-
1
-
-
84889419405
-
Epidemiology of cardiac arrest
-
In: Priori S.G., Zipes D.P. (eds.):. Malden, MA, Blackwell Publishing, pp.
-
Myerburg RJ, Wellens HJJ,. Epidemiology of cardiac arrest. In:, Priori SG, Zipes DP, (eds.): Sudden Cardiac Death. A Handbook for Clinical Practice. Malden, MA, Blackwell Publishing, 2006, pp. 3-20.
-
(2006)
Sudden Cardiac Death. A Handbook for Clinical Practice
, pp. 3-20
-
-
Myerburg, R.J.1
Wellens, H.J.J.2
-
2
-
-
0031940866
-
Family history as a risk factor for primary cardiac arrest
-
Friedlander Y, Siscovick DS, Weinmann S, Austin MA, Psaty BM, Lemaitre RN, Arbogast P, et al,. Family history as a risk factor for primary cardiac arrest. Circulation 1998; 97: 155-160. (Pubitemid 28124672)
-
(1998)
Circulation
, vol.97
, Issue.2
, pp. 155-160
-
-
Friedlander, Y.1
Siscovick, D.S.2
Weinmann, S.3
Austin, M.A.4
Psaty, B.M.5
Lemaitre, R.N.6
Arbogast, P.7
Raghunathan, T.E.8
Cobb, L.A.9
-
3
-
-
0033586647
-
Predicting sudden death in the population. The Paris prospective study I
-
Jouvan X, Desnos M, Guerot C, Ducimetière P,. Predicting sudden death in the population: The Paris Prospective Study I. Circulation 1999; 99: 1978-1983. (Pubitemid 29183894)
-
(1999)
Circulation
, vol.99
, Issue.15
, pp. 1978-1983
-
-
Jouven, X.1
Desnos, M.2
Guerot, C.3
Ducimetiere, P.4
-
4
-
-
33749527092
-
Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event
-
DOI 10.1161/CIRCULATIONAHA.106.624593, PII 0000301720061003000007
-
Kaikkonen KS, Kortelainen ML, Linna E, Huikuri HV,. Family history and the risk of sudden cardiac death as a manifestation of an acute coronary event. Circulation 2006; 114: 1462-1467. (Pubitemid 44527000)
-
(2006)
Circulation
, vol.114
, Issue.14
, pp. 1462-1467
-
-
Kaikkonen, K.S.1
Kortelainen, M.-L.2
Linna, E.3
Huikuri, H.V.4
-
5
-
-
33748640974
-
Familial sudden death is an important risk factor for primary ventricular fibrillation: A case-control study in acute myocardial infarction patients
-
DOI 10.1161/CIRCULATIONAHA.105.606145, PII 0000301720060912000005
-
Dekker LR, Bezzina CR, Henriques JP, Tanck MW, Koch KT, Alings MW, Arnold AER, et al,. Familial sudden death is an important risk factor for primary ventricular fibrillation: A case-control study in acute myocardial infarction patients. Circulation 2006; 114: 1140-1145. (Pubitemid 44386477)
-
(2006)
Circulation
, vol.114
, Issue.11
, pp. 1140-1145
-
-
Dekker, L.R.C.1
Bezzina, C.R.2
Henriques, J.P.S.3
Tanck, M.W.4
Koch, K.T.5
Alings, M.W.6
Arnold, A.E.R.7
De Boer, M.-J.8
Gorgels, A.P.M.9
Michels, H.R.10
Verkerk, A.11
Verheugt, F.W.A.12
Zijlstra, F.13
Wilde, A.A.M.14
-
6
-
-
0033514263
-
Low penetrance in the long-QT syndrome clinical impact
-
Priori SG, Napolitano C, Schwarz PJ,. Low penetrance in the long-QT syndrome: Clinical impact. Circulation 1999; 99: 529-533. (Pubitemid 29061868)
-
(1999)
Circulation
, vol.99
, Issue.4
, pp. 529-533
-
-
Priori, S.G.1
Napolitano, C.2
Schwartz, P.J.3
-
7
-
-
70449367296
-
Prevalence of the congenital long-QT syndrome
-
Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G, Gabbarini F, et al,. Prevalence of the congenital long-QT syndrome. Circulation 2009; 120: 1761-1767.
-
(2009)
Circulation
, vol.120
, pp. 1761-1767
-
-
Schwartz, P.J.1
Stramba-Badiale, M.2
Crotti, L.3
Pedrazzini, M.4
Besana, A.5
Bosi, G.6
Gabbarini, F.7
-
8
-
-
0032966760
-
A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome
-
DOI 10.1016/S0009-8981(98)00177-6, PII S0009898198001776
-
Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M,. A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome. Clin Chim Acta 1999; 280: 113-125. (Pubitemid 29094587)
-
(1999)
Clinica Chimica Acta
, vol.280
, Issue.1-2
, pp. 113-125
-
-
Larsen, L.A.1
Andersen, P.S.2
Kanters, J.K.3
Jacobsen, J.R.4
Vuust, J.5
Christiansen, M.6
-
9
-
-
17344389134
-
Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1
-
DOI 10.1006/geno.1998.5361
-
Splawski I, Shen J, Timothy KW, Vincent GM, Lehman MH, Keating MT,. Genomic structure of three long QT syndrome genes: KVLQT1, HERG and KCNE1. Genomics 1998; 51: 86-97. (Pubitemid 28373376)
-
(1998)
Genomics
, vol.51
, Issue.1
, pp. 86-97
-
-
Splawski, I.1
Shen, J.2
Timothy, K.W.3
Vincent, G.M.4
Lehmann, M.H.5
Keating, M.T.6
-
10
-
-
0034796020
-
Mutation detection in long QT syndrome: A comprehensive set of primers and PCR conditions [5]
-
Syrris P, Murray A, Carter ND, McKenna WM, Jeffery S,. Mutation detection in long QT syndrome: A comprehensive set of primers and PCR conditions. J Med Genet 2001; 38: 705-710. (Pubitemid 32946794)
-
(2001)
Journal of Medical Genetics
, vol.38
, Issue.10
, pp. 705-710
-
-
Syrris, P.1
Murray, A.2
Carter, N.D.3
McKenna, W.M.4
Jeffery, S.5
-
11
-
-
0034609531
-
Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
-
Splawski I, Shen J, Timothy KW, Lehmann MH, Priori SG, Robinson JL, Moss AJ, et al,. Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 2000; 102: 1178-1185.
-
(2000)
Circulation
, vol.102
, pp. 1178-1185
-
-
Splawski, I.1
Shen, J.2
Timothy, K.W.3
Lehmann, M.H.4
Priori, S.G.5
Robinson, J.L.6
Moss, A.J.7
-
12
-
-
7744243863
-
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
-
DOI 10.1016/j.hrthm.2004.07.013, PII S1547527104004047
-
Ackerman MJ, Splawski I, Makielski JC, Tester DJ, Will ML, Timothy KW, Keating MT, et al,. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing. Heart Rhythm 2004; 1: 600-607. (Pubitemid 39462721)
-
(2004)
Heart Rhythm
, vol.1
, Issue.5
, pp. 600-607
-
-
Ackerman, M.J.1
Splawski, I.2
Makielski, J.C.3
Tester, D.J.4
Will, M.L.5
Timothy, K.W.6
Keating, M.T.7
Jones, G.8
Chadha, M.9
Burrow, C.R.10
Stephens, J.C.11
Xu, C.12
Judson, R.13
Curran, M.E.14
-
13
-
-
33846425740
-
Cardiac sodium channel dysfunction in sudden infant death syndrome
-
DOI 10.1161/CIRCULATIONAHA.106.646513, PII 0000301720070123000015
-
Wang DW, Desai RR, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, et al,. Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation 2007; 115: 368-376. (Pubitemid 46148511)
-
(2007)
Circulation
, vol.115
, Issue.3
, pp. 368-376
-
-
Wang, D.W.1
Desai, R.R.2
Crotti, L.3
Arnestad, M.4
Insolia, R.5
Pedrazzini, M.6
Ferrandi, C.7
Vege, A.8
Rognum, T.9
Schwartz, P.J.10
George, A.L.11
-
14
-
-
33646777139
-
Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease
-
Stecker EC, Sono M, Wallace E, Gunson K, Jui J, Chugh SS,. Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease. Heart Rhythm 2006; 3: 697-700.
-
(2006)
Heart Rhythm
, vol.3
, pp. 697-700
-
-
Stecker, E.C.1
Sono, M.2
Wallace, E.3
Gunson, K.4
Jui, J.5
Chugh, S.S.6
-
15
-
-
37349080496
-
Cardiac sodium channel gene variants and sudden cardiac death in women
-
DOI 10.1161/CIRCULATIONAHA.107.736330
-
Albert CM, Nam EG, Rimm EB, Jin HW, Hajjar RJ, Hunter DJ, MacRae CA, et al,. Cardiac sodium channel gene variants and sudden cardiac death in women. Circulation 2008; 117: 16-23. (Pubitemid 350301143)
-
(2008)
Circulation
, vol.117
, Issue.1
, pp. 16-23
-
-
Albert, C.M.1
Nam, E.G.2
Rimm, E.B.3
Jin, H.W.4
Hajjar, R.J.5
Hunter, D.J.6
MacRae, C.A.7
Ellinor, P.T.8
-
16
-
-
84889341201
-
Clinical characteristics of sudden cardiac death victims and precipitating events
-
In: Priori S.G., Zipes D.P. (eds.):. Malden, MA, Blackwell Publishing, pp.
-
Albert MA, Cobbe SM,. Clinical characteristics of sudden cardiac death victims and precipitating events. In:, Priori SG, Zipes DP, (eds.): Sudden Cardiac Death. A Handbook for Clinical Practice. Malden, MA, Blackwell Publishing, 2006, pp. 74-87.
-
(2006)
Sudden Cardiac Death. A Handbook for Clinical Practice
, pp. 74-87
-
-
Albert, M.A.1
Cobbe, S.M.2
-
17
-
-
0032066007
-
Taking the idio out of idiosyncratic - Predicting torsades de pointes
-
Roden DM,. Taking the idio out of idiosyncratic-predicting torsades de pointes. Pacing Clin Electrophysiol 1998; 21: 1029-1034.
-
(1998)
Pacing Clin Electrophysiol
, vol.21
, pp. 1029-1034
-
-
Roden, D.M.1
-
19
-
-
33845383109
-
Modulation of HERG gating by a charge cluster in the N-terminal proximal domain
-
DOI 10.1529/biophysj.106.087247
-
Saenen JB, Labro AJ, Raes A, Snyders DJ,. Modulation of HERG gating by a charge cluster in the N-terminal proximal domain. Biophys J 2006; 91: 4381-4391. (Pubitemid 44904225)
-
(2006)
Biophysical Journal
, vol.91
, Issue.12
, pp. 4381-4391
-
-
Saenen, J.B.1
Labro, A.J.2
Raes, A.3
Snyders, D.J.4
-
20
-
-
0345690174
-
Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT Syndrome
-
Ackerman MJ, Tester DJ, Jones G, Will MK, Burrow CR, Curran M,. Ethnic differences in cardiac potassium channel variants: Implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome. Mayo Clin Proc 2003; 78: 1479-1487. (Pubitemid 37475631)
-
(2003)
Mayo Clinic Proceedings
, vol.78
, Issue.12
, pp. 1479-1487
-
-
Ackerman, M.J.1
Tester, D.J.2
Jones, G.S.3
Will, M.L.4
Burrow, C.R.5
Curran, M.E.6
-
21
-
-
15044363738
-
Single nucleotide polymorphism map of five long-QT genes
-
DOI 10.1007/s00109-004-0595-3
-
Aydin A, Bähring S, Dahm S, Guenther UP, Uhlmann R, Busjahn A, Luft FC,. Single nucleotide polymorphism map of five long-QT genes. J Mol Med 2005; 83: 159-165. (Pubitemid 40379304)
-
(2005)
Journal of Molecular Medicine
, vol.83
, Issue.2
, pp. 159-165
-
-
Aydin, A.1
Bahring, S.2
Dahm, S.3
Guenther, U.P.4
Uhlmann, R.5
Busjahn, A.6
Luft, F.C.7
-
22
-
-
34249088350
-
Genome-wide transcription and the implications for genomic organization
-
DOI 10.1038/nrg2083, PII NRG2083
-
Kapranov P, Willingham AT, Gingeras TR,. Genome-wide transcription and the implications for genomic organization. Nat Rev Genet 2007; 8: 413-423. (Pubitemid 46789245)
-
(2007)
Nature Reviews Genetics
, vol.8
, Issue.6
, pp. 413-423
-
-
Kapranov, P.1
Willingham, A.T.2
Gingeras, T.R.3
-
23
-
-
65349160903
-
Sudden cardiac death: The larger problem... The larger genome
-
Spooner PM,. Sudden cardiac death: The larger problem...the larger genome. J Cardiovasc Electrophysiol 2009; 20: 585-596.
-
(2009)
J Cardiovasc Electrophysiol
, vol.20
, pp. 585-596
-
-
Spooner, P.M.1
|