These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
440 related articles for article (PubMed ID: 26614543)
41. Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations. Xu X; Zhang Y; Sun H; Liu X; Yang X; Xiong H; Jiang Y; Bao X; Wang S; Yang Z; Wu Y; Qin J; Lin Q; Wu X Brain Dev; 2014 Sep; 36(8):676-81. PubMed ID: 24168886 [TBL] [Abstract][Full Text] [Related]
42. Case studies in neuroscience: a novel amino acid duplication in the NH Angus M; Peters CH; Poburko D; Brimble E; Spelbrink EM; Ruben PC J Neurophysiol; 2019 Nov; 122(5):1975-1980. PubMed ID: 31533007 [TBL] [Abstract][Full Text] [Related]
43. Dravet syndrome with autism inherited from a paternal mosaic heterozygous mutation on SCN1A. Xiong Z; Yi L; Cao D; He W; Chen J; Gao S; Sun X J Neurol Sci; 2016 Oct; 369():53-56. PubMed ID: 27653866 [No Abstract] [Full Text] [Related]
44. Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons. Jiao J; Yang Y; Shi Y; Chen J; Gao R; Fan Y; Yao H; Liao W; Sun XF; Gao S Hum Mol Genet; 2013 Nov; 22(21):4241-52. PubMed ID: 23773995 [TBL] [Abstract][Full Text] [Related]
45. A mutation in GABRB3 associated with Dravet syndrome. Le SV; Le PHT; Le TKV; Kieu Huynh TT; Hang Do TT Am J Med Genet A; 2017 Aug; 173(8):2126-2131. PubMed ID: 28544625 [TBL] [Abstract][Full Text] [Related]
46. Milder phenotype with SCN1A truncation mutation other than SMEI. Yu MJ; Shi YW; Gao MM; Deng WY; Liu XR; Chen L; Long YS; Yi YH; Liao WP Seizure; 2010 Sep; 19(7):443-5. PubMed ID: 20630778 [TBL] [Abstract][Full Text] [Related]
47. Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy. Kearney JA; Wiste AK; Stephani U; Trudeau MM; Siegel A; RamachandranNair R; Elterman RD; Muhle H; Reinsdorf J; Shields WD; Meisler MH; Escayg A Pediatr Neurol; 2006 Feb; 34(2):116-20. PubMed ID: 16458823 [TBL] [Abstract][Full Text] [Related]
48. Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI). Arlier Z; Bayri Y; Kolb LE; Erturk O; Ozturk AK; Bayrakli F; Bilguvar K; Moliterno JA; Dervent A; Demirbilek V; Yalcinkaya C; Korkmaz B; Tuysuz B; Gunel M J Child Neurol; 2010 Oct; 25(10):1265-8. PubMed ID: 20110217 [TBL] [Abstract][Full Text] [Related]
49. Dravet syndrome: a genetic epileptic disorder. Akiyama M; Kobayashi K; Ohtsuka Y Acta Med Okayama; 2012; 66(5):369-76. PubMed ID: 23093055 [TBL] [Abstract][Full Text] [Related]
50. Rescuing epileptic and behavioral alterations in a Dravet syndrome mouse model by inhibiting eukaryotic elongation factor 2 kinase (eEF2K). Beretta S; Gritti L; Ponzoni L; Scalmani P; Mantegazza M; Sala M; Verpelli C; Sala C Mol Autism; 2022 Jan; 13(1):1. PubMed ID: 34980259 [TBL] [Abstract][Full Text] [Related]
51. Development and Validation of a Prediction Model for Early Diagnosis of Brunklaus A; Pérez-Palma E; Ghanty I; Xinge J; Brilstra E; Ceulemans B; Chemaly N; de Lange I; Depienne C; Guerrini R; Mei D; Møller RS; Nabbout R; Regan BM; Schneider AL; Scheffer IE; Schoonjans AS; Symonds JD; Weckhuysen S; Kattan MW; Zuberi SM; Lal D Neurology; 2022 Mar; 98(11):e1163-e1174. PubMed ID: 35074891 [TBL] [Abstract][Full Text] [Related]
52. 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]