176 related articles for article (PubMed ID: 17086543)
1. Febrile seizures are associated with mutation of seizure-related (SEZ) 6, a brain-specific gene.
Yu ZL; Jiang JM; Wu DH; Xie HJ; Jiang JJ; Zhou L; Peng L; Bao GS
J Neurosci Res; 2007 Jan; 85(1):166-72. PubMed ID: 17086543
[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. Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.
Hedera P; Ma S; Blair MA; Taylor KA; Hamati A; Bradford Y; Abou-Khalil B; Haines JL
Epilepsia; 2006 Oct; 47(10):1622-8. PubMed ID: 17054683
[TBL] [Abstract][Full Text] [Related]
4. Genetic susceptibility to simple febrile seizures: interleukin-1beta promoter polymorphisms are associated with sporadic cases.
Kira R; Torisu H; Takemoto M; Nomura A; Sakai Y; Sanefuji M; Sakamoto K; Matsumoto S; Gondo K; Hara T
Neurosci Lett; 2005 Aug; 384(3):239-44. PubMed ID: 15916853
[TBL] [Abstract][Full Text] [Related]
5. Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.
Ma S; Abou-Khalil B; Blair MA; Sutcliffe JS; Haines JL; Hedera P
Neurosci Lett; 2006 Feb; 394(1):74-8. PubMed ID: 16256272
[TBL] [Abstract][Full Text] [Related]
6. New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p.
Nabbout R; Baulac S; Desguerre I; Bahi-Buisson N; Chiron C; Ruberg M; Dulac O; LeGuern E
Neurology; 2007 Apr; 68(17):1374-81. PubMed ID: 17452582
[TBL] [Abstract][Full Text] [Related]
7. [Clinical analysis of families with generalized epilepsy with febrile seizures plus].
Xi MJ; Huang XS; Wei JK; Zheng H; Jia YJ; Chamg XH; Zhang ZY; Fan YX; Gao L
Zhongguo Dang Dai Er Ke Za Zhi; 2007 Oct; 9(5):436-40. PubMed ID: 17937853
[TBL] [Abstract][Full Text] [Related]
8. A novel GABRG2 mutation associated with febrile seizures.
Audenaert D; Schwartz E; Claeys KG; Claes L; Deprez L; Suls A; Van Dyck T; Lagae L; Van Broeckhoven C; Macdonald RL; De Jonghe P
Neurology; 2006 Aug; 67(4):687-90. PubMed ID: 16924025
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.
Yoshioka M; Higuchi Y; Fujii T; Aiba H; Toda T
Brain Dev; 2008 Jan; 30(1):59-67. PubMed ID: 17597323
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients.
Nakayama J; Hamano K; Iwasaki N; Ohta M; Nakahara S; Matsui A; Arinami T
Neuropediatrics; 2003 Jun; 34(5):234-6. PubMed ID: 14598228
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A screening test for the prediction of Dravet syndrome before one year of age.
Hattori J; Ouchida M; Ono J; Miyake S; Maniwa S; Mimaki N; Ohtsuka Y; Ohmori I
Epilepsia; 2008 Apr; 49(4):626-33. PubMed ID: 18076640
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [A long-term follow-up of 234 children with febrile seizures].
Durá-Travé T; Yoldi-Petri ME
Rev Neurol; 2004 Dec 16-31; 39(12):1104-8. PubMed ID: 15625625
[TBL] [Abstract][Full Text] [Related]
18. Adult-onset epilepsy and history of childhood febrile seizures: a retrospective study.
Mohebbi MR; Navipour R; Seyedkazemi M; Zamanian H; Khamseh F
Neurol India; 2004 Dec; 52(4):463-5. PubMed ID: 15626834
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Interleukin-10 is associated with resistance to febrile seizures: genetic association and experimental animal studies.
Ishizaki Y; Kira R; Fukuda M; Torisu H; Sakai Y; Sanefuji M; Yukaya N; Hara T
Epilepsia; 2009 Apr; 50(4):761-7. PubMed ID: 19055487
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
