Von Willebrand’s Disease: Clinical Picture, Diagnosis, and Treatment
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry
Reference119 articles.
1. Shear rate dependence of platelet adhesions to collagenous surfaces in Willebrand factor-depleted blood;Baumgartner;Thromb. Haemostas.,1977
2. Pool s cryoprecipitate and exhausted plasma in the treatment of von Willebrand’s disease and factor-XI deficiency;Bennett;Lancet,1966
3. The treatment of haemorrhage in von Willebrand’s disease and the blood level of factor VIII (AHG);Biggs;Br. J. Haematol.,1963
4. Antihemophilic factor concentrate therapy in von Willebrand’s disease: Dissociation of bleeding time factor and ristocetin-cofactor activities;Blatt;J.A.M.A.,1976
5. Factor VIII on the vascular intima: Possible importance in haemostasis and thrombosis;Bloom;Nature,1973
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1. von Willebrand Disease in Childhood Chronic ITP;The Korean Journal of Hematology;2008
2. Multiple congenital coagulopathies co-expressed with Von Willebrand’s disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature;Haemophilia;2007-11
3. Diagnostik und klinischer Verlauf bei 10 Patienten mit erworbenem von-Willebrand-Syndrom;28. Hämophilie-Symposion Hamburg 1997;1999
4. Hemophilia;Emergency Medicine Clinics of North America;1993-05
5. Potentially catastrophic bleeding disorders;Postgraduate Medicine;1989-09
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