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- 1999
Mechanism-based pharmacokinetic-pharmacodynamic modeling of antilipolytic effects of adenosine A(1) receptor agonists in rats: prediction of tissue-dependent efficacy in vivo,
J Pharmacol Exp Ther, vol. 290, no. 2, pp. 702-9.
- 1998
Selectivity of action of 8-alkylamino analogues of N6-cyclopentyladenosine in vivo: haemodynamic versus anti-lipolytic responses in rats,
Br J Pharmacol, vol. 124, no. 3, pp. 607-18.
- 1997
Analysis of drug-receptor interactions in vivo: a new approach in pharmacokinetic-pharmacodynamic modelling,
Int J Clin Pharmacol Ther, vol. 35, no. 10, pp. 442-6.
8-Alkylamino-substituted analogs of N6-cyclopentyladenosine are partial agonists for the cardiovascular adenosine A1 receptors in vivo,
J Pharmacol Exp Ther, vol. 283, no. 2, pp. 800-8.
Pharmacokinetic-pharmacodynamic characterization of the cardiovascular, hypnotic, EEG and ventilatory responses to dexmedetomidine in the rat,
J Pharmacol Exp Ther, vol. 283, no. 3, pp. 1051-8.
Time course of action of three adenosine A1 receptor agonists with differing lipophilicity in rats: comparison of pharmacokinetic, haemodynamic and EEG effects,
Naunyn Schmiedebergs Arch Pharmacol, vol. 356, no. 6, pp. 827-37.
- 1996
Hemodynamic effects and histamine release elicited by the selective adenosine A3 receptor agonist 2-Cl-IB-MECA in conscious rats,
Eur J Pharmacol, vol. 308, no. 3, pp. 311-4.
Partial agonism of the nonselective adenosine receptor agonist 8-butylaminoadenosine at the A1 receptor in vivo,
J Pharmacol Exp Ther, vol. 279, no. 3, pp. 1439-46.
- 1995
Ribose-modified adenosine analogues as potential partial agonists for the adenosine receptor,
J Med Chem, vol. 38, no. 20, pp. 4000-6.
Deoxyribose analogues of N6-cyclopentyladenosine (CPA): partial agonists at the adenosine A1 receptor in vivo,
Br J Pharmacol, vol. 116, no. 3, pp. 1957-64.
8-substituted adenosine and theophylline-7-riboside analogues as potential partial agonists for the adenosine A1 receptor,
Eur J Pharmacol, vol. 290, no. 3, pp. 189-99.
Modelling of the pharmacodynamic interaction of an A1 adenosine receptor agonist and antagonist in vivo: N6-cyclopentyladenosine and 8-cyclopentyltheophylline,
Br J Pharmacol, vol. 115, no. 7, pp. 1253-9.
Pharmacokinetic-pharmacodynamic modelling of the cardiovascular effects of R- and S-N6-phenylisopropyladenosine in conscious normotensive rats,
J Pharmacol Exp Ther, vol. 273, no. 1, pp. 405-14.
- 1994
Pharmacokinetic-pharmacodynamic relationship of the cardiovascular effects of adenosine A1 receptor agonist N6-cyclopentyladenosine in the rat,
J Pharmacol Exp Ther, vol. 268, no. 2, pp. 616-24.
- 1993
A comparison of the concentration-effect relationships of midazolam for EEG-derived parameters and saccadic peak velocity,
Br J Clin Pharmacol, vol. 36, no. 2, pp. 109-15.
- 1992
Influence of single- and multiple-dose omeprazole treatment on nifedipine pharmacokinetics and effects in healthy subjects,
Eur J Clin Pharmacol, vol. 42, no. 3, pp. 319-24.
- 1988
Pharmacokinetics and hemodynamic effects of nisoldipine and its interaction with cimetidine,
Clin Pharmacol Ther, vol. 43, no. 3, pp. 332-41.
- 1987
Rate of increase in the plasma concentration of nifedipine as a major determinant of its hemodynamic effects in humans,
Clin Pharmacol Ther, vol. 41, no. 1, pp. 26-30.
- 1986
Nifedipine: kinetics and hemodynamic effects in patients with liver cirrhosis after intravenous and oral administration,
Clin Pharmacol Ther, vol. 40, no. 1, pp. 21-8.
- 1985
Nifedipine: influence of renal function on pharmacokinetic/hemodynamic relationship,
Clin Pharmacol Ther, vol. 37, no. 5, pp. 563-74.
- 1984
Variability in nifedipine pharmacokinetics and dynamics: a new oxidation polymorphism in man,
Biochem Pharmacol, vol. 33, no. 22, pp. 3721-4.



