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European Journal of Clinical Pharmacology|January 1, 1989
Quinidine inhibits the 2-hydroxylation of imipramine and desipramine but not the demethylation of imipramineK Brøsen, L F GramEuropean Journal of Clinical Pharmacology|January 1, 1989
Clinical significance of the sparteine/debrisoquine oxidation polymorphismK Brøsen, L F GramPharmacopsychiatry|January 1, 1986
Benzodiazepine suppression of cortisol secretion: a measure of anxiolytic activity?L F Gram, P ChristensenBritish Medical Journal|February 19, 1972
Drug interaction: inhibitory effect of neuroleptics on metabolism of tricyclic antidepressants in manL F Gram, K F OveroClinical Pharmacology and Therapeutics|September 1, 1975
First-pass metabolism of nortriptyline in manL F Gram, K F OveroActa Pharmacologica Et Toxicologica|February 1, 1982
Equilibrium dialysis for determination of protein binding or imipramine--evaluation of a methodC B Kristensen, L F GramActa Pharmacologica Et Toxicologica|February 1, 1982
Imipramine kinetics in the single pass rat liver perfusion modelE J Erlandsen, L F GramBritish Journal of Clinical Pharmacology|February 1, 1990
Quinidine kinetics after a single oral dose in relation to the sparteine oxidation polymorphism in manK Brøsen, F Davidsen, L F GramBritish Journal of Clinical Pharmacology|March 1, 1993
The N-demethylation of imipramine correlates with the oxidation of S-mephenytoin (S/R-ratio). A population studyE Skjelbo, L F Gram, K BrøsenUgeskrift for Laeger|November 25, 1996
[Serotonin syndrome and malignant neuroleptic syndrome. A review based on the material from the National Board of Adverse Drug Reactions]M G von Halling Laier, L F GramPageof 107