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Investigating the Genetic Basis of Type 3 of Von Willebrand Disease (VWD)
von Willebrand Disease (VWD) is the most common inherited bleeding disorder in humans, resulting from quantitative or qualitative deficiencies of von Willebrand factor (VWF). Type 3 VWD is the rarest and most severe form ...
Characterizing angiodysplasia in type 2 von Willebrand disease (VWD) using blood outgrowth endothelial cells (BOECs)
Gastrointestinal bleeding associated with angiodysplasia is a common, often intractable complication in patients with von Willebrand disease (VWD). von Willebrand factor (VWF), the protein deficient in VWD, was recently ...