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Bailliere'S Clinical Haematology|March 31, 1999
Acquired von Willebrand diseaseP J van Genderen, J J MichielsAngiology|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 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 GenderenSeminars 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 MichielsLeukemia & Lymphoma|September 1, 1996
Acquired von Willebrand disease in myeloproliferative disordersP J van Genderen, H Leenknegt, J J Michiels, et al.British Journal of Haematology|March 23, 1999
Thromboxane-dependent platelet activation in vivo precedes arterial thrombosis in thrombocythaemia: a rationale for the use of low-dose aspirin as an antithrombotic agentP J van Genderen, F J Prins, J J Michiels, et al.Leukemia & Lymphoma|September 1, 1996
Atypical transient ischemic attacks in thrombocythemia of various myeloproliferative disordersJ J Michiels, P J van Genderen, P H Jansen, et al.Pageof 13