Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
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 Group
E Aygören-Pürsün, I Scharrer
Haemostasis
|
September 1, 1994
Experience with Haemate P in von Willebrand's disease in adults
I Scharrer, T Vigh, E Aygören-Pürsün
International Archives of Allergy and Immunology
|
May 22, 2013
Challenges of C1-inhibitor concentrate self-administration
H 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 history
E 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 concentrates
H 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 thromboembolism
S 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 Survey
M Maurer, K Bork, I Martinez-Saguer, et al.
American Journal of Hematology
|
October 13, 2006
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusions
E 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 angioedema
T Gösswein, A Kocot, G Emmert, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 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 Group
E Aygören-Pürsün, I Scharrer
Haemostasis
|
September 1, 1994
Experience with Haemate P in von Willebrand's disease in adults
I Scharrer, T Vigh, E Aygören-Pürsün
International Archives of Allergy and Immunology
|
May 22, 2013
Challenges of C1-inhibitor concentrate self-administration
H 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 history
E 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 concentrates
H 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 thromboembolism
S 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 Survey
M Maurer, K Bork, I Martinez-Saguer, et al.
American Journal of Hematology
|
October 13, 2006
Retrochorionic hematoma in congenital afibrinogenemia: resolution with fibrinogen concentrate infusions
E 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 angioedema
T Gösswein, A Kocot, G Emmert, et al.
Page
of 2