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567 related items for PubMed ID: 26704558

  • 1. Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.
    Bagnall RD, Crompton DE, Petrovski S, Lam L, Cutmore C, Garry SI, Sadleir LG, Dibbens LM, Cairns A, Kivity S, Afawi Z, Regan BM, Duflou J, Berkovic SF, Scheffer IE, Semsarian C.
    Ann Neurol; 2016 Apr; 79(4):522-34. PubMed ID: 26704558
    [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. Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young.
    Bagnall RD, Das K J, Duflou J, Semsarian C.
    Heart Rhythm; 2014 Apr; 11(4):655-62. PubMed ID: 24440382
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 07; 21(2):201-8. PubMed ID: 20875080
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy.
    Leu C, Balestrini S, Maher B, Hernández-Hernández L, Gormley P, Hämäläinen E, Heggeli K, Schoeler N, Novy J, Willis J, Plagnol V, Ellis R, Reavey E, O'Regan M, Pickrell WO, Thomas RH, Chung SK, Delanty N, McMahon JM, Malone S, Sadleir LG, Berkovic SF, Nashef L, Zuberi SM, Rees MI, Cavalleri GL, Sander JW, Hughes E, Helen Cross J, Scheffer IE, Palotie A, Sisodiya SM.
    EBioMedicine; 2015 Sep 07; 2(9):1063-70. PubMed ID: 26501104
    [Abstract] [Full Text] [Related]

  • 7. Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?
    Bleakley LE, Soh MS, Bagnall RD, Sadleir LG, Gooley S, Semsarian C, Scheffer IE, Berkovic SF, Reid CA.
    Front Neurol; 2020 Sep 07; 11():925. PubMed ID: 33013630
    [Abstract] [Full Text] [Related]

  • 8. Cardiac arrhythmia and epilepsy genetic variants in sudden unexpected death in epilepsy.
    Aschner A, Keller A, Williams A, Whitney R, Cunningham K, Hamilton RM, Pollanen M, Donner E.
    Front Neurol; 2024 Sep 07; 15():1386730. PubMed ID: 38756210
    [Abstract] [Full Text] [Related]

  • 9. Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes.
    Shigemizu D, Aiba T, Nakagawa H, Ozaki K, Miya F, Satake W, Toda T, Miyamoto Y, Fujimoto A, Suzuki Y, Kubo M, Tsunoda T, Shimizu W, Tanaka T.
    PLoS One; 2015 Sep 07; 10(7):e0130329. PubMed ID: 26132555
    [Abstract] [Full Text] [Related]

  • 10. Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.
    Anderson JH, Tester DJ, Will ML, Ackerman MJ.
    Circ Cardiovasc Genet; 2016 Jun 07; 9(3):259-65. PubMed ID: 27114410
    [Abstract] [Full Text] [Related]

  • 11. Exome analysis focusing on epilepsy-related genes in children and adults with sudden unexplained death.
    Buerki SE, Haas C, Neubauer J.
    Seizure; 2023 Dec 07; 113():66-75. PubMed ID: 37995443
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.
    Altmann HM, Tester DJ, Will ML, Middha S, Evans JM, Eckloff BW, Ackerman MJ.
    Circulation; 2015 Jun 09; 131(23):2051-60. PubMed ID: 25922419
    [Abstract] [Full Text] [Related]

  • 14. Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected Death.
    Chahal CAA, Tester DJ, Fayyaz AU, Jaliparthy K, Khan NA, Lu D, Khan M, Sahoo A, Rajendran A, Knight JA, Simpson MA, Behr ER, So EL, St Louis EK, Reichard RR, Edwards WD, Ackerman MJ, Somers VK.
    J Am Heart Assoc; 2021 Dec 07; 10(23):e021170. PubMed ID: 34816733
    [Abstract] [Full Text] [Related]

  • 15. Mortality and SUDEP in epilepsy patients treated with vagus nerve stimulation.
    Granbichler CA, Nashef L, Selway R, Polkey CE.
    Epilepsia; 2015 Feb 07; 56(2):291-6. PubMed ID: 25580645
    [Abstract] [Full Text] [Related]

  • 16. Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series.
    Partemi S, Vidal MC, Striano P, Campuzano O, Allegue C, Pezzella M, Elia M, Parisi P, Belcastro V, Casellato S, Giordano L, Mastrangelo M, Pietrafusa N, Striano S, Zara F, Bianchi A, Buti D, La Neve A, Tassinari CA, Oliva A, Brugada R.
    Int J Legal Med; 2015 May 07; 129(3):495-504. PubMed ID: 25119684
    [Abstract] [Full Text] [Related]

  • 17. Increased risk of sudden unexpected death in epilepsy in females using lamotrigine: a nested, case-control study.
    Aurlien D, Larsen JP, Gjerstad L, Taubøll E.
    Epilepsia; 2012 Feb 07; 53(2):258-66. PubMed ID: 22126371
    [Abstract] [Full Text] [Related]

  • 18. Semiconductor Whole Exome Sequencing for the Identification of Genetic Variants in Colombian Patients Clinically Diagnosed with Long QT Syndrome.
    Burgos M, Arenas A, Cabrera R.
    Mol Diagn Ther; 2016 Aug 07; 20(4):353-62. PubMed ID: 27251404
    [Abstract] [Full Text] [Related]

  • 19. Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
    Nunn LM, Lopes LR, Syrris P, Murphy C, Plagnol V, Firman E, Dalageorgou C, Zorio E, Domingo D, Murday V, Findlay I, Duncan A, Carr-White G, Robert L, Bueser T, Langman C, Fynn SP, Goddard M, White A, Bundgaard H, Ferrero-Miliani L, Wheeldon N, Suvarna SK, O'Beirne A, Lowe MD, McKenna WJ, Elliott PM, Lambiase PD.
    Europace; 2016 Jun 07; 18(6):888-96. PubMed ID: 26498160
    [Abstract] [Full Text] [Related]

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