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E Aygören

Showing results (1-10 of 12) with videos related to

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Thrombosis and Haemostasis|January 4, 1998
A multicenter pharmacosurveillance study for the evaluation of the efficacy and safety of recombinant factor VIII in the treatment of patients with hemophilia A. German Kogenate Study GroupE Aygören-Pürsün, I Scharrer
Haemostasis|September 1, 1994
Experience with Haemate P in von Willebrand's disease in adultsI Scharrer, T Vigh, E Aygören-Pürsün
International Archives of Allergy and Immunology|May 22, 2013
Challenges of C1-inhibitor concentrate self-administrationH B Boysen, L Bouillet, E Aygören-Pürsün
Klinische Wochenschrift|January 1, 1990
[Lipoprotein(a): an indicator of risk in thromboembolic disease?]W März, E Aygören, M Trommlitz, et al.
Allergy|August 24, 2013
Risk of angioedema following invasive or surgical procedures in HAE type I and II--the natural historyE Aygören-Pürsün, I Martinez Saguer, W Kreuz, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1993
Two years' experience with two recombinant factor VIII concentratesH H Brackmann, E Aygören, I Scharrer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 1999
Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolismS Ehrenforth, M von Depka Prondsinski, E Aygören-Pürsün, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 4, 2018
Management of patients with hereditary angioedema in Germany: comparison with other countries in the Icatibant Outcome SurveyM Maurer, K Bork, I Martinez-Saguer, et al.
American Journal of Hematology|October 13, 2006
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusionsE Aygören-Pürsün, I Martinez Saguer, E Rusicke, et al.
Cytogenetic and Genome Research|September 2, 2008
Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedemaT Gösswein, A Kocot, G Emmert, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Thrombosis and Haemostasis|January 4, 1998
A multicenter pharmacosurveillance study for the evaluation of the efficacy and safety of recombinant factor VIII in the treatment of patients with hemophilia A. German Kogenate Study GroupE Aygören-Pürsün, I Scharrer
Haemostasis|September 1, 1994
Experience with Haemate P in von Willebrand's disease in adultsI Scharrer, T Vigh, E Aygören-Pürsün
International Archives of Allergy and Immunology|May 22, 2013
Challenges of C1-inhibitor concentrate self-administrationH B Boysen, L Bouillet, E Aygören-Pürsün
Klinische Wochenschrift|January 1, 1990
[Lipoprotein(a): an indicator of risk in thromboembolic disease?]W März, E Aygören, M Trommlitz, et al.
Allergy|August 24, 2013
Risk of angioedema following invasive or surgical procedures in HAE type I and II--the natural historyE Aygören-Pürsün, I Martinez Saguer, W Kreuz, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1993
Two years' experience with two recombinant factor VIII concentratesH H Brackmann, E Aygören, I Scharrer, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 1999
Study of the prothrombin gene 20201 GA variant in FV:Q506 carriers in relationship to the presence or absence of juvenile venous thromboembolismS Ehrenforth, M von Depka Prondsinski, E Aygören-Pürsün, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 4, 2018
Management of patients with hereditary angioedema in Germany: comparison with other countries in the Icatibant Outcome SurveyM Maurer, K Bork, I Martinez-Saguer, et al.
American Journal of Hematology|October 13, 2006
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusionsE Aygören-Pürsün, I Martinez Saguer, E Rusicke, et al.
Cytogenetic and Genome Research|September 2, 2008
Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedemaT Gösswein, A Kocot, G Emmert, et al.
Pageof 2