Genotyping might help therapeutic decision-making in patients with von Willebrand disease type 2 B
Author:
Affiliation:
1. Centre Regional de Traitement des Hemophiles; Hopital Louis Pradel; Bron France
2. Laboratoire Hématase; Hôpital E. Herriot; Lyon France
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12960/fullpdf
Reference11 articles.
1. Accelerated uptake of VWF/platelet complexes in macrophages contributes to VWD type 2B-associated thrombocytopenia;Casari;Blood,2013
2. The genetic basis of von Willebrand disease;Goodeve;Blood Rev,2010
3. Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients;Federici;Blood,2009
4. Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in type IIB von Willebrand's disease;Holmberg;N Engl J Med,1983
5. How I treat type 2 variant forms of von Willebrand disease;Tosetto;Blood,2015
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Updated overview on von Willebrand disease: focus on the interest of genotyping;Expert Review of Hematology;2019-10-06
2. Thrombocytopenia and GBA gene mutation in a patient with adult type 1 Gaucher disease;Platelets;2017-06-05
3. Differential diagnosis of neonatal alloimmune thrombocytopenia: Type 2B von Willebrand disease;Platelets;2017-04-24
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