Works matching IS 18832148 AND DT 2016 AND VI 32 AND IP 5
Results: 18
J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 315, doi. 10.1016/j.joa.2016.07.002
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Catheter ablation for ventricular tachyarrhythmia in patients with channelopathies.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 404, doi. 10.1016/j.joa.2016.01.011
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Characterization of the novel mutant A78T-HERG from a long QT syndrome type 2 patient: Instability of the mutant protein and stabilization by heat shock factor 1.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 433, doi. 10.1016/j.joa.2015.10.005
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Molecular genetics have opened a new era for arrhythmia research, but also Pandora׳s box?
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 313, doi. 10.1016/j.joa.2016.07.001
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Recent advances in genetic testing and counseling for inherited arrhythmias.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 389, doi. 10.1016/j.joa.2015.12.009
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Cardiac dynamics: Alternans and arrhythmogenesis.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 411, doi. 10.1016/j.joa.2016.02.009
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Current topics in catecholaminergic polymorphic ventricular tachycardia.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 344, doi. 10.1016/j.joa.2015.09.008
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Genetics of Brugada syndrome.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 418, doi. 10.1016/j.joa.2016.07.012
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Atrial arrhythmias in inherited arrhythmogenic disorders.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 366, doi. 10.1016/j.joa.2015.11.007
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Erratum to ‘2015 HRS/EHRA/APHRS/SOLAECE expert consensus statement on optimal implantable cardioverter-defibrillator programming and testing’ [Journal of Arrhythmia 32/1 (2016) 1–28].
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 441, doi. 10.1016/j.joa.2016.08.001
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Molecular pathogenesis of long QT syndrome type 2.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 373, doi. 10.1016/j.joa.2015.11.009
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Editorial Board.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. iii, doi. 10.1016/S1880-4276(16)30112-0
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- Article
Left cardiac sympathetic denervation: An important treatment option for patients with hereditary ventricular arrhythmias.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 340, doi. 10.1016/j.joa.2015.08.002
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The genetic background of arrhythmogenic right ventricular cardiomyopathy.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 398, doi. 10.1016/j.joa.2016.01.006
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Inherited bradyarrhythmia: A diverse genetic background.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 352, doi. 10.1016/j.joa.2015.09.009
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Molecular pathogenesis of long QT syndrome type 1.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 381, doi. 10.1016/j.joa.2015.12.006
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Molecular autopsy in victims of inherited arrhythmias.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 359, doi. 10.1016/j.joa.2015.09.010
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Autonomic and cardio-respiratory responses to exercise in Brugada Syndrome patients.
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- Journal of Arrhythmia, 2016, v. 32, n. 5, p. 426, doi. 10.1016/j.joa.2015.09.001
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- Article