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Journal Abstract Search

71 related items for PubMed ID: 15101840

  • 1. Febrile convulsions and genetic susceptibility: role of the neuronal nicotinic acetylcholine receptor alpha 4 subunit.
    Mulley J, Heron S, Scheffer I, Berkovic S.
    Epilepsia; 2004 May; 45(5):561; author reply 561-2. PubMed ID: 15101840
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  • 3. Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions.
    Chou IC, Lee CC, Huang CC, Wu JY, Tsai JJ, Tsai CH, Tsai FJ.
    Epilepsia; 2003 Aug; 44(8):1089-93. PubMed ID: 12887442
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  • 4. No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder.
    Lohoff FW, Ferraro TN, McNabb L, Schwebel C, Dahl JP, Doyle GA, Buono RJ, Berrettini WH.
    Psychiatry Res; 2005 Jun 30; 135(3):171-7. PubMed ID: 15996750
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  • 6. A fok1 polymorphism in the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene.
    Guipponi M, Baldy-Moulinier M, Malafosse A.
    Clin Genet; 1997 Jan 30; 51(1):78-9. PubMed ID: 9084944
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  • 9. Genetic susceptibility to simple febrile seizures: interleukin-1beta promoter polymorphisms are associated with sporadic cases.
    Kira R, Torisu H, Takemoto M, Nomura A, Sakai Y, Sanefuji M, Sakamoto K, Matsumoto S, Gondo K, Hara T.
    Neurosci Lett; 2005 Aug 26; 384(3):239-44. PubMed ID: 15916853
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  • 11. Dinucleotide polymorphism in the first intron of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene (CHRNA4).
    Weiland S, Steinlein O.
    Clin Genet; 1996 Nov 26; 50(5):433-4. PubMed ID: 9007339
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  • 13. A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus.
    Audenaert D, Claes L, Claeys KG, Deprez L, Van Dyck T, Goossens D, Del-Favero J, Van Paesschen W, Van Broeckhoven C, De Jonghe P.
    J Med Genet; 2005 Dec 26; 42(12):947-52. PubMed ID: 15827091
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  • 14. A novel GABRG2 mutation associated with febrile seizures.
    Audenaert D, Schwartz E, Claeys KG, Claes L, Deprez L, Suls A, Van Dyck T, Lagae L, Van Broeckhoven C, Macdonald RL, De Jonghe P.
    Neurology; 2006 Aug 22; 67(4):687-90. PubMed ID: 16924025
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  • 15. Genetic polymorphism at codon 129 of the prion protein gene is not associated with multiple sclerosis.
    Stüve O, Korth C, Gabatto P, Cameron EM, Hu W, Eagar TN, Monson NL, Frohman EM, Racke MK, Zabetian CP, Oksenberg JR.
    Arch Neurol; 2009 Feb 22; 66(2):280-1. PubMed ID: 19204171
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  • 17. Generalized epilepsy with febrile seizures plus-associated sodium channel beta1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function.
    Xu R, Thomas EA, Gazina EV, Richards KL, Quick M, Wallace RH, Harkin LA, Heron SE, Berkovic SF, Scheffer IE, Mulley JC, Petrou S.
    Neuroscience; 2007 Aug 10; 148(1):164-74. PubMed ID: 17629415
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  • 18. A novel intragenetic PvuII marker in the human neuronal nicotinic acetylcholine receptor a4 subunit gene (CHRNA4). Mutation and polymorphism report no. 62. Online.
    Iwata H, Hirose S, Akiyoshi H, Kaneko S, Mitsudome A.
    Hum Mutat; 1999 Aug 10; 14(1):93. PubMed ID: 10447275
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  • 19. Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design.
    Pereira AC, Xavier-Neto J, Mesquita SM, Mota GF, Lopes AA, Krieger JE.
    Int J Cardiol; 2005 Oct 20; 105(1):15-8. PubMed ID: 16207540
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