-
2
-
-
70349501483
-
The magnitude of sudden cardiac death in the young: A death certificate based review in England and Wales
-
Papadakis M, Sharma S, Cox S, et al. The magnitude of sudden cardiac death in the young: a death certificate based review in England and Wales. Europace 2009;11:1353-8.
-
(2009)
Europace
, vol.11
, pp. 1353-1358
-
-
Papadakis, M.1
Sharma, S.2
Cox, S.3
-
3
-
-
34247885947
-
Sudden arrhythmic death syndrome: A national survey of sudden unexplained cardiac death
-
DOI 10.1136/hrt.2006.099598
-
Behr ER, Casey A, Sheppard M, et al. Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death. Heart 2007;93:601-5. (Pubitemid 46707114)
-
(2007)
Heart
, vol.93
, Issue.5
, pp. 601-605
-
-
Behr, E.R.1
Casey, A.2
Sheppard, M.3
Wright, M.4
Bowker, T.J.5
Davies, M.J.6
McKenna, W.J.7
Wood, D.A.8
-
4
-
-
0037384929
-
Sudden, unexpected cardiac or unexplained death in England: A national survey
-
DOI 10.1093/qjmed/hcg038
-
Bowker TJ, Wood DA, Davies MJ, et al. Sudden, unexpected cardiac or unexplained death in England: a national survey. Q J Med 2003;96:269-79. (Pubitemid 36432386)
-
(2003)
QJM - Monthly Journal of the Association of Physicians
, vol.96
, Issue.4
, pp. 269-279
-
-
Bowker, T.J.1
Wood, D.A.2
Davies, M.J.3
Sheppard, M.N.4
Cary, N.R.B.5
Burton, J.D.K.6
Chambers, D.R.7
Dawling, S.8
Hobson, H.L.9
Pyke, S.D.M.10
Riemersma, R.A.11
Thompson, S.G.12
-
5
-
-
33846046495
-
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome
-
DOI 10.1161/CIRCULATIONAHA.106.658021, PII 0000301720070123000014
-
Arnestad M, Crotti L, Rognum TO, et al. Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation 2007;115:361-7. (Pubitemid 46148510)
-
(2007)
Circulation
, vol.115
, Issue.3
, pp. 361-367
-
-
Arnestad, M.1
Crotti, L.2
Rognum, T.O.3
Insolia, R.4
Pedrazzini, M.5
Ferrandi, C.6
Vege, A.7
Wang, D.W.8
Rhodes, T.E.9
George, A.L.10
Schwartz, P.J.11
-
6
-
-
0242329842
-
Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome
-
DOI 10.1016/S0140-6736(03)14692-2
-
Behr E, Wood DA, Wright M, et al. Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome. Lancet 2003;362:1457-9. (Pubitemid 37352884)
-
(2003)
Lancet
, vol.362
, Issue.9394
, pp. 1457-1459
-
-
Behr, E.1
Wood, D.A.2
Wright, M.3
Syrris, P.4
Sheppard, M.N.5
Casey, A.6
Davies, M.J.7
McKenna, W.8
-
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, W.A.C.4
Wilde, A.A.M.5
-
8
-
-
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, E.M.T.6
Rowland, E.7
Jeffery, S.8
McKenna, W.J.9
-
9
-
-
77957257904
-
Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: The experience of a tertiary referral center in the Netherlands
-
van der Werf C, Hofman N, Tan HL, et al. Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands. Heart Rhythm 2010;7:1383-9.
-
(2010)
Heart Rhythm
, vol.7
, pp. 1383-1389
-
-
Van Der Werf, C.1
Hofman, N.2
Tan, H.L.3
-
12
-
-
79959342278
-
The sudden arrhythmic death syndrome
-
Kumar D, Elliott P, eds. Oxford, UK: Oxford University Press
-
Lambiase P. The sudden arrhythmic death syndrome. In: Kumar D, Elliott P, eds. Principles and practice of clinical cardiovascular genetics. Oxford, UK: Oxford University Press, 2010:483-94.
-
(2010)
Principles and Practice of Clinical Cardiovascular Genetics
, pp. 483-494
-
-
Lambiase, P.1
-
13
-
-
79952715853
-
Genetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice
-
Tester DJ, Ackerman MJ. Genetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice. Circulation 2011;123:1021-37.
-
(2011)
Circulation
, vol.123
, pp. 1021-1037
-
-
Tester, D.J.1
Ackerman, M.J.2
-
14
-
-
0033044699
-
The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome
-
DOI 10.1053/euhj.1998.1332
-
Matsuo K, Kurita T, Inagaki M, et al. The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome. Eur Heart J 1999;20:465-70. (Pubitemid 29116543)
-
(1999)
European Heart Journal
, vol.20
, Issue.6
, pp. 465-470
-
-
Matsuo, K.1
Kurita, T.2
Inagaki, M.3
Kakishita, M.4
Aihara, N.5
Shimizu, W.6
Taguchi, A.7
Suyama, K.8
Kamakura, S.9
Shimomura, K.10
-
15
-
-
67449102308
-
Misdiagnosis of long QT syndrome as epilepsy at first presentation
-
MacCormick JM, McAlister H, Crawford J, et al. Misdiagnosis of long QT syndrome as epilepsy at first presentation. Ann Emerg Med 2009;54:26-32.
-
(2009)
Ann Emerg Med
, vol.54
, pp. 26-32
-
-
MacCormick, J.M.1
McAlister, H.2
Crawford, J.3
-
16
-
-
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
-
17
-
-
79959330271
-
Mutations in the Lamin A/C gene play a major role in sudden arrhythmic death syndrome
-
abstract
-
Moller DV, Behr ER, Hedley P, et al. Mutations in the Lamin A/C gene play a major role in sudden arrhythmic death syndrome [abstract]. Circulation 2010;122:A16108.
-
(2010)
Circulation
, vol.122
-
-
Moller, D.V.1
Behr, E.R.2
Hedley, P.3
-
18
-
-
70349338813
-
Yield of genetic screening in inherited cardiac channelopathies how to prioritize access to genetic testing
-
Bai R, Napolitano C, Bloise R, et al. Yield of genetic screening in inherited cardiac channelopathies how to prioritize access to genetic testing. Circ Arrhythm Electrophysiol 2009;2:6-15.
-
(2009)
Circ Arrhythm Electrophysiol
, vol.2
, pp. 6-15
-
-
Bai, R.1
Napolitano, C.2
Bloise, R.3
-
19
-
-
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
-
-
-
20
-
-
0022374027
-
The idiopathic long QT syndrome: Pathogenetic mechanisms and therapy
-
Schwartz PJ, Locati E. The idiopathic long QT syndrome: pathogenetic mechanisms and therapy. Eur Heart J 1985;6(Suppl D):103-14. (Pubitemid 16172260)
-
(1985)
European Heart Journal
, vol.6
, Issue.SUPPL. D
, pp. 103-114
-
-
Schwartz, P.J.1
Locati, E.2
-
21
-
-
77955248903
-
Heart Rhythm UK position statement on clinical indications for implantable cardioverter defibrillators in adult patients with familial sudden cardiac death syndromes
-
Garratt CJ, Elliott P, Behr E, et al. Heart Rhythm UK position statement on clinical indications for implantable cardioverter defibrillators in adult patients with familial sudden cardiac death syndromes. Europace 2010;12:1156-75.
-
(2010)
Europace
, vol.12
, pp. 1156-1175
-
-
Garratt, C.J.1
Elliott, P.2
Behr, E.3
-
22
-
-
0033533770
-
Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning
-
DOI 10.1056/NEJM199910073411504
-
Ackerman MJ, Tester DJ, Porter CJ, et al. Molecular diagnosis of the inherited long QT syndrome in a woman who died after near-drowning. N Engl J Med 1999;341:1121-5. (Pubitemid 29466224)
-
(1999)
New England Journal of Medicine
, vol.341
, Issue.15
, pp. 1121-1125
-
-
Ackerman, M.J.1
Tester, D.J.2
Porter, C.-B.J.3
Edwards, W.D.4
-
24
-
-
2342440911
-
Postmortem molecular screening in unexplained sudden death
-
DOI 10.1016/j.jacc.2003.11.052, PII S0735109704003146
-
Chugh SS, Senashova O, Watts A, et al. Postmortem molecular screening in unexplained sudden death. J Am Coll Cardiol 2004;43:1625-9. (Pubitemid 38561345)
-
(2004)
Journal of the American College of Cardiology
, vol.43
, Issue.9
, pp. 1625-1629
-
-
Chugh, S.S.1
Senashova, O.2
Watts, A.3
Tran, P.T.4
Zhou, Z.5
Gong, Q.6
Titus, J.L.7
Hayflick, S.J.8
-
25
-
-
2542613801
-
Postmortem molecular analysis in victims of sudden unexplained death
-
DOI 10.1097/01.paf.0000127406.20447.8a
-
Di Paolo M, Luchini D, Bloise R, et al. Postmortem molecular analysis in victims of sudden unexplained death. Am J Forensic Med Pathol 2004;25:182-4. (Pubitemid 38702550)
-
(2004)
American Journal of Forensic Medicine and Pathology
, vol.25
, Issue.2
, pp. 182-184
-
-
Di, P.M.1
Luchini, D.2
Bloise, R.3
Priori, S.G.4
-
26
-
-
7544230111
-
Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: A molecular autopsy of 49 medical examiner/coroner's cases
-
Tester DJ, Spoon DB, Valdivia HH, et al. Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases. Mayo Clin Proc 2004;79:1380-4. (Pubitemid 39453301)
-
(2004)
Mayo Clinic Proceedings
, vol.79
, Issue.11
, pp. 1380-1384
-
-
Tester, D.J.1
Spoon, D.B.2
Valdivia, H.H.3
Makielski, J.C.4
Ackerman, M.J.5
-
27
-
-
18244399334
-
Pathogenesis of unexplained drowning: New insights from a molecular autopsy
-
Tester DJ, Kopplin LJ, Creighton W, et al. Pathogenesis of unexplained drowning: new insights from a molecular autopsy. Mayo Clin Proc 2005;80:596-600. (Pubitemid 40628814)
-
(2005)
Mayo Clinic Proceedings
, vol.80
, Issue.5
, pp. 596-600
-
-
Tester, D.J.1
Kopplin, L.J.2
Creighton, W.3
Burke, A.P.4
Ackerman, M.J.5
-
28
-
-
32944473591
-
Identification of novel missense mutations of cardiac ryanodine receptor gene in exercise-induced sudden death at autopsy
-
DOI 10.2353/jmoldx.2006.050081
-
Creighton W, Virmani R, Kutys R, et al. Identification of novel missense mutations of cardiac ryanodine receptor gene in exercise-induced sudden death at autopsy. J Mol Diagn 2006;8:62-7. (Pubitemid 43257435)
-
(2006)
Journal of Molecular Diagnostics
, vol.8
, Issue.1
, pp. 62-67
-
-
Creighton, W.1
Virmani, R.2
Kutys, R.3
Burke, A.4
-
29
-
-
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
-
30
-
-
43949101679
-
Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians
-
DOI 10.1016/j.ijcard.2007.05.001, PII S0167527307008753
-
Doolan A, Langlois N, Chiu C, et al. Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians. Int J Cardiol 2008;127:138-41. (Pubitemid 351707517)
-
(2008)
International Journal of Cardiology
, vol.127
, Issue.1
, pp. 138-141
-
-
Doolan, A.1
Langlois, N.2
Chiu, C.3
Ingles, J.4
Lind, J.M.5
Semsarian, C.6
-
31
-
-
41649090413
-
Postmortem genetic testing for conventional autopsy-negative sudden unexplained death: An evaluation of different DNA extraction protocols and the feasibility of mutational analysis from archival paraffin-embedded heart tissue
-
DOI 10.1309/VLA7TT9EQ05FFVN4
-
Carturan E, Tester DJ, Brost BC, et al. Postmortem genetic testing for conventional autopsy-negative sudden unexplained death: an evaluation of different DNA extraction protocols and the feasibility of mutational analysis from archival paraffin-embedded heart tissue. Am J Clin Pathol 2008;129:391-7. (Pubitemid 352029291)
-
(2008)
American Journal of Clinical Pathology
, vol.129
, Issue.3
, pp. 391-397
-
-
Carturan, E.1
Tester, D.J.2
Brost, B.C.3
Basso, C.4
Thiene, G.5
Ackerman, M.J.6
-
32
-
-
37549007151
-
Guidelines for autopsy investigation of sudden cardiac death
-
Basso C, Burke M, Fornes P, et al. Guidelines for autopsy investigation of sudden cardiac death. Virchows Arch 2008;452:11-18.
-
(2008)
Virchows Arch
, vol.452
, pp. 11-18
-
-
Basso, C.1
Burke, M.2
Fornes, P.3
-
35
-
-
78650549525
-
Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals
-
Goldenberg I, Horr S, Moss AJ, et al. Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals. J Am Coll Cardiol 2011;57:51-9.
-
(2011)
J Am Coll Cardiol
, vol.57
, pp. 51-59
-
-
Goldenberg, I.1
Horr, S.2
Moss, A.J.3
-
36
-
-
24644515300
-
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome
-
DOI 10.1161/CIRCULATIONAHA.105.549071
-
Crotti L, Lundquist AL, Insolia R, et al. KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome. Circulation 2005;112:1251-8. (Pubitemid 41266719)
-
(2005)
Circulation
, vol.112
, Issue.9
, pp. 1251-1258
-
-
Crotti, L.1
Lundquist, A.L.2
Insolia, R.3
Pedrazzini, M.4
Ferrandi, C.5
De Ferrari, G.M.6
Vicentini, A.7
Yang, P.8
Roden, D.M.9
George Jr., A.L.10
Schwartz, P.J.11
-
37
-
-
70350540922
-
NOS1AP is a genetic modifier of the long-QT syndrome
-
Crotti L, Monti MC, Insolia R, et al. NOS1AP is a genetic modifier of the long-QT syndrome. Circulation 2009;120:1657-63.
-
(2009)
Circulation
, vol.120
, pp. 1657-1663
-
-
Crotti, L.1
Monti, M.C.2
Insolia, R.3
-
40
-
-
74849139235
-
Molecular autopsy in sudden cardiac death and its implication for families: Discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration
-
Michaud K, Fellmann F, Abriel H, et al. Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration. Swiss Med Wkly 2009;139:712-18.
-
(2009)
Swiss Med Wkly
, vol.139
, pp. 712-718
-
-
Michaud, K.1
Fellmann, F.2
Abriel, H.3
|