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Journal Abstract Search

540 related items for PubMed ID: 16380441

  • 21. Identification of two mutations in cis in the SCN1A gene in a family showing genetic epilepsy with febrile seizures plus (GEFS+) and idiopathic generalized epilepsy (IGE).
    Binini N, Sancini G, Villa C, Dal Magro R, Sansoni V, Rusconi R, Mantegazza M, Grioni D, Talpo F, Toselli M, Combi R.
    Brain Res; 2017 Dec 15; 1677():26-32. PubMed ID: 28951233
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  • 22. Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
    Marini C, Mei D, Temudo T, Ferrari AR, Buti D, Dravet C, Dias AI, Moreira A, Calado E, Seri S, Neville B, Narbona J, Reid E, Michelucci R, Sicca F, Cross HJ, Guerrini R.
    Epilepsia; 2007 Sep 15; 48(9):1678-1685. PubMed ID: 17561957
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  • 24. Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man.
    Alekov AK, Rahman MM, Mitrovic N, Lehmann-Horn F, Lerche H.
    Eur J Neurosci; 2001 Jun 15; 13(11):2171-6. PubMed ID: 11422459
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  • 25. 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 15; 52(5):1010-7. PubMed ID: 21480876
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  • 28. Molecular basis of an inherited epilepsy.
    Lossin C, Wang DW, Rhodes TH, Vanoye CG, George AL.
    Neuron; 2002 Jun 13; 34(6):877-84. PubMed ID: 12086636
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  • 30. Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: associated with loss of function of Na(v) 1.1.
    Liao WP, Shi YW, Long YS, Zeng Y, Li T, Yu MJ, Su T, Deng P, Lei ZG, Xu SJ, Deng WY, Liu XR, Sun WW, Yi YH, Xu ZC, Duan S.
    Epilepsia; 2010 Sep 13; 51(9):1669-78. PubMed ID: 20550552
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  • 36. A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
    Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH.
    Am J Hum Genet; 2001 Apr 13; 68(4):866-73. PubMed ID: 11254445
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  • 38. Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plus.
    Kumakura A, Ito M, Hata D, Oh N, Kurahashi H, Wang JW, Hirose S.
    Brain Dev; 2009 Feb 13; 31(2):179-82. PubMed ID: 18632234
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