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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

858 related articles for article (PubMed ID: 26188943)

  • 1. 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]  

  • 2. [Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].
    Xu XJ; Zhang YH; Sun HH; Liu XY; Wu HS; Wu XR
    Zhonghua Er Ke Za Zhi; 2012 Aug; 50(8):580-6. PubMed ID: 23158734
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SCN1A clinical spectrum includes the self-limited focal epilepsies of childhood.
    Kivity S; Oliver KL; Afawi Z; Damiano JA; Arsov T; Bahlo M; Berkovic SF
    Epilepsy Res; 2017 Mar; 131():9-14. PubMed ID: 28192756
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plus.
    Goldberg-Stern H; Aharoni S; Afawi Z; Bennett O; Appenzeller S; Pendziwiat M; Kuhlenbäumer G; Basel-Vanagaite L; Shuper A; Korczyn AD; Helbig I
    J Child Neurol; 2014 Feb; 29(2):221-6. PubMed ID: 24257433
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
    Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R
    Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures.
    Shi YW; Yu MJ; Long YS; Qin B; He N; Meng H; Liu XR; Deng WY; Gao MM; Yi YH; Li BM; Liao WP
    Genes Brain Behav; 2012 Mar; 11(2):170-6. PubMed ID: 22151702
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo SCN1A pathogenic variants in the GEFS+ spectrum: Not always a familial syndrome.
    Myers KA; Burgess R; Afawi Z; Damiano JA; Berkovic SF; Hildebrand MS; Scheffer IE
    Epilepsia; 2017 Feb; 58(2):e26-e30. PubMed ID: 28084635
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Gain of function SCN1A disease-causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication.
    Matricardi S; Cestèle S; Trivisano M; Kassabian B; Leroudier N; Vittorini R; Nosadini M; Cesaroni E; Siliquini S; Marinaccio C; Longaretti F; Podestà B; Operto FF; Luisi C; Sartori S; Boniver C; Specchio N; Vigevano F; Marini C; Mantegazza M
    Epilepsia; 2023 May; 64(5):1331-1347. PubMed ID: 36636894
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].
    Xu XJ; Zhang YH; Sun HH; Liu XY; Jiang YW; Wu XR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):625-30. PubMed ID: 23225037
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
    Scheffer IE; Zhang YH; Jansen FE; Dibbens L
    Brain Dev; 2009 May; 31(5):394-400. PubMed ID: 19203856
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: is there a common core deficit?
    Passamonti C; Petrelli C; Mei D; Foschi N; Guerrini R; Provinciali L; Zamponi N
    Epilepsy Behav; 2015 Feb; 43():89-92. PubMed ID: 25569746
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection.
    Surovy M; Soltysova A; Kolnikova M; Sykora P; Ilencikova D; Ficek A; Radvanszky J; Kadasi L
    Gen Physiol Biophys; 2016 Jul; 35(3):333-42. PubMed ID: 27045673
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).
    Ma H; Guo Y; Chen Z; Wang L; Tang Z; Zhang J; Miao Q; Zhai Q
    Seizure; 2021 May; 88():146-152. PubMed ID: 33895391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. One novel Dravet syndrome causing mutation and one recurrent MAE causing mutation in SCN1A gene.
    Yordanova I; Todorov T; Dimova P; Hristova D; Tincheva R; Litvinenko I; Yotovska O; Kremensky I; Todorova A
    Neurosci Lett; 2011 Apr; 494(2):180-3. PubMed ID: 21396429
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation spectrum of the SCN1A gene in a Hungarian population with epilepsy.
    Till Á; Zima J; Fekete A; Bene J; Czakó M; Szabó A; Melegh B; Hadzsiev K
    Seizure; 2020 Jan; 74():8-13. PubMed ID: 31765958
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.
    Carranza Rojo D; Harvey AS; Iona X; Dibbens LM; Damiano JA; Arsov T; Gill D; Freeman JL; Leventer RJ; Vincent A; Berkovic SF; McMahon JM; Scheffer IE
    Epilepsy Res; 2012 Jun; 100(1-2):194-8. PubMed ID: 22386634
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 43.