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Journal Abstract Search

1093 related items for PubMed ID: 20653139

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  • 4. Sudden death: managing the family, the role of genetics.
    Brugada R.
    Heart; 2011 Apr; 97(8):676-81. PubMed ID: 21421602
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  • 5. The role of molecular autopsy in unexplained sudden cardiac death.
    Tester DJ, Ackerman MJ.
    Curr Opin Cardiol; 2006 May; 21(3):166-72. PubMed ID: 16601452
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  • 6. 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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  • 10. Clinical and Genetic Diagnosis of Nonischemic Sudden Cardiac Death.
    Jiménez-Jáimez J, Alcalde Martínez V, Jiménez Fernández M, Bermúdez Jiménez F, Rodríguez Vázquez Del Rey MDM, Perin F, Oyonarte Ramírez JM, López Fernández S, de la Torre I, García Orta R, González Molina M, Cabrerizo EM, Álvarez Abril B, Álvarez M, Macías Ruiz R, Correa C, Tercedor L.
    Rev Esp Cardiol (Engl Ed); 2017 Oct; 70(10):808-816. PubMed ID: 28566242
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  • 15. Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.
    Hofman N, van Lochem LT, Wilde AA.
    Future Cardiol; 2010 May; 6(3):395-408. PubMed ID: 20462344
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  • 16. Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and children.
    Tester DJ, Ackerman MJ.
    Annu Rev Med; 2009 May; 60():69-84. PubMed ID: 18928334
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  • 18. Depolarization/repolarization, electrocardiographic abnormalities, and arrhythmias in cardiac channelopathies.
    Marcus FI.
    J Electrocardiol; 2005 Oct; 38(4 Suppl):60-3. PubMed ID: 16226076
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