-
1
-
-
0015417934
-
Ventricular fibrillation occurring on arousal from sleep by auditory stimuli
-
Wellens H.J.J., Vermeulen A., Durrer D. Ventricular fibrillation occurring on arousal from sleep by auditory stimuli. Circulation. 46:1972;661-665.
-
(1972)
Circulation
, vol.46
, pp. 661-665
-
-
Wellens, H.J.J.1
Vermeulen, A.2
Durrer, D.3
-
2
-
-
0028332312
-
Epinephrine-induced ventricular premature complexes due to early afterdepolarizations and effects of verapamil and propranolol in a patient with congenital long QT syndrome
-
Shimizu W., Ohe T., Kurita T., Tokuda T., Shimomura K. Epinephrine-induced ventricular premature complexes due to early afterdepolarizations and effects of verapamil and propranolol in a patient with congenital long QT syndrome. J Cardiovasc Electrophysiol. 5:1994;438-444.
-
(1994)
J Cardiovasc Electrophysiol
, vol.5
, pp. 438-444
-
-
Shimizu, W.1
Ohe, T.2
Kurita, T.3
Tokuda, T.4
Shimomura, K.5
-
3
-
-
0029016795
-
Auditory stimuli as a major cause of syncope in a patient with idiopathic long QT syndrome
-
Nakajima T., Misu K., Iwasawa K., et al. Auditory stimuli as a major cause of syncope in a patient with idiopathic long QT syndrome. Jpn Circ J. 59:1995;241-246.
-
(1995)
Jpn Circ J
, vol.59
, pp. 241-246
-
-
Nakajima, T.1
Misu, K.2
Iwasawa, K.3
-
4
-
-
0025847714
-
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
-
Keating M.T., Atkinson D.L., Dunn C., Timothy K.W., Vincent G.M., Leppert M. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science. 252:1991;704-706.
-
(1991)
Science
, vol.252
, pp. 704-706
-
-
Keating, M.T.1
Atkinson, D.L.2
Dunn, C.3
Timothy, K.W.4
Vincent, G.M.5
Leppert, M.6
-
5
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
Curran M.E., Splawski I., Timothy K.W., Vincent G.M., Green E.D., Keating M.T. A molecular basis for cardiac arrhythmia HERG mutations cause long QT syndrome. Cell. 80:1995;795-803.
-
(1995)
Cell
, vol.80
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
Vincent, G.M.4
Green, E.D.5
Keating, M.T.6
-
6
-
-
0028905566
-
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
-
Wang Q., Shen J., Splawski I., et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 80:1995;805-811.
-
(1995)
Cell
, vol.80
, pp. 805-811
-
-
Wang, Q.1
Shen, J.2
Splawski, I.3
-
7
-
-
0028819671
-
Mapping of a gene for long QT syndrome to chromosome 4q25-27
-
Schott J.J., Charpentier F., Peltier S., et al. Mapping of a gene for long QT syndrome to chromosome 4q25-27. Am J Hum Genet. 57:1995;1114-1122.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1114-1122
-
-
Schott, J.J.1
Charpentier, F.2
Peltier, S.3
-
8
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KvLQT1 mutations cause cardiac arrhythmias
-
Wang Q., Curran M.E., Splawski I., et al. Positional cloning of a novel potassium channel gene KvLQT1 mutations cause cardiac arrhythmias. Nat Genet. 12:1996;17-23.
-
(1996)
Nat Genet
, vol.12
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
-
10
-
-
0030247934
-
The roles of ion channels in an inherited heart disease: Molecular genetics of the long QT syndrome
-
Kass R.S., Davies M.P. The roles of ion channels in an inherited heart disease molecular genetics of the long QT syndrome. Cardiovasc Res. 32:1996;443-454.
-
(1996)
Cardiovasc Res
, vol.32
, pp. 443-454
-
-
Kass, R.S.1
Davies, M.P.2
-
11
-
-
0029847602
-
Multiple mechanisms in the long QT syndrome. Current knowledge, gaps, and future directions
-
Roden D.M., Lazzara R., Rosen M., et al. Multiple mechanisms in the long QT syndrome. Current knowledge, gaps, and future directions. Circulation. 94:1996;1996-2012.
-
(1996)
Circulation
, vol.94
, pp. 1996-2012
-
-
Roden, D.M.1
Lazzara, R.2
Rosen, M.3
-
12
-
-
0028861892
-
ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
-
Moss A.J., Zareba W., Benhorin J., et al. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome. Circulation. 92:1995;2929-2934.
-
(1995)
Circulation
, vol.92
, pp. 2929-2934
-
-
Moss, A.J.1
Zareba, W.2
Benhorin, J.3
-
13
-
-
0029824105
-
ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2)
-
Schultze-Bahr E., Haverkamp W., Breithardt G., Funke H., Wiebusch H., Assmann G. ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2). Circulation. 94:1996;2318-2319.
-
(1996)
Circulation
, vol.94
, pp. 2318-2319
-
-
Schultze-Bahr, E.1
Haverkamp, W.2
Breithardt, G.3
Funke, H.4
Wiebusch, H.5
Assmann, G.6
-
14
-
-
0001197981
-
Gene-specific influence on the triggers for cardiac arrest in the long QT syndrome
-
Schwartz PJ, Moss AJ, Priori SG, et al. Gene-specific influence on the triggers for cardiac arrest in the long QT syndrome [abstract]. Circulation 1997;96:I-212.
-
(1997)
Circulation
, vol.96
-
-
Schwartz, P.J.1
Moss, A.J.2
Priori, S.G.3
-
16
-
-
0024791277
-
An efficient salt-chloroform extraction of DNA from blood and tissues
-
Müllerbach R., Lagoda P.J.L., Welter C. An efficient salt-chloroform extraction of DNA from blood and tissues. Trends Genet. 5:1989;391.
-
(1989)
Trends Genet
, vol.5
, pp. 391
-
-
Müllerbach, R.1
Lagoda, P.J.L.2
Welter, C.3
-
17
-
-
0030924035
-
The long QT syndrome: A novel missense mutation in the S6 region of the KVLQT1 gene
-
Van den Berg M.H., Wilde A.A.M., Robles de Medina E.O., et al. The long QT syndrome a novel missense mutation in the S6 region of the KVLQT1 gene. Hum Genet. 100:1997;356-361.
-
(1997)
Hum Genet
, vol.100
, pp. 356-361
-
-
Van Den Berg, M.H.1
Wilde, A.A.M.2
Robles De Medina, E.O.3
-
19
-
-
0026759352
-
The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome
-
Vincent G.M., Timothy K.W., Leppert M., Keating M.T. The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome. N Engl J Med. 327:1992;846-852.
-
(1992)
N Engl J Med
, vol.327
, pp. 846-852
-
-
Vincent, G.M.1
Timothy, K.W.2
Leppert, M.3
Keating, M.T.4
-
20
-
-
0030016059
-
Evidence of a long QT founder gene with varying phenotypic expression in South African families
-
de Jager T., Corbett C.H., Badenhorst J.C.W., Brink P.A., Corfield V.A. Evidence of a long QT founder gene with varying phenotypic expression in South African families. J Med Genet. 33:1996;567-573.
-
(1996)
J Med Genet
, vol.33
, pp. 567-573
-
-
De Jager, T.1
Corbett, C.H.2
Badenhorst, J.C.W.3
Brink, P.A.4
Corfield, V.A.5
-
21
-
-
4243341517
-
Cellular basis for the electrocardiographic features of the LQT1 form of the long QT syndrome: Effects of β-adrenergic agonists, antagonists and sodium channel blockers on transmural dispersion of repolarization and torsades de pointes [abstract]
-
Shimizu W., Antzelevitch C. Cellular basis for the electrocardiographic features of the LQT1 form of the long QT syndrome effects of β-adrenergic agonists, antagonists and sodium channel blockers on transmural dispersion of repolarization and torsades de pointes [abstract]. J Am Coll Cardiol. 31:1998;2A.
-
(1998)
J Am Coll Cardiol
, vol.31
-
-
Shimizu, W.1
Antzelevitch, C.2
-
22
-
-
0029887380
-
+ channel blockade, β-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long QT syndrome
-
+ channel blockade, β-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long QT syndrome. Circ Res. 78:1996;1009-1015.
-
(1996)
Circ Res
, vol.78
, pp. 1009-1015
-
-
Priori, S.G.1
Napolitano, C.2
Cantu, F.3
Brown, A.M.4
Schwartz, P.J.5
-
23
-
-
0030819433
-
Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsades de pointes in LQT2 and LQT3 models of the long QT syndrome
-
Shimizu W., Antzelevitch C. Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsades de pointes in LQT2 and LQT3 models of the long QT syndrome. Circulation. 96:1997;2038-2047.
-
(1997)
Circulation
, vol.96
, pp. 2038-2047
-
-
Shimizu, W.1
Antzelevitch, C.2
-
24
-
-
0030298484
-
Mode of onset of torsades de pointes in congenital long QT syndrome
-
Viskin S., Alla S.R., Barron H.V., et al. Mode of onset of torsades de pointes in congenital long QT syndrome. J Am Coll Cardiol. 28:1996;1262-1268.
-
(1996)
J Am Coll Cardiol
, vol.28
, pp. 1262-1268
-
-
Viskin, S.1
Alla, S.R.2
Barron, H.V.3
-
25
-
-
0030218890
-
A mutation in HERG associated with notched T-waves in long QT syndrome
-
Dausse E., Berthet M., Denjoy I., et al. A mutation in HERG associated with notched T-waves in long QT syndrome. J Mol Cell Cardiol. 28:1996;1609-1615.
-
(1996)
J Mol Cell Cardiol
, vol.28
, pp. 1609-1615
-
-
Dausse, E.1
Berthet, M.2
Denjoy, I.3
-
26
-
-
0013516545
-
Differences in precipitators of cardiac arrest and sudden death in chromosome 11 versus 7 genotype long QT syndrome patients
-
Timothy KW, Zhang L, Meyer KJ, Vincent GM. Differences in precipitators of cardiac arrest and sudden death in chromosome 11 versus 7 genotype long QT syndrome patients [abstract]. Circulation 1996;94:I-204.
-
(1996)
Circulation
, vol.94
-
-
Timothy, K.W.1
Zhang, L.2
Meyer, K.J.3
Vincent, G.M.4
-
27
-
-
0001383792
-
Identification in a mutational hot spot in HERG-related long QT syndrome (LQT2): Phenotypic implications
-
Napolitano C, Priori SG, Schwartz PJ, et al. Identification in a mutational hot spot in HERG-related long QT syndrome (LQT2): phenotypic implications [abstract]. Circulation 1997;96:I-212.
-
(1997)
Circulation
, vol.96
-
-
Napolitano, C.1
Priori, S.G.2
Schwartz, P.J.3
-
28
-
-
0025940097
-
Early afterdepolarizations induced by isoproterenol in patients with congenital long QT syndrome
-
Shimizu W., Ohe T., Kurita T., et al. Early afterdepolarizations induced by isoproterenol in patients with congenital long QT syndrome. Circulation. 84:1991;1915-1923.
-
(1991)
Circulation
, vol.84
, pp. 1915-1923
-
-
Shimizu, W.1
Ohe, T.2
Kurita, T.3
-
30
-
-
0025963987
-
Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes: Mechanism of action
-
Sanguinetti M.C., Jurkiewicz N.K., Scott A., Siegl P.K.S. Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes mechanism of action. Circ Res. 68:1991;77-84.
-
(1991)
Circ Res
, vol.68
, pp. 77-84
-
-
Sanguinetti, M.C.1
Jurkiewicz, N.K.2
Scott, A.3
Siegl, P.K.S.4
-
32
-
-
0032076162
-
+ current, on repolarization in human and guinea pig ventricular myocytes
-
+ current, on repolarization in human and guinea pig ventricular myocytes. Cardiovasc Res. 38:1998;441-450.
-
(1998)
Cardiovasc Res
, vol.38
, pp. 441-450
-
-
Bosch, R.F.1
Gaspo, R.2
Busch, A.E.3
Lang, H.J.4
Li, G.R.5
Nattel, S.6
-
33
-
-
0029024749
-
+ current in ventricular myocytes of the guinea pig type: Theoretical formulation and their role in repolarization
-
+ current in ventricular myocytes of the guinea pig type theoretical formulation and their role in repolarization. Circ Res. 77:1995;140-152.
-
(1995)
Circ Res
, vol.77
, pp. 140-152
-
-
Zeng, J.1
Laurita, K.R.2
Rosenbaum, D.S.3
Rudy, Y.4
|