196 related articles for article (PubMed ID: 26311622)
1. Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures.
Saitoh M; Ishii A; Ihara Y; Hoshino A; Terashima H; Kubota M; Kikuchi K; Yamanaka G; Amemiya K; Hirose S; Mizuguchi M
Epilepsy Res; 2015 Nov; 117():1-6. PubMed ID: 26311622
[TBL] [Abstract][Full Text] [Related]
2. SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes.
van Hugte EJH; Lewerissa EI; Wu KM; Scheefhals N; Parodi G; van Voorst TW; Puvogel S; Kogo N; Keller JM; Frega M; Schubert D; Schelhaas HJ; Verhoeven J; Majoie M; van Bokhoven H; Nadif Kasri N
Brain; 2023 Dec; 146(12):5153-5167. PubMed ID: 37467479
[TBL] [Abstract][Full Text] [Related]
3. Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.
Kwong AK; Fung CW; Chan SY; Wong VC
PLoS One; 2012; 7(7):e41802. PubMed ID: 22848613
[TBL] [Abstract][Full Text] [Related]
4. Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series.
Sahli M; Zrhidri A; Elaloui SC; Smaili W; Lyahyai J; Oudghiri FZ; Sefiani A
J Med Case Rep; 2019 Aug; 13(1):266. PubMed ID: 31439038
[TBL] [Abstract][Full Text] [Related]
5. A missense mutation of the gene encoding voltage-dependent sodium channel (Nav1.1) confers susceptibility to febrile seizures in rats.
Mashimo T; Ohmori I; Ouchida M; Ohno Y; Tsurumi T; Miki T; Wakamori M; Ishihara S; Yoshida T; Takizawa A; Kato M; Hirabayashi M; Sasa M; Mori Y; Serikawa T
J Neurosci; 2010 Apr; 30(16):5744-53. PubMed ID: 20410126
[TBL] [Abstract][Full Text] [Related]
6. Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.
Volkers L; Kahlig KM; Verbeek NE; Das JH; van Kempen MJ; Stroink H; Augustijn P; van Nieuwenhuizen O; Lindhout D; George AL; Koeleman BP; Rook MB
Eur J Neurosci; 2011 Oct; 34(8):1268-75. PubMed ID: 21864321
[TBL] [Abstract][Full Text] [Related]
7. Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome.
Lenge M; Balestrini S; Mei D; Macconi L; Caligiuri ME; Cuccarini V; Aquino D; Mazzi F; d'Incerti L; Darra F; Bernardina BD; Guerrini R
Cereb Cortex; 2023 Aug; 33(16):9532-9541. PubMed ID: 37344172
[TBL] [Abstract][Full Text] [Related]
8. [Clinical and imaging features of acute encephalopathy with biphasic seizures and late reduced diffusion in children].
Zhang MJ; Lin L; Wang WH; Li WH; Wei CJ; Xie H; Zhang QP; Wu Y; Xiong H; Zhou SZ; Yang B; Bao XH
Zhonghua Er Ke Za Zhi; 2023 Nov; 61(11):989-994. PubMed ID: 37899338
[No Abstract] [Full Text] [Related]
9. A serial analysis of serum aspartate aminotransferase levels in patients with acute encephalopathy with biphasic seizures and late reduced diffusion and prolonged febrile seizure.
Kasai A; Motobayashi M; Nishioka M; Fukuyama T; Inaba Y
Brain Dev; 2023 Oct; 45(9):487-494. PubMed ID: 37357027
[TBL] [Abstract][Full Text] [Related]
10. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Kasperaviciute D; Catarino CB; Matarin M; Leu C; Novy J; Tostevin A; Leal B; Hessel EV; Hallmann K; Hildebrand MS; Dahl HH; Ryten M; Trabzuni D; Ramasamy A; Alhusaini S; Doherty CP; Dorn T; Hansen J; Krämer G; Steinhoff BJ; Zumsteg D; Duncan S; Kälviäinen RK; Eriksson KJ; Kantanen AM; Pandolfo M; Gruber-Sedlmayr U; Schlachter K; Reinthaler EM; Stogmann E; Zimprich F; Théâtre E; Smith C; O'Brien TJ; Meng Tan K; Petrovski S; Robbiano A; Paravidino R; Zara F; Striano P; Sperling MR; Buono RJ; Hakonarson H; Chaves J; Costa PP; Silva BM; da Silva AM; de Graan PN; Koeleman BP; Becker A; Schoch S; von Lehe M; Reif PS; Rosenow F; Becker F; Weber Y; Lerche H; Rössler K; Buchfelder M; Hamer HM; Kobow K; Coras R; Blumcke I; Scheffer IE; Berkovic SF; Weale ME; ; Delanty N; Depondt C; Cavalleri GL; Kunz WS; Sisodiya SM
Brain; 2013 Oct; 136(Pt 10):3140-50. PubMed ID: 24014518
[TBL] [Abstract][Full Text] [Related]
11. Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic children: A protocol for systematic review and meta-analysis.
Wen Z; Chen J; Zhu B; Lu Y; Chen L
Medicine (Baltimore); 2021 May; 100(20):e25831. PubMed ID: 34011048
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of three Chinese pedigrees affected with Genetic epilepsy with febrile seizures plus due to variants of SCN1A gene].
Yang Z; Wang Y; Chen G; Song L; Ma Y; Zhang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Mar; 41(3):284-288. PubMed ID: 38448015
[TBL] [Abstract][Full Text] [Related]
13. [Correlation between clinical phenotypes and genotypes among 46 children with SCN1A-related developmental epileptic encephalopathy].
Peng B; Zhu H; Tian Y; Li X; Wang X; Gao Y; Zhang Y; Shen H; Chen W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Apr; 41(4):426-431. PubMed ID: 38565507
[TBL] [Abstract][Full Text] [Related]
14. SCN1A Gene Mutations in Indian Children With Epilepsy: Single Center Experience.
Maruthi G; Dhayalan P; Kumaran P; Soundraoandiyan J; Gambhir P
Indian Pediatr; 2023 Aug; 60(8):648-650. PubMed ID: 37209046
[TBL] [Abstract][Full Text] [Related]
15. Effect of SCN1Aand SCN2A gene polymorphisms on the efficacy of valproic acid treatment in Chinese children with epilepsy.
Bao Z; Li H; Hu J; Zhao R; Yan L; Zheng A
PLoS One; 2024; 19(6):e0304869. PubMed ID: 38837984
[TBL] [Abstract][Full Text] [Related]
16. Genetic exploration of Dravet syndrome: two case report.
Triono A; Herini ES; Gunadi
J Med Case Rep; 2024 Apr; 18(1):215. PubMed ID: 38649973
[TBL] [Abstract][Full Text] [Related]
17. Cerebral hemiatrophy and hemiparesis following hemiclonic status epilepticus in Dravet syndrome.
Caraballo R; Guzman A; Beltrán L; Espeche A
Epileptic Disord; 2024 Feb; 26(1):121-125. PubMed ID: 37815756
[TBL] [Abstract][Full Text] [Related]
18. Inherited SCN1A missense mutation in a Dravet Syndrome family: Neuropathological correlation, family screening and implications for adult carriers.
Sierra-Marcos A; Ribosa-Nogué R; Vidal-Robau N; Aldecoa I; Turón E; Rodríguez-Santiago B; Turón M; Boronat S; Molina-Porcel L
Epilepsy Res; 2024 Jan; 199():107266. PubMed ID: 38061235
[TBL] [Abstract][Full Text] [Related]
19. Core Features Differentiate Dravet Syndrome from Febrile Seizures.
Nordli DR; Nordli DR; Galan FN
J Pediatr; 2023 Jul; 258():113416. PubMed ID: 37030608
[TBL] [Abstract][Full Text] [Related]
20. Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis: A case report with a novel missense variant of SCN1A.
Okubo Y; Shibuya M; Nakamura H; Kawashima A; Kodama K; Endo W; Inui T; Togashi N; Aihara Y; Shirota M; Funayama R; Niihori T; Fujita A; Nakayama K; Aoki Y; Matsumoto N; Kure S; Kikuchi A; Haginoya K
Brain Dev; 2023 Oct; 45(9):505-511. PubMed ID: 37442734
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
