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von Willebrand Disease: A Concise Review and Update for the Practicing Physician

Clinical and Applied Thrombosis/Hemostasis, 2017
Varinder Kaur
exaly  

Classification and Characterization of Hereditary Types 2A, 2B, 2C, 2D, 2E, 2M, 2N, and 2U (Unclassifiable) von Willebrand Disease

Clinical and Applied Thrombosis/Hemostasis, 2006
Zwi N Berneman   +2 more
exaly  

Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology

Best Practice and Research in Clinical Haematology, 2001
C Mazurier   +2 more
exaly  

Von Willebrand factor and von Willebrand disease

Von Willebrand disease (vWD) is an autosomally inherited bleeding disorder caused by a deficiency or abnormality of von Willebrand factor (vWF). vWF is a large multimeric glycoprotein that mediates platelet adhesion at the site of vessel injury. Also, it protects factor VIII from proteolytic degradation in the circulation. vWD has a prevalence of about
openaire   +1 more source

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