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Brugada, R
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Marian, AJ
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Authors:
Li, DX
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Roberts, R
Citation: Dx. Li et al., Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy, CIRCULATION, 104(18), 2001, pp. 2188-2193
Citation: J. Brugada et al., Other genetic disorders and primary arrhythmias: The Brugada syndrome, MYOCARDIAL REPOLARIZATION: FROM GENE TO BEDSIDE, 2001, pp. 269-277
Authors:
Bowles, KR
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Brugada, R
Zintz, C
Comeaux, J
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Citation: Kr. Bowles et al., Construction of a high-resolution physical map of the chromosome 10q22-q23dilated cardiomyopathy locus and analysis of candidate genes, GENOMICS, 67(2), 2000, pp. 109-127
Citation: J. Brugada et al., Sudden death in Brugada syndrome and right ventricular cardiomyopathies. Similarities and differences, REV ESP CAR, 53(2), 2000, pp. 275-285
Citation: P. Brugada et al., Sudden death in patients and relatives with the syndrome of right bundle branch block, ST segment elevation in the precordial leads V-1 to V-3 and sudden death, EUR HEART J, 21(4), 2000, pp. 321-326
Citation: J. Brugada et al., Pharmacological and device approach to therapy of inherited cardiac diseases associated with cardiac arrhythmias and sudden death, J ELCARDIOL, 33, 2000, pp. 41-47
Authors:
Brugada, R
Brugada, J
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Kirsch, GE
Potenza, D
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Brugada, P
Citation: R. Brugada et al., Sodium channel blockers identify risk for sudden death in patients with ST-Segment elevation and right bundle branch block but structurally normal hearts, CIRCULATION, 101(5), 2000, pp. 510-515
Citation: J. Brugada et al., The syndrome of right bundle branch block ST segment elevation in V-1 to V-3 and sudden death - the Brugada syndrome, EUROPACE, 1(3), 1999, pp. 156-166
Citation: P. Brugada et al., The puzzle behind electrical chaos and sudden cardiac death in the structurally normal heart, EUR HEART J, 20(6), 1999, pp. 401-402