-
1
-
-
3042800339
-
Genetics of cardiac arrhythmias and sudden cardiac death
-
S. Priori, and C. Napolitano Genetics of cardiac arrhythmias and sudden cardiac death Ann N Y Acad Sci 1015 2004 96
-
(2004)
Ann N Y Acad Sci
, vol.1015
, pp. 96
-
-
Priori, S.1
Napolitano, C.2
-
2
-
-
0034487308
-
Idiopathic short QT interval: A new clinical syndrome?
-
I. Gussak, P. Brugada, and J. Brugada Idiopathic short QT interval: a new clinical syndrome? Cardiology 94 2000 99
-
(2000)
Cardiology
, vol.94
, pp. 99
-
-
Gussak, I.1
Brugada, P.2
Brugada, J.3
-
3
-
-
13444300924
-
Brugada syndrome. Report of the second consensus conference
-
C. Anztelevitch, P. Brugada, and M. Borggrefe Brugada syndrome. Report of the second consensus conference Circulation 111 2005 659
-
(2005)
Circulation
, vol.111
, pp. 659
-
-
Anztelevitch, C.1
Brugada, P.2
Borggrefe, M.3
-
4
-
-
2442698830
-
Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis
-
C. Antzelevitch Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis Ann Med 36 Suppl 1 2004 5
-
(2004)
Ann Med
, vol.36
, Issue.1 SUPPL.
, pp. 5
-
-
Antzelevitch, C.1
-
5
-
-
2442712549
-
Genes, exercise and sudden death: Molecular basis of familial catecholaminergic polymorphic ventricular tachycardia
-
P.J. Laitinen, H. Swan, and K. Piippo Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia Ann Med 36 Suppl. 1 2004 81
-
(2004)
Ann Med
, vol.36
, Issue.1 SUPPL.
, pp. 81
-
-
Laitinen, P.J.1
Swan, H.2
Piippo, K.3
-
6
-
-
20044374511
-
Double SCN5A mutation underlying asymptomatic Brugada syndrome
-
H. Yokoi, N. Makita, and K. Sasaki Double SCN5A mutation underlying asymptomatic Brugada syndrome Heart Rhythm 2 2005 285
-
(2005)
Heart Rhythm
, vol.2
, pp. 285
-
-
Yokoi, H.1
Makita, N.2
Sasaki, K.3
-
7
-
-
0037027484
-
Ambulatory electrocardiographic evidence of transmural dispersion of repolarization in patients with long-QT syndrome type 1 and 2
-
M. Viitasalo, L. Oikarinen, and H. Swan Ambulatory electrocardiographic evidence of transmural dispersion of repolarization in patients with long-QT syndrome type 1 and 2 Circulation 106 2002 2473
-
(2002)
Circulation
, vol.106
, pp. 2473
-
-
Viitasalo, M.1
Oikarinen, L.2
Swan, H.3
-
8
-
-
0035909898
-
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family
-
F. Kyndt, V. Probst, and F. Potet Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family Circulation 104 2001 3081
-
(2001)
Circulation
, vol.104
, pp. 3081
-
-
Kyndt, F.1
Probst, V.2
Potet, F.3
-
9
-
-
0037428218
-
KCNQ1 gain-of-function mutation in familial atrial fibrillation
-
Y.H. Chen, S.J. Xu, and S. Bendahhou KCNQ1 gain-of-function mutation in familial atrial fibrillation Science 299 2003 251
-
(2003)
Science
, vol.299
, pp. 251
-
-
Chen, Y.H.1
Xu, S.J.2
Bendahhou, S.3
-
10
-
-
0346727397
-
Sudden death associated with short-QT syndrome linked to mutations in HERG
-
R. Brugada, K. Hong, and R. Dumaine Sudden death associated with short-QT syndrome linked to mutations in HERG Circulation 109 2004 30
-
(2004)
Circulation
, vol.109
, pp. 30
-
-
Brugada, R.1
Hong, K.2
Dumaine, R.3
-
11
-
-
19944433739
-
Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG
-
C. Wolpert, R. Schimpf, and C. Giustetto Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG J Cardiovasc Electrophysiol 16 2005 54
-
(2005)
J Cardiovasc Electrophysiol
, vol.16
, pp. 54
-
-
Wolpert, C.1
Schimpf, R.2
Giustetto, C.3
-
12
-
-
14744273673
-
Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RYR2 mutations
-
H. Swan, P. Laitinen, K. Kontula, and L. Toivonen Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RYR2 mutations J Cardiovasc Electrophysiol 16 2005 162
-
(2005)
J Cardiovasc Electrophysiol
, vol.16
, pp. 162
-
-
Swan, H.1
Laitinen, P.2
Kontula, K.3
Toivonen, L.4
-
13
-
-
0037454049
-
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease
-
V. Probst, F. Kyndt, and F. Potet Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease J Am Coll Cardiol 41 2003 643
-
(2003)
J Am Coll Cardiol
, vol.41
, pp. 643
-
-
Probst, V.1
Kyndt, F.2
Potet, F.3
-
14
-
-
0036324229
-
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
-
M. Tristani-Firouzi, J.L. Jensen, and M.R. Donaldson Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) J Clin Invest 110 2002 381
-
(2002)
J Clin Invest
, vol.110
, pp. 381
-
-
Tristani-Firouzi, M.1
Jensen, J.L.2
Donaldson, M.R.3
-
16
-
-
0242713010
-
A new oral therapy for long QT syndrome. Long-term oral potassium improves repolarization in patients with HERG mutations
-
S.P. Etheridge, S.J. Compton, M. Tristani-Firouzi, and J.W. Mason A new oral therapy for long QT syndrome. Long-term oral potassium improves repolarization in patients with HERG mutations J Am Coll Cardiol 42 2003 1777
-
(2003)
J Am Coll Cardiol
, vol.42
, pp. 1777
-
-
Etheridge, S.P.1
Compton, S.J.2
Tristani-Firouzi, M.3
Mason, J.W.4
-
17
-
-
2442662544
-
Novel therapeutics for treatment of long-QT syndrome and torsade de pointes
-
I.A. Khan, and R.M. Gowda Novel therapeutics for treatment of long-QT syndrome and torsade de pointes Int J Cardiol 95 2004 1
-
(2004)
Int J Cardiol
, vol.95
, pp. 1
-
-
Khan, I.A.1
Gowda, R.M.2
-
19
-
-
20044368228
-
Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome
-
C. Wolpert, C. Echternach, and C. Veltmann Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome Heart Rhythm 2 2005 254
-
(2005)
Heart Rhythm
, vol.2
, pp. 254
-
-
Wolpert, C.1
Echternach, C.2
Veltmann, C.3
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