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.
4. From focal epilepsy to Dravet syndrome--Heterogeneity of the phenotype due to SCN1A mutations of the p.Arg1596 amino acid residue in the Nav1.1 subunit. Hoffman-Zacharska D; Szczepanik E; Terczynska I; Goszczanska-Ciuchta A; Zalewska-Miszkurka Z; Tataj R; Bal J Neurol Neurochir Pol; 2015; 49(4):258-66. PubMed ID: 26188943 [TBL] [Abstract][Full Text] [Related]
5. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome? Lim BC; Hwang H; Kim H; Chae JH; Choi J; Kim KJ; Hwang YS; Yum MS; Ko TS Epilepsy Res; 2015 Jan; 109():34-9. PubMed ID: 25524840 [TBL] [Abstract][Full Text] [Related]
6. Transmantle sign in focal cortical dysplasia: a unique radiological entity with excellent prognosis for seizure control. Wang DD; Deans AE; Barkovich AJ; Tihan T; Barbaro NM; Garcia PA; Chang EF J Neurosurg; 2013 Feb; 118(2):337-44. PubMed ID: 23216463 [TBL] [Abstract][Full Text] [Related]
7. Long-term outcome after epilepsy surgery for focal cortical dysplasia. Cohen-Gadol AA; Ozduman K; Bronen RA; Kim JH; Spencer DD J Neurosurg; 2004 Jul; 101(1):55-65. PubMed ID: 15255252 [TBL] [Abstract][Full Text] [Related]
8. Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE). Bonduelle T; Hartlieb T; Baldassari S; Sim NS; Kim SH; Kang HC; Kobow K; Coras R; Chipaux M; Dorfmüller G; Adle-Biassette H; Aronica E; Lee JH; Blumcke I; Baulac S Acta Neuropathol Commun; 2021 Jan; 9(1):3. PubMed ID: 33407896 [TBL] [Abstract][Full Text] [Related]
9. Repeat surgery for focal cortical dysplasias in children: indications and outcomes. Sacino MF; Ho CY; Whitehead MT; Kao A; Depositario-Cabacar D; Myseros JS; Magge SN; Keating RF; Gaillard WD; Oluigbo CO J Neurosurg Pediatr; 2017 Feb; 19(2):174-181. PubMed ID: 27834621 [TBL] [Abstract][Full Text] [Related]
10. Cortical dysplastic lesions in children with intractable epilepsy: role of complete resection. Hader WJ; Mackay M; Otsubo H; Chitoku S; Weiss S; Becker L; Snead OC; Rutka JT J Neurosurg; 2004 Feb; 100(2 Suppl Pediatrics):110-7. PubMed ID: 14758938 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Long-term outcome characteristics in mesial temporal lobe epilepsy with and without associated cortical dysplasia. Schmeiser B; Hammen T; Steinhoff BJ; Zentner J; Schulze-Bonhage A Epilepsy Res; 2016 Oct; 126():147-56. PubMed ID: 27500381 [TBL] [Abstract][Full Text] [Related]
13. Medically resistant pediatric insular-opercular/perisylvian epilepsy. Part 2: outcome following resective surgery. Weil AG; Le NM; Jayakar P; Resnick T; Miller I; Fallah A; Duchowny M; Bhatia S J Neurosurg Pediatr; 2016 Nov; 18(5):523-535. PubMed ID: 27472665 [TBL] [Abstract][Full Text] [Related]
14. Early resective surgery causes favorable seizure outcome in malformations of cortical development. Radhakrishnan A; Menon R; Menon D; Singh A; Radhakrishnan N; Vilanilam G; Abraham M; Thomas B; Kesavadas C; Varma RP; Thomas SV Epilepsy Res; 2016 Aug; 124():1-11. PubMed ID: 27156173 [TBL] [Abstract][Full Text] [Related]
15. [Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy]. Zhang YH; Sun HH; Liu XY; Ma XW; Yang ZX; Xiong H; Qin J; Lin Q; Wu XR Zhonghua Er Ke Za Zhi; 2008 Oct; 46(10):769-73. PubMed ID: 19099883 [TBL] [Abstract][Full Text] [Related]
16. Seizure outcome in surgically treated drug-resistant mesial temporal lobe epilepsy based on the recent histopathological classifications. Giulioni M; Marucci G; Martinoni M; Volpi L; Riguzzi P; Marliani AF; Bisulli F; Tinuper P; Tassinari CA; Michelucci R; Rubboli G J Neurosurg; 2013 Jul; 119(1):37-47. PubMed ID: 23641822 [TBL] [Abstract][Full Text] [Related]
17. Seizures with tonic posturing: Semiologic difference between supplementary sensorimotor area (SSMA) origin and extra-SSMA origin. Sitthinamsuwan B; Usui N; Tottori T; Terada K; Kondo A; Matsuda K; Baba K; Inoue Y Epilepsia; 2016 Feb; 57(2):e39-44. PubMed ID: 26660199 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Focal epilepsy in SCN1A-mutation carrying patients: is there a role for epilepsy surgery? Vezyroglou A; Varadkar S; Bast T; Hirsch E; Strobl K; Harvey AS; ; Scheffer IE; Sisodiya SM; Cross JH Dev Med Child Neurol; 2020 Nov; 62(11):1331-1335. PubMed ID: 32538476 [TBL] [Abstract][Full Text] [Related]
20. Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasia. Choi SA; Kim SY; Kim H; Kim WJ; Kim H; Hwang H; Choi JE; Lim BC; Chae JH; Chong S; Lee JY; Phi JH; Kim SK; Wang KC; Kim KJ Epilepsy Res; 2018 Jan; 139():54-59. PubMed ID: 29197666 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]