Platelet von Willebrand factor in inherited and acquired bleeding disorders.
- 28 March 1995
- journal article
- editorial
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 92 (7) , 2428-2432
- https://doi.org/10.1073/pnas.92.7.2428
Abstract
No abstract availableThis publication has 52 references indexed in Scilit:
- Purification and characterization of human platelet von Willebrand factorBritish Journal of Haematology, 1994
- The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand diseaseBritish Journal of Haematology, 1994
- Multimeric pattern of plasma and platelet von willebrand factor is normal in uremic patientsAmerican Journal of Hematology, 1993
- Type I von Willebrand disease, subtype ‘platelet low’: decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cellsBritish Journal of Haematology, 1993
- Effect of deletion of the A1 domain of von Willebrand factor on its binding to heparin, collagen and platelets in the presence of ristocetinEuropean Journal of Biochemistry, 1991
- Collagen type III induced ex vivo thrombogenesis in humans. Role of platelets and leukocytes in deposition of fibrin.Arteriosclerosis: An Official Journal of the American Heart Association, Inc., 1990
- Correction of the bleeding time in treated patients with severe von willebrand disease is not solely dependent on the normal multimeric structure of plasma von willebrand factorAmerican Journal of Hematology, 1987
- Transplantation of normal bone marrow into a pig with severe von Willebrand's disease.Journal of Clinical Investigation, 1986
- Variant von Willebrand's DiseaseJournal of Clinical Investigation, 1980
- Presence of factor VIII-related antigen in blood platelets of patients with Von Willebrand's diseaseNature, 1975