The Molecular Basis of Von Willebrand Disease

Luciano Baronciani, Pier Mannuccio Mannucci

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

Original languageEnglish
Title of host publicationMolecular Hematology: Third Edition
PublisherWiley-Blackwell
Pages233-245
Number of pages13
ISBN (Print)9781405182317
DOIs
Publication statusPublished - 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)

Cite this

Baronciani, L., & Mannucci, P. M. (2010). The Molecular Basis of Von Willebrand Disease. In Molecular Hematology: Third Edition (pp. 233-245). Wiley-Blackwell. https://doi.org/10.1002/9781444318531.ch19

The Molecular Basis of Von Willebrand Disease. / Baronciani, Luciano; Mannucci, Pier Mannuccio.

Molecular Hematology: Third Edition. Wiley-Blackwell, 2010. p. 233-245.

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

Baronciani, L & Mannucci, PM 2010, The Molecular Basis of Von Willebrand Disease. in Molecular Hematology: Third Edition. Wiley-Blackwell, pp. 233-245. https://doi.org/10.1002/9781444318531.ch19
Baronciani L, Mannucci PM. The Molecular Basis of Von Willebrand Disease. In Molecular Hematology: Third Edition. Wiley-Blackwell. 2010. p. 233-245 https://doi.org/10.1002/9781444318531.ch19
Baronciani, Luciano ; Mannucci, Pier Mannuccio. / The Molecular Basis of Von Willebrand Disease. Molecular Hematology: Third Edition. Wiley-Blackwell, 2010. pp. 233-245
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