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Journal Abstract Search

101 related items for PubMed ID: 21059181

  • 1. Polymorphisms of adrenergic cardiovascular control genes are associated with adolescent chronic fatigue syndrome.
    Sommerfeldt L, Portilla H, Jacobsen L, Gjerstad J, Wyller VB.
    Acta Paediatr; 2011 Feb; 100(2):293-8. PubMed ID: 21059181
    [Abstract] [Full Text] [Related]

  • 2. Moderate exercise increases expression for sensory, adrenergic, and immune genes in chronic fatigue syndrome patients but not in normal subjects.
    Light AR, White AT, Hughen RW, Light KC.
    J Pain; 2009 Oct; 10(10):1099-112. PubMed ID: 19647494
    [Abstract] [Full Text] [Related]

  • 3. Autoantibodies, polymorphisms in the serotonin pathway, and human leukocyte antigen class II alleles in chronic fatigue syndrome: are they associated with age at onset and specific symptoms?
    Ortega-Hernandez OD, Cuccia M, Bozzini S, Bassi N, Moscavitch S, Diaz-Gallo LM, Blank M, Agmon-Levin N, Shoenfeld Y.
    Ann N Y Acad Sci; 2009 Sep; 1173():589-99. PubMed ID: 19758204
    [Abstract] [Full Text] [Related]

  • 4. Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome.
    Goertzel BN, Pennachin C, de Souza Coelho L, Gurbaxani B, Maloney EM, Jones JF.
    Pharmacogenomics; 2006 Apr; 7(3):475-83. PubMed ID: 16610957
    [Abstract] [Full Text] [Related]

  • 5. Glucocorticoid receptor polymorphisms and haplotypes associated with chronic fatigue syndrome.
    Rajeevan MS, Smith AK, Dimulescu I, Unger ER, Vernon SD, Heim C, Reeves WC.
    Genes Brain Behav; 2007 Mar; 6(2):167-76. PubMed ID: 16740143
    [Abstract] [Full Text] [Related]

  • 6. An integrated approach to infer causal associations among gene expression, genotype variation, and disease.
    Lee E, Cho S, Kim K, Park T.
    Genomics; 2009 Oct; 94(4):269-77. PubMed ID: 19540336
    [Abstract] [Full Text] [Related]

  • 7. Genetic evaluation of the serotonergic system in chronic fatigue syndrome.
    Smith AK, Dimulescu I, Falkenberg VR, Narasimhan S, Heim C, Vernon SD, Rajeevan MS.
    Psychoneuroendocrinology; 2008 Feb; 33(2):188-97. PubMed ID: 18079067
    [Abstract] [Full Text] [Related]

  • 8. [Catechol-O-methyltransferase gene rs6267 polymorphism in children with attention deficit hyperactivity disorder].
    Zhang YB, Luo XR, Liu X, Zhong Y, Zhu F, Chen LY.
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Feb; 13(2):127-30. PubMed ID: 21342622
    [Abstract] [Full Text] [Related]

  • 9. Genetic variation in catechol-O-methyltransferase modifies effects of clonidine treatment in chronic fatigue syndrome.
    Hall KT, Kossowsky J, Oberlander TF, Kaptchuk TJ, Saul JP, Wyller VB, Fagermoen E, Sulheim D, Gjerstad J, Winger A, Mukamal KJ.
    Pharmacogenomics J; 2016 Oct; 16(5):454-60. PubMed ID: 27457818
    [Abstract] [Full Text] [Related]

  • 10. Polymorphism in COMT is associated with IgG3 subclass level and susceptibility to infection in patients with chronic fatigue syndrome.
    Löbel M, Mooslechner AA, Bauer S, Günther S, Letsch A, Hanitsch LG, Grabowski P, Meisel C, Volk HD, Scheibenbogen C.
    J Transl Med; 2015 Aug 14; 13():264. PubMed ID: 26272340
    [Abstract] [Full Text] [Related]

  • 11. An angiotensin-1 converting enzyme polymorphism is associated with allostatic load mediated by C-reactive protein, interleukin-6 and cortisol.
    Smith AK, Maloney EM, Falkenberg VR, Dimulescu I, Rajeevan MS.
    Psychoneuroendocrinology; 2009 May 14; 34(4):597-606. PubMed ID: 19081678
    [Abstract] [Full Text] [Related]

  • 12. 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 14; 23(3):104-7. PubMed ID: 12739038
    [Abstract] [Full Text] [Related]

  • 13. Genetic polymorphisms of estrogen receptor alpha, CYP19, catechol-O-methyltransferase are associated with familial prostate carcinoma risk in a Japanese population.
    Suzuki K, Nakazato H, Matsui H, Koike H, Okugi H, Kashiwagi B, Nishii M, Ohtake N, Nakata S, Ito K, Yamanaka H.
    Cancer; 2003 Oct 01; 98(7):1411-6. PubMed ID: 14508827
    [Abstract] [Full Text] [Related]

  • 14. Catecholamine-o-methyltransferase polymorphisms are associated with postoperative pain intensity.
    Lee PJ, Delaney P, Keogh J, Sleeman D, Shorten GD.
    Clin J Pain; 2011 Feb 01; 27(2):93-101. PubMed ID: 20842020
    [Abstract] [Full Text] [Related]

  • 15. Pharmacogenetics and obstetric anesthesia.
    Landau R.
    Int Anesthesiol Clin; 2007 Feb 01; 45(1):1-15. PubMed ID: 17215696
    [No Abstract] [Full Text] [Related]

  • 16. Association of medically unexplained fatigue with ACE insertion/deletion polymorphism in Gulf War veterans.
    Vladutiu GD, Natelson BH.
    Muscle Nerve; 2004 Jul 01; 30(1):38-43. PubMed ID: 15221876
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 58(3):291-6. PubMed ID: 17482701
    [Abstract] [Full Text] [Related]

  • 18. Association of mannose-binding lectin gene polymorphisms with antiphospholipid syndrome, cardiovascular disease and chronic damage in patients with systemic lupus erythematosus.
    Font J, Ramos-Casals M, Brito-Zerón P, Nardi N, Ibañez A, Suarez B, Jiménez S, Tàssies D, García-Criado A, Ros E, Sentís J, Reverter JC, Lozano F.
    Rheumatology (Oxford); 2007 Jan 01; 46(1):76-80. PubMed ID: 16801331
    [Abstract] [Full Text] [Related]

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  • 20. Mirrored symptoms in mother and child with chronic fatigue syndrome.
    van de Putte EM, van Doornen LJ, Engelbert RH, Kuis W, Kimpen JL, Uiterwaal CS.
    Pediatrics; 2006 Jun 01; 117(6):2074-9. PubMed ID: 16740850
    [Abstract] [Full Text] [Related]

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