vWF, von Willebrand factor
Predictors of Bleeding from Esophageal Varices: The Role of Factor VII and von Willebrand Factor (vWF)
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Superiority of the Rapid Von Willebrand Factor (VWF) VWF:GPIbR and VWF:GPIbM Assays in Type 2A, 2B and 2M Von Willebrand Disease
12
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease
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Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress induced platelet aggregation
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Role of serum ADAMTS13 and Von Willebrand Factor (VWF) as early Prognostic Markers in Identifying the Disease Course in Dengue Fever
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Immunohistochemistry comparing endoscopic vein harvesting vs. open vein harvesting on saphenous vein endothelium
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Severe Plasmodium falciparum malaria is associated with circulating ultra-large von willebrand multimers and ADAMTS13 inhibition
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Time course of soluble P-selectin and von Willebrand factor levels in trauma patients: a prospective observational study
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Variance of matrix metalloproteinase (MMP) and tissue inhibitor of metalloproteinase (TIMP) concentrations in activated, concentrated platelets from healthy male donors
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Von Willebrand's disease with spontaneous platelet aggregation induced by an abnormal plasma von Willebrand factor
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Rapid activation of endothelial cells enables Plasmodium falciparum adhesion to platelet-decorated von Willebrand factor strings.
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Fibrin induces release of von Willebrand factor from endothelial cells
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Relationship between ABO blood group and von Willebrand factor levels: from biology to clinical implications
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Unusually large von Willebrand factor multimers increase adhesion of sickle erythrocytes to human endothelial cells under controlled flow
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Abstract
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O linked carbohydrate of recombinant von Willebrand factor influences ristocetin induced binding to platelet glycoprotein 1b
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Gray platelet syndrome Dissociation between abnormal sorting in megakaryocyte alpha granules and normal sorting in Weibel Palade bodies of endothelial cells
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Demonstration and characterization of specific binding sites for factor VIII/von Willebrand factor on human platelets
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Subunit composition of plasma von Willebrand factor Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE)
6
Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin Role of platelet activation, fibrinogen, and two distinct membrane receptors
9