-
2
-
-
0000387603
-
A new familial cardiac syndrome in children
-
Ward O.C. A new familial cardiac syndrome in children. J Irish Med Assoc. 54:1964;103-106.
-
(1964)
J Irish Med Assoc
, vol.54
, pp. 103-106
-
-
Ward, O.C.1
-
3
-
-
49749174698
-
Congenital deaf-mutism, functional heart disease with prolongation of the QT interval and sudden death
-
Jervell A., Lang-Nielsen F. Congenital deaf-mutism, functional heart disease with prolongation of the QT interval and sudden death. Am Heart J. 54:1957;59-68.
-
(1957)
Am Heart J
, vol.54
, pp. 59-68
-
-
Jervell, A.1
Lang-Nielsen, F.2
-
5
-
-
0001127258
-
An analysis of the time-relations of electrocardiograms
-
Bazett H.C. An analysis of the time-relations of electrocardiograms. Heart. 7:1920;353-370.
-
(1920)
Heart
, vol.7
, pp. 353-370
-
-
Bazett, H.C.1
-
7
-
-
0026759352
-
The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome
-
Vincent M.G., Timothy W.K., Leppert M., Keating M. 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, M.G.1
Timothy, W.K.2
Leppert, M.3
Keating, M.4
-
9
-
-
0025336051
-
QT dispersion: An indication of arrhythmia risk in patients with long QT intervals
-
Day C.P., McComb J.M., Campbell R.W.F. QT dispersion An indication of arrhythmia risk in patients with long QT intervals . Br Heart J. 63:1990;342-344.
-
(1990)
Br Heart J
, vol.63
, pp. 342-344
-
-
Day, C.P.1
McComb, J.M.2
Campbell, R.W.F.3
-
10
-
-
0028097678
-
QT dispersion and sudden death in heart failure
-
Barr C.S., Naas A., Freeman M., Lang C.C., Struthers A.D. QT dispersion and sudden death in heart failure. Lancet. 343:1994;327-329.
-
(1994)
Lancet
, vol.343
, pp. 327-329
-
-
Barr, C.S.1
Naas, A.2
Freeman, M.3
Lang, C.C.4
Struthers, A.D.5
-
11
-
-
0029001048
-
Dispersion of QT interval in patients with and without susceptibility to ventricular tachyarrhythmias after previous myocardial infarction
-
Perkiomaki J.S., Koistinen J., Yli-Mayry S., Huikuri H.V. Dispersion of QT interval in patients with and without susceptibility to ventricular tachyarrhythmias after previous myocardial infarction. J Am Coll Cardiol. 267:1995;174-179.
-
(1995)
J Am Coll Cardiol
, vol.267
, pp. 174-179
-
-
Perkiomaki, J.S.1
Koistinen, J.2
Yli-Mayry, S.3
Huikuri, H.V.4
-
12
-
-
0017650689
-
The role of local disparity in conduction and recovery time or ventricular vulnerability to fibrillation
-
Merx W., Yoon M.S., Han J. The role of local disparity in conduction and recovery time or ventricular vulnerability to fibrillation. Am Heart J. 94:1977;603-610.
-
(1977)
Am Heart J
, vol.94
, pp. 603-610
-
-
Merx, W.1
Yoon, M.S.2
Han, J.3
-
13
-
-
0022409811
-
Mechanism of ventricular arrhythmias caused by increased dispersion of repolarization
-
Kuo C.S., Reddy C.P., Munakata K., Surawicz B. Mechanism of ventricular arrhythmias caused by increased dispersion of repolarization. Eur Heart J. 6:(Suppl D):1985;63-70.
-
(1985)
Eur Heart J
, vol.6
, Issue.SUPPL. D
, pp. 63-70
-
-
Kuo, C.S.1
Reddy, C.P.2
Munakata, K.3
Surawicz, B.4
-
14
-
-
0024271358
-
Nonuniform recovery of excitability in the left ventricle
-
Vassallo J.A., Cassidy D.M., Kindwall K.E., Marchlinski F.E., Josephson M.E. Nonuniform recovery of excitability in the left ventricle. Circulation. 78:1988;1365-1372.
-
(1988)
Circulation
, vol.78
, pp. 1365-1372
-
-
Vassallo, J.A.1
Cassidy, D.M.2
Kindwall, K.E.3
Marchlinski, F.E.4
Josephson, M.E.5
-
15
-
-
0000878601
-
Genetics aspects of the cardioauditory syndrome of Jervell and Lange-Nielsen (congenital deafness and electrocardiographic abnormalities)
-
Fraser G.R., Froggat P., Murphy T. Genetics aspects of the cardioauditory syndrome of Jervell and Lange-Nielsen (congenital deafness and electrocardiographic abnormalities). Ann Hum Genet. 28:1964;133-157.
-
(1964)
Ann Hum Genet
, vol.28
, pp. 133-157
-
-
Fraser, G.R.1
Froggat, P.2
Murphy, T.3
-
16
-
-
0018257185
-
Hereditary QT prolongation syndrome in Japan: Genetic analysis and pathologic findings of the conducting system
-
Hashiba K. Hereditary QT prolongation syndrome in Japan Genetic analysis and pathologic findings of the conducting system . Jpn Circ J. 42:1978;1133-1139.
-
(1978)
Jpn Circ J
, vol.42
, pp. 1133-1139
-
-
Hashiba, K.1
-
17
-
-
0031936234
-
Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome
-
Duggal P., Vesely M.R., Wattanasirichaigoon D., Villafane J., Kaushik V. Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome. Circulation. 97:1998;142-146.
-
(1998)
Circulation
, vol.97
, pp. 142-146
-
-
Duggal, P.1
Vesely, M.R.2
Wattanasirichaigoon, D.3
Villafane, J.4
Kaushik, V.5
-
18
-
-
0028035198
-
The Jervell and Lange-Nielsen syndrome
-
Komsuoglu B., Goldeli O., Kulan K., et al. The Jervell and Lange-Nielsen syndrome. Int J Cardiol. 47:1994;189-192.
-
(1994)
Int J Cardiol
, vol.47
, pp. 189-192
-
-
Komsuoglu, B.1
Goldeli, O.2
Kulan, K.3
-
19
-
-
0027411504
-
Idiopathic long QT syndrome: Asking the right question
-
Balbir S., Saad A.S., Moh'd A.H., Saleh M.D., Nabil B. Idiopathic long QT syndrome Asking the right question . Lancet. 341:1993;741-742.
-
(1993)
Lancet
, vol.341
, pp. 741-742
-
-
Balbir, S.1
Saad, A.S.2
Moh'D, A.H.3
Saleh, M.D.4
Nabil, B.5
-
20
-
-
0031054075
-
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen syndrome
-
Neyround N., Tesson F., Denjoy I. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen syndrome. Nat Genet. 15:1997;186-189.
-
(1997)
Nat Genet
, vol.15
, pp. 186-189
-
-
Neyround, N.1
Tesson, F.2
Denjoy, I.3
-
21
-
-
0025847714
-
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
-
Keating M., Atkinson D., Dunn C., Timothy K., 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.1
Atkinson, D.2
Dunn, C.3
Timothy, K.4
Vincent, G.M.5
Leppert, M.6
-
22
-
-
0027306762
-
Locus heterogeneity of dominant long QT syndrome
-
Curran M.E., Atkinson D., Timothy K., et al. Locus heterogeneity of dominant long QT syndrome. J Clin Invest. 92:1993;799-803.
-
(1993)
J Clin Invest
, vol.92
, pp. 799-803
-
-
Curran, M.E.1
Atkinson, D.2
Timothy, K.3
-
23
-
-
0027507884
-
Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome
-
Dean J.C., Cross S., Jennings K. Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome. J Med Genet. 30:1993;947-950.
-
(1993)
J Med Genet
, vol.30
, pp. 947-950
-
-
Dean, J.C.1
Cross, S.2
Jennings, K.3
-
24
-
-
0027601119
-
Linkage analysis in a Japanese long QT syndrome family
-
Akimoto K., Matsuoka R., Kasanuki H., et al. Linkage analysis in a Japanese long QT syndrome family. Kokyuto Junkan. 41:1993;463-465.
-
(1993)
Kokyuto Junkan
, vol.41
, pp. 463-465
-
-
Akimoto, K.1
Matsuoka, R.2
Kasanuki, H.3
-
25
-
-
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
-
26
-
-
9044240040
-
Positional cloning of the novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang Q., Curran M.E., Splawski I., et al. Positional cloning of the 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
-
27
-
-
0028905566
-
SCNA5 mutations associated with inherited cardiac arrhythmia, long QT syndrome
-
Wang Q., Shen J., Splawski I., et al. SCNA5 mutations associated with 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
-
28
-
-
0028819671
-
Mapping of a gene for long QT syndrome to chromosome 4q25-27
-
Schott 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.1
Charpentier, F.2
Peltier, S.3
-
29
-
-
0025769189
-
Left cardiac sympathetic denervation in the therapy of the congenital long QT syndrome: A worldwide report
-
Schwartz P.J., Locati E., Moss A.J. Left cardiac sympathetic denervation in the therapy of the congenital long QT syndrome A worldwide report . Circulation. 84:1991;503-511.
-
(1991)
Circulation
, vol.84
, pp. 503-511
-
-
Schwartz, P.J.1
Locati, E.2
Moss, A.J.3
-
30
-
-
0029164889
-
Long QT syndrome: An indication for cervicothoracic sympathectomy
-
Ouriel K., Moss A.J. Long QT syndrome An indication for cervicothoracic sympathectomy . Cardiovasc Surg. 3:1995;475-478.
-
(1995)
Cardiovasc Surg
, vol.3
, pp. 475-478
-
-
Ouriel, K.1
Moss, A.J.2
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