Search Results - "Tamminga, Wim J"

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    Absorption, Metabolism, and Excretion of Intravenously and Orally Administered [14C]Telmisartan in Healthy Volunteers by Stangier, Joachim, Schmid, Jochen, Türck, Dietrich, Switek, Heinz, Verhagen, Aalt, Peeters, Pierre A. M., van Marle, Sjoerd P., Tamminga, Wim J., Sollie, Frans A. E., Jonkman, Jan H. G.

    Published in Journal of clinical pharmacology (01-12-2000)
    “…The study was conducted in healthy male volunteers to evaluate the absorption, metabolic pattern, and mode of elimination of telmisartan, a nonpeptide…”
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    Polymorphic drug metabolism (CYP2D6) and utilisation of psychotropic drugs in hospitalised psychiatric patients: a retrospective study by TAMMINGA, Wim J, WEMER, Johan, OOSTERHUIS, Berend, DE BOER, Anthonius, VRANCKX, Stan, DRENTH, Ben F. H, DE ZEEUW, Rokus A, DE LEIJ, Lou F. M. H, JONKMAN, Jan H. G

    Published in European journal of clinical pharmacology (01-05-2003)
    “…The aim of the current retrospective study was to assess the influence of polymorphic drug metabolism as assessed by genotyping, on the on the utilisation of…”
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    Inhibitory Effect of Telmisartan on the Blood Pressure Response to Angiotensin II Challenge by Stangier, Joachim, Su, Chung-An P. F, van Heiningen, Pauline N. M, Meinicke, Thomas, van Lier, Jan J, de Bruin, Henrieke, Tamminga, Wim J, Jonkman, Jan H. G

    Published in Journal of cardiovascular pharmacology (01-11-2001)
    “…Telmisartan is a new angiotensin receptor antagonist possessing potent, selective, and insurmountable inhibitory activity specific to the angiotensin II type 1…”
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    An optimized methodology for combined phenotyping and genotyping on CYP2D6 and CYP2C19 by TAMMINGA, Wim J, WEMER, Johan, OOSTERHUIS, Berend, BRAKENHOFF, Jan P. G, GERRITS, Mireille G. F, DE ZEEUW, Rokus A, DE LEIJ, Lou F. M. H, JONKMAN, Jan H. G

    Published in European journal of clinical pharmacology (01-05-2001)
    “…A method for simultaneous phenotyping and genotyping for CYP2D6 and CYP2C19 was tested. Six healthy volunteers were selected (three extensive and three poor…”
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  7. 7

    Mephenytoin as a probe for CYP2C19 phenotyping:effect of sample storage, intra‐individual reproducibility and occurrence of adverse events by Tamminga, Wim J., Wemer, Johan, Oosterhuis, Berend, Wieling, Jaap, Touw, Daan J., De Zeeuw, Rokus A., De Leij, Lou F. M. H., Jonkman, Jan H. G.

    Published in British journal of clinical pharmacology (01-05-2001)
    “…Aims  To further evaluate mephenytoin as a probe for CYP2C19 phenotyping. Methods  Healthy subjects (n = 2638) were phenotyped using the urinary…”
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  8. 8

    The prevalence of CYP2C19 genotypes in a population of healthy Dutch volunteers and apparent gender differences in phenotypes by Tamminga, Wim J., Wemer, Johan, Oosterhuis, Berend, De Zeeuw, Rokus A., De Leij, Lou F. M. H., Jonkman, Jan H. G.

    Published in British journal of clinical pharmacology (01-05-2002)
    “…We reported the prevalence of poor metabolizers of CYP2C19 to be 1.8% in a sample of the Dutch population (n=4301; [1]). These data were obtained by…”
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  9. 9

    Evaluation of analytical and clinical performance of a dual-probe phenotyping method for CYP2D6 polymorphism and CYP3A4 activity screening by WIELING, J, TAMMINGA, W. J, SAKIMAN, E. P, OOSTERHUIS, B, WEMER, J, JONKMAN, J. H. G

    Published in Therapeutic drug monitoring (01-08-2000)
    “…A bioanalytical method for the determination of dextromethorphan (DEX) and its metabolites dextrorphan (DTX), 3-methoxymorphinan (3MM), and 3-hydroxymorphinan…”
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  10. 10

    Clopidogrel, a novel antiplatelet agent, and digoxin: absence of pharmacodynamic and pharmacokinetic interaction by Peeters, P A, Crijns, H J, Tamminga, W J, Jonkman, J H, Dickinson, J P, Necciari, J

    “…The safety, and the pharmacodynamic and pharmacokinetic compatibility of clopidogrel, 75 mg daily, with the cardiac glycoside digoxin, were assessed in 12…”
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