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PUBMED FOR HANDHELDS

Journal Abstract Search


203 related items for PubMed ID: 9327906

  • 1. Catechol O-methyltransferase: characterization of the protein, its gene, and the preclinical pharmacology of COMT inhibitors.
    Männistö PT.
    Adv Pharmacol; 1998; 42():324-8. PubMed ID: 9327906
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  • 3. Positron emission tomography in drug evaluation: influence of three different catechol-O-methyltransferase inhibitors on metabolism of [NCA] 6-[18F]fluoro-L-dopa in rhesus monkey.
    Günther I, Psylla M, Reddy GN, Antonini A, Vontobel P, Reist HW, Zollinger A, Nickles RJ, Beer HF, Schubiger PA.
    Nucl Med Biol; 1995 Oct; 22(7):921-7. PubMed ID: 8547890
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  • 4. Different in vivo properties of three new inhibitors of catechol O-methyltransferase in the rat.
    Männistö PT, Tuomainen P, Tuominen RK.
    Br J Pharmacol; 1992 Mar; 105(3):569-74. PubMed ID: 1628144
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  • 5. COMT inhibition: a new treatment strategy for Parkinson's disease.
    Kurth MC, Adler CH.
    Neurology; 1998 May; 50(5 Suppl 5):S3-14. PubMed ID: 9591516
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  • 8. Effects of three types of catechol O-methylation inhibitors on L-3,4-dihydroxyphenylalanine-induced circling behaviour in rats.
    Törnwall M, Männistö PT.
    Eur J Pharmacol; 1993 Nov 30; 250(1):77-84. PubMed ID: 8119326
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  • 9. COMT inhibition in the treatment of Parkinson's disease.
    Ruottinen HM, Rinne UK.
    J Neurol; 1998 Nov 30; 245(11 Suppl 3):P25-34. PubMed ID: 9808337
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  • 11. A systematic review of catechol-0-methyltransferase inhibitors: efficacy and safety in clinical practice.
    Marsala SZ, Gioulis M, Ceravolo R, Tinazzi M.
    Clin Neuropharmacol; 2012 Nov 30; 35(4):185-90. PubMed ID: 22805229
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  • 13. COMT inhibitors: management of Parkinson's disease.
    Mov Disord; 2002 Nov 30; 17 Suppl 4():S45-51. PubMed ID: 12211139
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  • 14. [Inhibition of catechol-O-methyltransferase. Optimizing dopaminergic therapy in idiopathic Parkinson syndrome with entacapone].
    Arnold G, Kupsch A.
    Nervenarzt; 2000 Feb 30; 71(2):78-83. PubMed ID: 10703007
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  • 15. Effects of peripheral and central catechol-O-methyltransferase inhibition on striatal extracellular levels of dopamine: a microdialysis study in freely moving rats.
    Napolitano A, Bellini G, Borroni E, Zürcher G, Bonuccelli U.
    Parkinsonism Relat Disord; 2003 Jan 30; 9(3):145-50. PubMed ID: 12573869
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  • 16. Effects of selective catechol-O-methyltransferase inhibitors on single-trial passive avoidance retention in male rats.
    Khromova I, Voronina T, Kraineva VA, Zolotov N, Männistö PT.
    Behav Brain Res; 1997 Jun 30; 86(1):49-57. PubMed ID: 9105581
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  • 17. The central catechol-O-methyltransferase inhibitor tolcapone increases striatal hydroxyl radical production in L-DOPA/carbidopa treated rats.
    Gerlach M, Xiao AY, Kuhn W, Lehnfeld R, Waldmeier P, Sontag KH, Riederer P.
    J Neural Transm (Vienna); 2001 Jun 30; 108(2):189-204. PubMed ID: 11314772
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  • 18. Modulation of rat brain endogenous dopamine metabolism by new inhibitors of catechol O-methyltransferase.
    Törnwall M, Tuomainen P, Männistö PT.
    Eur J Pharmacol; 1993 Aug 03; 239(1-3):39-45. PubMed ID: 8223912
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  • 19. COMT inhibition with tolcapone does not affect carbidopa pharmacokinetics in parkinsonian patients in levodopa/carbidopa (Sinemet).
    Jorga KM, Nicholl DJ.
    Br J Clin Pharmacol; 1999 Sep 03; 48(3):449-52. PubMed ID: 10510160
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