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study subject pantoprazole intragastric effect omeprazole intragastric ph genotype esomeprazole treatment aliment pharmacol pantoprazole 40 mg pharmacol signi day 1 *1/*1 mutation *1/*17 therapy percentage level esomeprazole 40 mg administration pharmacokinetic cyp 2c baseline haga teaching hospital signi ficantly pylori *1/*2 period caucasian aliment pylori-negative value ficant increase acid-inhibitory effect patient wt ⁄ wt cyp 2c genotype evidence acid-inhibitory population study b day 6 lansoprazole proton inhibitor metabolism acid production 24- *2/*17 ficantly cyp 2c polymorphism rebound acid hypersecretion acid-inhibition result ppi treatment *2/*2 table omeprazole 20 mg gastrin acidity *17 difference rebound dosing helicobacter hospital acid secretion lansoprazole 15 mg 24- h period publishing blackwell signi ficant acid-inhibition pylori status pylori-negative subjects polymorphism pharmacodynamic
3 Most Recent Publications
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A comparison of the acid-inhibitory effects of esomeprazole and pantoprazole in relation to pharmacokinetics and CYP2C19 polymorphism
(Article)
Hunfeld, N.G. Touw, D.J. Mathot, R.A. Mulder, P.G.H. Schaik, R.H.N. van Kuipers, E.J. Kooiman, J.C. Geus, W.P. |
2010-01-01
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Effect of CYP2C19*2 and *17 mutations on pharmacodynamics and kinetics of proton pump inhibitors in Caucasians
(Article)
Hunfeld, N.G. Mathot, R.A. Touw, D.J. Schaik, R.H.N. van Mulder, P.G.H. Franck, P.F. Kuipers, E.J. Geus, W.P. |
2008-05-01
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Systematic review: Rebound acid hypersecretion after therapy with proton pump inhibitors
(Article)
Hunfeld, N.G. Geus, W.P. Kuipers, E.J. |
2007-01-01
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