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KW - Von Willebrand disease and its classification

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The Molecular Basis of Von Willebrand Disease

Keywords

ASJC Scopus subject areas

Access to Document

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