檢索結果 - PH Reitsma

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  1. 1
    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 thrombosis

    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 thrombosis 由 SR Poort, FR Rosendaal, PH Reitsma, R M Bertina

    出版 1996
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  2. 2
    High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance) [see comments]

    High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance) [see comments] 由 FR Rosendaal, Ted Koster, Jan P. Vandenbroucke, PH Reitsma

    出版 1995
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  3. 3
    Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families

    Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families 由 BP Koeleman, PH Reitsma, C.F. Allaart, R M Bertina

    出版 1994
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  4. 4
    The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects

    The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects 由 PH Reitsma, SR Poort, C.F. Allaart, E Briët, R M Bertina

    出版 1991
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  5. 5
    The putative factor IX gene promoter in hemophilia B Leyden

    The putative factor IX gene promoter in hemophilia B Leyden 由 PH Reitsma, R M Bertina, JK Ploos van Amstel, Anja Riemens, E Briët

    出版 1988
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  6. 6
    Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor

    Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor 由 Jeroen Eikenboom, Tadashi Matsushita, PH Reitsma, EA Tuley, Giancarlo Castaman, E Briët, J. Evan Sadler

    出版 1996
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  7. 7
    Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients

    Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients 由 VR Arruda, W C Pieneman, PH Reitsma, PP Deutz-Terlouw, JM Annichino-Bizzacchi, E Briët, FF Costa

    出版 1995
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  8. 8
    Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients

    Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients 由 VR Arruda, W C Pieneman, PH Reitsma, PP Deutz-Terlouw, JM Annichino-Bizzacchi, E Briët, FF Costa

    出版 1995
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  9. 9
    Apparent different thrombotic tendency in patients with factor V Leiden and protein C deficiency due to selection of patients

    Apparent different thrombotic tendency in patients with factor V Leiden and protein C deficiency due to selection of patients 由 RP Lensen, Frits R. Rosendaal, Ted Koster, C.F. Allaart, Hans de Ronde, Jan P. Vandenbroucke, PH Reitsma, RM Bertina

    出版 1996
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  10. 10
    Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study) [see comments]

    Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study) [see comments] 由 Ted Koster, Frits R. Rosendaal, E Briët, FJ van der Meer, LP Colly, PH Trienekens, SR Poort, PH Reitsma, Jan P. Vandenbroucke

    出版 1995
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  11. 11
    Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460

    Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460 由 R M Bertina, HK Ploos van Amstel, A van Wijngaarden, J Coenen, MP Leemhuis, PP Deutz-Terlouw, IK van der Linden, PH Reitsma

    出版 1990
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