353 related articles for article (PubMed ID: 23311867)
21. Scn1a and Cacna1a mutations mutually alter their original phenotypes in rats.
Ohmori I; Kobayashi K; Ouchida M
Neurochem Int; 2020 Dec; 141():104859. PubMed ID: 33045260
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
Lossin C; Rhodes TH; Desai RR; Vanoye CG; Wang D; Carniciu S; Devinsky O; George AL
J Neurosci; 2003 Dec; 23(36):11289-95. PubMed ID: 14672992
[TBL] [Abstract][Full Text] [Related]
25. Outcomes and comorbidities of SCN1A-related seizure disorders.
de Lange IM; Gunning B; Sonsma ACM; van Gemert L; van Kempen M; Verbeek NE; Sinoo C; Nicolai J; Knoers NVAM; Koeleman BPC; Brilstra EH
Epilepsy Behav; 2019 Jan; 90():252-259. PubMed ID: 30527252
[TBL] [Abstract][Full Text] [Related]
26. SCN1A-related phenotypes: Epilepsy and beyond.
Scheffer IE; Nabbout R
Epilepsia; 2019 Dec; 60 Suppl 3():S17-S24. PubMed ID: 31904117
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. A two-hit story: Seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsies.
Salgueiro-Pereira AR; Duprat F; Pousinha PA; Loucif A; Douchamps V; Regondi C; Ayrault M; Eugie M; Stunault MI; Escayg A; Goutagny R; Gnatkovsky V; Frassoni C; Marie H; Bethus I; Mantegazza M
Neurobiol Dis; 2019 May; 125():31-44. PubMed ID: 30659983
[TBL] [Abstract][Full Text] [Related]
30. Exaggerated Nighttime Sleep and Defective Sleep Homeostasis in a Drosophila Knock-In Model of Human Epilepsy.
Petruccelli E; Lansdon P; Kitamoto T
PLoS One; 2015; 10(9):e0137758. PubMed ID: 26361221
[TBL] [Abstract][Full Text] [Related]
31. SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.
Silvennoinen K; Gawel K; Tsortouktzidis D; Pitsch J; Alhusaini S; van Loo KMJ; Picardo R; Michalak Z; Pagni S; Martins Custodio H; Mills J; Whelan CD; de Zubicaray GI; McMahon KL; van der Ent W; Kirstein-Smardzewska KJ; Tiraboschi E; Mudge JM; Frankish A; Thom M; Wright MJ; Thompson PM; Schoch S; Becker AJ; Esguerra CV; Sisodiya SM
Acta Neuropathol; 2022 Jul; 144(1):107-127. PubMed ID: 35551471
[TBL] [Abstract][Full Text] [Related]
32. Orexin Receptor Antagonism Improves Sleep and Reduces Seizures in Kcna1-null Mice.
Roundtree HM; Simeone TA; Johnson C; Matthews SA; Samson KK; Simeone KA
Sleep; 2016 Feb; 39(2):357-68. PubMed ID: 26446112
[TBL] [Abstract][Full Text] [Related]
33. Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.
Rhodes TH; Vanoye CG; Ohmori I; Ogiwara I; Yamakawa K; George AL
J Physiol; 2005 Dec; 569(Pt 2):433-45. PubMed ID: 16210358
[TBL] [Abstract][Full Text] [Related]
34. A knock-in model of human epilepsy in Drosophila reveals a novel cellular mechanism associated with heat-induced seizure.
Sun L; Gilligan J; Staber C; Schutte RJ; Nguyen V; O'Dowd DK; Reenan R
J Neurosci; 2012 Oct; 32(41):14145-55. PubMed ID: 23055484
[TBL] [Abstract][Full Text] [Related]
35. Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
Hawkins NA; Zachwieja NJ; Miller AR; Anderson LL; Kearney JA
PLoS Genet; 2016 Oct; 12(10):e1006398. PubMed ID: 27768696
[TBL] [Abstract][Full Text] [Related]
36. Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.
Arican P; Dundar NO; Cavusoglu D; Ozdemır TR; Gencpinar P
Childs Nerv Syst; 2017 Apr; 33(4):677-680. PubMed ID: 27889818
[TBL] [Abstract][Full Text] [Related]
37. SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations.
Usluer S; Salar S; Arslan M; Yiş U; Kara B; Tektürk P; Baykan B; Meral C; Türkdoğan D; Bebek N; Yalçın Çapan Ö; Gündoğdu Eken A; Çağlayan SH
Seizure; 2016 Jul; 39():34-43. PubMed ID: 27236449
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Escayg A; Goldin AL
Epilepsia; 2010 Sep; 51(9):1650-8. PubMed ID: 20831750
[TBL] [Abstract][Full Text] [Related]
40. Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families.
Brunklaus A; Ellis R; Stewart H; Aylett S; Reavey E; Jefferson R; Jain R; Chakraborty S; Jayawant S; Zuberi SM
Eur J Paediatr Neurol; 2015 Jul; 19(4):484-8. PubMed ID: 25795284
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
