Differential identification of a rare form of platelet-type (pseudo-) von Willebrand disease (VWD) from Type 2B VWD using a simplified ristocetin-induced-platelet-agglutination mixing assay and confirmed by genetic analysis-Reference-Cited by-同舟云学术

Differential identification of a rare form of platelet-type (pseudo-) von Willebrand disease (VWD) from Type 2B VWD using a simplified ristocetin-induced-platelet-agglutination mixing assay and confirmed by genetic analysis

Published:2007-11 Issue:4 Volume:139 Page:623-626
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Favaloro Emmanuel J.,Patterson David,Denholm Anna,Mead Scott,Gilbert Ann,Collins Anne,Estell Jane,George Peter M.,Smith Mark P.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2007.06850.x/fullpdf

Reference7 articles.

1. Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance

2. 2B or not 2B? Differential identification of type 2B, versus pseudo-von Willebrand disease

3. Laboratory Identification of von Willebrand Disease: Technical and Scientific Perspectives

4. Identification of a novel point mutation in platelet glycoprotein Ibalpha, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease

5. A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene

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