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Journal Abstract Search

500 related items for PubMed ID: 26749013

  • 1. Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention.
    Goldman AM, Behr ER, Semsarian C, Bagnall RD, Sisodiya S, Cooper PN.
    Epilepsia; 2016 Jan; 57 Suppl 1(Suppl 1):17-25. PubMed ID: 26749013
    [Abstract] [Full Text] [Related]

  • 2. Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing.
    Coll M, Allegue C, Partemi S, Mates J, Del Olmo B, Campuzano O, Pascali V, Iglesias A, Striano P, Oliva A, Brugada R.
    Int J Legal Med; 2016 Mar; 130(2):331-9. PubMed ID: 26423924
    [Abstract] [Full Text] [Related]

  • 3. Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases.
    Tu E, Bagnall RD, Duflou J, Semsarian C.
    Brain Pathol; 2011 Mar; 21(2):201-8. PubMed ID: 20875080
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  • 5. Molecular autopsy for sudden unexplained death? Time to discuss pros and cons.
    Mazzanti A, Priori SG.
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1099-102. PubMed ID: 22966897
    [No Abstract] [Full Text] [Related]

  • 6. Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia-Related Genes.
    Chahal CAA, Salloum MN, Alahdab F, Gottwald JA, Tester DJ, Anwer LA, So EL, Murad MH, St Louis EK, Ackerman MJ, Somers VK.
    J Am Heart Assoc; 2020 Jan 07; 9(1):e012264. PubMed ID: 31865891
    [Abstract] [Full Text] [Related]

  • 7. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J.
    J Cardiovasc Electrophysiol; 2012 Oct 07; 23(10):1092-8. PubMed ID: 22882672
    [Abstract] [Full Text] [Related]

  • 8. Rare sudden unexpected death in epilepsy SCN5A variants cause changes in channel function implicating cardiac arrhythmia as a cause of death.
    Soh MS, Bagnall RD, Semsarian C, Scheffer IE, Berkovic SF, Reid CA.
    Epilepsia; 2022 Jun 07; 63(6):e57-e62. PubMed ID: 35397174
    [Abstract] [Full Text] [Related]

  • 9. Explaining sudden infant death with cardiac arrhythmias: Complete exon sequencing of nine cardiac arrhythmia genes in Dutch SIDS cases highlights new and known DNA variants.
    Liebrechts-Akkerman G, Liu F, van Marion R, Dinjens WNM, Kayser M.
    Forensic Sci Int Genet; 2020 May 07; 46():102266. PubMed ID: 32145446
    [Abstract] [Full Text] [Related]

  • 10. Molecular genetic basis of sudden cardiac death.
    Towbin JA.
    Pediatr Clin North Am; 2004 Oct 07; 51(5):1229-55. PubMed ID: 15331282
    [Abstract] [Full Text] [Related]

  • 11. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
    Wang D, Shah KR, Um SY, Eng LS, Zhou B, Lin Y, Mitchell AA, Nicaj L, Prinz M, McDonald TV, Sampson BA, Tang Y.
    Forensic Sci Int; 2014 Apr 07; 237():90-9. PubMed ID: 24631775
    [Abstract] [Full Text] [Related]

  • 12. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C, Zhao Q, Su T, Tang S, Lv G, Liu H, Quan L, Cheng J.
    Forensic Sci Int; 2013 Sep 10; 231(1-3):82-7. PubMed ID: 23890619
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  • 14. Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
    Son MK, Ki CS, Park SJ, Huh J, Kim JS, On YK.
    J Korean Med Sci; 2013 Jul 10; 28(7):1021-6. PubMed ID: 23853484
    [Abstract] [Full Text] [Related]

  • 15. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 Jul 10; 49():263-74. PubMed ID: 9509262
    [Abstract] [Full Text] [Related]

  • 16. Genetic analysis of hyperpolarization-activated cyclic nucleotide-gated cation channels in sudden unexpected death in epilepsy cases.
    Tu E, Waterhouse L, Duflou J, Bagnall RD, Semsarian C.
    Brain Pathol; 2011 Nov 10; 21(6):692-8. PubMed ID: 21615589
    [Abstract] [Full Text] [Related]

  • 17. High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.
    Klassen TL, Bomben VC, Patel A, Drabek J, Chen TT, Gu W, Zhang F, Chapman K, Lupski JR, Noebels JL, Goldman AM.
    Epilepsia; 2014 Feb 10; 55(2):e6-12. PubMed ID: 24372310
    [Abstract] [Full Text] [Related]

  • 18. Common variants in cardiac ion channel genes are associated with sudden cardiac death.
    Albert CM, MacRae CA, Chasman DI, VanDenburgh M, Buring JE, Manson JE, Cook NR, Newton-Cheh C.
    Circ Arrhythm Electrophysiol; 2010 Jun 10; 3(3):222-9. PubMed ID: 20400777
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  • 19. Long QT and Brugada syndrome gene mutations in New Zealand.
    Chung SK, MacCormick JM, McCulley CH, Crawford J, Eddy CA, Mitchell EA, Shelling AN, French JK, Skinner JR, Rees MI.
    Heart Rhythm; 2007 Oct 10; 4(10):1306-14. PubMed ID: 17905336
    [Abstract] [Full Text] [Related]

  • 20. Neuron-specific Kv1.1 deficiency is sufficient to cause epilepsy, premature death, and cardiorespiratory dysregulation.
    Trosclair K, Dhaibar HA, Gautier NM, Mishra V, Glasscock E.
    Neurobiol Dis; 2020 Apr 10; 137():104759. PubMed ID: 31978607
    [Abstract] [Full Text] [Related]

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