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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

778 related items for PubMed ID: 26230511

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  • 5. [Genetic and molecular basis for sodium channel-mediated Brugada syndrome].
    Barajas-Martínez H, Hu D, Antzelevitch C.
    Arch Cardiol Mex; 2013; 83(4):295-302. PubMed ID: 24269159
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  • 7. 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; 18(6):888-96. PubMed ID: 26498160
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  • 8. High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.
    Risgaard B, Jabbari R, Refsgaard L, Holst AG, Haunsø S, Sadjadieh A, Winkel BG, Olesen MS, Tfelt-Hansen J.
    Clin Genet; 2013 Nov; 84(5):489-95. PubMed ID: 23414114
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  • 10. Genetic analysis of sudden unexplained death: a multidisciplinary approach.
    Kauferstein S, Kiehne N, Jenewein T, Biel S, Kopp M, König R, Erkapic D, Rothschild M, Neumann T.
    Forensic Sci Int; 2013 Jun 10; 229(1-3):122-7. PubMed ID: 23683917
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  • 11. Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort.
    Koopmann TT, Beekman L, Alders M, Meregalli PG, Mannens MM, Moorman AF, Wilde AA, Bezzina CR.
    Heart Rhythm; 2007 Jun 10; 4(6):752-5. PubMed ID: 17556197
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  • 14. Dual phenotypic transmission in Brugada syndrome.
    Hermida JS, Arnalsteen-Dassonvalle E, Kubala M, Mathiron A, Traulle S, Anbazhagan K, Hermida A, Rochette J.
    Arch Cardiovasc Dis; 2013 Jun 10; 106(6-7):366-72. PubMed ID: 23810369
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