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Journal Abstract Search

393 related items for PubMed ID: 15277629

  • 21.
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  • 23. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
    Bonanni P, Malcarne M, Moro F, Veggiotti P, Buti D, Ferrari AR, Parrini E, Mei D, Volzone A, Zara F, Heron SE, Bordo L, Marini C, Guerrini R.
    Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
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  • 24. Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A.
    Mahoney K, Moore SJ, Buckley D, Alam M, Parfrey P, Penney S, Merner N, Hodgkinson K, Young TL.
    Seizure; 2009 Sep; 18(7):492-7. PubMed ID: 19464195
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  • 27. [Progress in molecular genetics of generalized epilepsy with febrile seizures plus].
    Sun HH, Zhang YH.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2008 Apr; 40(2):229-33. PubMed ID: 18458705
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  • 28. Therapy for hyperthermia-induced seizures in Scn1a mutant rats.
    Hayashi K, Ueshima S, Ouchida M, Mashimo T, Nishiki T, Sendo T, Serikawa T, Matsui H, Ohmori I.
    Epilepsia; 2011 May; 52(5):1010-7. PubMed ID: 21480876
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  • 29. Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy.
    Rhodes TH, Lossin C, Vanoye CG, Wang DW, George AL.
    Proc Natl Acad Sci U S A; 2004 Jul 27; 101(30):11147-52. PubMed ID: 15263074
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  • 32. Sodium channel SCN1A and epilepsy: mutations and mechanisms.
    Escayg A, Goldin AL.
    Epilepsia; 2010 Sep 27; 51(9):1650-8. PubMed ID: 20831750
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  • 34. SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.
    Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X.
    J Hum Genet; 2008 Sep 27; 53(8):769-774. PubMed ID: 18566737
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  • 36. Milder phenotype with SCN1A truncation mutation other than SMEI.
    Yu MJ, Shi YW, Gao MM, Deng WY, Liu XR, Chen L, Long YS, Yi YH, Liao WP.
    Seizure; 2010 Sep 27; 19(7):443-5. PubMed ID: 20630778
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