-
1
-
-
0025935591
-
The long QT syndrome: Prospective longitudinal study of 328 families
-
A.J. Moss, P.J. Schwartz, and R.S. Crampton The long QT syndrome: prospective longitudinal study of 328 families Circulation 84 1991 1136 1144
-
(1991)
Circulation
, vol.84
, pp. 1136-1144
-
-
Moss, A.J.1
Schwartz, P.J.2
Crampton, R.S.3
-
2
-
-
84860120316
-
Sudden cardiac death and genetic ion channelopathies: Long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation
-
C. Napolitano, R. Bloise, N. Monteforte, and S.G. Priori Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation Circulation 125 2012 2027 2034
-
(2012)
Circulation
, vol.125
, pp. 2027-2034
-
-
Napolitano, C.1
Bloise, R.2
Monteforte, N.3
Priori, S.G.4
-
3
-
-
23644450590
-
Genetics of acquired long QT syndrome
-
D.M. Roden, and P.C. Viswanathan Genetics of acquired long QT syndrome J Clin Invest 115 2005 2025 2032
-
(2005)
J Clin Invest
, vol.115
, pp. 2025-2032
-
-
Roden, D.M.1
Viswanathan, P.C.2
-
4
-
-
0034609531
-
Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
-
I. Splawski, J. Shen, and K.W. Timothy Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2 Circulation 102 2000 1178 1185
-
(2000)
Circulation
, vol.102
, pp. 1178-1185
-
-
Splawski, I.1
Shen, J.2
Timothy, K.W.3
-
5
-
-
0036217325
-
Characterization of a novel missense mutation E637K in the pore-S6 loop of HERG in a patient with long QT syndrome
-
K. Hayashi, M. Shimizu, and H. Ino Characterization of a novel missense mutation E637K in the pore-S6 loop of HERG in a patient with long QT syndrome Cardiovasc Res 54 2002 67 76
-
(2002)
Cardiovasc Res
, vol.54
, pp. 67-76
-
-
Hayashi, K.1
Shimizu, M.2
Ino, H.3
-
6
-
-
4043181187
-
Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG
-
K. Hayashi, M. Shimizu, and H. Ino Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG Clin Sci (Lond) 107 2004 175 182
-
(2004)
Clin Sci (Lond)
, vol.107
, pp. 175-182
-
-
Hayashi, K.1
Shimizu, M.2
Ino, H.3
-
7
-
-
74549172996
-
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome
-
H. Itoh, T. Sakaguchi, and W.G. Ding Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome Circ Arrhythm Electrophysiol 2 2009 511 523
-
(2009)
Circ Arrhythm Electrophysiol
, vol.2
, pp. 511-523
-
-
Itoh, H.1
Sakaguchi, T.2
Ding, W.G.3
-
8
-
-
0037133307
-
Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether -A-go-go-related gene potassium channel
-
A.J. Moss, W. Zareba, and E.S. Kaufman Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel Circulation 105 2002 794 799
-
(2002)
Circulation
, vol.105
, pp. 794-799
-
-
Moss, A.J.1
Zareba, W.2
Kaufman, E.S.3
-
9
-
-
71849098104
-
Genotype-phenotype aspects of type 2 long QT syndrome
-
W. Shimizu, A.J. Moss, and A.A. Wilde Genotype-phenotype aspects of type 2 long QT syndrome J Am Coll Cardiol 54 2009 2052 2062
-
(2009)
J Am Coll Cardiol
, vol.54
, pp. 2052-2062
-
-
Shimizu, W.1
Moss, A.J.2
Wilde, A.A.3
-
10
-
-
78650825624
-
A KCR1 variant implicated in susceptibility to the long QT syndrome
-
K. Hayashi, N. Fujino, and H. Ino A KCR1 variant implicated in susceptibility to the long QT syndrome J Mol Cell Cardiol 50 2011 50 57
-
(2011)
J Mol Cell Cardiol
, vol.50
, pp. 50-57
-
-
Hayashi, K.1
Fujino, N.2
Ino, H.3
-
11
-
-
0642364448
-
The IKr drug response is modulated by KCR1 in transfected cardiac and noncardiac cell lines
-
S. Kupershmidt, I.C. Yang, and K. Hayashi The IKr drug response is modulated by KCR1 in transfected cardiac and noncardiac cell lines FASEB J 17 2003 2263 2265
-
(2003)
FASEB J
, vol.17
, pp. 2263-2265
-
-
Kupershmidt, S.1
Yang, I.C.2
Hayashi, K.3
-
12
-
-
34247111885
-
HERG is protected from pharmacological block by alpha-1,2- glucosyltransferase function
-
T. Nakajima, K. Hayashi, and P.C. Viswanathan HERG is protected from pharmacological block by alpha-1,2-glucosyltransferase function J Biol Chem 282 2007 5506 5513
-
(2007)
J Biol Chem
, vol.282
, pp. 5506-5513
-
-
Nakajima, T.1
Hayashi, K.2
Viswanathan, P.C.3
-
13
-
-
0033615646
-
January CT. Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome: Pharmacological and temperature effects
-
Z. Zhou, and Q. Gong January CT. Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome: pharmacological and temperature effects J Biol Chem 274 1999 31123 31126
-
(1999)
J Biol Chem
, vol.274
, pp. 31123-31126
-
-
Zhou, Z.1
Gong, Q.2
-
14
-
-
0042817907
-
Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C
-
B.P. Delisle, C.L. Anderson, and R.C. Balijepalli Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C J Biol Chem 278 2003 35749 35754
-
(2003)
J Biol Chem
, vol.278
, pp. 35749-35754
-
-
Delisle, B.P.1
Anderson, C.L.2
Balijepalli, R.C.3
-
15
-
-
33644851751
-
Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism
-
C.L. Anderson, B.P. Delisle, and B.D. Anson Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism Circulation 113 2006 365 373
-
(2006)
Circulation
, vol.113
, pp. 365-373
-
-
Anderson, C.L.1
Delisle, B.P.2
Anson, B.D.3
-
16
-
-
67449102308
-
Misdiagnosis of long QT syndrome as epilepsy at first presentation
-
J.M. MacCormick, H. McAlister, and J. Crawford Misdiagnosis of long QT syndrome as epilepsy at first presentation Ann Emerg Med 54 2009 26 32
-
(2009)
Ann Emerg Med
, vol.54
, pp. 26-32
-
-
MacCormick, J.M.1
McAlister, H.2
Crawford, J.3
-
17
-
-
59649127401
-
Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy
-
J.N. Johnson, N. Hofman, and C.M. Haglund Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy Neurology 72 2009 224 231
-
(2009)
Neurology
, vol.72
, pp. 224-231
-
-
Johnson, J.N.1
Hofman, N.2
Haglund, C.M.3
-
18
-
-
0030058329
-
Diurnal pattern of QTc interval: How long is prolonged? Possible relation to circadian triggers of cardiovascular events
-
J. Molnar, F. Zhang, J. Weiss, F.A. Ehlert, and J.E. Rosenthal Diurnal pattern of QTc interval: how long is prolonged? Possible relation to circadian triggers of cardiovascular events J Am Coll Cardiol 27 1996 76 83
-
(1996)
J Am Coll Cardiol
, vol.27
, pp. 76-83
-
-
Molnar, J.1
Zhang, F.2
Weiss, J.3
Ehlert, F.A.4
Rosenthal, J.E.5
-
19
-
-
0035050390
-
Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: Experience in 101 related family members
-
E.S. Kaufman, S.G. Priori, and C. Napolitano Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family members J Cardiovasc Electrophysiol 12 2001 455 461
-
(2001)
J Cardiovasc Electrophysiol
, vol.12
, pp. 455-461
-
-
Kaufman, E.S.1
Priori, S.G.2
Napolitano, C.3
-
20
-
-
33747878246
-
Corrected QT variability in serial electrocardiograms in long QT syndrome: The importance of the maximum corrected QT for risk stratification
-
I. Goldenberg, J. Mathew, and A.J. Moss Corrected QT variability in serial electrocardiograms in long QT syndrome: the importance of the maximum corrected QT for risk stratification J Am Coll Cardiol 48 2006 1047 1052
-
(2006)
J Am Coll Cardiol
, vol.48
, pp. 1047-1052
-
-
Goldenberg, I.1
Mathew, J.2
Moss, A.J.3
-
22
-
-
70349208609
-
+ concentration controls cell surface density of IKr in rabbit hearts and of the HERG channel in human cell lines
-
+ concentration controls cell surface density of IKr in rabbit hearts and of the HERG channel in human cell lines J Clin Invest 119 2009 2745 2757
-
(2009)
J Clin Invest
, vol.119
, pp. 2745-2757
-
-
Guo, J.1
Massaeli, H.2
Xu, J.3
-
25
-
-
34547580639
-
Retrospective analysis of electrocardiographic changes after administration of oral or intravenous garenoxacin in five phase I, placebo-controlled studies in healthy volunteers
-
Z. Wang, D.M. Grasela, and G. Krishna Retrospective analysis of electrocardiographic changes after administration of oral or intravenous garenoxacin in five phase I, placebo-controlled studies in healthy volunteers Clin Ther 29 2007 1098 1106
-
(2007)
Clin Ther
, vol.29
, pp. 1098-1106
-
-
Wang, Z.1
Grasela, D.M.2
Krishna, G.3
-
26
-
-
77952876759
-
Torsades de pointes induced by a combination of garenoxacin and disopyramide and other cytochrome P450, family 3, subfamily A polypeptide-4-influencing drugs during hypokalemia due to licorice
-
K. Miyamoto, H. Kawai, and R. Aoyama Torsades de pointes induced by a combination of garenoxacin and disopyramide and other cytochrome P450, family 3, subfamily A polypeptide-4-influencing drugs during hypokalemia due to licorice Clin Exp Nephrol 14 2010 164 167
-
(2010)
Clin Exp Nephrol
, vol.14
, pp. 164-167
-
-
Miyamoto, K.1
Kawai, H.2
Aoyama, R.3
-
27
-
-
33644832519
-
Syndrome: Reduced repolarization reserve and the genetic link
-
D.M. Roden, and Q.T. Long syndrome: reduced repolarization reserve and the genetic link J Intern Med 259 2006 59 69
-
(2006)
J Intern Med
, vol.259
, pp. 59-69
-
-
Roden, D.M.1
Long, Q.T.2
-
28
-
-
0034546344
-
Long QT syndrome: Cellular basis and arrhythmia mechanism in LQT2
-
CT January, Q Gong, and Z Zhou Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2 J Cardiovasc Electrophysiol 11 2000 1413 1418
-
(2000)
J Cardiovasc Electrophysiol
, vol.11
, pp. 1413-1418
-
-
January, C.T.1
Gong, Q.2
Zhou, Z.3
-
29
-
-
55249088583
-
A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope
-
G. Christe, O. Theriault, and M. Chahine A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope Heart Rhythm 5 2008 1577 1586
-
(2008)
Heart Rhythm
, vol.5
, pp. 1577-1586
-
-
Christe, G.1
Theriault, O.2
Chahine, M.3
-
30
-
-
84855897480
-
Partially dominant mutant channel defect corresponding with intermediate LQT2 phenotype
-
Y. Krishnan, R. Zheng, C. Walsh, Y. Tang, and T.V. McDonald Partially dominant mutant channel defect corresponding with intermediate LQT2 phenotype Pacing Clin Electrophysiol 35 2012 3 16
-
(2012)
Pacing Clin Electrophysiol
, vol.35
, pp. 3-16
-
-
Krishnan, Y.1
Zheng, R.2
Walsh, C.3
Tang, Y.4
McDonald, T.V.5
-
31
-
-
68549128742
-
HERG-F463L potassium channels linked to long QT syndrome reduce I(Kr) current by a trafficking-deficient mechanism
-
H.T. Yang, C.F. Sun, and C.C. Cui HERG-F463L potassium channels linked to long QT syndrome reduce I(Kr) current by a trafficking-deficient mechanism Clin Exp Pharmacol Physiol 36 2009 822 827
-
(2009)
Clin Exp Pharmacol Physiol
, vol.36
, pp. 822-827
-
-
Yang, H.T.1
Sun, C.F.2
Cui, C.C.3
-
33
-
-
0032563717
-
Novel mechanism of HERG current suppression in LQT2: Shift in voltage dependence of HERG inactivation
-
T. Nakajima, T. Furukawa, and T. Tanaka Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation Circ Res 83 1998 415 422
-
(1998)
Circ Res
, vol.83
, pp. 415-422
-
-
Nakajima, T.1
Furukawa, T.2
Tanaka, T.3
-
34
-
-
3242717751
-
Pharmacological rescue of trafficking defective HERG channels formed by coassembly of wild-type and long QT mutant N470D subunits
-
Q. Gong, and C.L. Anderson January CT, Zhou Z. Pharmacological rescue of trafficking defective HERG channels formed by coassembly of wild-type and long QT mutant N470D subunits Am J Physiol Heart Circ Physiol 287 2004 H652 H658
-
(2004)
Am J Physiol Heart Circ Physiol
, vol.287
-
-
Gong, Q.1
Anderson, C.L.2
January C.T.Zhou, Z.3
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