-
1
-
-
33749367428
-
Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program
-
DOI 10.1001/jama.296.13.1593
-
Corrado D, Basso C, Pavei A, et al. Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program. JAMA 2006;296:1593-601. (Pubitemid 44515020)
-
(2006)
Journal of the American Medical Association
, vol.296
, Issue.13
, pp. 1593-1601
-
-
Corrado, D.1
Basso, C.2
Pavei, A.3
Michieli, P.4
Schiavon, M.5
Thiene, G.6
-
2
-
-
62649113485
-
Sudden deaths in young competitive athletes: Analysis of 1866 deaths in the United States, 1980-2006
-
Maron BJ, Doerer JJ, Haas TS, et al. Sudden deaths in young competitive athletes: Analysis of 1866 deaths in the United States, 1980-2006. Circulation 2009;119:1085-92.
-
(2009)
Circulation
, vol.119
, pp. 1085-1092
-
-
Maron, B.J.1
Doerer, J.J.2
Haas, T.S.3
-
3
-
-
0042734704
-
Sudden death in young athletes
-
DOI 10.1056/NEJMra022783
-
Maron BJ. Sudden death in young athletes. N Engl J Med 2003;349:1064-75. (Pubitemid 37098275)
-
(2003)
New England Journal of Medicine
, vol.349
, Issue.11
, pp. 1064-1075
-
-
Maron, B.J.1
-
4
-
-
0032491031
-
Screening for hypertrophic cardiomyopathy in young athletes
-
DOI 10.1056/NEJM199808063390602
-
Corrado D, Basso C, Schiavon M, et al. Screening for hypertrophic cardiomyopathy in young athletes. N Engl J Med 1998;339:364-9. (Pubitemid 28363798)
-
(1998)
New England Journal of Medicine
, vol.339
, Issue.6
, pp. 364-369
-
-
Corrado, D.1
Basso, C.2
Schiavon, M.3
Thiene, G.4
-
5
-
-
56849111744
-
Pre-participation screening of young competitive athletes for prevention of sudden cardiac death
-
Corrado D, Basso C, Schiavon M, et al. Pre-participation screening of young competitive athletes for prevention of sudden cardiac death. J Am Coll Cardiol 2008;52:1981-9.
-
(2008)
J Am Coll Cardiol
, vol.52
, pp. 1981-1989
-
-
Corrado, D.1
Basso, C.2
Schiavon, M.3
-
6
-
-
46849110148
-
Sudden arrhythmic death syndrome: Familial evaluation identifies inheritable heart disease in the majority of families
-
DOI 10.1093/eurheartj/ehn219
-
Behr ER, Dalageorgou C, Christiansen M, et al. Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families. Eur Heart J 2008;29:1670-80. (Pubitemid 351957547)
-
(2008)
European Heart Journal
, vol.29
, Issue.13
, pp. 1670-1680
-
-
Behr, E.R.1
Dalageorgou, C.2
Christiansen, M.3
Syrris, P.4
Hughes, S.5
Tome Esteban, M.T.6
Rowland, E.7
Jeffery, S.8
McKenna, W.J.9
-
7
-
-
22144439771
-
Sudden unexplained death: Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives
-
DOI 10.1161/CIRCULATIONAHA.104.522581
-
Tan HL, Hofman N, van Langen IM, et al. Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives. Circulation 2005;112:207-13. (Pubitemid 40982303)
-
(2005)
Circulation
, vol.112
, Issue.2
, pp. 207-213
-
-
Tan, H.L.1
Hofman, N.2
Van Langen, I.M.3
Van Der Wal, A.C.4
Wilde, A.A.M.5
-
8
-
-
0035830365
-
Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias
-
Schwartz PJ, Priori SG, Spazzolini C, et al. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation 2001;103:89-95. (Pubitemid 32050441)
-
(2001)
Circulation
, vol.103
, Issue.1
, pp. 89-95
-
-
Schwartz, P.J.1
Priori, S.G.2
Spazzolini, C.3
Moss, A.J.4
Michael Vincent, G.5
Napolitano, C.6
Denjoy, I.7
Guicheney, P.8
Breithardt, G.9
Keating, M.T.10
Towbin, J.A.11
Beggs, A.H.12
Brink, P.13
Wilde, A.A.M.14
Toivonen, L.15
Zareba, W.16
Robinson, J.L.17
Timothy, K.W.18
Corfield, V.19
Wattanasirichaigoon, D.20
Corbett, C.21
Haverkamp, W.22
Schulze-Bahr, E.23
Lehmann, M.H.24
Schwartz, K.25
Coumel, P.26
Bloise, R.27
more..
-
9
-
-
13444300924
-
Brugada syndrome: Report of the second consensus conference: Endorsed by the heart rhythm society and the European heart rhythm association
-
Antzelevitch C, Brugada P, Borggrefe M, et al. Brugada syndrome: Report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005;111:659-70.
-
(2005)
Circulation
, vol.111
, pp. 659-670
-
-
Antzelevitch, C.1
Brugada, P.2
Borggrefe, M.3
-
10
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
Fatkin D, MacRae C, Sasaki T, et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med 1999;341:1715-24.
-
(1999)
N Engl J Med
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
-
11
-
-
0003096674
-
Cardiac conduction defects associate with mutations in SCN5A
-
Schott JJ, Alshinawi C, Kyndt F, et al. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet 1999;23:20-1.
-
(1999)
Nat Genet
, vol.23
, pp. 20-21
-
-
Schott, J.J.1
Alshinawi, C.2
Kyndt, F.3
-
12
-
-
2942530660
-
Hypertrophic cardiomyopathy
-
DOI 10.1016/S0140-6736(04)16358-7, PII S0140673604163587
-
Elliott P, McKenna WJ. Hypertrophic cardiomyopathy. Lancet 2004;363:1881-91. (Pubitemid 38748646)
-
(2004)
Lancet
, vol.363
, Issue.9424
, pp. 1881-1891
-
-
Elliott, P.1
McKenna, W.J.2
-
13
-
-
0030842476
-
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population
-
Charron P, Dubourg O, Desnos M, et al. Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in a genotyped adult population. Circulation 1997;96:214-19. (Pubitemid 27298423)
-
(1997)
Circulation
, vol.96
, Issue.1
, pp. 214-219
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
Isnard, R.4
Hagege, A.5
Millaire, A.6
Carrier, L.7
Bonne, G.8
Tesson, F.9
Richard, P.10
Bouhour, J.-B.11
Schwartz, K.12
Komajda, M.13
-
14
-
-
64049101148
-
Arrhythmogenic right ventricular cardiomyopathy
-
Basso C, Corrado D, Marcus FI, et al. Arrhythmogenic right ventricular cardiomyopathy. Lancet 2009;373:1289-300.
-
(2009)
Lancet
, vol.373
, pp. 1289-1300
-
-
Basso, C.1
Corrado, D.2
Marcus, F.I.3
-
15
-
-
0027267765
-
Diagnostic criteria for the long QT syndrome: An update
-
Schwartz PJ, Moss AJ, Vincent GM, et al. Diagnostic criteria for the long QT syndrome. An update. Circulation 1993;88:782-4. (Pubitemid 23228078)
-
(1993)
Circulation
, vol.88
, Issue.2
, pp. 782-784
-
-
Schwartz, P.J.1
Moss, A.J.2
Vincent, G.M.3
Crampton, R.S.4
-
17
-
-
34247485039
-
Diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia
-
DOI 10.1016/j.hrthm.2006.12.048, PII S1547527106023630
-
Napolitano C, Priori SG. Diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm 2007;4:675-8. (Pubitemid 46655581)
-
(2007)
Heart Rhythm
, vol.4
, Issue.5
, pp. 675-678
-
-
Napolitano, C.1
Priori, S.G.2
-
18
-
-
0030067707
-
Signal-averaged electrocardiography
-
Cain ME, Anderson JL, Arnsdorf MF, et al. Signal-averaged electrocardiography. J Am Coll Cardiol 1996;27:238-49. (Pubitemid 26018938)
-
(1996)
Journal of the American College of Cardiology
, vol.27
, Issue.1
, pp. 238-249
-
-
Cain, M.E.1
Anderson, J.L.2
Arnsdorf, M.F.3
Mason, J.W.4
Scheinman, M.M.5
Waldo, A.L.6
-
19
-
-
0037134671
-
Late potentials and the Brugada syndrome
-
Antzelevitch C. Late potentials and the Brugada syndrome. J Am Coll Cardiol 2002;39:1996-9.
-
(2002)
J Am Coll Cardiol
, vol.39
, pp. 1996-1999
-
-
Antzelevitch, C.1
-
20
-
-
33749047246
-
Epinephrine QT stress testing in congenital long QT syndrome
-
DOI 10.1016/j.jelectrocard.2006.05.013, PII S0022073606001361, Research and Technology Transfer in Computerized Electrocardiology
-
Vyas H, Ackerman MJ. Epinephrine QT stress testing in congenital long QT syndrome. J Electrocardiol 2006;39:S107-13. (Pubitemid 44465954)
-
(2006)
Journal of Electrocardiology
, vol.39
, Issue.4 SUPPL.
-
-
Vyas, H.1
Ackerman, M.J.2
-
21
-
-
26844448690
-
Diagnosis of unexplained cardiac arrest: Role of adrenaline and procainamide infusion
-
DOI 10.1161/CIRCULATIONAHA.105.552166
-
Krahn AD, Gollob M, Yee R, et al. Diagnosis of unexplained cardiac arrest: Role of adrenaline and procainamide infusion. Circulation 2005;112:2228-34. (Pubitemid 41464564)
-
(2005)
Circulation
, vol.112
, Issue.15
, pp. 2228-2234
-
-
Krahn, A.D.1
Gollob, M.2
Yee, R.3
Gula, L.J.4
Skanes, A.C.5
Walker, B.D.6
Klein, G.J.7
-
22
-
-
33645302141
-
Role of genetic analyses in cardiology: Part I: Mendelian diseases: Cardiac channelopathies
-
Priori SG, Napolitano C. Role of genetic analyses in cardiology: part I: mendelian diseases: Cardiac channelopathies. Circulation 2006;113:1130-5.
-
(2006)
Circulation
, vol.113
, pp. 1130-1135
-
-
Priori, S.G.1
Napolitano, C.2
-
23
-
-
41149114636
-
Clinical indications for genetic testing in familial sudden cardiac death syndromes: An HRUK position statement
-
Heart Rhythm UK Familial Sudden Death Syndromes Statement Development Group
-
Heart Rhythm UK Familial Sudden Death Syndromes Statement Development Group. Clinical indications for genetic testing in familial sudden cardiac death syndromes: An HRUK position statement. Heart 2008;94:502-7.
-
(2008)
Heart
, vol.94
, pp. 502-507
-
-
-
24
-
-
33748141992
-
The role of molecular autopsy in unexplained sudden cardiac death
-
DOI 10.1097/01.hco.0000221576.33501.83, PII 0000157320060500000004
-
Tester DJ, Ackerman MJ. The role of molecular autopsy in unexplained sudden cardiac death. Curr Opin Cardiol 2006;21:166-72. (Pubitemid 44315078)
-
(2006)
Current Opinion in Cardiology
, vol.21
, Issue.3
, pp. 166-172
-
-
Tester, D.J.1
Ackerman, M.J.2
-
25
-
-
33750348298
-
Postmortem Long QT Syndrome Genetic Testing for Sudden Unexplained Death in the Young
-
DOI 10.1016/j.jacc.2006.10.010, PII S0735109706024776
-
Tester DJ, Ackerman MJ. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young. J Am Coll Cardiol 2007;49:240-6. (Pubitemid 46054388)
-
(2007)
Journal of the American College of Cardiology
, vol.49
, Issue.2
, pp. 240-246
-
-
Tester, D.J.1
Ackerman, M.J.2
-
26
-
-
0035860984
-
Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome
-
Ackerman MJ, Siu BL, Sturner WQ, et al. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome. JAMA 2001;286:2264-9. (Pubitemid 33063149)
-
(2001)
Journal of the American Medical Association
, vol.286
, Issue.18
, pp. 2264-2269
-
-
Ackerman, M.J.1
Siu, B.L.2
Sturner, W.Q.3
Tester, D.J.4
Valdivia, C.R.5
Makielski, J.C.6
Towbin, J.A.7
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