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0015223506
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Unilateral cervicothoracic sympathetic ganglionectomy for the treatment of long QT interval syndrome
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Moss AJ, McDonald J. Unilateral cervicothoracic sympathetic ganglionectomy for the treatment of long QT interval syndrome. N Engl J Med. 1971;285:903-904.
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Electrical alternation of the T-wave: Clinical and experimental evidence of its relationship with the sympathetic nervous system and with the long Q-T syndrome
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Schwartz PJ, Malliani A. Electrical alternation of the T-wave: clinical and experimental evidence of its relationship with the sympathetic nervous system and with the long Q-T syndrome. Am Heart J. 1975;89:45-50.
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Sudden death and the idiopathic long Q-T syndrome
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Moss AJ, Schwartz PJ. Sudden death and the idiopathic long Q-T syndrome. Am J Med. 1979;66:6-7.
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6
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0025847714
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Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
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Keating M, Atkinson D, Dunn C, Timothy K, Vincent GM, Leppert M. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science. 1991;252:704-706.
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Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11
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Keating M, Dunn C, Atkinson D, Timothy K, Vincent GM, Leppert M. Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. Am J Hum Genet. 1991;49:1335-1339.
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8
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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
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Wang Q, Shen J, Splawski I, Atkinson D, Li Z, Robinson JL, Moss AJ, Towbin JA, Keating MT. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 1995;80:805-811.
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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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Curran ME, Splawski I, Timothy KW, Vincent GM, Green ED, Keating MT. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell. 1995;80:795-803.
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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
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Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Towbin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet. 1996;12:17-23.
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11
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Delayed repolarization (QT or QTU prolongation) and malignant ventricular arrhythmias
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Moss AJ, Schwartz PJ. Delayed repolarization (QT or QTU prolongation) and malignant ventricular arrhythmias. Modern Concepts Cardiovasc Dis. 1982;51:85-90.
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The long QT syndrome: A prospective international study
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Moss AJ, Schwartz PJ, Crampton RS, Locati E, Carleen E. The long QT syndrome: a prospective international study. Circulation. 1985;71:17-21.
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13
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0025935591
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The long QT syndrome: Prospective longitudinal study of 328 families
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Moss AJ, Schwartz PJ, Crampton RS, Tzivoni D, Locati EH, MacCluer J, Hall WJ, Weitkamp L, Vincent GM, Garson A Jr, Robinson JL, Benhorin J, Choi S. The long QT syndrome: prospective longitudinal study of 328 families. Circulation. 1991;84:1136-1144.
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14
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0032499656
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Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: Findings from the International LQTS Registry
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Locati EH, Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Lehmann GM, Towbin JA, Priori SG, Napolitano C, Robinson JL, Andrews M, Timothy K, Hall WJ. Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry. Circulation. 1998;97:2237-2244.
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15
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0032502041
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Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome
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Rashba EJ, Zareba W, Moss AJ, Hall WJ, Robinson J, Locati EH, Schwartz PJ, Andrews M, for the LQTS Investigators. Influence of pregnancy on the risk for cardiac events in patients with hereditary long QT syndrome. Circulation. 1998;97:451-456.
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16
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0028861892
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ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
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Moss AJ, Zareba W, Benhorin J, Locati EH, Hall WJ, Robinson JL, Schwartz PJ, Towbin JA, Vincent GM, Lehmann MH, Keating MT, MacCluer JW, Timothy KW. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome. Circulation. 1995;92:2929-2934.
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17
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Influence of genotype on the clinical course of the long-QT syndrome
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Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Robinson JL, Priori SG, Benhorin J, Locati EH, Towbin JA, Keating MT, Lehmann MH, Hall WJ, for the International Long-QT Syndrome Registry Research Group. Influence of genotype on the clinical course of the long-QT syndrome. N Engl J Med. 1998;339:960-965.
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Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
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Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT. Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation. 2000;102:1178-1185.
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19
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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
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Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z. 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. 2002;105:794-799.
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20
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0032874978
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Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome
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Moss AJ, Robinson JL, Gessman L, Gillespie R, Zareba W, Schwartz PJ, Vincent GM, Benhorin J, Locati Heilbron E, Towbin JA, Priori SG, Napolitano C, Zhang L, Medina A, Andrews ML, Timothy K. Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome. Am J Cardiol. 1999;84:876-879.
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21
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0033962980
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Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome
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Ali RHH, Zareba W, Moss AJ, Schwartz PJ, Benhorin J, Vincent GM, Locati EH, Priori SG, Napolitano C, Towbin JA, Hall WJ, Robinson JL, Andrews ML, Zhang L, Timothy K, Medina A. Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome. Am J Cardiol. 2000;85:457-461.
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22
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Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias
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Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating MT, Towbin JA, Beggs AH, Brink P, Wilde AAM, Toivonen L, Zareba W, Robinson JL, Timothy KW, Corfield V, Wattanasirichaigoon D, Corbett C, Haverkamp W, Schulze-Bahr E, Lehmann MH, Schwartz K, Coumel P, Bloise R. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation. 2001;103:89-95.
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Wattanasirichaigoon, D.20
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Lehmann, M.H.24
Schwartz, K.25
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Bloise, R.27
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Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome
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Moss AJ, Zareba W, Hall WJ, Schwartz PJ, Crampton RS, Benhorin J, Vincent GM, Locati EH, Priori SG, Napolitano C, Medina A, Zhang L, Robinson JL, Timothy K, Towbin JA, Andrews ML. Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome. Circulation. 2000;101:616-623.
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Benhorin, J.6
Vincent, G.M.7
Locati, E.H.8
Priori, S.G.9
Napolitano, C.10
Medina, A.11
Zhang, L.12
Robinson, J.L.13
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Andrews, M.L.16
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+ channel blockade and to increases in heart rate: Implications for gene-specific therapy
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+ channel blockade and to increases in heart rate: implications for gene-specific therapy. Circulation. 1995;92:3381-3386.
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25
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0035022511
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Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:ΔKPQ mutation
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Windle JR, Geletka RC, Moss AJ, Zareba W, Atkins DL. Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:ΔKPQ mutation. Ann Noninvasive Electrocardiol. 2001;6:153-158.
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Ann Noninvasive Electrocardiol
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Windle, J.R.1
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Atkins, D.L.5
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26
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0037623309
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Implantable cardioverter defibrillator in high-risk long QT syndrome patients
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Zareba W, Moss AJ, Daubert JP, Hall WJ, Robinson JL, Andrews M. Implantable cardioverter defibrillator in high-risk long QT syndrome patients. J Cardiovasc Electrophysiol. 2003;14:337-341.
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J Cardiovasc Electrophysiol
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Andrews, M.6
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27
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11144356780
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Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome
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Schwartz PJ, Priori SG, Cerrone M, Spazzolini C, Odero A, Napolitano C, Bloise R, De Ferrari GM, Klersy C, Moss AJ, Zareba W, Robinson JL, Hall WJ, Brink PA, Toivonen L, Epstein AE, Li C, Hu D. Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome. Circulation. 2004;109:1826-1833.
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Schwartz, P.J.1
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Napolitano, C.6
Bloise, R.7
De Ferrari, G.M.8
Klersy, C.9
Moss, A.J.10
Zareba, W.11
Robinson, J.L.12
Hall, W.J.13
Brink, P.A.14
Toivonen, L.15
Epstein, A.E.16
Li, C.17
Hu, D.18
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