I Pabinger-Fasching|K Lechner - JoVE Visualize

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Blut|November 1, 1990

Hemostatic and fibrinolytic parameters in patients with acute myeloid leukemia: activation of blood coagulation, fibrinolysis and unspecific proteolysisW Speiser, I Pabinger-Fasching, P A Kyrle, et al.

Blut|November 1, 1984

Efficacy of the M-2 protocol in previously untreated patients with advanced multiple myelomaH Gössinger, P Bettelheim, E Neumann, et al.

Thrombosis and Haemostasis|July 1, 1994

Six novel and three recurrent mutations in nine Austrian patients with hemophilia BJ Walter, I Pabinger-Fasching, H H Watzke

Cardiology in the Young|May 29, 2000

Is there a possible role for haemostasis in the development of perigraft reaction complicating the modified Blalock Taussig shunt?U Salzer-Muhar, I Pabinger-Fasching, S Zacherl-Wightman

Thrombosis and Haemostasis|June 30, 1989

High risk of acquired immune deficiency syndrome (AIDS) and of AIDS related complex (ARC) in hemophiliacs seropositive for more than 5 yearsC Stain, I Pabinger-Fasching, K Guggenberger, et al.

Annals of Hematology|April 23, 2003

Fibrinolytic therapy with rt-PA in a patient with paroxysmal nocturnal hemoglobinuria and Budd-Chiari syndromeA C Hauser, A Brichta, I Pabinger-Fasching, et al.

Annals of Hematology|May 1, 1994

Symptomatic hereditary type-II protein C deficiency caused by a missense mutation in exon IX of the protein C gene (Gly381 to Ser)E Wittmann, J Walter, I Pabinger-Fasching, et al.

International Journal of Clinical & Laboratory Research|February 24, 2001

Evaluation of a highly specific functional test for the detection of factor V LeidenP Quenhenberger, S Handler, C Mannhalter, et al.

Padiatrie Und Padologie|January 1, 1991

[Warfarin embryopathy in maternal coumarin therapy for protein S deficiency]S Freude, I Pabinger-Fasching, D Kozel-Lachmann, et al.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1993

Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiencyS R Poort, I Pabinger-Fasching, C Mannhalter, et al.

Pageof 40

Showing results (11-20 of 397) with videos related to

Sort By:

Pageof 40

Blut|November 1, 1990

Hemostatic and fibrinolytic parameters in patients with acute myeloid leukemia: activation of blood coagulation, fibrinolysis and unspecific proteolysisW Speiser, I Pabinger-Fasching, P A Kyrle, et al.

Blut|November 1, 1984

Efficacy of the M-2 protocol in previously untreated patients with advanced multiple myelomaH Gössinger, P Bettelheim, E Neumann, et al.

Thrombosis and Haemostasis|July 1, 1994

Six novel and three recurrent mutations in nine Austrian patients with hemophilia BJ Walter, I Pabinger-Fasching, H H Watzke

Cardiology in the Young|May 29, 2000

Is there a possible role for haemostasis in the development of perigraft reaction complicating the modified Blalock Taussig shunt?U Salzer-Muhar, I Pabinger-Fasching, S Zacherl-Wightman

Thrombosis and Haemostasis|June 30, 1989

High risk of acquired immune deficiency syndrome (AIDS) and of AIDS related complex (ARC) in hemophiliacs seropositive for more than 5 yearsC Stain, I Pabinger-Fasching, K Guggenberger, et al.

Annals of Hematology|April 23, 2003

Fibrinolytic therapy with rt-PA in a patient with paroxysmal nocturnal hemoglobinuria and Budd-Chiari syndromeA C Hauser, A Brichta, I Pabinger-Fasching, et al.

Annals of Hematology|May 1, 1994

Symptomatic hereditary type-II protein C deficiency caused by a missense mutation in exon IX of the protein C gene (Gly381 to Ser)E Wittmann, J Walter, I Pabinger-Fasching, et al.

International Journal of Clinical & Laboratory Research|February 24, 2001

Evaluation of a highly specific functional test for the detection of factor V LeidenP Quenhenberger, S Handler, C Mannhalter, et al.

Padiatrie Und Padologie|January 1, 1991

[Warfarin embryopathy in maternal coumarin therapy for protein S deficiency]S Freude, I Pabinger-Fasching, D Kozel-Lachmann, et al.

Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1993

Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiencyS R Poort, I Pabinger-Fasching, C Mannhalter, et al.

Pageof 40