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Clinical Pharmacology and Therapeutics
|
May 15, 2007
Time for quantitative clinical pharmacology: a proposal for a pharmacometrics curriculum
N Holford, M O Karlsson
Clinical Pharmacokinetics
|
July 4, 2001
Concentration-controlled or effect-controlled trials: useful alternatives to conventional dose-controlled trials?
A Grahnén, M O Karlsson
Molecular Pharmacology
|
January 1, 1989
Estimation of ligand binding parameters by simultaneous fitting of association and dissociation data: a Monte Carlo simulation study
M O Karlsson, A Neil
Biopharmaceutics & Drug Disposition
|
November 1, 1991
In vivo evaluation of the semi-simultaneous method for bioavailability estimation using controlled intravenous infusion as an 'extravascular' route of administration
U Bredberg, M O Karlsson
CPT: Pharmacometrics & Systems Pharmacology
|
July 10, 2013
Best practices in population modeling should always be evolving
M O Karlsson, F Mentré
Pharmaceutical Research
|
September 1, 1989
Estimation of bioavailability on a single occasion after semisimultaneous drug administration
M O Karlsson, U Bredberg
Journal of Pharmacokinetics and Biopharmaceutics
|
April 1, 1990
Bioavailability estimation by semisimultaneous drug administration: a Monte Carlo simulation study
M O Karlsson, U Bredberg
European Journal of Pharmacology
|
March 22, 1988
Estimation of binding parameters by kinetic data analysis: differentiation between one and two binding sites
M O Karlsson, A Neil
The Journal of Pharmacy and Pharmacology
|
February 1, 1990
Serum protein binding of noscapine: influence of a reversible hydrolysis
M O Karlsson, B Dahlström
Journal of Pharmacokinetics and Biopharmaceutics
|
August 1, 1990
Comparison of methods to calculate cyclosporine A bioavailability from consecutive oral and intravenous doses
M O Karlsson, A Lindberg-Freijs
Page
of 13
Search research articles
Search
Showing results (1-10 of 121) with videos related to
Sort By:
Page
of 13
Clinical Pharmacology and Therapeutics
|
May 15, 2007
Time for quantitative clinical pharmacology: a proposal for a pharmacometrics curriculum
N Holford, M O Karlsson
Clinical Pharmacokinetics
|
July 4, 2001
Concentration-controlled or effect-controlled trials: useful alternatives to conventional dose-controlled trials?
A Grahnén, M O Karlsson
Molecular Pharmacology
|
January 1, 1989
Estimation of ligand binding parameters by simultaneous fitting of association and dissociation data: a Monte Carlo simulation study
M O Karlsson, A Neil
Biopharmaceutics & Drug Disposition
|
November 1, 1991
In vivo evaluation of the semi-simultaneous method for bioavailability estimation using controlled intravenous infusion as an 'extravascular' route of administration
U Bredberg, M O Karlsson
CPT: Pharmacometrics & Systems Pharmacology
|
July 10, 2013
Best practices in population modeling should always be evolving
M O Karlsson, F Mentré
Pharmaceutical Research
|
September 1, 1989
Estimation of bioavailability on a single occasion after semisimultaneous drug administration
M O Karlsson, U Bredberg
Journal of Pharmacokinetics and Biopharmaceutics
|
April 1, 1990
Bioavailability estimation by semisimultaneous drug administration: a Monte Carlo simulation study
M O Karlsson, U Bredberg
European Journal of Pharmacology
|
March 22, 1988
Estimation of binding parameters by kinetic data analysis: differentiation between one and two binding sites
M O Karlsson, A Neil
The Journal of Pharmacy and Pharmacology
|
February 1, 1990
Serum protein binding of noscapine: influence of a reversible hydrolysis
M O Karlsson, B Dahlström
Journal of Pharmacokinetics and Biopharmaceutics
|
August 1, 1990
Comparison of methods to calculate cyclosporine A bioavailability from consecutive oral and intravenous doses
M O Karlsson, A Lindberg-Freijs
Page
of 13