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P H Reitsma

Showing results (141-150 of 275) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|April 22, 2005
Evaluation of the von Willebrand factor Y1584C polymorphism as a potential risk factor for bleeding in patients receiving anticoagulant treatment with vitamin K antagonistsP Tjernberg, J F Van Der Heijden, J C J Eikenboom, et al.
Thrombosis and Haemostasis|June 1, 1997
Tissue factor expression during monocyte-macrophage differentiationM M van den Eijnden, S I Steenhauer, P H Reitsma, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1994
Expression of tissue factor and tissue factor pathway inhibitor in monocytes in response to bacterial lipopolysaccharide and phorbolesterC P van der Logt, R J Dirven, P H Reitsma, et al.
Thrombosis and Haemostasis|June 1, 1994
Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S geneE Gómez, M R Ledford, C H Pegelow, et al.
Blood|August 15, 1991
The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effectsP H Reitsma, S R Poort, C F Allaart, et al.
Thrombosis and Haemostasis|August 1, 1995
Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families?B P Koeleman, D van Rumpt, K Hamulyák, 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.
Thrombosis and Haemostasis|August 24, 1999
The 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene is not associated with myocardial infarctionC J Doggen, R M Bertina, V M Cats, et al.
Calcified Tissue International|January 1, 1980
Kinetic studies of bone and mineral metabolism during treatment with (3-amino-1-hydroxypropylidene)-1,1-bisphosphonate (APD) in ratsP H Reitsma, O L Bijvoet, H Verlinden-Ooms, et al.
Atherosclerosis|December 24, 1998
The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosisB J Verhoeff, M D Trip, M H Prins, et al.
Pageof 28

Showing results (141-150 of 275) with videos related to

Sort By:
Pageof 28
Journal of Thrombosis and Haemostasis : JTH|April 22, 2005
Evaluation of the von Willebrand factor Y1584C polymorphism as a potential risk factor for bleeding in patients receiving anticoagulant treatment with vitamin K antagonistsP Tjernberg, J F Van Der Heijden, J C J Eikenboom, et al.
Thrombosis and Haemostasis|June 1, 1997
Tissue factor expression during monocyte-macrophage differentiationM M van den Eijnden, S I Steenhauer, P H Reitsma, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1994
Expression of tissue factor and tissue factor pathway inhibitor in monocytes in response to bacterial lipopolysaccharide and phorbolesterC P van der Logt, R J Dirven, P H Reitsma, et al.
Thrombosis and Haemostasis|June 1, 1994
Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S geneE Gómez, M R Ledford, C H Pegelow, et al.
Blood|August 15, 1991
The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effectsP H Reitsma, S R Poort, C F Allaart, et al.
Thrombosis and Haemostasis|August 1, 1995
Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families?B P Koeleman, D van Rumpt, K Hamulyák, 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.
Thrombosis and Haemostasis|August 24, 1999
The 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene is not associated with myocardial infarctionC J Doggen, R M Bertina, V M Cats, et al.
Calcified Tissue International|January 1, 1980
Kinetic studies of bone and mineral metabolism during treatment with (3-amino-1-hydroxypropylidene)-1,1-bisphosphonate (APD) in ratsP H Reitsma, O L Bijvoet, H Verlinden-Ooms, et al.
Atherosclerosis|December 24, 1998
The effect of a common methylenetetrahydrofolate reductase mutation on levels of homocysteine, folate, vitamin B12 and on the risk of premature atherosclerosisB J Verhoeff, M D Trip, M H Prins, et al.
Pageof 28