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Keywords: von Willebrand disease type 3
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Journal Articles

Current Management of Patients with Severe von Willebrand Disease Type 3: A 2012 Update

Subject Area:
Hematology , Oncology
Augusto B. Federici, Paula James
Journal: Acta Haematologica
Acta Haematol (2012) 128 (2): 88–99.
https://doi.org/10.1159/000338208
Published Online: 15 August 2012
...Augusto B. Federici; Paula James Von Willebrand disease type 3 (VWD3) is the most severe form of this bleeding disorder due to the almost complete deficiency of von Willebrand factor (VWF). VWD3 is inherited as an autosomal recessive trait. While heterozygous carriers exhibit mild or no bleeding...
View article titled, Current Management of Patients with Severe <span class="search-highlight">von</span> <span class="search-highlight">Willebrand</span> <span class="search-highlight">Disease</span> <span class="search-highlight">Type</span> <span class="search-highlight">3</span>: A 2012 Update
Open the PDF for Current Management of Patients with Severe <span class="search-highlight">von</span> <span class="search-highlight">Willebrand</span> <span class="search-highlight">Disease</span> <span class="search-highlight">Type</span> <span class="search-highlight">3</span>: A 2012 Update in another window
Journal Articles

Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene: A Single Center Experience on Molecular Heterogeneity and Laboratory Features in 12 Families

Subject Area:
Hematology , Oncology
G. Castaman, S. Giacomelli, F. Rodeghiero
Journal: Acta Haematologica
Acta Haematol (2009) 121 (2-3): 106–110.
https://doi.org/10.1159/000214850
Published Online: 08 June 2009
... von Willebrand disease type 3 von Willebrand disease (VWD) is an inherited bleeding disorder caused by a deficiency in or abnormal function of von Willebrand factor (VWF), a multimeric protein which promotes platelet adhesion to the subendothelium and acts as a carrier for factor VIII (FVIII...
View article titled, Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene: A Single Center Experience on Molecular Heterogeneity and Laboratory Features in 12 Families
Open the PDF for Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene: A Single Center Experience on Molecular Heterogeneity and Laboratory Features in 12 Families in another window