-
1
-
-
0024205817
-
Community study of the causes of "natural" sudden death
-
Thomas AC, Knapman PA, Krikler DM, et al. Community study of the causes of "natural" sudden death. BMJ 1988;297:1453-6.
-
(1988)
BMJ
, vol.297
, pp. 1453-1456
-
-
Thomas, A.C.1
Knapman, P.A.2
Krikler, D.M.3
-
2
-
-
0026669899
-
Unexplained death in fit young people
-
Davies MJ. Unexplained death in fit young people. BMJ 1992;305:538-9.
-
(1992)
BMJ
, vol.305
, pp. 538-539
-
-
Davies, M.J.1
-
3
-
-
0037384929
-
Sudden, unexpected cardiac or unexplained death in England: A national survey
-
Bowker TJ, Wood DA, Davies MJ, et al. Sudden, unexpected cardiac or unexplained death in England: a national survey. QJM 2003;96:269-79.
-
(2003)
QJM
, vol.96
, pp. 269-279
-
-
Bowker, T.J.1
Wood, D.A.2
Davies, M.J.3
-
4
-
-
0029068145
-
Sudden unexpected nontraumatic death in 54 young adults: A 30-year population-based study
-
Shen WK, Edwards WD, Hammill SC, et al. Sudden unexpected nontraumatic death in 54 young adults: a 30-year population-based study. Am J Cardiol 1995;76:148-52.
-
(1995)
Am J Cardiol
, vol.76
, pp. 148-152
-
-
Shen, W.K.1
Edwards, W.D.2
Hammill, S.C.3
-
5
-
-
0025748647
-
Sudden unexpected death in persons less than 40 years of age
-
Drory Y, Turetz Y, Hiss Y, et al. Sudden unexpected death in persons less than 40 years of age. Am J Cardiol 1991;68:1388- 92.
-
(1991)
Am J Cardiol
, vol.68
, pp. 1388-1392
-
-
Drory, Y.1
Turetz, Y.2
Hiss, Y.3
-
6
-
-
0032939409
-
Cardiovascular causes of sudden death in young individuals including athletes
-
Basso C, Corrado D, Thiene G. Cardiovascular causes of sudden death in young individuals including athletes. Cardiol Rev 1999;7:127-35.
-
(1999)
Cardiol Rev
, vol.7
, pp. 127-135
-
-
Basso, C.1
Corrado, D.2
Thiene, G.3
-
7
-
-
49749174698
-
Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death
-
Jervell A, Lange-Nielsen F. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death. Am Heart J 1957;54:59.
-
(1957)
Am Heart J
, vol.54
, pp. 59
-
-
Jervell, A.1
Lange-Nielsen, F.2
-
9
-
-
0000387603
-
New familial cardiac syndrome in children
-
Ward OC. New familial cardiac syndrome in children. J Irish Med Assoc 1964;54:103.
-
(1964)
J Irish Med Assoc
, vol.54
, pp. 103
-
-
Ward, O.C.1
-
10
-
-
0242329842
-
Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome
-
Behr E, Wood DA, Wright M, et al. Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome. Lancet 2003;362:1457-9.
-
(2003)
Lancet
, vol.362
, pp. 1457-1459
-
-
Behr, E.1
Wood, D.A.2
Wright, M.3
-
11
-
-
0021129260
-
Hypertrophic cardiomyopathy: An important cause of sudden death
-
McKenna WJ, Deanfield JE. Hypertrophic cardiomyopathy: an important cause of sudden death. Arch Dis Child 1984;59:971-5.
-
(1984)
Arch Dis Child
, vol.59
, pp. 971-975
-
-
McKenna, W.J.1
Deanfield, J.E.2
-
12
-
-
0036153781
-
Hypertrophic cardiomyopathy: Management, risk stratification, and prevention of sudden death
-
McKenna WJ, Behr ER. Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death. Heart 2002;87:169-76.
-
(2002)
Heart
, vol.87
, pp. 169-176
-
-
McKenna, W.J.1
Behr, E.R.2
-
14
-
-
22144439771
-
Sudden unexplained death: Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives
-
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.
-
(2005)
Circulation
, vol.112
, pp. 207-213
-
-
Tan, H.L.1
Hofman, N.2
van Langen, I.M.3
-
15
-
-
0035969990
-
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
-
Laitinen PJ, Brown KM, Piippo K, et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 2001;103:485-90.
-
(2001)
Circulation
, vol.103
, pp. 485-490
-
-
Laitinen, P.J.1
Brown, K.M.2
Piippo, K.3
-
16
-
-
0035895322
-
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
-
Priori SG, Napolitano C, Tiso N, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 2001;103:196-200.
-
(2001)
Circulation
, vol.103
, pp. 196-200
-
-
Priori, S.G.1
Napolitano, C.2
Tiso, N.3
-
17
-
-
0035205336
-
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
-
Lahat H, Pras E, Olender T, et al. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am J Hum Genet 2001;69:1378-84.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1378-1384
-
-
Lahat, H.1
Pras, E.2
Olender, T.3
-
18
-
-
0034609531
-
Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
-
Splawski I, Shen J, Timothy KW, et al. Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 2000;102:1178-85.
-
(2000)
Circulation
, vol.102
, pp. 1178-1185
-
-
Splawski, I.1
Shen, J.2
Timothy, K.W.3
-
19
-
-
0026466921
-
Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. A multicenter report
-
Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol 1992;20:1391-6.
-
(1992)
J Am Coll Cardiol
, vol.20
, pp. 1391-1396
-
-
Brugada, P.1
Brugada, J.2
-
20
-
-
0034649298
-
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families
-
Priori SG, Napolitano C, Gasparini M, et al. Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: a prospective evaluation of 52 families. Circulation 2000;102:2509-15.
-
(2000)
Circulation
, vol.102
, pp. 2509-2515
-
-
Priori, S.G.1
Napolitano, C.2
Gasparini, M.3
-
21
-
-
0032546384
-
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
-
Chen Q, Kirsch GE, Zhang D, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 1998;392:293-6.
-
(1998)
Nature
, vol.392
, pp. 293-296
-
-
Chen, Q.1
Kirsch, G.E.2
Zhang, D.3
-
22
-
-
0030712343
-
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: A multicenter study
-
Corrado D, Basso C, Thiene G, et al. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. J Am Coll Cardiol 1997;30:1512-20.
-
(1997)
J Am Coll Cardiol
, vol.30
, pp. 1512-1520
-
-
Corrado, D.1
Basso, C.2
Thiene, G.3
-
23
-
-
0028347223
-
Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology
-
McKenna WJ, Thiene G, Nava A, et al. Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology. Br Heart J 1994;71:215-18.
-
(1994)
Br Heart J
, vol.71
, pp. 215-218
-
-
McKenna, W.J.1
Thiene, G.2
Nava, A.3
-
25
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
Curran ME, Splawski I, Timothy KW, et al. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 1995;80:795-803.
-
(1995)
Cell
, vol.80
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
-
26
-
-
0346727397
-
Sudden death associated with short-QT syndrome linked to mutations in HERG
-
Brugada R, Hong K, Dumaine R, et al. Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation 2004;109:30-5.
-
(2004)
Circulation
, vol.109
, pp. 30-35
-
-
Brugada, R.1
Hong, K.2
Dumaine, R.3
-
27
-
-
0042859880
-
Short QT syndrome: A familial cause of sudden death
-
Gaita F, Giustetto C, Bianchi F, et al. Short QT syndrome: a familial cause of sudden death. Circulation 2003;108:965-70.
-
(2003)
Circulation
, vol.108
, pp. 965-970
-
-
Gaita, F.1
Giustetto, C.2
Bianchi, F.3
-
28
-
-
2342440911
-
Postmortem molecular screening in unexplained sudden death
-
Chugh SS, Senashova O, Watts A, et al. Postmortem molecular screening in unexplained sudden death. J Am Coll Cardiol 2004;43:1625-9.
-
(2004)
J Am Coll Cardiol
, vol.43
, pp. 1625-1629
-
-
Chugh, S.S.1
Senashova, O.2
Watts, A.3
-
29
-
-
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.
-
(2004)
Mayo Clin Proc
, vol.79
, pp. 1380-1384
-
-
Tester, D.J.1
Spoon, D.B.2
Valdivia, H.H.3
-
30
-
-
2942695712
-
A cardiac arrhythmia syndrome caused by loss of ankyrin-B function
-
Mohler PJ, Splawski I, Napolitano C, et al. A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. Proc Natl Acad Sci USA 2004;101:9137-142.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 9137-9142
-
-
Mohler, P.J.1
Splawski, I.2
Napolitano, C.3
-
31
-
-
0242464931
-
Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death
-
Mohler PJ, Schott JJ, Gramolini AO, et al. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature 2003;421:634-9.
-
(2003)
Nature
, vol.421
, pp. 634-639
-
-
Mohler, P.J.1
Schott, J.J.2
Gramolini, A.O.3
-
32
-
-
0035907032
-
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
-
Plaster NM, Tawil R, Tristani-Firouzi M, et al. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. Cell 2001;105:511-19.
-
(2001)
Cell
, vol.105
, pp. 511-519
-
-
Plaster, N.M.1
Tawil, R.2
Tristani-Firouzi, M.3
-
33
-
-
5344223383
-
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
-
Splawski I, Timothy KW, Sharpe LM, et al. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Cell 2004;119:19-31.
-
(2004)
Cell
, vol.119
, pp. 19-31
-
-
Splawski, I.1
Timothy, K.W.2
Sharpe, L.M.3
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