-
2
-
-
0029097799
-
Molecular mechanism for an inherited cardiac arrhythmia
-
Bennett PB, Yazawa K, Makita N, George AL. Molecular mechanism for an inherited cardiac arrhythmia. Nature. 1995;376:683-685.
-
(1995)
Nature
, vol.376
, pp. 683-685
-
-
Bennett, P.B.1
Yazawa, K.2
Makita, N.3
George, A.L.4
-
3
-
-
0032546384
-
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
-
Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 1998;392:293-296.
-
(1998)
Nature
, vol.392
, pp. 293-296
-
-
Chen, Q.1
Kirsch, G.E.2
Zhang, D.3
Brugada, R.4
Brugada, J.5
Brugada, P.6
Potenza, D.7
Moya, A.8
Borggrefe, M.9
Breithardt, G.10
Ortiz-Lopez, R.11
Wang, Z.12
Antzelevitch, C.13
O'Brien, R.E.14
Schulze-Bahr, E.15
Keating, M.T.16
Towbin, J.A.17
Wang, Q.18
-
4
-
-
0037376563
-
Genetic control of sodium channel function
-
Tan HL, Bezzina CR, Smits JP, Verkerk AO, Wilde AA. Genetic control of sodium channel function. Cardiovasc Res. 2003;57:961-973.
-
(2003)
Cardiovasc Res
, vol.57
, pp. 961-973
-
-
Tan, H.L.1
Bezzina, C.R.2
Smits, J.P.3
Verkerk, A.O.4
Wilde, A.A.5
-
5
-
-
0003096674
-
Cardiac conduction defects associate with mutations in SCN5A
-
Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AAM, Escande D, Mannens MMAM, Le Marec H. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet. 1999;23:20-21.
-
(1999)
Nat Genet
, vol.23
, pp. 20-21
-
-
Schott, J.J.1
Alshinawi, C.2
Kyndt, F.3
Probst, V.4
Hoorntje, T.M.5
Hulsbeek, M.6
Wilde, A.A.M.7
Escande, D.8
Mannens, M.M.A.M.9
Le Marec, H.10
-
6
-
-
0242317397
-
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)
-
Benson DW, Wang DW, Dyment M, Knilans TK, Fish FA, Strieper MJ, Rhodes TH, George AL. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). J Clin Invest. 2003;112:1019-1028.
-
(2003)
J Clin Invest
, vol.112
, pp. 1019-1028
-
-
Benson, D.W.1
Wang, D.W.2
Dyment, M.3
Knilans, T.K.4
Fish, F.A.5
Strieper, M.J.6
Rhodes, T.H.7
George, A.L.8
-
7
-
-
0033533990
-
+ channel mutation causing both long-QT and Brugada syndromes
-
+ channel mutation causing both long-QT and Brugada syndromes. Circ Res. 1999;85:1206 -1213.
-
(1999)
Circ Res
, vol.85
, pp. 1206-1213
-
-
Bezzina, C.R.1
Veldkamp, M.W.2
Van Den Berg, M.P.3
Postma, A.V.4
Rook, M.B.5
Viersma, J.W.6
Van Langen, I.M.7
Tan-Sindhunata, G.8
Bink-Boelkens, M.T.E.9
Van Der Hout, A.H.10
Mannens, M.M.11
Wilde, A.A.12
-
8
-
-
0034981834
-
Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome
-
Van den Berg MP, Wilde AAM, Viersma JW, Brouwer J, Haaksma J, van der Hout AH, Stolte-Dijkstra I, Bezzina CR, van Langen IM, Beaufort-Knol GCM, Cornel JH, Crijns HJ. Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome. J Cardiovasc Electrophysiol. 2001;12:630-636.
-
(2001)
J Cardiovasc Electrophysiol
, vol.12
, pp. 630-636
-
-
Van Den Berg, M.P.1
Wilde, A.A.M.2
Viersma, J.W.3
Brouwer, J.4
Haaksma, J.5
Van Der Hout, A.H.6
Stolte-Dijkstra, I.7
Bezzina, C.R.8
Van Langen, I.M.9
Beaufort-Knol, G.C.M.10
Cornel, J.H.11
Crijns, H.J.12
-
9
-
-
0035909898
-
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family
-
Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baró I, Moisan JP, Boisseau P, Schott JJ, Escande D, Le Marec H. Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family. Circulation. 2001;104:3081-3086.
-
(2001)
Circulation
, vol.104
, pp. 3081-3086
-
-
Kyndt, F.1
Probst, V.2
Potet, F.3
Demolombe, S.4
Chevallier, J.C.5
Baró, I.6
Moisan, J.P.7
Boisseau, P.8
Schott, J.J.9
Escande, D.10
Le Marec, H.11
-
10
-
-
0036801529
-
Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation
-
Grant AO, Carboni MP, Neplioueva V, Starmer CF, Memmi M, Napolitano C, Priori S. Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. J Clin Invest. 2002;110:1201-1209.
-
(2002)
J Clin Invest
, vol.110
, pp. 1201-1209
-
-
Grant, A.O.1
Carboni, M.P.2
Neplioueva, V.3
Starmer, C.F.4
Memmi, M.5
Napolitano, C.6
Priori, S.7
-
11
-
-
7744228426
-
Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death
-
Rossenbacker T, Carroll SJ, Liu H, Kuipéri C, de Ravel TJL, Devriendt K, Carmeliet P, Kass RS, Heidbüchel H. Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death. Heart Rhythm. 2004;1:610-615.
-
(2004)
Heart Rhythm
, vol.1
, pp. 610-615
-
-
Rossenbacker, T.1
Carroll, S.J.2
Liu, H.3
Kuipéri, C.4
De Ravel, T.J.L.5
Devriendt, K.6
Carmeliet, P.7
Kass, R.S.8
Heidbüchel, H.9
-
12
-
-
21144438184
-
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families
-
Smits JPP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MMAM, Balser JR, Tan HL, Bezzina CR, Wilde AAM. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families. J Mol Cell Cardiol. 2005;38:969-981.
-
(2005)
J Mol Cell Cardiol
, vol.38
, pp. 969-981
-
-
Smits, J.P.P.1
Koopmann, T.T.2
Wilders, R.3
Veldkamp, M.W.4
Opthof, T.5
Bhuiyan, Z.A.6
Mannens, M.M.A.M.7
Balser, J.R.8
Tan, H.L.9
Bezzina, C.R.10
Wilde, A.A.M.11
-
13
-
-
0034730085
-
The elusive link between LQT3 and Brugada syndrome. The role of flecainide challenge
-
Priori SG, Napolitano C, Schwartz PJ, Bloise R, Crotti L, Ronchetti E. The elusive link between LQT3 and Brugada syndrome. The role of flecainide challenge. Circulation. 2000;102:945-947.
-
(2000)
Circulation
, vol.102
, pp. 945-947
-
-
Priori, S.G.1
Napolitano, C.2
Schwartz, P.J.3
Bloise, R.4
Crotti, L.5
Ronchetti, E.6
-
15
-
-
0031944052
-
Measurement of heart rate and Q-T interval in the conscious mouse
-
Mitchell GF, Jeron A, Koren G. Measurement of heart rate and Q-T interval in the conscious mouse. Am J Physiol. 1998;274:H747-H751.
-
(1998)
Am J Physiol
, vol.274
-
-
Mitchell, G.F.1
Jeron, A.2
Koren, G.3
-
16
-
-
0021273027
-
Maximal upstroke velocity as an index of available sodium conductance. Comparison of maximal upstroke velocity and voltage clamp measurements of sodium current in rabbit Purkinje fibers
-
Cohen CJ, Bean BP, Tsien RW. Maximal upstroke velocity as an index of available sodium conductance. Comparison of maximal upstroke velocity and voltage clamp measurements of sodium current in rabbit Purkinje fibers. Circ Res. 1984;54:636-651.
-
(1984)
Circ Res
, vol.54
, pp. 636-651
-
-
Cohen, C.J.1
Bean, B.P.2
Tsien, R.W.3
-
17
-
-
0037134843
-
Epicardial electrograms of the right ventricular outflow tract in patients with the Brugada syndrome: Using the epicardial lead
-
Nagase S, Kusano KF, Morita H, Fujimoto Y, Kakishita M, Nakamura K, Emori T, Matsubara H, Ohe T. Epicardial electrograms of the right ventricular outflow tract in patients with the Brugada syndrome: using the epicardial lead. J Am Coll Cardiol. 2002;39:1992-1995.
-
(2002)
J Am Coll Cardiol
, vol.39
, pp. 1992-1995
-
-
Nagase, S.1
Kusano, K.F.2
Morita, H.3
Fujimoto, Y.4
Kakishita, M.5
Nakamura, K.6
Emori, T.7
Matsubara, H.8
Ohe, T.9
-
18
-
-
1642416093
-
Delay in right ventricular activation contributes to Brugada syndrome
-
Tukkie R, Sogaard P, Vleugels J, de Groot IKLM, Wilde AAM, Tan HL. Delay in right ventricular activation contributes to Brugada syndrome. Circulation. 2004;109:1272-1277.
-
(2004)
Circulation
, vol.109
, pp. 1272-1277
-
-
Tukkie, R.1
Sogaard, P.2
Vleugels, J.3
De Groot, I.K.L.M.4
Wilde, A.A.M.5
Tan, H.L.6
-
19
-
-
2942610914
-
Changes in body surface potential distributions induced by isoproterenol and Na blockers in patients with the Brugada syndrome
-
Izumida N, Asano Y, Doi S, Wakimoto H, Fukamizu S, Kimura T, Ueyama T, Sakurada H, Kawano S, Sawanobori T, Hiraoka M. Changes in body surface potential distributions induced by isoproterenol and Na blockers in patients with the Brugada syndrome. Int J Cardiol. 2004;95:261-268.
-
(2004)
Int J Cardiol
, vol.95
, pp. 261-268
-
-
Izumida, N.1
Asano, Y.2
Doi, S.3
Wakimoto, H.4
Fukamizu, S.5
Kimura, T.6
Ueyama, T.7
Sakurada, H.8
Kawano, S.9
Sawanobori, T.10
Hiraoka, M.11
-
20
-
-
27844591399
-
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: A combined electrophysiologic, genetic, histopathologic and computational study
-
Coronel R, Casini S, Koopmann TT, Wilms-Schopman FJG, Verkerk AO, de Groot JR, Bhuiyan Z, Bezzina CR, Veldkamp MW, Linnenbank AC, van der Wal AC, Tan HL, Brugada P, Wilde AA, de Bakker JM. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiologic, genetic, histopathologic and computational study. Circulation. 2005;112:2769-2777.
-
(2005)
Circulation
, vol.112
, pp. 2769-2777
-
-
Coronel, R.1
Casini, S.2
Koopmann, T.T.3
Wilms-Schopman, F.J.G.4
Verkerk, A.O.5
De Groot, J.R.6
Bhuiyan, Z.7
Bezzina, C.R.8
Veldkamp, M.W.9
Linnenbank, A.C.10
Van Der Wal, A.C.11
Tan, H.L.12
Brugada, P.13
Wilde, A.A.14
De Bakker, J.M.15
-
21
-
-
25444509189
-
Impaired impulse propagation in Scn5a-knockout mice. Combined contribution of excitability, connexin expression, and tissue architecture in relation to aging
-
Van Veen TAB, Stein M, Royer A, Le Quang K, Charpentier F, Colledge WH, Huang CLH, Wilders R, Grace AA, Escande D, de Bakker JM, van Rijen HV. Impaired impulse propagation in Scn5a-knockout mice. Combined contribution of excitability, connexin expression, and tissue architecture in relation to aging. Circulation. 2005;112:1927-1935.
-
(2005)
Circulation
, vol.112
, pp. 1927-1935
-
-
Van Veen, T.A.B.1
Stein, M.2
Royer, A.3
Le Quang, K.4
Charpentier, F.5
Colledge, W.H.6
Huang, C.L.H.7
Wilders, R.8
Grace, A.A.9
Escande, D.10
De Bakker, J.M.11
Van Rijen, H.V.12
-
22
-
-
0033379061
-
Transmural dispersion of repolarization and arrhythmogenicity: The Brugada syndrome versus the long QT syndrome
-
Antzelevitch C, Yan GX, Shimizu W. Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome. J Electrocardiol. 1999;32(Suppl):158-165.
-
(1999)
J Electrocardiol
, vol.32
, Issue.SUPPL.
, pp. 158-165
-
-
Antzelevitch, C.1
Yan, G.X.2
Shimizu, W.3
-
23
-
-
0034700276
-
Anisoptropic reentry in a perfused 2-dimensional layer of rabbit ventricular myocardium
-
Schalij MJ, Boersma L, Huijberts M, Allessie MA. Anisoptropic reentry in a perfused 2-dimensional layer of rabbit ventricular myocardium. Circulation. 2000;102:2650-2658.
-
(2000)
Circulation
, vol.102
, pp. 2650-2658
-
-
Schalij, M.J.1
Boersma, L.2
Huijberts, M.3
Allessie, M.A.4
-
24
-
-
0037066036
-
+ channel mutation that causes both Brugada and long-QT syndrome phenotypes. A simulation study of mechanism
-
+ channel mutation that causes both Brugada and long-QT syndrome phenotypes. A simulation study of mechanism. Circulation. 2002;105:1208-1213.
-
(2002)
Circulation
, vol.105
, pp. 1208-1213
-
-
Clancy, C.E.1
Rudy, Y.2
-
25
-
-
0034800266
-
Abrupt rate accelerations or premature beats cause life-threatening arrhythmias in mice with long-QT3 syndrome
-
Nuyens D, Stengl M, Dugarmaa S, Rossenbacker T, Compernolle V, Rudy Y, Smits JF, Flameng W, Clancy CE, Moons L, Vos MA, Dewerchin M, Benndorf K, Collen D, Carmeliet E, Carmeliet P. Abrupt rate accelerations or premature beats cause life-threatening arrhythmias in mice with long-QT3 syndrome. Nat Med. 2001;7:1021-1027.
-
(2001)
Nat Med
, vol.7
, pp. 1021-1027
-
-
Nuyens, D.1
Stengl, M.2
Dugarmaa, S.3
Rossenbacker, T.4
Compernolle, V.5
Rudy, Y.6
Smits, J.F.7
Flameng, W.8
Clancy, C.E.9
Moons, L.10
Vos, M.A.11
Dewerchin, M.12
Benndorf, K.13
Collen, D.14
Carmeliet, E.15
Carmeliet, P.16
-
26
-
-
24944471422
-
Sinus node dysfunction following targeted disruption of the murine cardiac sodium channel gene Scn5a
-
Lei M, Goddard C, Liu J, Léoni AL, Royer A, Fung SSM, Xiao G, Ma A, Zhang H, Charpentier F, Vandenberg JI, Colledge WH, Grace AA, Huang CL. Sinus node dysfunction following targeted disruption of the murine cardiac sodium channel gene Scn5a. J Physiol. 2005;567:387-400.
-
(2005)
J Physiol
, vol.567
, pp. 387-400
-
-
Lei, M.1
Goddard, C.2
Liu, J.3
Léoni, A.L.4
Royer, A.5
Fung, S.S.M.6
Xiao, G.7
Ma, A.8
Zhang, H.9
Charpentier, F.10
Vandenberg, J.I.11
Colledge, W.H.12
Grace, A.A.13
Huang, C.L.14
-
27
-
-
18344362987
-
Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a
-
Papadatos GA, Wallerstein PMR, Head CEG, Ratcliff R, Brady PA, Benndorf K, Saumarez RC, Trezise AEO, Huang CLH, Vandenberg JI, Colledge WH, Grace AA. Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a. Proc Natl Acad Sci U S A. 2002;99:6210-6215.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 6210-6215
-
-
Papadatos, G.A.1
Wallerstein, P.M.R.2
Head, C.E.G.3
Ratcliff, R.4
Brady, P.A.5
Benndorf, K.6
Saumarez, R.C.7
Trezise, A.E.O.8
Huang, C.L.H.9
Vandenberg, J.I.10
Colledge, W.H.11
Grace, A.A.12
-
28
-
-
0037539913
-
Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families
-
Veldkamp MW, Wilders R, Baartscheer A, Zegers JG, Bezzina CR, Wilde AAM. Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families. Circ Res. 2003;92:976-983.
-
(2003)
Circ Res
, vol.92
, pp. 976-983
-
-
Veldkamp, M.W.1
Wilders, R.2
Baartscheer, A.3
Zegers, J.G.4
Bezzina, C.R.5
Wilde, A.A.M.6
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