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 *

264 related articles for article (PubMed ID: 28565819)

  • 1. Genetic basis of pediatric epilepsy syndromes.
    Zhang D; Liu X; Deng X
    Exp Ther Med; 2017 May; 13(5):2129-2133. PubMed ID: 28565819
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies.
    Zhou P; He N; Zhang JW; Lin ZJ; Wang J; Yan LM; Meng H; Tang B; Li BM; Liu XR; Shi YW; Zhai QX; Yi YH; Liao WP
    Genes Brain Behav; 2018 Nov; 17(8):e12456. PubMed ID: 29314583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Na+ channelopathies and epilepsy: recent advances and new perspectives.
    Marini C; Mantegazza M
    Expert Rev Clin Pharmacol; 2010 May; 3(3):371-84. PubMed ID: 22111617
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Epileptic Encephalopathies as Neurodegenerative Disorders.
    Helbig I; von Deimling M; Marsh ED
    Adv Neurobiol; 2017; 15():295-315. PubMed ID: 28674986
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Understanding Genotypes and Phenotypes in Epileptic Encephalopathies.
    Helbig I; Tayoun AA
    Mol Syndromol; 2016 Sep; 7(4):172-181. PubMed ID: 27781027
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dravet Syndrome: A Developmental and Epileptic Encephalopathy.
    Lopez-Santiago L; Isom LL
    Epilepsy Curr; 2019 Jan; 19(1):51-53. PubMed ID: 30838929
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes.
    Mastrangelo M
    Pediatr Neurol; 2015 Aug; 53(2):119-29. PubMed ID: 26073591
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Current understanding and neurobiology of epileptic encephalopathies.
    Auvin S; Cilio MR; Vezzani A
    Neurobiol Dis; 2016 Aug; 92(Pt A):72-89. PubMed ID: 26992889
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features.
    Liang JS; Lin LJ; Yang MT; Wang JS; Lu JF
    Brain Dev; 2017 Nov; 39(10):877-881. PubMed ID: 28709814
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnostic Approach to Genetic Causes of Early-Onset Epileptic Encephalopathy.
    Gürsoy S; Erçal D
    J Child Neurol; 2016 Mar; 31(4):523-32. PubMed ID: 26271793
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
    Gerald B; Ramsey K; Belnap N; Szelinger S; Siniard AL; Balak C; Russell M; Richholt R; De Both M; Claasen AM; Schrauwen I; Huentelman MJ; Craig DW; Rangasamy S; Narayanan V
    Semin Pediatr Neurol; 2018 Jul; 26():28-32. PubMed ID: 29961512
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Infantile epileptic encephalopathies: what matters is genetics].
    Garcia-Penas JJ; Jimenez-Legido M
    Rev Neurol; 2017 May; 64(s03):S65-S69. PubMed ID: 28524223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genes of early-onset epileptic encephalopathies: from genotype to phenotype.
    Mastrangelo M; Leuzzi V
    Pediatr Neurol; 2012 Jan; 46(1):24-31. PubMed ID: 22196487
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epileptic Encephalopathies-Clinical Syndromes and Pathophysiological Concepts.
    von Deimling M; Helbig I; Marsh ED
    Curr Neurol Neurosci Rep; 2017 Feb; 17(2):10. PubMed ID: 28229394
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights.
    Ng AC; Chahine M; Scantlebury MH; Appendino JP
    J Neurol; 2024 Jun; 271(6):3063-3094. PubMed ID: 38607431
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.
    Mei D; Cetica V; Marini C; Guerrini R
    Epilepsia; 2019 Dec; 60 Suppl 3():S2-S7. PubMed ID: 31904125
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.