E L Saenko|S W Pipe - JoVE Visualize

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The Journal of Pediatrics|May 1, 1996

Neonatal purpura fulminans in association with factor V R506Q mutationS W Pipe, A H Schmaier, W C Nichols, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|September 9, 2011

Outcomes of mentored, grant-funded fellowship training in haemostasis /thrombosis: findings from a nested case-control survey studyN A Goldenberg, R Kruse-Jarres, N Frick, et al.

Journal of Thrombosis and Haemostasis : JTH|May 19, 2006

Factor V C2 domain contains a major thrombin-binding site responsible for thrombin-catalyzed factor V activationH Suzuki, M Shima, K Nogami, et al.

Thrombosis Research|April 12, 2001

In hemophilia A and autoantibody inhibitor patients: the factor VIII A2 domain and light chain are most immunogenicD H Scandella, H Nakai, M Felch, et al.

Blood|September 18, 1997

Loss of tolerance to exogenous and endogenous factor VIII in a mild hemophilia A patient with an Arg593 to Cys mutationA R Thompson, M E Murphy, M Liu, et al.

The Journal of Biological Chemistry|June 16, 1995

Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIIIJ F Healey, I M Lubin, H Nakai, et al.

Biokhimiia (Moscow, Russia)|October 1, 1989

[Protective effect rendered by human ceruloplasmin on erythrocytes in hepatocerebral dystrophy]E L Saenko, O V Skorobogat'ko, T I Mzhel'skaia, et al.

Vox Sanguinis|August 31, 2002

Molecular defects in coagulation Factor VIII and their impact on Factor VIII functionE L Saenko, N Ananyeva, D Kouiavskaia, et al.

The Journal of Biological Chemistry|June 1, 2000

Factor VIII C2 domain contains the thrombin-binding site responsible for thrombin-catalyzed cleavage at Arg1689K Nogami, M Shima, K Hosokawa, et al.

Thrombosis and Haemostasis|February 12, 1999

Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chainR Laub, M Di Giambattista, P Fondu, et al.

Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:

Pageof 9

The Journal of Pediatrics|May 1, 1996

Neonatal purpura fulminans in association with factor V R506Q mutationS W Pipe, A H Schmaier, W C Nichols, et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia|September 9, 2011

Outcomes of mentored, grant-funded fellowship training in haemostasis /thrombosis: findings from a nested case-control survey studyN A Goldenberg, R Kruse-Jarres, N Frick, et al.

Journal of Thrombosis and Haemostasis : JTH|May 19, 2006

Factor V C2 domain contains a major thrombin-binding site responsible for thrombin-catalyzed factor V activationH Suzuki, M Shima, K Nogami, et al.

Thrombosis Research|April 12, 2001

In hemophilia A and autoantibody inhibitor patients: the factor VIII A2 domain and light chain are most immunogenicD H Scandella, H Nakai, M Felch, et al.

Blood|September 18, 1997

Loss of tolerance to exogenous and endogenous factor VIII in a mild hemophilia A patient with an Arg593 to Cys mutationA R Thompson, M E Murphy, M Liu, et al.

The Journal of Biological Chemistry|June 16, 1995

Residues 484-508 contain a major determinant of the inhibitory epitope in the A2 domain of human factor VIIIJ F Healey, I M Lubin, H Nakai, et al.

Biokhimiia (Moscow, Russia)|October 1, 1989

[Protective effect rendered by human ceruloplasmin on erythrocytes in hepatocerebral dystrophy]E L Saenko, O V Skorobogat'ko, T I Mzhel'skaia, et al.

Vox Sanguinis|August 31, 2002

Molecular defects in coagulation Factor VIII and their impact on Factor VIII functionE L Saenko, N Ananyeva, D Kouiavskaia, et al.

The Journal of Biological Chemistry|June 1, 2000

Factor VIII C2 domain contains the thrombin-binding site responsible for thrombin-catalyzed cleavage at Arg1689K Nogami, M Shima, K Hosokawa, et al.

Thrombosis and Haemostasis|February 12, 1999

Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chainR Laub, M Di Giambattista, P Fondu, et al.

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