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Keywords: Desmopressin response
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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
... concentrates. Therefore, a DDAVP trial is also warranted in patients with recessive inheritance and measurable FVIII/VWF par-ameters. Autosomal recessive disease C2362F Desmopressin response Multimeric patterns von Willebrand disease type 3 ...
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
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Journal Articles

Autosomal Dominant von Willebrand Disease Type 2M

Subject Area:
Hematology , Oncology
Cedric Hermans, Javier Batlle
Journal: Acta Haematologica
Acta Haematol (2009) 121 (2-3): 139–144.
https://doi.org/10.1159/000214854
Published Online: 08 June 2009
.... Desmopressin response Multimeric patterns Phenotype Platelet adhesion Type 2M von Willebrand disease von Willebrand disease (VWD) is a common, congenital bleeding disorder caused by a deficiency in or dysfunction of von Willebrand factor (VWF). VWF is a large, multimeric plasma glycoprotein...
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