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In vitro characterization of clobazam metabolism by recombinant cytochrome P450 enzymes: importance of CYP2C19.
- C. Giraud, A. Tran, E. Rey, J. Vincent, J. Treluyer, G. Pons
- Chemistry, Medicine
- Drug metabolism and disposition: the biological…
- 1 November 2004
The specific cytochrome P450 (P450) isoforms mediating the biotransformations of clobazam (CLB) and those of its major metabolites, N-desmethylclobazam (NCLB) and 4'-hydroxyclobazam were identified… Expand
Retention of Plasmodium falciparum ring-infected erythrocytes in the slow, open microcirculation of the human spleen.
The current paradigm in Plasmodium falciparum malaria pathogenesis states that young, ring-infected erythrocytes (rings) circulate in peripheral blood and that mature stages are sequestered in the… Expand
IN VITRO AND IN VIVO INHIBITORY EFFECT OF STIRIPENTOL ON CLOBAZAM METABOLISM
- C. Giraud, J. Treluyer, +4 authors A. Tran
- Chemistry, Medicine
- Drug Metabolism and Disposition
- 1 April 2006
A metabolic interaction between stiripentol (STP), an anticonvulsant agent that inhibits the activity of several cytochromes P450 (P450s), and clobazam (CLB), a 1,5-benzodiazepine, used in… Expand
Universal antiretroviral therapy for pregnant and breast-feeding HIV-1-infected women: towards the elimination of mother-to-child transmission of HIV-1 in resource-limited settings.
- R. Becquet, D. Ekouevi, +8 authors F. Dabis
- Clinical infectious diseases : an official…
- 15 December 2009
Prevention of mother-to-child transmission (MTCT) of human immunodeficiency virus type 1 (HIV-1) remains a challenge in most resource-limited settings, particularly in Africa. Single-dose and… Expand
An optimized ibuprofen dosing scheme for preterm neonates with patent ductus arteriosus, based on a population pharmacokinetic and pharmacodynamic study.
- D. Hirt, B. van Overmeire, +5 authors S. Urien
- British journal of clinical pharmacology
- 1 May 2008
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT Ibuprofen is a nonsteroidal anti-inflammatory agent that induces closure of the patent ductus arteriosus in neonates. Few studies of ibuprofen… Expand
Penetration of enfuvirtide, tenofovir, efavirenz, and protease inhibitors in the genital tract of HIV-1-infected men
One likely mechanism of virological failure is poor antiretroviral drug diffusion in sites of viral replication such as the genital tract. We measured antiretroviral drug concentrations in blood and… Expand
Maternal-Fetal Transfer and Amniotic Fluid Accumulation of Nucleoside Analogue Reverse Transcriptase Inhibitors in Human Immunodeficiency Virus-Infected Pregnant Women
- H. Chappuy, J. Treluyer, +6 authors L. Mandelbrot
- Antimicrobial Agents and Chemotherapy
- 1 November 2004
ABSTRACT This study was performed to investigate placental transfer of nucleoside analogue reverse transcriptase inhibitors (NRTIs) and their concentrations in amniotic fluid when given to human… Expand
Treatment of oxaliplatin-induced peripheral neuropathy by intravenous mangafodipir.
- R. Coriat, J. Alexandre, +11 authors F. Batteux
- The Journal of clinical investigation
- 2 January 2014
BACKGROUND The majority of patients receiving the platinum-based chemotherapy drug oxaliplatin develop peripheral neurotoxicity. Because this neurotoxicity involves ROS production, we investigated… Expand
Population pharmacokinetics of metformin in obese and non-obese patients with type 2 diabetes mellitus
- C. Bardin, E. Nobécourt, E. Larger, F. Chast, J. Treluyer, S. Urien
- European Journal of Clinical Pharmacology
- 25 January 2012
PurposeThe objective of this study was to develop a population pharmacokinetic model and investigate the effect of several demographic covariates on metformin pharmacokinetics in patients with type 2… Expand
Pharmacokinetic Optimisation of Benzodiazepine Therapy for Acute Seizures
All benzodiazepines enter cerebral tissue rapidly. However, the duration of action is short for diazepam (<2 hours) and midazolam (3 to 4 hours) and longer for clonazepam (24 hours) and lorazepam (up… Expand