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Y Plusquellec

Showing results (11-20 of 33) with videos related to

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Arzneimittel-Forschung|October 1, 1992
The amount of drug remaining in the body at the time Tmax after simultaneous extravascular and intravenous administrationY Plusquellec, G Houin
Journal of Biomedical Engineering|May 1, 1993
Mean residence time in multicompartmental models with time delaysY Plusquellec, G Houin
Journal of Biomedical Engineering|July 1, 1991
Relationship between loading dose and infusion rate to achieve any fraction of the steady-state level in any compartment modelY Plusquellec, G Houin
European Journal of Drug Metabolism and Pharmacokinetics|March 15, 2000
Consequence of equal absorption, distribution and/or elimination rate constantsY Plusquellec, F Courbon, S Nogarede
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|June 26, 1999
Concentration at steady-state after periodic and non-uniform administration of drugY Plusquellec, J De Biasi, J Souhait
Medical Engineering & Physics|February 15, 2000
A pharmacokinetic model for multiple sites discontinuous gastrointestinal absorptionY Plusquellec, C Efthymiopoulos, P Duthil, et al.
Arzneimittel-Forschung|March 1, 1996
Minimal experimental requirements for structural identifiability in linear compartmental models. The software 'IDEXMIN'J A Mérino, J de Biasi, Y Plusquellec, et al.
Arzneimittel-Forschung|January 1, 1984
Isoniazid plasma and lymph kinetics after intravenous injection in dogsM Blanc, J L Steimer, C Boyer, et al.
Arzneimittel-Forschung|November 1, 1993
Effect of drug transit time between exchange locus with plasma and sampling siteY Plusquellec, L Bousquet, J de Biasi, et al.
Journal of Pharmaceutical Sciences|March 1, 1982
A time-lag model for pharmacokinetics of drugs subject to enterohepatic circulationJ L Steimer, Y Plusquellec, A Guillaume, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Arzneimittel-Forschung|October 1, 1992
The amount of drug remaining in the body at the time Tmax after simultaneous extravascular and intravenous administrationY Plusquellec, G Houin
Journal of Biomedical Engineering|May 1, 1993
Mean residence time in multicompartmental models with time delaysY Plusquellec, G Houin
Journal of Biomedical Engineering|July 1, 1991
Relationship between loading dose and infusion rate to achieve any fraction of the steady-state level in any compartment modelY Plusquellec, G Houin
European Journal of Drug Metabolism and Pharmacokinetics|March 15, 2000
Consequence of equal absorption, distribution and/or elimination rate constantsY Plusquellec, F Courbon, S Nogarede
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|June 26, 1999
Concentration at steady-state after periodic and non-uniform administration of drugY Plusquellec, J De Biasi, J Souhait
Medical Engineering & Physics|February 15, 2000
A pharmacokinetic model for multiple sites discontinuous gastrointestinal absorptionY Plusquellec, C Efthymiopoulos, P Duthil, et al.
Arzneimittel-Forschung|March 1, 1996
Minimal experimental requirements for structural identifiability in linear compartmental models. The software 'IDEXMIN'J A Mérino, J de Biasi, Y Plusquellec, et al.
Arzneimittel-Forschung|January 1, 1984
Isoniazid plasma and lymph kinetics after intravenous injection in dogsM Blanc, J L Steimer, C Boyer, et al.
Arzneimittel-Forschung|November 1, 1993
Effect of drug transit time between exchange locus with plasma and sampling siteY Plusquellec, L Bousquet, J de Biasi, et al.
Journal of Pharmaceutical Sciences|March 1, 1982
A time-lag model for pharmacokinetics of drugs subject to enterohepatic circulationJ L Steimer, Y Plusquellec, A Guillaume, et al.
Pageof 4