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PUBMED FOR HANDHELDS

Journal Abstract Search


143 related items for PubMed ID: 403278

  • 1. Concentration-time effects of quinidine disposition kinetics in rhesus monkeys.
    Ueda CT, Ballard B, Rowland M.
    J Pharmacol Exp Ther; 1977 Mar; 200(3):459-68. PubMed ID: 403278
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  • 3. Disposition kinetics of dihydroquinidine following quinidine administration.
    Ueda CT, Williamson BJ, Dzindzio BS.
    Res Commun Chem Pathol Pharmacol; 1976 Jun; 14(2):215-25. PubMed ID: 940955
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  • 4. Dose-dependent kinetics of quinidine in the perfused rat liver preparation. Kinetics of formation of active metabolites.
    Yu VC, de Lamirande E, Horning MG, Pang KS.
    Drug Metab Dispos; 1982 Jun; 10(6):568-72. PubMed ID: 6130901
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  • 5. Analysis of iosulamide in plasma and urine: application to intravenous pharmacokinetics in rhesus monkey.
    Park GB, Biddlecome CE, Rowe EA, Kullberg MP, Edelson J.
    Drug Metab Dispos; 1981 Jun; 9(1):43-7. PubMed ID: 6111430
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  • 6. Effect of plasma protein binding on quinidine kinetics in the rabbit.
    Guentert TW, Oie S.
    J Pharmacol Exp Ther; 1980 Oct; 215(1):165-71. PubMed ID: 7452481
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  • 7. Modulation of effect of dietary salt on prehepatic first-pass metabolism: effects of beta-blockade and intravenous salt loading.
    Fromm MF, Darbar D, Dell'Orto S, Roden DM.
    J Pharmacol Exp Ther; 1999 Jul; 290(1):253-8. PubMed ID: 10381784
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  • 8. Pharmacokinetic disposition of guanabenz in the rhesus monkey.
    Meacham RH, Chiang ST, Kick CJ, Sisenwine SF, Jusko WJ, Ruelius HW.
    Drug Metab Dispos; 1981 Jul; 9(6):509-14. PubMed ID: 6120807
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  • 9. Disposition of the angiotensin II receptor antagonist L-158,809 in rats and rhesus monkeys.
    Colletti AE, Krieter PA.
    Drug Metab Dispos; 1994 Jul; 22(2):183-8. PubMed ID: 8013272
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  • 10. The pharmacology of verapamil. I. Elimination kinetics in dogs and correlation of plasma levels with effect on the eletrocardiogram.
    McAllister RG, Bourne DW, Dittert LW.
    J Pharmacol Exp Ther; 1977 Jul; 202(1):38-44. PubMed ID: 874818
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  • 11. Orally active inhibitors of human leukocyte elastase. II. Disposition of L-694,458 in rats and rhesus monkeys.
    Vincent SH, Painter SK, Luffer-Atlas D, Karanam BV, McGowan E, Cioffe C, Doss G, Chiu SH.
    Drug Metab Dispos; 1997 Aug; 25(8):932-9. PubMed ID: 9280401
    [Abstract] [Full Text] [Related]

  • 12. Rapid elimination of quinidine in pediatric patients.
    Szefler SJ, Pieroni DR, Gingell RL, Shen DD.
    Pediatrics; 1982 Sep; 70(3):370-5. PubMed ID: 7110810
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  • 16. Disposition kinetics of quinidine.
    Ueda CT, Hirschfeld DS, Scheinman MM, Rowland M, Williamson BJ, Dzindzio BS.
    Clin Pharmacol Ther; 1976 Jan; 19(1):30-6. PubMed ID: 1245091
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  • 17. [Distribution, absorption and elimination of radioactivity following oral and intravenous application of 2'-14C-labelled cyproterone acetate to rhesus monkeys (author's transl)].
    Schulz V.
    Arzneimittelforschung; 1976 Apr; 26(4):544-6. PubMed ID: 821492
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  • 19. The influence of diazepam on the pharmacokinetics of intravenous and epidural bupivacaine in the rhesus monkey.
    Thompson GA, Turner PA, Bridenbaugh PO, Stuebing RC, Denson DD.
    Anesth Analg; 1986 Feb; 65(2):151-5. PubMed ID: 3942302
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