subject area of
- 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