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Journal Abstract Search

146 related items for PubMed ID: 22578703

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  • 2. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
    Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Zumsteg D, Duncan S, Kälviäinen RK, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Théâtre E, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Chaves J, Costa PP, Silva BM, da Silva AM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Rössler K, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME, UK Brain Expression Consortium, Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM.
    Brain; 2013 Oct; 136(Pt 10):3140-50. PubMed ID: 24014518
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  • 6. Major vault protein (MVP) gene polymorphisms and drug resistance in mesial temporal lobe epilepsy with hippocampal sclerosis.
    Balan S, Radhab SK, Sathyan S, Vijai J, Banerjee M, Radhakrishnan K.
    Gene; 2013 Sep 10; 526(2):449-53. PubMed ID: 23751308
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  • 9. Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.
    Manna I, Labate A, Mumoli L, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A.
    Epilepsy Res; 2013 Sep 10; 106(1-2):284-7. PubMed ID: 23623847
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  • 10. SCN1A rs3812718 polymorphism and susceptibility to epilepsy with febrile seizures: a meta-analysis.
    Tang L, Lu X, Tao Y, Zheng J, Zhao P, Li K, Li L.
    Gene; 2014 Jan 01; 533(1):26-31. PubMed ID: 24076350
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  • 11. Increased frequency of interleukin-1beta-511T allele in patients with temporal lobe epilepsy, hippocampal sclerosis, and prolonged febrile convulsion.
    Kanemoto K, Kawasaki J, Yuasa S, Kumaki T, Tomohiro O, Kaji R, Nishimura M.
    Epilepsia; 2003 Jun 01; 44(6):796-9. PubMed ID: 12790892
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  • 13. Epilepsy: Genetic variant in subtype of MTLE.
    Kingwell K.
    Nat Rev Neurol; 2013 Nov 01; 9(11):603. PubMed ID: 24126623
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  • 16. Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures.
    Jamali S, Salzmann A, Perroud N, Ponsole-Lenfant M, Cillario J, Roll P, Roeckel-Trevisiol N, Crespel A, Balzar J, Schlachter K, Gruber-Sedlmayr U, Pataraia E, Baumgartner C, Zimprich A, Zimprich F, Malafosse A, Szepetowski P.
    PLoS One; 2010 Sep 16; 5(9):. PubMed ID: 20862287
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  • 17. Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation.
    Colosimo E, Gambardella A, Mantegazza M, Labate A, Rusconi R, Schiavon E, Annesi F, Cassulini RR, Carrideo S, Chifari R, Canevini MP, Canger R, Franceschetti S, Annesi G, Wanke E, Quattrone A.
    Epilepsia; 2007 Sep 16; 48(9):1691-1696. PubMed ID: 17565594
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