175 related articles for article (PubMed ID: 29429462)
1. [Association between SCN1A rs3812718 polymorphism and generalized epilepsy with febrile seizures plus].
Ma QL; Wang B; Chen GF; Huang JL; Li Y; Cao DZ; Liu RT
Zhongguo Dang Dai Er Ke Za Zhi; 2018 Feb; 20(2):130-133. PubMed ID: 29429462
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. De-novo mutations and genetic variation in the SCN1A gene in Malaysian patients with generalized epilepsy with febrile seizures plus (GEFS+).
Tan EH; Razak SA; Abdullah JM; Mohamed Yusoff AA
Epilepsy Res; 2012 Dec; 102(3):210-5. PubMed ID: 22944210
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis.
Balan S; Vellichirammal NN; Banerjee M; Radhakrishnan K
Epilepsy Res; 2012 Sep; 101(3):288-92. PubMed ID: 22578703
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
Marini C; Mei D; Temudo T; Ferrari AR; Buti D; Dravet C; Dias AI; Moreira A; Calado E; Seri S; Neville B; Narbona J; Reid E; Michelucci R; Sicca F; Cross HJ; Guerrini R
Epilepsia; 2007 Sep; 48(9):1678-1685. PubMed ID: 17561957
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. A novel inherited SCN1A mutation associated with GEFS+ in benign and encephalopathic epilepsy.
Gauthier AC; Manganas LN; Mattson RH
J Clin Neurosci; 2017 Jun; 40():82-84. PubMed ID: 28262406
[TBL] [Abstract][Full Text] [Related]
10. A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
Escayg A; Heils A; MacDonald BT; Haug K; Sander T; Meisler MH
Am J Hum Genet; 2001 Apr; 68(4):866-73. PubMed ID: 11254445
[TBL] [Abstract][Full Text] [Related]
11. SCN1A rs3812718 polymorphism and susceptibility to epilepsy with febrile seizures: a meta-analysis.
Tang L; Lu X; Tao Y; Zheng J; Zhao P; Li K; Li L
Gene; 2014 Jan; 533(1):26-31. PubMed ID: 24076350
[TBL] [Abstract][Full Text] [Related]
12. De novo truncating mutation in SCN1A as a cause of febrile seizures plus (FS+).
Jaimes A; Guerrero-López R; González-Giráldez B; Serratosa JM
Epileptic Disord; 2020 Jun; 22(3):323-326. PubMed ID: 32540801
[TBL] [Abstract][Full Text] [Related]
13. Identification of two mutations in cis in the SCN1A gene in a family showing genetic epilepsy with febrile seizures plus (GEFS+) and idiopathic generalized epilepsy (IGE).
Binini N; Sancini G; Villa C; Dal Magro R; Sansoni V; Rusconi R; Mantegazza M; Grioni D; Talpo F; Toselli M; Combi R
Brain Res; 2017 Dec; 1677():26-32. PubMed ID: 28951233
[TBL] [Abstract][Full Text] [Related]
14. A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.
Cui X; Zeng F; Liu Y; Zhang J; Archacki S; Zhan T; Du R; Tang Z; Liu J; Wang QK; Liu M
Neurosci Lett; 2011 Sep; 503(1):27-30. PubMed ID: 21843600
[TBL] [Abstract][Full Text] [Related]
15. Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.
Zhang C; Wong V; Ng PW; Lui CH; Sin NC; Wong KS; Baum L; Kwan P
Epilepsia; 2010 Sep; 51(9):1878-81. PubMed ID: 20477842
[TBL] [Abstract][Full Text] [Related]
16. Novel mutation of SCN1A in familial generalized epilepsy with febrile seizures plus.
Li N; Zhang J; Guo JF; Yan XX; Xia K; Tang BS
Neurosci Lett; 2010 Aug; 480(3):211-4. PubMed ID: 20600615
[TBL] [Abstract][Full Text] [Related]
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; 50(3):228-32. PubMed ID: 24405698
[TBL] [Abstract][Full Text] [Related]
18. Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A.
Mahoney K; Moore SJ; Buckley D; Alam M; Parfrey P; Penney S; Merner N; Hodgkinson K; Young TL
Seizure; 2009 Sep; 18(7):492-7. PubMed ID: 19464195
[TBL] [Abstract][Full Text] [Related]
19. Single-Base Gene Variants in
Buainain RP; Sodré AR; Dos Santos JS; Takazaki KAG; Queiroz LS; de Oliveira CTP; de Aguiar PHP; Marson FAL; Ortega MM
Int J Mol Sci; 2024 May; 25(11):. PubMed ID: 38892194
[TBL] [Abstract][Full Text] [Related]
20. SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus.
Bisulli F; Licchetta L; Baldassari S; Muccioli L; Marconi C; Cantalupo G; Myers C; Menghi V; Minardi R; Caporali L; Marini C; Guerrini R; Mefford HC; Tinuper P; Pippucci T
Epileptic Disord; 2019 Apr; 21(2):185-191. PubMed ID: 30977726
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
