274 related articles for article (PubMed ID: 15715999)
1. A family of generalized epilepsy with febrile seizures plus type 2-a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures.
Nagao Y; Mazaki-Miyazaki E; Okamura N; Takagi M; Igarashi T; Yamakawa K
Epilepsy Res; 2005 Feb; 63(2-3):151-6. PubMed ID: 15715999
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
Wallace RH; Wang DW; Singh R; Scheffer IE; George AL; Phillips HA; Saar K; Reis A; Johnson EW; Sutherland GR; Berkovic SF; Mulley JC
Nat Genet; 1998 Aug; 19(4):366-70. PubMed ID: 9697698
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Gene symbol: SCN1A. Disease: Generalized epilepsy with febrile seizures plus.
Sun H; Zhang Y; Liang J; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
Hum Genet; 2008 Oct; 124(3):298. PubMed ID: 18846618
[No Abstract] [Full Text] [Related]
10. A case of extended spectrum GEFS+.
Grant AC; Vazquez B
Epilepsia; 2005; 46 Suppl 10():39-40. PubMed ID: 16359470
[TBL] [Abstract][Full Text] [Related]
11. [Linkage location and mutation analysis of generalized epilepsy with febrile seizures plus].
Lin H; Wang YP; Wang MY; Wu LW
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(45):3177-81. PubMed ID: 19171087
[TBL] [Abstract][Full Text] [Related]
12. Myoclonic seizures in the context of generalized epilepsy with febrile seizures plus (GEFS+).
Baulac M; Gourfinkel-An I; Baulac S; Leguern E
Adv Neurol; 2005; 95():119-25. PubMed ID: 15508917
[No Abstract] [Full Text] [Related]
13. 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]
14. [Clinical analysis and screening for SCN1A gene mutation in two pedigrees of generalized epilepsies with febrile seizures plus].
Wang XH; Zhou SZ; Guo Q; Sun DK
Zhonghua Er Ke Za Zhi; 2009 Aug; 47(8):570-4. PubMed ID: 19951487
[TBL] [Abstract][Full Text] [Related]
15. Novel de novo mutation of a conserved SCN1A amino-acid residue (R1596).
Dlugos DJ; Ferraro TN; Buono RJ
Pediatr Neurol; 2007 Oct; 37(4):303-5. PubMed ID: 17903680
[TBL] [Abstract][Full Text] [Related]
16. Focal epilepsy resulting from a de novo SCN1A mutation.
Okumura A; Kurahashi H; Hirose S; Okawa N; Watanabe K
Neuropediatrics; 2007 Oct; 38(5):253-6. PubMed ID: 18330841
[TBL] [Abstract][Full Text] [Related]
17. Phenotypes and genotypes in epilepsy with febrile seizures plus.
Ito M; Yamakawa K; Sugawara T; Hirose S; Fukuma G; Kaneko S
Epilepsy Res; 2006 Aug; 70 Suppl 1():S199-205. PubMed ID: 16884893
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
Escayg A; MacDonald BT; Meisler MH; Baulac S; Huberfeld G; An-Gourfinkel I; Brice A; LeGuern E; Moulard B; Chaigne D; Buresi C; Malafosse A
Nat Genet; 2000 Apr; 24(4):343-5. PubMed ID: 10742094
[No Abstract] [Full Text] [Related]
[Next] [New Search]