H. Vliet

发表

Factor VII coagulant activity is related to blood lipids in the elderly. The Rotterdam study

A. Hofman, D. Grobbee, M. Bots, 1994 .

Acquired von Willebrand disease as a cause of recurrent mucocutaneous bleeding in primary thrombocythemia: Relationship with platelet count

J. Michiels, P. V. Genderen, H. Vliet, 1994, Annals of Hematology.

Erythromelalgia and Arterial Thrombophilia in Thrombocythemia

J. Michiels, P. V. Genderen, H. Vliet, 1994, Annals of the New York Academy of Sciences.

Acquired haemophilia A in women postpartum: management of bleeding episodes and natural history of the factor VIII inhibitor

I. Nováková, H. Nieuwenhuis, I. Novàkovà, 1997, European journal of haematology.

Pseudothrombocytopenia: a cold autoantibody against platelet glycoprotein GP IIb

M. Kappers-Klunne, J. Abels, H. Vliet, 1986, British journal of haematology.

Antibodies against glycosphingolipids in sera of patients with idiopathic thrombocytopenic purpura

M. Kappers-Klunne, J. Abels, H. Vliet, 1987, British journal of haematology.

The in vitro effect of the new antithrombotic drug candidate ALX-0081 on blood samples of patients undergoing percutaneous coronary intervention

M. Simoons, P. D. de Groot, F. Leebeek, 2011, Thrombosis and Haemostasis.

PREDICTION OF BLEEDING RISK BY HAEMOSTASIS TESTS

E. Brommer, A. Boks, S. Schalm, 1988 .

Acquired von Willebrand disease caused by an autoantibody selectively inhibiting the binding of von Willebrand factor to collagen.

P. V. van Genderen, J. Sixma, T. Vink, 1994, Blood.

Heparin-induced thrombocytopenia and antithrombotic therapy

M. Kappers-Klunne, J. Michiels, D. Boon, 1994, The Lancet.