529 related articles for article (PubMed ID: 22386634)
1. 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; 100(1-2):194-8. PubMed ID: 22386634
[TBL] [Abstract][Full Text] [Related]
2. Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations.
Appenzeller S; Helbig I; Stephani U; Häusler M; Kluger G; Bungeroth M; Müller S; Kuhlenbäumer G; van Baalen A
Dev Med Child Neurol; 2012 Dec; 54(12):1144-8. PubMed ID: 23066759
[TBL] [Abstract][Full Text] [Related]
3. Genetic epilepsies with febrile seizures plus: clinical spectrum of Polish patients with SCN1A mutation - preliminary report.
Terczyńska I; Szczepanik E; Duszyc K; Górka P; Tataj R; Hoffman-Zacharska D
Dev Period Med; 2014; 18(4):426-31. PubMed ID: 25874779
[TBL] [Abstract][Full Text] [Related]
4. 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; 50(3):228-32. PubMed ID: 24405698
[TBL] [Abstract][Full Text] [Related]
5. Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.
Mulley JC; Hodgson B; McMahon JM; Iona X; Bellows S; Mullen SA; Farrell K; Mackay M; Sadleir L; Bleasel A; Gill D; Webster R; Wirrell EC; Harbord M; Sisodiya S; Andermann E; Kivity S; Berkovic SF; Scheffer IE; Dibbens LM
Epilepsia; 2013 Sep; 54(9):e122-6. PubMed ID: 23895530
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. 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; 58(2):e26-e30. PubMed ID: 28084635
[TBL] [Abstract][Full Text] [Related]
8. 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; 49(4):258-66. PubMed ID: 26188943
[TBL] [Abstract][Full Text] [Related]
9. Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus.
Goldberg-Stern H; Aharoni S; Afawi Z; Bennett O; Appenzeller S; Pendziwiat M; Kuhlenbäumer G; Basel-Vanagaite L; Shuper A; Korczyn AD; Helbig I
J Child Neurol; 2014 Feb; 29(2):221-6. PubMed ID: 24257433
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].
Xu XJ; Zhang YH; Sun HH; Liu XY; Wu HS; Wu XR
Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):580-6. PubMed ID: 23158734
[TBL] [Abstract][Full Text] [Related]
12. SCN1A testing for epilepsy: application in clinical practice.
Hirose S; Scheffer IE; Marini C; De Jonghe P; Andermann E; Goldman AM; Kauffman M; Tan NC; Lowenstein DH; Sisodiya SM; Ottman R; Berkovic SF;
Epilepsia; 2013 May; 54(5):946-52. PubMed ID: 23586701
[TBL] [Abstract][Full Text] [Related]
13. 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; 74():8-13. PubMed ID: 31765958
[TBL] [Abstract][Full Text] [Related]
14. Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome.
Kim DW; Lim BC; Kim KJ; Chae JH; Lee R; Lee SK
Epilepsy Res; 2013 Oct; 106(3):440-5. PubMed ID: 23916143
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.
Wang JW; Shi XY; Kurahashi H; Hwang SK; Ishii A; Higurashi N; Kaneko S; Hirose S;
Epilepsy Res; 2012 Dec; 102(3):195-200. PubMed ID: 23195492
[TBL] [Abstract][Full Text] [Related]
16. SCN1A-related phenotypes: Epilepsy and beyond.
Scheffer IE; Nabbout R
Epilepsia; 2019 Dec; 60 Suppl 3():S17-S24. PubMed ID: 31904117
[TBL] [Abstract][Full Text] [Related]
17. Outcomes and comorbidities of SCN1A-related seizure disorders.
de Lange IM; Gunning B; Sonsma ACM; van Gemert L; van Kempen M; Verbeek NE; Sinoo C; Nicolai J; Knoers NVAM; Koeleman BPC; Brilstra EH
Epilepsy Behav; 2019 Jan; 90():252-259. PubMed ID: 30527252
[TBL] [Abstract][Full Text] [Related]
18. Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline.
Kim YO; Bellows S; McMahon JM; Iona X; Damiano J; Dibbens L; Kelley K; Gill D; Cross JH; Berkovic SF; Scheffer IE
Dev Med Child Neurol; 2014 Jan; 56(1):85-90. PubMed ID: 24328833
[TBL] [Abstract][Full Text] [Related]
19. CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy.
Nabbout R; Depienne C; Chipaux M; Girard B; Souville I; Trouillard O; Dulac O; Chelly J; Afenjar A; Héron D; Leguern E; Beldjord C; Bienvenu T; Bahi-Buisson N
Epilepsy Res; 2009 Nov; 87(1):25-30. PubMed ID: 19734009
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]