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Annals of Hematology|January 8, 2010
Acquired haemophilia caused by non-haemophilic factor VIII gene variantsAndreas Tiede, Roswith Eisert, Andreas Czwalinna, et al.Journal of Neurosurgery|May 15, 2002
Application of recombinant activated factor VII during surgery for a giant skull base hemangiopericytoma to achieve safe hemostasis. Case reportRüdiger Gerlach, Gerhard Marquardt, Heimo Wissing, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 20, 2009
Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defectsWolfgang Miesbach, Inge Scharrer, Agnes Henschen, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 30, 2003
Combined plasmapheresis and immunosuppression as rescue treatment of a patient with catastrophic antiphospholipid syndrome occurring despite anticoagulation: a case reportSteffen Koschmieder, Wolfgang Miesbach, Florian Fauth, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 12, 2006
Cold storage of citrated whole blood induces drastic time-dependent losses in factor VIII and von Willebrand factor: potential for misdiagnosis of haemophilia and von Willebrand diseaseMartina Böhm, Susanne Täschner, Evelyne Kretzschmar, et al.Thrombosis and Haemostasis|February 1, 2007
Addition of rituximab to standard therapy improves response rate and progression-free survival in relapsed or refractory thrombotic thrombocytopenic purpura and autoimmune haemolytic anaemiaFlorian Heidel, Daniel B Lipka, Charis von Auer, et al.Thrombosis Research|December 4, 2003
ADAMTS-13 activity in patients with brain and prostate tumors is mildly reduced, but not correlated to stage of malignancy and metastasisMartina Böhm, Rüdiger Gerlach, Wolf-Dietrich Beecken, et al.Journal of Clinical Medicine|January 22, 2021
Influence of Personality, Resilience and Life Conditions on Depression and Anxiety in 104 Patients Having Survived Acute Autoimmune Thrombotic Thrombocytopenic PurpuraTanja Falter, Sibylle Böschen, Markus Schepers, et al.Thrombosis and Haemostasis|April 30, 2003
The deletion polymorphism in the angiotensin-converting enzyme gene is a moderate risk factor for venous thromboembolismMario von Depka, Andreas Czwalinna, Cornelia Wermes, et al.British Journal of Haematology|May 27, 2005
The course of ADAMTS-13 activity and inhibitor titre in the treatment of thrombotic thrombocytopenic purpura with plasma exchange and vincristineMartina Böhm, Christoph Betz, Wolfgang Miesbach, et al.Pageof 6