BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

615 related articles for article (PubMed ID: 24902755)

  • 1. Co-occurring malformations of cortical development and SCN1A gene mutations.
    Barba C; Parrini E; Coras R; Galuppi A; Craiu D; Kluger G; Parmeggiani A; Pieper T; Schmitt-Mechelke T; Striano P; Giordano F; Blumcke I; Guerrini R
    Epilepsia; 2014 Jul; 55(7):1009-19. PubMed ID: 24902755
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy.
    Skjei KL; Church EW; Harding BN; Santi M; Holland-Bouley KD; Clancy RR; Porter BE; Heuer GG; Marsh ED
    J Neurosurg Pediatr; 2015 Dec; 16(6):668-74. PubMed ID: 26339958
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SCN1A testing for epilepsy: application in clinical practice.
    Hirose S; Scheffer IE; Marini C; De Jonghe P; Andermann E; Goldman AM; Kauffman M; Tan NC; Lowenstein DH; Sisodiya SM; Ottman R; Berkovic SF;
    Epilepsia; 2013 May; 54(5):946-52. PubMed ID: 23586701
    [TBL] [Abstract][Full Text] [Related]  

  • 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. 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]  

  • 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. 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]  

  • 8. Epileptogenic focal lesions in Dravet syndrome: A warning to investigators.
    Ventura R; Beltrán-Corbellini Á; Toledano R; Román IS; García-Morales I; Gil-Nagel A
    Epileptic Disord; 2024 Apr; 26(2):173-180. PubMed ID: 38116874
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The spectrum of SCN1A-related infantile epileptic encephalopathies.
    Harkin LA; McMahon JM; Iona X; Dibbens L; Pelekanos JT; Zuberi SM; Sadleir LG; Andermann E; Gill D; Farrell K; Connolly M; Stanley T; Harbord M; Andermann F; Wang J; Batish SD; Jones JG; Seltzer WK; Gardner A; ; Sutherland G; Berkovic SF; Mulley JC; Scheffer IE
    Brain; 2007 Mar; 130(Pt 3):843-52. PubMed ID: 17347258
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Malformations of cortical development (MCDs) and epilepsy: experience from a tertiary care center in south India.
    Mathew T; Srikanth SG; Satishchandra P
    Seizure; 2010 Apr; 19(3):147-52. PubMed ID: 20144553
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome.
    Kim DW; Lim BC; Kim KJ; Chae JH; Lee R; Lee SK
    Epilepsy Res; 2013 Oct; 106(3):440-5. PubMed ID: 23916143
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Epilepsy surgery in children with focal cortical dysplasia (FCD): results of long-term seizure outcome.
    Kloss S; Pieper T; Pannek H; Holthausen H; Tuxhorn I
    Neuropediatrics; 2002 Feb; 33(1):21-6. PubMed ID: 11930272
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Large-scale structural alteration of brain in epileptic children with
    Lee YJ; Yum MS; Kim MJ; Shim WH; Yoon HM; Yoo IH; Lee J; Lim BC; Kim KJ; Ko TS
    Neuroimage Clin; 2017; 15():594-600. PubMed ID: 28664031
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mesial temporal sclerosis in a cohort of children with SCN1A gene mutation.
    Van Poppel K; Patay Z; Roberts D; Clarke DF; McGregor A; Perkins FF; Wheless JW
    J Child Neurol; 2012 Jul; 27(7):893-7. PubMed ID: 22532537
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline.
    Kim YO; Bellows S; McMahon JM; Iona X; Damiano J; Dibbens L; Kelley K; Gill D; Cross JH; Berkovic SF; Scheffer IE
    Dev Med Child Neurol; 2014 Jan; 56(1):85-90. PubMed ID: 24328833
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Focal cortical dysplasias: surgical outcome in 67 patients in relation to histological subtypes and dual pathology.
    Fauser S; Schulze-Bonhage A; Honegger J; Carmona H; Huppertz HJ; Pantazis G; Rona S; Bast T; Strobl K; Steinhoff BJ; Korinthenberg R; Rating D; Volk B; Zentner J
    Brain; 2004 Nov; 127(Pt 11):2406-18. PubMed ID: 15319274
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.