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PUBMED FOR HANDHELDS

Journal Abstract Search


647 related items for PubMed ID: 20608822

  • 1. The genetic and clinical features of cardiac channelopathies.
    Roberts JD, Gollob MH.
    Future Cardiol; 2010 Jul; 6(4):491-506. PubMed ID: 20608822
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  • 3. Arrhythmogenic hereditary syndromes: Brugada Syndrome, long QT syndrome, short QT syndrome and CPVT.
    Schimpf R, Veltmann C, Wolpert C, Borggrefe M.
    Minerva Cardioangiol; 2010 Dec; 58(6):623-36. PubMed ID: 21135804
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  • 5. Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.
    Napolitano C, Bloise R, Monteforte N, Priori SG.
    Circulation; 2012 Apr 24; 125(16):2027-34. PubMed ID: 22529064
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  • 6. [Cardiac channelopathies in the context of hereditary arrhythmia syndromes].
    Huttelmaier MT, Fischer TH.
    Inn Med (Heidelb); 2024 Aug 24; 65(8):787-797. PubMed ID: 38977442
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  • 7. [Cardiac ion channelopathies: A potential link between cardiomyopathies and cardiac arrhythmias].
    Schimpf R, Rudic B, Tülümen E, Papavassiliu T, Dösch C, Borggrefe M.
    Dtsch Med Wochenschr; 2013 Mar 24; 138(12):591-7. PubMed ID: 23483420
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  • 12. Short QT syndrome: a review.
    Patel U, Pavri BB.
    Cardiol Rev; 2009 Mar 24; 17(6):300-3. PubMed ID: 19829181
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  • 15. Ion channel diseases in children: manifestations and management.
    Schwartz PJ, Crotti L.
    Curr Opin Cardiol; 2008 May 24; 23(3):184-91. PubMed ID: 18382205
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  • 16. [Sudden cardiac death in athletes with an apparently normal heart: the channelopathies].
    Giustetto C, Gaita F.
    G Ital Cardiol (Rome); 2008 Oct 24; 9(10 Suppl 1):78S-82S. PubMed ID: 19195312
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  • 17. Ion Channel Disorders and Sudden Cardiac Death.
    Garcia-Elias A, Benito B.
    Int J Mol Sci; 2018 Feb 28; 19(3):. PubMed ID: 29495624
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  • 18. A clinical approach to inherited arrhythmias.
    Cerrone M, Cummings S, Alansari T, Priori SG.
    Circ Cardiovasc Genet; 2012 Oct 01; 5(5):581-90. PubMed ID: 23074337
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  • 19. Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.
    Hofman N, van Lochem LT, Wilde AA.
    Future Cardiol; 2010 May 01; 6(3):395-408. PubMed ID: 20462344
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  • 20. Amplification of spatial dispersion of repolarization underlies sudden cardiac death associated with catecholaminergic polymorphic VT, long QT, short QT and Brugada syndromes.
    Antzelevitch C, Oliva A.
    J Intern Med; 2006 Jan 01; 259(1):48-58. PubMed ID: 16336513
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