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P H Reitsma

Showing results (211-220 of 275) with videos related to

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Blood|October 15, 1995
Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patientsV R Arruda, W C Pieneman, P H Reitsma, et al.
The New England Journal of Medicine|March 21, 1996
Hyperhomocysteinemia as a risk factor for deep-vein thrombosisM den Heijer, T Koster, H J Blom, et al.
Journal of Thrombosis and Haemostasis : JTH|November 25, 2018
High levels of coagulation factors and venous thrombosis risk: strongest association for factor VIII and von Willebrand factorI M Rietveld, W M Lijfering, S le Cessie, et al.
British Journal of Haematology|June 1, 1996
Activated protein C resistance: a comparison between two clotting assays and their relationship to the presence of the factor V Leiden mutationC Legnani, G Palareti, R Biagi, et al.
Journal of Thrombosis and Haemostasis : JTH|February 5, 2015
No evidence for a direct effect of von Willebrand factor's ABH blood group antigens on von Willebrand factor clearanceD J Groeneveld, T van Bekkum, K L Cheung, et al.
British Journal of Haematology|February 23, 1999
The 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseR F Franco, M D Trip, H ten Cate, et al.
The Journal of Biological Chemistry|September 29, 2001
Apolipoprotein A-V: a novel apolipoprotein associated with an early phase of liver regenerationH N van der Vliet, M G Sammels, A C Leegwater, et al.
Journal of Thrombosis and Haemostasis : JTH|April 14, 2011
Genetic variants of F11, statin use and venous thrombosisL A Bare, A R Arellano, C H Tong, et al.
The Journal of Biological Chemistry|July 5, 1990
Mutations in hemophilia Bm occur at the Arg180-Val activation site or in the catalytic domain of factor IXR M Bertina, I K van der Linden, P M Mannucci, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiencyMaria Pintao, A A Garcia, D Borgel, et al.
Pageof 28

Showing results (211-220 of 275) with videos related to

Sort By:
Pageof 28
Blood|October 15, 1995
Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patientsV R Arruda, W C Pieneman, P H Reitsma, et al.
The New England Journal of Medicine|March 21, 1996
Hyperhomocysteinemia as a risk factor for deep-vein thrombosisM den Heijer, T Koster, H J Blom, et al.
Journal of Thrombosis and Haemostasis : JTH|November 25, 2018
High levels of coagulation factors and venous thrombosis risk: strongest association for factor VIII and von Willebrand factorI M Rietveld, W M Lijfering, S le Cessie, et al.
British Journal of Haematology|June 1, 1996
Activated protein C resistance: a comparison between two clotting assays and their relationship to the presence of the factor V Leiden mutationC Legnani, G Palareti, R Biagi, et al.
Journal of Thrombosis and Haemostasis : JTH|February 5, 2015
No evidence for a direct effect of von Willebrand factor's ABH blood group antigens on von Willebrand factor clearanceD J Groeneveld, T van Bekkum, K L Cheung, et al.
British Journal of Haematology|February 23, 1999
The 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseR F Franco, M D Trip, H ten Cate, et al.
The Journal of Biological Chemistry|September 29, 2001
Apolipoprotein A-V: a novel apolipoprotein associated with an early phase of liver regenerationH N van der Vliet, M G Sammels, A C Leegwater, et al.
Journal of Thrombosis and Haemostasis : JTH|April 14, 2011
Genetic variants of F11, statin use and venous thrombosisL A Bare, A R Arellano, C H Tong, et al.
The Journal of Biological Chemistry|July 5, 1990
Mutations in hemophilia Bm occur at the Arg180-Val activation site or in the catalytic domain of factor IXR M Bertina, I K van der Linden, P M Mannucci, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiencyMaria Pintao, A A Garcia, D Borgel, et al.
Pageof 28