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Journal Abstract Search

109 related items for PubMed ID: 17885758

  • 1. Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia?
    Gürsoy S, Erdal E, Sezgin M, Barlas IO, Aydeniz A, Alaşehirli B, Sahin G.
    Rheumatol Int; 2008 Feb; 28(4):307-11. PubMed ID: 17885758
    [Abstract] [Full Text] [Related]

  • 2. No evidence for an association between the Glu298Asp polymorphism of the endothelial nitric oxide synthase gene and fibromyalgia syndrome.
    Alaşehirli B, Demiryürek S, Arica E, Gürsoy S, Demiryürek AT.
    Rheumatol Int; 2007 Jan; 27(3):275-80. PubMed ID: 16951945
    [Abstract] [Full Text] [Related]

  • 3. The association between fibromyalgia and polymorphism of monoamine oxidase A and interleukin-4.
    Su SY, Chen JJ, Lai CC, Chen CM, Tsai FJ.
    Clin Rheumatol; 2007 Jan; 26(1):12-6. PubMed ID: 16547693
    [Abstract] [Full Text] [Related]

  • 4. Association between sequence variations of the Mediterranean fever gene and fibromyalgia syndrome in a cohort of Turkish patients.
    Karakus N, Yigit S, Inanir A, Inanir S, Toprak H, Okan S.
    Clin Chim Acta; 2012 Dec 24; 414():36-40. PubMed ID: 23010357
    [Abstract] [Full Text] [Related]

  • 5. Association between fibromyalgia syndrome and polymorphism of the IL-4 gene in a Turkish population.
    Yigit S, Inanir A, Tekcan A, Inanir S, Tural S, Ates O.
    Gene; 2013 Sep 15; 527(1):62-4. PubMed ID: 23644020
    [Abstract] [Full Text] [Related]

  • 6. Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome.
    Gürsoy S, Erdal E, Herken H, Madenci E, Alaşehirli B, Erdal N.
    Rheumatol Int; 2003 May 15; 23(3):104-7. PubMed ID: 12739038
    [Abstract] [Full Text] [Related]

  • 7. Association analysis of the functional MAOA gene promoter and MAOB gene intron 13 polymorphisms in tension type headache patients.
    Edgnülü TG, Özge A, Erdal N, Kuru O, Erdal ME.
    Adv Clin Exp Med; 2014 May 15; 23(6):901-6. PubMed ID: 25618115
    [Abstract] [Full Text] [Related]

  • 8. [Association study of the polymorphisms of monoamine oxidase A genes with schizophrenia].
    Shi YZ, Wang CH, Lv LX, Wang YH, Zhang HX, Lou BY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 15; 24(4):457-9. PubMed ID: 17680543
    [Abstract] [Full Text] [Related]

  • 9. Analysis of monoamine oxidase A (MAO-A) promoter polymorphism in male heroin-dependent subjects: behavioural and personality correlates.
    Gerra G, Garofano L, Bosari S, Pellegrini C, Zaimovic A, Moi G, Bussandri M, Moi A, Brambilla F, Mameli A, Pizzamiglio M, Donnini C.
    J Neural Transm (Vienna); 2004 May 15; 111(5):611-21. PubMed ID: 15088154
    [Abstract] [Full Text] [Related]

  • 10. Relationship between FokI polymorphism in the vitamin D receptor gene and fibromyalgia syndrome.
    Maraslı E, Ozdolap S, Sarıkaya S.
    Int J Rheum Dis; 2016 Nov 15; 19(11):1063-1068. PubMed ID: 27135653
    [Abstract] [Full Text] [Related]

  • 11. [Polymorphism of MAO-B gene and NAD(P)H: quinone oxidoreductase gene in Parkinson's disease].
    Shao M, Liu Z, Tao E, Chen B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr 15; 18(2):122-4. PubMed ID: 11295131
    [Abstract] [Full Text] [Related]

  • 12. Clinical symptoms in fibromyalgia are associated to catechol-O-methyltransferase (COMT) gene Val158Met polymorphism.
    Inanir A, Karakus N, Ates O, Sezer S, Bozkurt N, Inanir S, Yigit S.
    Xenobiotica; 2014 Oct 15; 44(10):952-6. PubMed ID: 24762091
    [Abstract] [Full Text] [Related]

  • 13. Studies of the DXS7 polymorphism at the MAO loci in unipolar depression.
    Qian Y, Lin S, Jiang S, Jiang K, Wu X, Tang G, Wang D.
    Am J Med Genet; 1999 Dec 15; 88(6):598-600. PubMed ID: 10581474
    [Abstract] [Full Text] [Related]

  • 14. Detection and analysis of four polymorphic markers at the human monoamine oxidase (MAO) gene in Japanese controls and patients with Parkinson's disease.
    Nakatome M, Tun Z, Shimada S, Honda K.
    Biochem Biophys Res Commun; 1998 Jun 18; 247(2):452-6. PubMed ID: 9642149
    [Abstract] [Full Text] [Related]

  • 15. Monoamine oxidase (MAO) intron 13 polymorphism and platelet MAO-B activity in combat-related posttraumatic stress disorder.
    Pivac N, Knezevic J, Kozaric-Kovacic D, Dezeljin M, Mustapic M, Rak D, Matijevic T, Pavelic J, Muck-Seler D.
    J Affect Disord; 2007 Nov 18; 103(1-3):131-8. PubMed ID: 17289152
    [Abstract] [Full Text] [Related]

  • 16. Genotype combinations for monoamine oxidase-B intron 13 polymorphism and dopamine D2 receptor TaqIB polymorphism are associated with ever-smoking status among men.
    Costa-Mallen P, Costa LG, Checkoway H.
    Neurosci Lett; 2005 Sep 09; 385(2):158-62. PubMed ID: 15955630
    [Abstract] [Full Text] [Related]

  • 17. Association of A/G polymorphism in intron 13 of the monoamine oxidase B gene with schizophrenia in a Spanish population.
    Gassó P, Bernardo M, Mas S, Crescenti A, Garcia C, Parellada E, Lafuente A.
    Neuropsychobiology; 2008 Sep 09; 58(2):65-70. PubMed ID: 18832861
    [Abstract] [Full Text] [Related]

  • 18. Assessment of opioid receptor μ1 gene A118G polymorphism and its association with pain intensity in patients with fibromyalgia.
    Solak Ö, Erdoğan MÖ, Yıldız H, Ulaşlı AM, Yaman F, Terzi ES, Ulu S, Dündar Ü, Solak M.
    Rheumatol Int; 2014 Sep 09; 34(9):1257-61. PubMed ID: 24671502
    [Abstract] [Full Text] [Related]

  • 19. Association of a monoamine oxidase B allele with Parkinson's disease.
    Kurth JH, Kurth MC, Poduslo SE, Schwankhaus JD.
    Ann Neurol; 1993 Apr 09; 33(4):368-72. PubMed ID: 8489207
    [Abstract] [Full Text] [Related]

  • 20. Genetic polymorphism of monoamine oxidase B and susceptibility of Parkinson's disease.
    Hwang WJ, Lai ML, Tsai TT, Lai MD.
    Zhonghua Yi Xue Za Zhi (Taipei); 1997 Sep 09; 60(3):137-41. PubMed ID: 9419949
    [Abstract] [Full Text] [Related]

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