-
1
-
-
43049105386
-
Cardiac sodium channel overlap syndromes: Different faces of SCN5A mutations
-
Remme CA, Wilde AAM, Bezzina CR. Cardiac sodium channel overlap syndromes: Different faces of SCN5A mutations. Trend Cardiovasc Med 2008; 18: 78-87.
-
(2008)
Trend Cardiovasc Med
, vol.18
, pp. 78-87
-
-
Remme, C.A.1
Wilde, A.A.M.2
Bezzina, C.R.3
-
3
-
-
0033533990
-
A single Na+ channel mutation causing both long-QT and Brugada syndromes
-
Bezzina C, Veldkamp MW, van den Berg MP, Postma AV, Rook MB, Viersma J-W, et al. A single Na+ 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.1
Veldkamp, M.W.2
van den Berg, M.P.3
Postma, A.V.4
Rook, M.B.5
Viersma, J.-W.6
-
4
-
-
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 F, Memmi M, Napolitano C, et al. 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, F.4
Memmi, M.5
Napolitano, C.6
-
5
-
-
45749132521
-
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
-
Makita N, Behr E, Shimizu W, Horie M, Sunami A, Crotti L, et al. The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. J Clin Invest 2008; 118: 2219-2229.
-
(2008)
J Clin Invest
, vol.118
, pp. 2219-2229
-
-
Makita, N.1
Behr, E.2
Shimizu, W.3
Horie, M.4
Sunami, A.5
Crotti, L.6
-
6
-
-
84899621833
-
Flecainide provocation reveals concealed Brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A
-
Kanters JK, Yuan L, Hedley PL, Stoevring B, Jons C, Thomsen PEB, et al. Flecainide provocation reveals concealed Brugada syndrome in a long QT syndrome family with a novel L1786Q mutation in SCN5A. Circ J 2014; 78: 1136-1143.
-
(2014)
Circ J
, vol.78
, pp. 1136-1143
-
-
Kanters, J.K.1
Yuan, L.2
Hedley, P.L.3
Stoevring, B.4
Jons, C.5
Thomsen, P.E.B.6
-
7
-
-
84891708821
-
Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes
-
Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace 2013; 15: 1389-1406.
-
(2013)
Europace
, vol.15
, pp. 1389-1406
-
-
Priori, S.G.1
Wilde, A.A.2
Horie, M.3
Cho, Y.4
Behr, E.R.5
Berul, C.6
-
8
-
-
84888239192
-
Update of diagnosis and management of inherited cardiac arrhythmias
-
Shimizu W. Update of diagnosis and management of inherited cardiac arrhythmias. Circ J 2013; 77: 2867-2872.
-
(2013)
Circ J
, vol.77
, pp. 2867-2872
-
-
Shimizu, W.1
-
9
-
-
84870570379
-
Brugada syndrome: Two decades of progress
-
Veerakul G, Nademanee K. Brugada syndrome: Two decades of progress. Circ J 2012; 76: 2713-2722.
-
(2012)
Circ J
, vol.76
, pp. 2713-2722
-
-
Veerakul, G.1
Nademanee, K.2
-
10
-
-
33646386662
-
Molecular basis of ranolazine block of LQT-3 mutant sodium channels: Evidence for site of action
-
Fredj S, Sampson KJ, Liu H, Kass RS. Molecular basis of ranolazine block of LQT-3 mutant sodium channels: Evidence for site of action. Br J Pharmacol 2006; 148: 16-24
-
(2006)
Br J Pharmacol
, vol.148
, pp. 16-24
-
-
Fredj, S.1
Sampson, K.J.2
Liu, H.3
Kass, R.S.4
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