1234 related articles for article (PubMed ID: 19203856)
1. Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
Scheffer IE; Zhang YH; Jansen FE; Dibbens L
Brain Dev; 2009 May; 31(5):394-400. PubMed ID: 19203856
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?
Sijben AE; Sithinamsuwan P; Radhakrishnan A; Badawy RA; Dibbens L; Mazarib A; Lev D; Lerman-Sagie T; Straussberg R; Berkovic SF; Scheffer IE
Epilepsia; 2009 Apr; 50(4):953-6. PubMed ID: 19292758
[TBL] [Abstract][Full Text] [Related]
4. Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+.
Selmer KK; Egeland T; Solaas MH; Nakken KO; Kjeldsen MJ; Friis ML; Brandal K; Corey LA; Undlien DE
Acta Neurol Scand; 2008 Apr; 117(4):289-92. PubMed ID: 17927801
[TBL] [Abstract][Full Text] [Related]
5. Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients.
Herini ES; Gunadi ; Harahap IS; Yusoff S; Morikawa S; Patria SY; Nishimura N; Sunartini ; Sutaryo ; Takada S; Matsuo M; Nishio H
Epilepsy Res; 2010 Jun; 90(1-2):132-9. PubMed ID: 20452746
[TBL] [Abstract][Full Text] [Related]
6. Clinical spectrum of SCN1A mutations.
Gambardella A; Marini C
Epilepsia; 2009 May; 50 Suppl 5():20-3. PubMed ID: 19469841
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Progress in searching for the febrile seizure susceptibility genes.
Nakayama J
Brain Dev; 2009 May; 31(5):359-65. PubMed ID: 19201561
[TBL] [Abstract][Full Text] [Related]
9. Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene.
Guerrini R; Cellini E; Mei D; Metitieri T; Petrelli C; Pucatti D; Marini C; Zamponi N
Epilepsia; 2010 Dec; 51(12):2474-7. PubMed ID: 21204810
[TBL] [Abstract][Full Text] [Related]
10. 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; 51(9):1669-78. PubMed ID: 20550552
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. One novel Dravet syndrome causing mutation and one recurrent MAE causing mutation in SCN1A gene.
Yordanova I; Todorov T; Dimova P; Hristova D; Tincheva R; Litvinenko I; Yotovska O; Kremensky I; Todorova A
Neurosci Lett; 2011 Apr; 494(2):180-3. PubMed ID: 21396429
[TBL] [Abstract][Full Text] [Related]
13. Severe epilepsy syndromes of early childhood: the link between genetics and pathophysiology with a focus on SCN1A mutations.
Stafstrom CE
J Child Neurol; 2009 Aug; 24(8 Suppl):15S-23S. PubMed ID: 19666879
[TBL] [Abstract][Full Text] [Related]
14. A case report of a family with overlapping features of autosomal dominant febrile seizures and GEFS+.
Hindocha N; Nabbout R; Elmslie F; Makoff A; Al-Chalabi A; Nashef L
Epilepsia; 2009 Apr; 50(4):937-42. PubMed ID: 19054398
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Epilepsy with a de novo missense mutation in the sodium channel a1 subunit: a case report.
Stefanaki E; Aggelakou V; Orfanou M; Kokori E; Boutoufianakis S
Acta Paediatr; 2006 Dec; 95(12):1703-6. PubMed ID: 17129991
[TBL] [Abstract][Full Text] [Related]
17. Generalized epilepsy with febrile seizures plus: novel SCN1A mutation.
Dimova PS; Yordanova I; Bojinova V; Jordanova A; Kremenski I
Pediatr Neurol; 2010 Feb; 42(2):137-40. PubMed ID: 20117752
[TBL] [Abstract][Full Text] [Related]
18. [Severe myoclonic epilepsy in infancy (Dravet's syndrome). Some genetic aspects].
Herranz JL
Rev Neurol; 2003 Jul 1-15; 37(1):60-3. PubMed ID: 12861511
[TBL] [Abstract][Full Text] [Related]
19. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R
Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
[TBL] [Abstract][Full Text] [Related]
20. A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.
Livingston JH; Cross JH; Mclellan A; Birch R; Zuberi SM
J Child Neurol; 2009 Apr; 24(4):503-8. PubMed ID: 19339291
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
