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Seminars in Thrombosis and Hemostasis|January 1, 1997
Acquired von Willebrand disease in patients with high platelet countsU Budde, P J van GenderenAngiology|June 1, 1994
Arterial thrombophilia in primary thrombocythemia. A case reportP J van Genderen, J J MichielsPresse Medicale (Paris, France : 1983)|January 22, 1994
Erythromelalgic, thrombotic and haemorrhagic manifestations of thrombocythaemiaP J van Genderen, J J MichielsBailliere'S Clinical Haematology|March 31, 1999
Acquired von Willebrand diseaseP J van Genderen, J J MichielsSeminars in Thrombosis and Hemostasis|January 1, 1997
Erythromelalgia: a pathognomonic microvascular thrombotic complication in essential thrombocythemia and polycythemia veraP J van Genderen, J J MichielsSeminars in Thrombosis and Hemostasis|January 1, 1997
Essential thrombocythemia in childhoodJ J Michiels, P J Van GenderenDrugs & Aging|September 13, 2000
Polycythaemia vera and essential thrombocythaemia in the elderlyP J van Genderen, M M TroostThrombosis Research|February 15, 1994
The reliability of Hickman catheter blood for the assessment of activation markers of coagulation and fibrinolysis in patients with hematological malignanciesP J van Genderen, M Gomes, J StibbeSeminars in Thrombosis and Hemostasis|January 1, 1997
The paradox of bleeding and thrombosis in thrombocythemia: is von Willebrand factor the link?P J van Genderen, H Leenknegt, J J MichielsAngiology|June 1, 1994
Thrombocythemic erythromelalgia, primary erythermalgia, and secondary erythermalgia: three distinct clinicopathologic entitiesJ P Drenth, P J van Genderen, J J MichielsPageof 4