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Journal Abstract Search

215 related items for PubMed ID: 20488458

  • 1. Heterozygosity at catechol-O-methyltransferase Val158Met and schizophrenia: new data and meta-analysis.
    Costas J, Sanjuán J, Ramos-Ríos R, Paz E, Agra S, Ivorra JL, Páramo M, Brenlla J, Arrojo M.
    J Psychiatr Res; 2011 Jan; 45(1):7-14. PubMed ID: 20488458
    [Abstract] [Full Text] [Related]

  • 2. Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women.
    Sazci A, Ergul E, Kucukali I, Kilic G, Kaya G, Kara I.
    Brain Res Mol Brain Res; 2004 Dec 06; 132(1):51-6. PubMed ID: 15548428
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  • 5. COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia.
    Haraldsson HM, Ettinger U, Magnusdottir BB, Sigmundsson T, Sigurdsson E, Ingason A, Petursson H.
    Psychiatry Res; 2009 Sep 30; 169(2):173-5. PubMed ID: 19647329
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  • 6. Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.
    Borroni B, Grassi M, Costanzi C, Zanetti M, Archetti S, Franzoni S, Caimi L, Padovani A.
    Neurobiol Aging; 2007 Aug 30; 28(8):1231-8. PubMed ID: 16837108
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  • 8. COMT Association Data in Schizophrenia: New Caveats.
    Sand PG, Eichhammer P, Langguth B, Hajak G.
    Biol Psychiatry; 2006 Sep 15; 60(6):663-4; author reply 664-5. PubMed ID: 16899231
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  • 9. Anorexia nervosa and the Val158Met polymorphism of the COMT gene: meta-analysis and new data.
    Brandys MK, Slof-Op't Landt MC, van Elburg AA, Ophoff R, Verduijn W, Meulenbelt I, Middeldorp CM, Boomsma DI, van Furth EF, Slagboom E, Kas MJ, Adan RA.
    Psychiatr Genet; 2012 Jun 15; 22(3):130-6. PubMed ID: 22366815
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  • 10. COMT Val158Met polymorphism in schizophrenia with obsessive-compulsive disorder: a case-control study.
    Poyurovsky M, Michaelovsky E, Frisch A, Knoll G, Amir I, Finkel B, Buniak F, Hermesh H, Weizman R.
    Neurosci Lett; 2005 Nov 25; 389(1):21-4. PubMed ID: 16043283
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  • 11. No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.
    Nunokawa A, Watanabe Y, Muratake T, Kaneko N, Koizumi M, Someya T.
    Neurosci Res; 2007 Jul 25; 58(3):291-6. PubMed ID: 17482701
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  • 12. Analysis of association between the catechol-O-methyltransferase (COMT) gene and negative symptoms in chronic schizophrenia.
    Wang Y, Fang Y, Shen Y, Xu Q.
    Psychiatry Res; 2010 Sep 30; 179(2):147-50. PubMed ID: 20483479
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  • 13. The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia.
    Ohnishi T, Hashimoto R, Mori T, Nemoto K, Moriguchi Y, Iida H, Noguchi H, Nakabayashi T, Hori H, Ohmori M, Tsukue R, Anami K, Hirabayashi N, Harada S, Arima K, Saitoh O, Kunugi H.
    Brain; 2006 Feb 30; 129(Pt 2):399-410. PubMed ID: 16330500
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  • 14. Catechol-O-methyltransferase val108/158met genotype predicts working memory response to antipsychotic medications.
    Weickert TW, Goldberg TE, Mishara A, Apud JA, Kolachana BS, Egan MF, Weinberger DR.
    Biol Psychiatry; 2004 Nov 01; 56(9):677-82. PubMed ID: 15522252
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  • 15. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
    Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I.
    Int Clin Psychopharmacol; 2010 Jul 01; 25(4):218-27. PubMed ID: 20531207
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  • 16. Meta-analysis of association between genetic variants in COMT and schizophrenia: an update.
    Okochi T, Ikeda M, Kishi T, Kawashima K, Kinoshita Y, Kitajima T, Yamanouchi Y, Tomita M, Inada T, Ozaki N, Iwata N.
    Schizophr Res; 2009 May 01; 110(1-3):140-8. PubMed ID: 19329282
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  • 17. Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population.
    Liang S, Liu X, Fan P, Liu R, Zhang J, He G, Liu Y, Bai H.
    Arch Med Res; 2012 Feb 01; 43(2):154-8. PubMed ID: 22475780
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  • 18. Association study on catechol-O-methyltransferase (COMT) Val158Met gene polymorphism and NEO-FFI.
    Aoki J, Iwahashi K, Ishigooka J, Ikeda K.
    Psychiatry Res; 2011 May 15; 187(1-2):312-3. PubMed ID: 21051090
    [No Abstract] [Full Text] [Related]

  • 19. Clinical involvement of catechol-O-methyltransferase polymorphisms in schizophrenia spectrum disorders: influence on the severity of psychotic symptoms and on the response to neuroleptic treatment.
    Molero P, Ortuño F, Zalacain M, Patiño-García A.
    Pharmacogenomics J; 2007 Dec 15; 7(6):418-26. PubMed ID: 17363961
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  • 20. COMT gene val158met polymorphism in patients with dyspeptic symptoms.
    Tahara T, Arisawa T, Shibata T, Nakamura M, Wang F, Hirata I.
    Hepatogastroenterology; 2008 Dec 15; 55(84):979-82. PubMed ID: 18705311
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