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Journal Abstract Search

324 related items for PubMed ID: 11904235

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  • 4. Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.
    Lü JJ, Zhang YH, Pan H, Chen YC, Liu XY, Jiang YW, Bao XH, Shen Y, Wu HS, Xu KM, Wu XR.
    Chin Med J (Engl); 2004 Oct; 117(10):1497-501. PubMed ID: 15498372
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  • 8. [Association analysis of childhood absence epilepsy by microsatellite DNA].
    Lu J, Chen Y, Pan H, Zhang Y, Jiang Y, Di W, Shen Y, Xu K, Wu H, Wu X.
    Zhonghua Yi Xue Za Zhi; 2002 Aug 10; 82(15):1029-32. PubMed ID: 12194792
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  • 9. Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map.
    Sugimoto Y, Morita R, Amano K, Fong CY, Shah PU, Castroviejo IP, Khan S, Delgado-Escueta AV, Yamakawa K.
    Genomics; 2000 Sep 15; 68(3):264-72. PubMed ID: 10995568
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  • 10. Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15.
    Sander T, Kretz R, Williamson MP, Elmslie FV, Rees M, Hildmann T, Bianchi A, Bauer G, Sailer U, Scaramelli A, Schmitz B, Gardiner RM, Janz D, Beck-Mannagetta G.
    Acta Neurol Scand; 1997 Jul 15; 96(1):1-7. PubMed ID: 9262125
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  • 11. Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
    Delgado-Escueta AV, Medina MT, Serratosa JM, Castroviejo IP, Gee MN, Weissbecker K, Westling BW, Fong CY, Alonso ME, Cordova S, Shah P, Khan S, Sainz J, Rubio-Donnadieu F, Sparkes RS.
    Adv Neurol; 1999 Jul 15; 79():351-74. PubMed ID: 10514826
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  • 12. Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity.
    Durner M, Zhou G, Fu D, Abreu P, Shinnar S, Resor SR, Moshe SL, Rosenbaum D, Cohen J, Harden C, Kang H, Wallace S, Luciano D, Ballaban-Gil K, Klotz I, Dicker E, Greenberg DA.
    Am J Hum Genet; 1999 May 15; 64(5):1411-9. PubMed ID: 10205274
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  • 13. Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.
    Sander T, Hildmann T, Janz D, Wienker TF, Bianchi A, Bauer G, Sailer U, Scaramelli A, Neitzel H, Schmitz B, Bailey ME, Beck-Mannagetta G, Johnson KJ, Darlison MG.
    Epilepsy Res; 1996 Apr 15; 23(3):235-44. PubMed ID: 8739126
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  • 14. Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.
    Chioza BA, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley JM, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis ML, Guerrini R, Kjeldsen MJ, Nabbout R, Nashef L, Sander T, Sirén A, Wirrell E, McKeigue P, Robinson R, Gardiner RM, Everett KV.
    Epilepsy Res; 2009 Dec 15; 87(2-3):247-55. PubMed ID: 19837565
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  • 15. Replication analysis of a putative susceptibility locus (EGI) for idiopathic generalized epilepsy on chromosome 8q24.
    Sander T, Kretz R, Schulz H, Sailer U, Bauer G, Scaramelli A, Epplen JT, Riess O, Janz D.
    Epilepsia; 1998 Jul 15; 39(7):715-20. PubMed ID: 9670899
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  • 18. The gamma-aminobutyric acid receptor gamma 3 subunit gene (GABRG3) is tightly linked to the alpha 5 subunit gene (GABRA5) on human chromosome 15q11-q13 and is transcribed in the same orientation.
    Greger V, Knoll JH, Woolf E, Glatt K, Tyndale RF, DeLorey TM, Olsen RW, Tobin AJ, Sikela JM, Nakatsu Y.
    Genomics; 1995 Mar 20; 26(2):258-64. PubMed ID: 7601451
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  • 19. Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.
    Tanaka M, Olsen RW, Medina MT, Schwartz E, Alonso ME, Duron RM, Castro-Ortega R, Martinez-Juarez IE, Pascual-Castroviejo I, Machado-Salas J, Silva R, Bailey JN, Bai D, Ochoa A, Jara-Prado A, Pineda G, Macdonald RL, Delgado-Escueta AV.
    Am J Hum Genet; 2008 Jun 20; 82(6):1249-61. PubMed ID: 18514161
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  • 20. The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.
    Sander T, Peters C, Janz D, Bianchi A, Bauer G, Wienker TF, Hildmann T, Epplen JT, Riess O.
    Epilepsy Res; 1998 Jan 20; 29(2):115-22. PubMed ID: 9477143
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