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U Harbrecht

Showing results (11-20 of 20) with videos related to

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Journal of Internal Medicine|March 6, 1998
Increased sensitivity of factor IX to phenprocoumon as a cause of bleeding in a patient with antiphospholipid antibody associated thrombosisU Harbrecht, J Oldenburg, P Klein, et al.
Virchows Archiv : an International Journal of Pathology|February 9, 2000
Segmental hepatic vein thrombosis associated with heparin-induced thrombocytopenia III Theuerkauf, L Lickfett, U Harbrecht, et al.
Neurology|April 13, 2005
Heparin-induced thrombocytopenia in neurologic patients treated with low-molecular-weight heparinC Pohl, A Kredteck, B Bastians, et al.
Neurology|April 4, 2000
Neurologic complications in immune-mediated heparin-induced thrombocytopeniaC Pohl, U Harbrecht, A Greinacher, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 14, 2015
Congenital combined deficiency of coagulation factors VII and X--different genetic mechanismsA Pavlova, B Preisler, J Driesen, et al.
European Journal of Neurology|August 2, 2005
Common genetic variants of homocysteine metabolism in ischemic stroke: a case-control studyM Linnebank, M Montenarh, H Kölsch, et al.
British Journal of Haematology|July 1, 1997
Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapyJ Oldenburg, E M Quenzel, U Harbrecht, et al.
Neurology|December 30, 2004
Polymorphisms in glutathione S-transferase omega-1 and AD, vascular dementia, and strokeH Kölsch, M Linnebank, D Lütjohann, et al.
Thrombosis and Haemostasis|January 12, 2001
Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complexJ Oldenburg, B von Brederlow, A Fregin, et al.
Hamostaseologie|June 7, 2014
[Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]R Knöfler, W Eberl, H Schulze, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Internal Medicine|March 6, 1998
Increased sensitivity of factor IX to phenprocoumon as a cause of bleeding in a patient with antiphospholipid antibody associated thrombosisU Harbrecht, J Oldenburg, P Klein, et al.
Virchows Archiv : an International Journal of Pathology|February 9, 2000
Segmental hepatic vein thrombosis associated with heparin-induced thrombocytopenia III Theuerkauf, L Lickfett, U Harbrecht, et al.
Neurology|April 13, 2005
Heparin-induced thrombocytopenia in neurologic patients treated with low-molecular-weight heparinC Pohl, A Kredteck, B Bastians, et al.
Neurology|April 4, 2000
Neurologic complications in immune-mediated heparin-induced thrombocytopeniaC Pohl, U Harbrecht, A Greinacher, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 14, 2015
Congenital combined deficiency of coagulation factors VII and X--different genetic mechanismsA Pavlova, B Preisler, J Driesen, et al.
European Journal of Neurology|August 2, 2005
Common genetic variants of homocysteine metabolism in ischemic stroke: a case-control studyM Linnebank, M Montenarh, H Kölsch, et al.
British Journal of Haematology|July 1, 1997
Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapyJ Oldenburg, E M Quenzel, U Harbrecht, et al.
Neurology|December 30, 2004
Polymorphisms in glutathione S-transferase omega-1 and AD, vascular dementia, and strokeH Kölsch, M Linnebank, D Lütjohann, et al.
Thrombosis and Haemostasis|January 12, 2001
Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complexJ Oldenburg, B von Brederlow, A Fregin, et al.
Hamostaseologie|June 7, 2014
[Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]R Knöfler, W Eberl, H Schulze, et al.
Pageof 2