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5. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified. Zucca C; Redaelli F; Epifanio R; Zanotta N; Romeo A; Lodi M; Veggiotti P; Airoldi G; Panzeri C; Romaniello R; De Polo G; Bonanni P; Cardinali S; Baschirotto C; Martorell L; Borgatti R; Bresolin N; Bassi MT Arch Neurol; 2008 Apr; 65(4):489-94. PubMed ID: 18413471 [TBL] [Abstract][Full Text] [Related]
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7. [Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy]. Sun H; Zhang Y; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):121-7. PubMed ID: 19350499 [TBL] [Abstract][Full Text] [Related]
8. A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. Kimura K; Sugawara T; Mazaki-Miyazaki E; Hoshino K; Nomura Y; Tateno A; Hachimori K; Yamakawa K; Segawa M Brain Dev; 2005 Sep; 27(6):424-30. PubMed ID: 16122630 [TBL] [Abstract][Full Text] [Related]
9. 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; 19(7):443-5. PubMed ID: 20630778 [TBL] [Abstract][Full Text] [Related]
10. Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies. Fujiwara T Epilepsy Res; 2006 Aug; 70 Suppl 1():S223-30. PubMed ID: 16806826 [TBL] [Abstract][Full Text] [Related]
11. 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; 48(9):1678-1685. PubMed ID: 17561957 [TBL] [Abstract][Full Text] [Related]
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13. [Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy]. Zhang YH; Sun HH; Liu XY; Ma XW; Yang ZX; Xiong H; Qin J; Lin Q; Wu XR Zhonghua Er Ke Za Zhi; 2008 Oct; 46(10):769-73. PubMed ID: 19099883 [TBL] [Abstract][Full Text] [Related]
14. Alleged cases of vaccine encephalopathy rediagnosed years later as Dravet syndrome. Reyes IS; Hsieh DT; Laux LC; Wilfong AA Pediatrics; 2011 Sep; 128(3):e699-702. PubMed ID: 21844054 [TBL] [Abstract][Full Text] [Related]
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16. Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy. Nabbout R; Gennaro E; Dalla Bernardina B; Dulac O; Madia F; Bertini E; Capovilla G; Chiron C; Cristofori G; Elia M; Fontana E; Gaggero R; Granata T; Guerrini R; Loi M; La Selva L; Lispi ML; Matricardi A; Romeo A; Tzolas V; Valseriati D; Veggiotti P; Vigevano F; Vallée L; Dagna Bricarelli F; Bianchi A; Zara F Neurology; 2003 Jun; 60(12):1961-7. PubMed ID: 12821740 [TBL] [Abstract][Full Text] [Related]
17. Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy. Ceulemans BP; Claes LR; Lagae LG Pediatr Neurol; 2004 Apr; 30(4):236-43. PubMed ID: 15087100 [TBL] [Abstract][Full Text] [Related]
19. Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancy. Depienne C; Arzimanoglou A; Trouillard O; Fedirko E; Baulac S; Saint-Martin C; Ruberg M; Dravet C; Nabbout R; Baulac M; Gourfinkel-An I; LeGuern E Hum Mutat; 2006 Apr; 27(4):389. PubMed ID: 16541393 [TBL] [Abstract][Full Text] [Related]
20. 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; 31(2):179-82. PubMed ID: 18632234 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]