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A pregnancy physiologically based pharmacokinetic (p‐PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4

British journal of clinical pharmacology, 2012-11, Vol.74 (5), p.873-885

2012

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Pharmacogenetics of artemether‐lumefantrine influence on nevirapine disposition: Clinically significant drug–drug interaction?

British journal of clinical pharmacology, 2019-03, Vol.85 (3), p.540-550

2019

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Interaction between ABCG2 421C>A polymorphism and valproate in their effects on steady‐state disposition of lamotrigine in adults with epilepsy

British journal of clinical pharmacology, 2018-09, Vol.84 (9), p.2106-2119

2018

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Drug disposition and modelling before and after gastric bypass: immediate and controlled‐release metoprolol formulations

British journal of clinical pharmacology, 2015-11, Vol.80 (5), p.1021-1030

2015

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Effect of rifampin on enantioselective disposition and anti‐hypertensive effect of benidipine

British journal of clinical pharmacology, 2019-04, Vol.85 (4), p.737-745

2019

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Human disposition, metabolism and excretion of etamicastat, a reversible, peripherally selective dopamine β‐hydroxylase inhibitor

British journal of clinical pharmacology, 2014-06, Vol.77 (6), p.1017-1026

2014

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Stereoselective disposition of fluoxetine and norfluoxetine during pregnancy and breast‐feeding

British journal of clinical pharmacology, 2006-02, Vol.61 (2), p.155-163

2006

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Effects of proton pump inhibitors, esomeprazole and vonoprazan, on the disposition of proguanil, a CYP2C19 substrate, in healthy volunteers

British journal of clinical pharmacology, 2019-07, Vol.85 (7), p.1454-1463

2019

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Influence of SLCO1B3 haplotype‐tag SNPs on docetaxel disposition in Chinese nasopharyngeal cancer patients

British journal of clinical pharmacology, 2012-04, Vol.73 (4), p.606-618

2012

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Trans‐3′‐hydroxycotinine: Disposition kinetics, effects and plasma levels during cigarette smoking

British journal of clinical pharmacology, 2001-01, Vol.51 (1), p.53-59

2001

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Relationship of CYP3A5 genotype and ABCB1 diplotype to tacrolimus disposition in Brazilian kidney transplant patients

British journal of clinical pharmacology, 2014-08, Vol.78 (2), p.364-372

2014

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Doxazosin treatment of phaeochromocytoma during pregnancy: placental transfer and disposition in breast milk

British journal of clinical pharmacology, 2016-08, Vol.82 (2), p.568-569

2016

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Bioavailability and disposition of azelastine and fluticasone propionate when delivered by MP29‐02, a novel aqueous nasal spray

British journal of clinical pharmacology, 2012-07, Vol.74 (1), p.125-133

2012

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Artesunate/dihydroartemisinin pharmacokinetics in acute falciparum malaria in pregnancy: absorption, bioavailability, disposition and disease effects

British journal of clinical pharmacology, 2012-03, Vol.73 (3), p.467-477

2012

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Albendazole‐praziquantel interaction in healthy volunteers: kinetic disposition, metabolism and enantioselectivity

British journal of clinical pharmacology, 2011-04, Vol.71 (4), p.528-535

2011

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Comparison of caffeine disposition following administration by oral solution (energy drink) and inspired powder (AeroShot) in human subjects

British journal of clinical pharmacology, 2017-12, Vol.83 (12), p.2687-2694

2017

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Enantioselective disposition of fexofenadine with the P‐glycoprotein inhibitor verapamil

British journal of clinical pharmacology, 2009-05, Vol.67 (5), p.535-540

2009

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The effect of ABCG2 V12M, Q141K and Q126X, known functional variants in vitro, on the disposition of lamivudine

British journal of clinical pharmacology, 2007-11, Vol.64 (5), p.645-654

2007

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Disposition and metabolism of the flavonoid chrysin in normal volunteers

British journal of clinical pharmacology, 2001-02, Vol.51 (2), p.143-146

2001

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Use of Entero‐Test, a simple approach for non‐invasive clinical evaluation of the biliary disposition of drugs

British journal of clinical pharmacology, 2011-07, Vol.72 (1), p.133-142

2011

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Tobramycin disposition in ICU patients receiving a once daily regimen: population approach and dosage simulations

British journal of clinical pharmacology, 2011-01, Vol.71 (1), p.61-71

2011

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Interphenotype differences in disposition and effect on gastrin levels of omeprazole—suitability of omeprazole as a probe for CYP2C19

British journal of clinical pharmacology, 1995-05, Vol.39 (5), p.511-518

1995

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Contribution of the activities of CYP3A, CYP2D6, CYP1A2 and other potential covariates to the disposition of methadone in patients undergoing methadone maintenance treatment

British journal of clinical pharmacology, 2009-01, Vol.67 (1), p.29-37

2009

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Enantioselective disposition of rabeprazole in relation to CYP2C19 genotypes

British journal of clinical pharmacology, 2006-03, Vol.61 (3), p.315-320

2006

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Enantiomeric disposition of inhaled, intravenous and oral racemic‐salbutamol in man — no evidence of enantioselective lung metabolism

British journal of clinical pharmacology, 2000-01, Vol.49 (1), p.15-22

2000

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Zeitschrift / SerieThe American Journal Of Emergency Medicine

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A pregnancy physiologically based pharmacokinetic (p‐PBPK) model for disposition of drugs metabolized by CYP1A2, CYP2D6 and CYP3A4

Pharmacogenetics of artemether‐lumefantrine influence on nevirapine disposition: Clinically significant drug–drug interaction?

Interaction between ABCG2 421C>A polymorphism and valproate in their effects on steady‐state disposition of lamotrigine in adults with epilepsy

Drug disposition and modelling before and after gastric bypass: immediate and controlled‐release metoprolol formulations

Effect of rifampin on enantioselective disposition and anti‐hypertensive effect of benidipine

Human disposition, metabolism and excretion of etamicastat, a reversible, peripherally selective dopamine β‐hydroxylase inhibitor

Stereoselective disposition of fluoxetine and norfluoxetine during pregnancy and breast‐feeding

Effects of proton pump inhibitors, esomeprazole and vonoprazan, on the disposition of proguanil, a CYP2C19 substrate, in healthy volunteers

Influence of SLCO1B3 haplotype‐tag SNPs on docetaxel disposition in Chinese nasopharyngeal cancer patients

Trans‐3′‐hydroxycotinine: Disposition kinetics, effects and plasma levels during cigarette smoking

Relationship of CYP3A5 genotype and ABCB1 diplotype to tacrolimus disposition in Brazilian kidney transplant patients

Doxazosin treatment of phaeochromocytoma during pregnancy: placental transfer and disposition in breast milk

Bioavailability and disposition of azelastine and fluticasone propionate when delivered by MP29‐02, a novel aqueous nasal spray

Artesunate/dihydroartemisinin pharmacokinetics in acute falciparum malaria in pregnancy: absorption, bioavailability, disposition and disease effects

Albendazole‐praziquantel interaction in healthy volunteers: kinetic disposition, metabolism and enantioselectivity

Comparison of caffeine disposition following administration by oral solution (energy drink) and inspired powder (AeroShot) in human subjects

Enantioselective disposition of fexofenadine with the P‐glycoprotein inhibitor verapamil

The effect of ABCG2 V12M, Q141K and Q126X, known functional variants in vitro, on the disposition of lamivudine

Disposition and metabolism of the flavonoid chrysin in normal volunteers

Use of Entero‐Test, a simple approach for non‐invasive clinical evaluation of the biliary disposition of drugs

Tobramycin disposition in ICU patients receiving a once daily regimen: population approach and dosage simulations

Interphenotype differences in disposition and effect on gastrin levels of omeprazole—suitability of omeprazole as a probe for CYP2C19

Contribution of the activities of CYP3A, CYP2D6, CYP1A2 and other potential covariates to the disposition of methadone in patients undergoing methadone maintenance treatment

Enantioselective disposition of rabeprazole in relation to CYP2C19 genotypes

Enantiomeric disposition of inhaled, intravenous and oral racemic‐salbutamol in man — no evidence of enantioselective lung metabolism

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