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• A new congenital platelet abnormality characterized by spontaneous platelet aggregation, enhanced von Willebrand factor platelet interaction, and the presence of all von Willebrand factor multimers in plasma  Academic Article
• Causes of thrombophilia yet to be discovered: A personal view  Academic Article
• Gastrointestinal angiodysplasia in congenital platelet dysfunction  Academic Article
• Glanzmann thrombasthenia: deficient binding of von Willebrand factor to thrombin-stimulated platelets  Academic Article
• Nonsense mutation in the glycoprotein Ib alpha coding sequence associated with Bernard-Soulier syndrome  Academic Article
• Platelet dysfunction and a high bone mass phenotype in a murine model of platelet-type von Willebrand disease  Academic Article
• Platelet receptor structures and polymorphisms  Academic Article
• The clinical impact of platelet-function testing  Academic Article
• Variant Bernard-Soulier syndrome type bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex  Academic Article