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Journal Abstract Search
168 related items for PubMed ID: 8513845
1. Inhibition by paroxetine of desipramine metabolism in extensive but not in poor metabolizers of sparteine. Brøsen K, Hansen JG, Nielsen KK, Sindrup SH, Gram LF. Eur J Clin Pharmacol; 1993; 44(4):349-55. PubMed ID: 8513845 [Abstract] [Full Text] [Related]
2. Single-dose kinetics of clomipramine: relationship to the sparteine and S-mephenytoin oxidation polymorphisms. Nielsen KK, Brøsen K, Hansen MG, Gram LF. Clin Pharmacol Ther; 1994 May; 55(5):518-27. PubMed ID: 8181196 [Abstract] [Full Text] [Related]
3. The relationship between paroxetine and the sparteine oxidation polymorphism. Sindrup SH, Brøsen K, Gram LF, Hallas J, Skjelbo E, Allen A, Allen GD, Cooper SM, Mellows G, Tasker TC. Clin Pharmacol Ther; 1992 Mar; 51(3):278-87. PubMed ID: 1531950 [Abstract] [Full Text] [Related]
7. The influence of the sparteine/debrisoquine genetic polymorphism on the disposition of dexfenfluramine. Gross AS, Phillips AC, Rieutord A, Shenfield GM. Br J Clin Pharmacol; 1996 Apr; 41(4):311-7. PubMed ID: 8730977 [Abstract] [Full Text] [Related]
16. Metabolism, pharmacokinetics, and excretion of a highly selective N-methyl-D-aspartate receptor antagonist, traxoprodil, in human cytochrome P450 2D6 extensive and poor metabolizers. Johnson K, Shah A, Jaw-Tsai S, Baxter J, Prakash C. Drug Metab Dispos; 2003 Jan; 31(1):76-87. PubMed ID: 12485956 [Abstract] [Full Text] [Related]