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Journal Abstract Search

281 related items for PubMed ID: 25697436

  • 1. [Complex febrile Seizures or Dravet syndrome?: Description of 3 case reports].
    Hernández M, Pedraza M, Mesa T, Troncoso M.
    Rev Chil Pediatr; 2014 Oct; 85(5):588-93. PubMed ID: 25697436
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  • 3. Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.
    Xu X, Zhang Y, Sun H, Liu X, Yang X, Xiong H, Jiang Y, Bao X, Wang S, Yang Z, Wu Y, Qin J, Lin Q, Wu X.
    Brain Dev; 2014 Sep; 36(8):676-81. PubMed ID: 24168886
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  • 4. Child Neurology: Dravet syndrome: when to suspect the diagnosis.
    Millichap JJ, Koh S, Laux LC, Nordli DR.
    Neurology; 2009 Sep 29; 73(13):e59-62. PubMed ID: 19786689
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  • 7. Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.
    Carranza Rojo D, Harvey AS, Iona X, Dibbens LM, Damiano JA, Arsov T, Gill D, Freeman JL, Leventer RJ, Vincent A, Berkovic SF, McMahon JM, Scheffer IE.
    Epilepsy Res; 2012 Jun 29; 100(1-2):194-8. PubMed ID: 22386634
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  • 9. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS.
    Epilepsy Res; 2015 Jan 29; 109():34-9. PubMed ID: 25524840
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  • 10. From focal epilepsy to Dravet syndrome--Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit.
    Hoffman-Zacharska D, Szczepanik E, Terczynska I, Goszczanska-Ciuchta A, Zalewska-Miszkurka Z, Tataj R, Bal J.
    Neurol Neurochir Pol; 2015 Jan 29; 49(4):258-66. PubMed ID: 26188943
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  • 11. [Dravet syndrome is a rare genetic epileptic disorder that can be mistaken for fever cramps].
    Johannesen KM, Hansen MB.
    Ugeskr Laeger; 2014 Mar 31; 176(14):. PubMed ID: 25350058
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  • 14. De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome.
    Myers KA, Burgess R, Afawi Z, Damiano JA, Berkovic SF, Hildebrand MS, Scheffer IE.
    Epilepsia; 2017 Feb 31; 58(2):e26-e30. PubMed ID: 28084635
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  • 15. Dravet syndrome with SCN1B gene mutation: A rare entity.
    Mukherjee D, Mukherjee S, Niyogi P, Mahapatra M.
    Neurol India; 2017 Feb 31; 65(4):801-803. PubMed ID: 28681755
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  • 16. 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 31; 30(4):236-43. PubMed ID: 15087100
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  • 17. Vaccination and occurrence of seizures in SCN1A mutation-positive patients: a multicenter Italian study.
    Zamponi N, Passamonti C, Petrelli C, Veggiotti P, Baldassari C, Verrotti A, Capovilla G, Viri M, Coppola G, Vignoli A.
    Pediatr Neurol; 2014 Mar 31; 50(3):228-32. PubMed ID: 24405698
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  • 19. Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy.
    Till Á, Zima J, Fekete A, Bene J, Czakó M, Szabó A, Melegh B, Hadzsiev K.
    Seizure; 2020 Jan 31; 74():8-13. PubMed ID: 31765958
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  • 20. Dravet syndrome, what is new?
    Al-Baradie RS.
    Neurosciences (Riyadh); 2013 Jan 31; 18(1):11-7. PubMed ID: 23291792
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