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Journal Abstract Search


168 related items for PubMed ID: 16530959

  • 1. Genetic analysis of the GABRA1 gene in patients with essential tremor.
    Deng H, Xie WJ, Le WD, Huang MS, Jankovic J.
    Neurosci Lett; 2006 Jun 19; 401(1-2):16-9. PubMed ID: 16530959
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial DNA in patients with essential tremor.
    Yoo YM, Lee CJ, Lee U, Kim YJ.
    Neurosci Lett; 2008 Mar 21; 434(1):29-34. PubMed ID: 18262358
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  • 3. Dopamine receptor D3 (DRD3) genotype and allelic variants and risk for essential tremor.
    García-Martín E, Martínez C, Alonso-Navarro H, Benito-León J, Puertas I, Rubio L, López-Alburquerque T, Agúndez JA, Jiménez-Jiménez FJ.
    Mov Disord; 2009 Oct 15; 24(13):1910-5. PubMed ID: 19645064
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  • 4. HS1-BP3 gene variant is common in familial essential tremor.
    Higgins JJ, Lombardi RQ, Pucilowska J, Jankovic J, Golbe LI, Verhagen L.
    Mov Disord; 2006 Mar 15; 21(3):306-9. PubMed ID: 16211613
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  • 5. Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor.
    García-Martín E, Martínez C, Alonso-Navarro H, Benito-León J, Lorenzo-Betancor O, Pastor P, Puertas I, Rubio L, López-Alburquerque T, Agúndez JA, Jiménez-Jiménez FJ.
    Pharmacogenet Genomics; 2011 Jul 15; 21(7):436-9. PubMed ID: 21422964
    [Abstract] [Full Text] [Related]

  • 6. Evidence of association between gamma-aminobutyric acid type A receptor genes located on 5q34 and female patients with mood disorders.
    Yamada K, Watanabe A, Iwayama-Shigeno Y, Yoshikawa T.
    Neurosci Lett; 2003 Sep 25; 349(1):9-12. PubMed ID: 12946574
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  • 7. A variant in the HS1-BP3 gene is associated with familial essential tremor.
    Shatunov A, Jankovic J, Elble R, Sambuughin N, Singleton A, Hallett M, Goldfarb L.
    Neurology; 2005 Dec 27; 65(12):1995; author reply 1995. PubMed ID: 16380635
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  • 9. Alternative splicing and promoter use in the human GABRA2 gene.
    Tian H, Chen HJ, Cross TH, Edenberg HJ.
    Brain Res Mol Brain Res; 2005 Jun 13; 137(1-2):174-83. PubMed ID: 15950776
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  • 10. Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
    Petryshen TL, Middleton FA, Tahl AR, Rockwell GN, Purcell S, Aldinger KA, Kirby A, Morley CP, McGann L, Gentile KL, Waggoner SG, Medeiros HM, Carvalho C, Macedo A, Albus M, Maier W, Trixler M, Eichhammer P, Schwab SG, Wildenauer DB, Azevedo MH, Pato MT, Pato CN, Daly MJ, Sklar P.
    Mol Psychiatry; 2005 Dec 13; 10(12):1074-88, 1057. PubMed ID: 16172613
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  • 12. Human GABA(B) receptor 1 gene: eight novel sequence variants.
    Hisama FM, Gruen JR, Choi J, Huseinovic M, Grigorenko EL, Pauls D, Mattson RH, Gelernter J, Wood FB, Goei VL.
    Hum Mutat; 2001 Apr 13; 17(4):349-50. PubMed ID: 11295833
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  • 13. Novel allelic variants in the human serotonin transporter gene linked polymorphism (5-HTTLPR) among depressed patients with suicide attempt.
    Segal J, Schenkel LC, Oliveira MH, Salum GA, Bau CH, Manfro GG, Leistner-Segal S.
    Neurosci Lett; 2009 Feb 13; 451(1):79-82. PubMed ID: 19103261
    [Abstract] [Full Text] [Related]

  • 14. Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
    Ma S, Davis TL, Blair MA, Fang JY, Bradford Y, Haines JL, Hedera P.
    Mov Disord; 2006 Sep 13; 21(9):1368-74. PubMed ID: 16721753
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  • 15. Association analysis of brain-derived neurotrophic factor (BDNF) gene 196 A/G polymorphism with Alzheimer's disease (AD) in mainland Chinese.
    Bian JT, Zhang JW, Zhang ZX, Zhao HL.
    Neurosci Lett; 2005 Oct 14; 387(1):11-6. PubMed ID: 16054753
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  • 16. Familial essential tremor is not associated with SCA-12 mutation in southern Italy.
    Nicoletti G, Annesi G, Carrideo S, Tomaino C, Di Costanzo A, Zappia M, Quattrone A.
    Mov Disord; 2002 Jul 14; 17(4):837-8. PubMed ID: 12210890
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  • 20. Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.
    Ma S, Abou-Khalil B, Blair MA, Sutcliffe JS, Haines JL, Hedera P.
    Neurosci Lett; 2006 Feb 06; 394(1):74-8. PubMed ID: 16256272
    [Abstract] [Full Text] [Related]


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