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P H Reitsma

Showing results (111-120 of 275) with videos related to

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Thrombosis and Haemostasis|May 1, 1997
Location on the human genetic linkage map of 26 genes involved in blood coagulationB P Koeleman, P H Reitsma, E Bakker, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1994
Haemophilia B Leyden: the effect of mutations at position +13 on the liver-specific transcription of the factor IX geneM J Reijnen, D Maasdam, R M Bertina, et al.
Thrombosis and Haemostasis|February 3, 1992
Alternative splicing is responsible for the presence of two tissue factor mRNA species in LPS stimulated human monocytesC P van der Logt, P H Reitsma, R M Bertina
The Journal of Clinical Investigation|February 1, 1994
Three novel mutations in five unrelated subjects with hereditary protein S deficiency type IP H Reitsma, H K Ploos van Amstel, R M Bertina
Nucleic Acids Research|October 11, 1990
RFLP for the human prothrombin (F2) geneM de Vetten, H K Ploos van Amstel, P H Reitsma
Blood|November 15, 1996
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosisS R Poort, F R Rosendaal, P H Reitsma, et al.
British Journal of Haematology|March 1, 1995
A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopeniaG Castaman, J C Eikenboom, F Rodeghiero, et al.
Thrombosis and Haemostasis|December 1, 1994
Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorderS R Poort, J J Michiels, P H Reitsma, et al.
Blood|August 15, 1994
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient familiesB P Koeleman, P H Reitsma, C F Allaart, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1992
Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B LeydenM J Reijnen, F M Sladek, R M Bertina, et al.
Pageof 28

Showing results (111-120 of 275) with videos related to

Sort By:
Pageof 28
Thrombosis and Haemostasis|May 1, 1997
Location on the human genetic linkage map of 26 genes involved in blood coagulationB P Koeleman, P H Reitsma, E Bakker, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1994
Haemophilia B Leyden: the effect of mutations at position +13 on the liver-specific transcription of the factor IX geneM J Reijnen, D Maasdam, R M Bertina, et al.
Thrombosis and Haemostasis|February 3, 1992
Alternative splicing is responsible for the presence of two tissue factor mRNA species in LPS stimulated human monocytesC P van der Logt, P H Reitsma, R M Bertina
The Journal of Clinical Investigation|February 1, 1994
Three novel mutations in five unrelated subjects with hereditary protein S deficiency type IP H Reitsma, H K Ploos van Amstel, R M Bertina
Nucleic Acids Research|October 11, 1990
RFLP for the human prothrombin (F2) geneM de Vetten, H K Ploos van Amstel, P H Reitsma
Blood|November 15, 1996
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosisS R Poort, F R Rosendaal, P H Reitsma, et al.
British Journal of Haematology|March 1, 1995
A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopeniaG Castaman, J C Eikenboom, F Rodeghiero, et al.
Thrombosis and Haemostasis|December 1, 1994
Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorderS R Poort, J J Michiels, P H Reitsma, et al.
Blood|August 15, 1994
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient familiesB P Koeleman, P H Reitsma, C F Allaart, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1992
Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B LeydenM J Reijnen, F M Sladek, R M Bertina, et al.
Pageof 28