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Volumn 18, Issue 2, 2000, Pages 309-325

Long QT syndrome

Author keywords

[No Author keywords available]

Indexed keywords

AMIODARONE; AMITRIPTYLINE; AMOXAPINE; AMPICILLIN; ANTIANGINA PECTORIS AGENT; ANTIARRHYTHMIC AGENT; ANTIBIOTIC AGENT; ANTIDEPRESSANT AGENT; ANTIHISTAMINIC AGENT; ASTEMIZOLE; CHLORPROMAZINE; CISAPRIDE; CLARITHROMYCIN; CLEMASTINE FUMARATE; CLOMIPRAMINE; DESIPRAMINE; DIPHENHYDRAMINE; DISOPYRAMIDE PHOSPHATE; DOXEPIN; ERYTHROMYCIN; FLECAINIDE ACETATE; FLUDROCORTISONE; FLUPHENAZINE; HALOPERIDOL; IBUTILIDE FUMARATE; IMIPRAMINE; INDAPAMIDE; MAPROTILINE; MORACIZINE; NEUROLEPTIC AGENT; NORTRIPTYLINE; PENTAERYTHRITYL TETRANITRATE; PENTAMIDINE; PENTAMIDINE ISETHIONATE; PERPHENAZINE; PIMOZIDE; UNINDEXED DRUG;

EID: 0034112322     PISSN: 07338651     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0733-8651(05)70143-0     Document Type: Article
Times cited : (73)

References (100)
  • 1
    • 0033574273 scopus 로고    scopus 로고
    • MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmias
    • G.W. Abbott F. Sesti I. Splawski MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmias Cell 97 1999 175 187
    • (1999) Cell , vol.97 , pp. 175-187
    • Abbott, G.W.1    Sesti, F.2    Splawski, I.3
  • 3
    • 0344966743 scopus 로고
    • The autonomic nervous system in relation to electrocardiographic waveform and cardiac rhythm
    • J.A. Abildskov G.M. Vincent The autonomic nervous system in relation to electrocardiographic waveform and cardiac rhythm Randall W.C. Neural Regulation of the Heart 1977 Oxford University Press Boston 409 424
    • (1977) , pp. 409-424
    • Abildskov, J.A.1    Vincent, G.M.2
  • 4
    • 0028082351 scopus 로고
    • Clinical relevance of cardiac arrhythmias generated by afterdepolarizations: Role of M cells in the generation of U waves, triggered activity and torsade de pointes [review]
    • C. Antzelevitch S. Sicouri Clinical relevance of cardiac arrhythmias generated by afterdepolarizations: Role of M cells in the generation of U waves, triggered activity and torsade de pointes [review] J Am Coll Cardiol 23 1994 259 277
    • (1994) J Am Coll Cardiol , vol.23 , pp. 259-277
    • Antzelevitch, C.1    Sicouri, S.2
  • 5
    • 0029618150 scopus 로고
    • Role of M cells in acquired long QT syndrome, U waves, and torsade de pointes
    • C. Antzelevitch V.V. Nesterenko G.X. Yan Role of M cells in acquired long QT syndrome, U waves, and torsade de pointes J Electrocardiol 28 suppl 1995 131 138
    • (1995) J Electrocardiol , vol.28 , Issue.suppl , pp. 131-138
    • Antzelevitch, C.1    Nesterenko, V.V.2    Yan, G.X.3
  • 6
    • 0003087023 scopus 로고
    • Regional differences in the electrophysiology of ventricular cells: Physiological and clinical implications
    • C. Antzelevitch S. Sicouri A. Lukas Regional differences in the electrophysiology of ventricular cells: Physiological and clinical implications Zipes D.P. Jalife J. Cardiac Electrophysiology: From Cell to Bedside 1995 WB Saunders Philadelphia 228 245
    • (1995) , pp. 228-245
    • Antzelevitch, C.1    Sicouri, S.2    Lukas, A.3
  • 7
    • 0030888769 scopus 로고    scopus 로고
    • Optical mapping of drug-induced polymorphic arrhythmias and torsade de pointes in the isolated rabbit heart
    • Y. Asano J.M. Davidenko W.T. Baxter Optical mapping of drug-induced polymorphic arrhythmias and torsade de pointes in the isolated rabbit heart J Am Coll Cardiol 29 1997 831 842
    • (1997) J Am Coll Cardiol , vol.29 , pp. 831-842
    • Asano, Y.1    Davidenko, J.M.2    Baxter, W.T.3
  • 8
    • 0029952101 scopus 로고    scopus 로고
    • KvLQT1 and IsK (minK) proteins associate to form the IKs cardiac potassium current
    • J. Barhanin F. Lesage E. Guillemare KvLQT1 and IsK (minK) proteins associate to form the IKs cardiac potassium current Nature 384 1996 78 80
    • (1996) Nature , vol.384 , pp. 78-80
    • Barhanin, J.1    Lesage, F.2    Guillemare, E.3
  • 9
    • 0029097799 scopus 로고    scopus 로고
    • Molecular mechanism for an inherited cardiac arrhythmia
    • P.B. Bennett K. Yazawa N. Makita Molecular mechanism for an inherited cardiac arrhythmia Nature 376 1996 683 685
    • (1996) Nature , vol.376 , pp. 683-685
    • Bennett, P.B.1    Yazawa, K.2    Makita, N.3
  • 10
    • 0021715880 scopus 로고
    • Efficacy of left cardiac sympathectomy in the treatment of patients with the long QT syndrome
    • A.K. Bhandari M.M. Scheinman F. Morady Efficacy of left cardiac sympathectomy in the treatment of patients with the long QT syndrome Circulation 70 1984 1018 1023
    • (1984) Circulation , vol.70 , pp. 1018-1023
    • Bhandari, A.K.1    Scheinman, M.M.2    Morady, F.3
  • 11
    • 0029028063 scopus 로고
    • Nicorandil suppresses a hump on the monophasic action potential and torsades de pointes in a patient with idiopathic long QT syndrome
    • M. Chinushi Y. Aizawa H. Furushima Nicorandil suppresses a hump on the monophasic action potential and torsades de pointes in a patient with idiopathic long QT syndrome Jpn Heart J 36 1995 477 481
    • (1995) Jpn Heart J , vol.36 , pp. 477-481
    • Chinushi, M.1    Aizawa, Y.2    Furushima, H.3
  • 12
    • 0029831629 scopus 로고    scopus 로고
    • Genetically defined therapy of inherited long-QT syndrome: Correction of abnormal repolarization by potassium
    • S.J. Compton R.L. Lux M.R. Ramsey Genetically defined therapy of inherited long-QT syndrome: Correction of abnormal repolarization by potassium Circulation 94 1996 1018 1022
    • (1996) Circulation , vol.94 , pp. 1018-1022
    • Compton, S.J.1    Lux, R.L.2    Ramsey, M.R.3
  • 13
    • 0028914969 scopus 로고
    • A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
    • M.E. Curran I. Splawski K.W. Timothy 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
  • 14
    • 19244371485 scopus 로고    scopus 로고
    • KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome
    • C. Donger I. Denjoy M. Berthet KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome Circulation 96 1997 2778 2781
    • (1997) Circulation , vol.96 , pp. 2778-2781
    • Donger, C.1    Denjoy, I.2    Berthet, M.3
  • 15
    • 0032957468 scopus 로고    scopus 로고
    • The long QT syndrome and torsades de pointes [review]
    • N. El-Sherif G. Turitto The long QT syndrome and torsades de pointes [review] Pacing Clin Electrophysiol 22 1999 91 110
    • (1999) Pacing Clin Electrophysiol , vol.22 , pp. 91-110
    • El-Sherif, N.1    Turitto, G.2
  • 16
    • 0033117020 scopus 로고    scopus 로고
    • Mechanism of arrhythmogenicity of the short-long cardiac sequence that precedes ventricular tachyarrhythmias in the long QT syndrome
    • N. El-Sherif E.B. Caref M. Chinushi Mechanism of arrhythmogenicity of the short-long cardiac sequence that precedes ventricular tachyarrhythmias in the long QT syndrome J Am Coll Cardiol 33 1999 1415 1423
    • (1999) J Am Coll Cardiol , vol.33 , pp. 1415-1423
    • El-Sherif, N.1    Caref, E.B.2    Chinushi, M.3
  • 17
    • 0031467877 scopus 로고    scopus 로고
    • Electrophysiological mechanism of the characteristic electrocardiographic morphology of torsade de pointes tachyarrhythmias in the long-QT syndrome: Detailed analysis of ventricular tridimensional activation patterns
    • N. El-Sherif M. Chinushi E.B. Caref Electrophysiological mechanism of the characteristic electrocardiographic morphology of torsade de pointes tachyarrhythmias in the long-QT syndrome: Detailed analysis of ventricular tridimensional activation patterns Circulation 96 1997 4392 4399
    • (1997) Circulation , vol.96 , pp. 4392-4399
    • El-Sherif, N.1    Chinushi, M.2    Caref, E.B.3
  • 18
    • 0029871675 scopus 로고    scopus 로고
    • Diabetic autonomic neuropathy and the heart
    • D.J. Ewing Diabetic autonomic neuropathy and the heart Diabetes Res Clin Pract 30 suppl 1996 31 36
    • (1996) Diabetes Res Clin Pract , vol.30 , Issue.suppl , pp. 31-36
    • Ewing, D.J.1
  • 19
    • 0027273764 scopus 로고
    • The long QT syndrome in children: An international study of 287 patients
    • Garson A. Jr Dick M. Fournier A. The long QT syndrome in children: An international study of 287 patients Circulation 87 1993 1866 1872
    • (1993) Circulation , vol.87 , pp. 1866-1872
    • Garson, A.1    Dick, M.2    Fournier, A.3
  • 20
    • 0028908741 scopus 로고
    • Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene SCN5A to band 3p21
    • George A.L. Jr Varkony T.A. Drabkin H.A. Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene SCN5A to band 3p21 Cytogenet Cell Genet 68 1995 67 70
    • (1995) Cytogenet Cell Genet , vol.68 , pp. 67-70
    • George, A.L.1    Varkony, T.A.2    Drabkin, H.A.3
  • 21
    • 0343416890 scopus 로고    scopus 로고
    • Time- and rate-dependent alterations of the QT interval precede the onset of torsade de pointes in patients with acquired QT prolongation
    • R.F.J. Gilmour M.L. Riccio E.H. Locati Time- and rate-dependent alterations of the QT interval precede the onset of torsade de pointes in patients with acquired QT prolongation J Am Coll Cardiol 30 1997 209 217
    • (1997) J Am Coll Cardiol , vol.30 , pp. 209-217
    • Gilmour, R.F.J.1    Riccio, M.L.2    Locati, E.H.3
  • 22
    • 0017286697 scopus 로고
    • Cardiac arrhythmias in acute central nervous system disease
    • M.A. Grossman Cardiac arrhythmias in acute central nervous system disease Arch Intern Med 136 1976 203 207
    • (1976) Arch Intern Med , vol.136 , pp. 203-207
    • Grossman, M.A.1
  • 23
    • 0039880271 scopus 로고    scopus 로고
    • Long QT genotype can be identified by ECG phenotype
    • L.C. Guili L. Zhang K.W. Timothy Long QT genotype can be identified by ECG phenotype J Am Coll Cardiol 31 1998 192A
    • (1998) J Am Coll Cardiol , vol.31 , pp. 192A
    • Guili, L.C.1    Zhang, L.2    Timothy, K.W.3
  • 25
    • 0024556795 scopus 로고
    • Early afterdepolarizations: Mechanism of induction and block: A role for L-type Ca2+ current
    • C.T. January J.M. Riddle Early afterdepolarizations: Mechanism of induction and block: A role for L-type Ca2+ current Circ Res 64 1989 977 990
    • (1989) Circ Res , vol.64 , pp. 977-990
    • January, C.T.1    Riddle, J.M.2
  • 26
    • 49749174698 scopus 로고
    • Congenital deaf-mutism, functional heart disease with prolongation of the QT interval, and sudden death
    • A. Jervell F. Lange-Nielsen 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    Lange-Nielsen, F.2
  • 27
    • 0013973537 scopus 로고
    • The surdo-cardiac syndrome: Three new cases of congenital deafness with syncopal attacks and Q-T prolongation in the electrocardiogram
    • A. Jervell R. Thingstad T.O. Endsjo The surdo-cardiac syndrome: Three new cases of congenital deafness with syncopal attacks and Q-T prolongation in the electrocardiogram Am Heart J 72 1966 582
    • (1966) Am Heart J , vol.72 , pp. 582
    • Jervell, A.1    Thingstad, R.2    Endsjo, T.O.3
  • 28
    • 0027186122 scopus 로고
    • Rate-dependent prolongation of cardiac action potentials by a methanesulfonanilide class III antiarrhythmic agent: Specific block of IKr by dofetilide
    • N.K. Jurkiewicz M. Sanguinetti Rate-dependent prolongation of cardiac action potentials by a methanesulfonanilide class III antiarrhythmic agent: Specific block of IKr by dofetilide Circ Res 72 1993 75 83
    • (1993) Circ Res , vol.72 , pp. 75-83
    • Jurkiewicz, N.K.1    Sanguinetti, M.2
  • 29
    • 0023158294 scopus 로고
    • QT interval prolongation and sudden cardiac death in diabetic autonomic neuropathy
    • J.K. Kahn J. Sisson A. Vinik QT interval prolongation and sudden cardiac death in diabetic autonomic neuropathy J Clin Endocrinol Metab 64 1987 751 754
    • (1987) J Clin Endocrinol Metab , vol.64 , pp. 751-754
    • Kahn, J.K.1    Sisson, J.2    Vinik, A.3
  • 30
    • 0029589933 scopus 로고
    • Abnormal response to exercise, face immersion, and isoproterenol in children with the long QT syndrome
    • M. Katagiri-Kawade T. Ohe Y. Arakaki Abnormal response to exercise, face immersion, and isoproterenol in children with the long QT syndrome Pacing Clin Electrophysiol 18 1995 2128 2134
    • (1995) Pacing Clin Electrophysiol , vol.18 , pp. 2128-2134
    • Katagiri-Kawade, M.1    Ohe, T.2    Arakaki, Y.3
  • 31
    • 84909848820 scopus 로고
    • Consistent linkage of the long QT syndrome to the Harvey ras-1 locus on chromosome 11
    • M.T. Keating C.K. Dunn D.L. Atkinson Consistent linkage of the long QT syndrome to the Harvey ras-1 locus on chromosome 11 Circulation 84 1991 II 414
    • (1991) Circulation , vol.84 , pp. II-414
    • Keating, M.T.1    Dunn, C.K.2    Atkinson, D.L.3
  • 32
    • 0029964083 scopus 로고    scopus 로고
    • Mechanisms and management of congenital and acquired long QT syndromes
    • R. Lazzara Mechanisms and management of congenital and acquired long QT syndromes Arch Mal Coeur Vaiss 89 spec no 1 1996 51 55
    • (1996) Arch Mal Coeur Vaiss , vol.89 , Issue.spec no 1 , pp. 51-55
    • Lazzara, R.1
  • 33
    • 0021919042 scopus 로고
    • The long QT syndrome: A prospective international study
    • A.J. Moss P.J. Schwartz R.S. Crampton The long QT syndrome: A prospective international study Circulation 71 1985 17 21
    • (1985) Circulation , vol.71 , pp. 17-21
    • Moss, A.J.1    Schwartz, P.J.2    Crampton, R.S.3
  • 34
    • 0028861892 scopus 로고
    • ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
    • A.J. Moss W. Zareba J. Benhorin 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
  • 35
    • 13144267750 scopus 로고    scopus 로고
    • Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome
    • N. Neyroud I. Denjoy C. Donger Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome Eur J Hum Genet 6 1998 129 133
    • (1998) Eur J Hum Genet , vol.6 , pp. 129-133
    • Neyroud, N.1    Denjoy, I.2    Donger, C.3
  • 36
    • 0031054075 scopus 로고    scopus 로고
    • A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    • N. Neyroud F. Tesson I. Denjoy A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome Nat Genet 15 1997 186 189
    • (1997) Nat Genet , vol.15 , pp. 186-189
    • Neyroud, N.1    Tesson, F.2    Denjoy, I.3
  • 37
    • 0025677749 scopus 로고
    • Electrocardiographic and electrophysiologic studies in patients with torsades de pointes: Role of monophasic action potentials
    • T. Ohe T. Kurita N. Aihara Electrocardiographic and electrophysiologic studies in patients with torsades de pointes: Role of monophasic action potentials Jpn Circ J 54 1990 1323 1330
    • (1990) Jpn Circ J , vol.54 , pp. 1323-1330
    • Ohe, T.1    Kurita, T.2    Aihara, N.3
  • 38
    • 0033514263 scopus 로고    scopus 로고
    • Low penetrance in the long QT syndrome: Clinical impact
    • S.G. Priori C. Napolitano P.J. Schwartz Low penetrance in the long QT syndrome: Clinical impact Circulation 99 1999 529 533
    • (1999) Circulation , vol.99 , pp. 529-533
    • Priori, S.G.1    Napolitano, C.2    Schwartz, P.J.3
  • 39
    • 0033514256 scopus 로고    scopus 로고
    • Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management: Parts I and II
    • S.G. Priori J. Barhanin R.N. Hauer Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management: Parts I and II Circulation 99 1999 518 528
    • (1999) Circulation , vol.99 , pp. 518-528
    • Priori, S.G.1    Barhanin, J.2    Hauer, R.N.3
  • 40
    • 0033537474 scopus 로고    scopus 로고
    • Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management: Part III
    • S.G. Priori J. Barhanin R.N. Hauer Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management: Part III Circulation 99 1999 674 681
    • (1999) Circulation , vol.99 , pp. 674-681
    • Priori, S.G.1    Barhanin, J.2    Hauer, R.N.3
  • 41
    • 0029887380 scopus 로고    scopus 로고
    • Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long QT syndrome
    • S.G. Priori C. Napolitano F. Cantu Differential response to Na+ channel blockade, beta-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
  • 42
    • 0002759673 scopus 로고    scopus 로고
    • KvLQT1 mutation in drug induced torsades de pointes [abstract]
    • S.G. Priori C. Napolitano P.J. Schwartz KvLQT1 mutation in drug induced torsades de pointes [abstract] Eur Heart J 18 1997 324
    • (1997) Eur Heart J , vol.18 , pp. 324
    • Priori, S.G.1    Napolitano, C.2    Schwartz, P.J.3
  • 43
    • 0001172012 scopus 로고    scopus 로고
    • The risk of sudden death as first cardiac event in asymptomatic patients with the long QT syndrome [abstract]
    • S.G. Priori C. Napolitano P.J. Schwartz The risk of sudden death as first cardiac event in asymptomatic patients with the long QT syndrome [abstract] Circulation 98 1998 777
    • (1998) Circulation , vol.98 , pp. 777
    • Priori, S.G.1    Napolitano, C.2    Schwartz, P.J.3
  • 44
    • 0027374247 scopus 로고
    • Electrophysiological mechanisms in a canine model of erythromycin-associated long QT syndrome
    • M. Rubart M.L. Pressler H.P. Pride Electrophysiological mechanisms in a canine model of erythromycin-associated long QT syndrome Circulation 88 1993 1832 1844
    • (1993) Circulation , vol.88 , pp. 1832-1844
    • Rubart, M.1    Pressler, M.L.2    Pride, H.P.3
  • 45
    • 0029925480 scopus 로고    scopus 로고
    • Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia
    • M.C. Sanguinetti M.E. Curran P.S. Spector Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia Proc Natl Acad Sci U S A 93 1996 2208 2212
    • (1996) Proc Natl Acad Sci U S A , vol.93 , pp. 2208-2212
    • Sanguinetti, M.C.1    Curran, M.E.2    Spector, P.S.3
  • 46
    • 0029002969 scopus 로고
    • A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel
    • M.C. Sanguinetti C. Jiang M.E. Curran A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel Cell 81 1995 299 307
    • (1995) Cell , vol.81 , pp. 299-307
    • Sanguinetti, M.C.1    Jiang, C.2    Curran, M.E.3
  • 47
    • 0025963987 scopus 로고
    • Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes: Mechanism of action
    • M.C. Sanguinetti N.K. Jurkiewicz A. Scott 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
  • 48
    • 0028819671 scopus 로고
    • Mapping of a gene for long QT syndrome to chromosome 4q25-27
    • J.J. Schott F. Charpentier S. Peltier 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
  • 49
    • 0031426535 scopus 로고    scopus 로고
    • Autosomal recessive long-QT syndrome (Jervell Lange–Nielsen syndrome) is genetically heterogeneous
    • E. Schulze-Bahr W. Haverkamp H. Wedekind Autosomal recessive long-QT syndrome (Jervell Lange–Nielsen syndrome) is genetically heterogeneous Hum Genet 100 1997 573 576
    • (1997) Hum Genet , vol.100 , pp. 573-576
    • Schulze-Bahr, E.1    Haverkamp, W.2    Wedekind, H.3
  • 50
    • 0031278313 scopus 로고    scopus 로고
    • KCNE1 mutations cause Jervell and Lange-Nielsen syndrome
    • E. Schulze-Bahr Q. Wang H. Wedekind KCNE1 mutations cause Jervell and Lange-Nielsen syndrome Nat Genet 17 1997 267 268
    • (1997) Nat Genet , vol.17 , pp. 267-268
    • Schulze-Bahr, E.1    Wang, Q.2    Wedekind, H.3
  • 51
    • 0017264676 scopus 로고
    • Cardiac sympathetic innervation and the sudden infant death syndrome: A possible pathogenetic link [review]
    • P.J. Schwartz Cardiac sympathetic innervation and the sudden infant death syndrome: A possible pathogenetic link [review] Am J Med 60 1976 167 172
    • (1976) Am J Med , vol.60 , pp. 167-172
    • Schwartz, P.J.1
  • 52
    • 0026730293 scopus 로고
    • Pathogenesis and therapy of the idiopathic long QT syndrome
    • P.J. Schwartz O. Bonazzi E.H. Locati Pathogenesis and therapy of the idiopathic long QT syndrome Ann NY Acad Sci 644 1992 112
    • (1992) Ann NY Acad Sci , vol.644 , pp. 112
    • Schwartz, P.J.1    Bonazzi, O.2    Locati, E.H.3
  • 53
    • 0001197981 scopus 로고    scopus 로고
    • Gene-specific influence on the triggers for cardiac arrest in the long QT syndrome
    • P.J. Schwartz A.J. Moss S.G. Priori Gene-specific influence on the triggers for cardiac arrest in the long QT syndrome Circulation 96 suppl I 1997 204
    • (1997) Circulation , vol.96 , Issue.suppl I , pp. 204
    • Schwartz, P.J.1    Moss, A.J.2    Priori, S.G.3
  • 54
    • 0028874658 scopus 로고
    • Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate: Implications for gene-specific therapy
    • P.J. Schwartz S.G. Priori E.H. Locati Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate: Implications for gene-specific therapy Circulation 92 1995 3381 3386
    • (1995) Circulation , vol.92 , pp. 3381-3386
    • Schwartz, P.J.1    Priori, S.G.2    Locati, E.H.3
  • 55
    • 17144450747 scopus 로고    scopus 로고
    • Prolongation of the QT interval and the sudden infant death syndrome
    • P.J. Schwartz M. Stramba-Badiale A. Segantini Prolongation of the QT interval and the sudden infant death syndrome N Engl J Med 338 1998 1709 1714
    • (1998) N Engl J Med , vol.338 , pp. 1709-1714
    • Schwartz, P.J.1    Stramba-Badiale, M.2    Segantini, A.3
  • 56
    • 0344863069 scopus 로고    scopus 로고
    • Cellular basis for the ECG features of the LQT1 form of the long-QT syndrome: Effects of beta-adrenergic agonists and antagonists and sodium channel blockers on transmural dispersion of repolarization and torsade de pointes
    • W. Shimizu C. Antzelevitch Cellular basis for the ECG features of the LQT1 form of the long-QT syndrome: Effects of beta-adrenergic agonists and antagonists and sodium channel blockers on transmural dispersion of repolarization and torsade de pointes Circulation 98 1998 2314 2322
    • (1998) Circulation , vol.98 , pp. 2314-2322
    • Shimizu, W.1    Antzelevitch, C.2
  • 57
    • 0030819433 scopus 로고    scopus 로고
    • Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsade de pointes in LQT2 and LQT3 models of the long-QT syndrome
    • W. Shimizu C. Antzelevitch Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsade 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
  • 58
    • 0344450692 scopus 로고
    • Effects of K+ channel opener on repolarization abnormalities demonstrated by monophasic action potential in patients with long QT syndrome
    • W. Shimizu T. Kurita Y. Arakaki Effects of K+ channel opener on repolarization abnormalities demonstrated by monophasic action potential in patients with long QT syndrome Circulation 92 suppl I 1995 275
    • (1995) Circulation , vol.92 , Issue.suppl I , pp. 275
    • Shimizu, W.1    Kurita, T.2    Arakaki, Y.3
  • 59
    • 0028839535 scopus 로고
    • Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome
    • W. Shimizu T. Ohe T. Kurita Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome J Am Coll Cardiol 26 1995 1299 1309
    • (1995) J Am Coll Cardiol , vol.26 , pp. 1299-1309
    • Shimizu, W.1    Ohe, T.2    Kurita, T.3
  • 60
    • 0030025308 scopus 로고    scopus 로고
    • The inward rectification mechanism of the HERG cardiac potassium channel
    • P.L. Smith T. Baukrowitz G. Yellen The inward rectification mechanism of the HERG cardiac potassium channel Nature 379 1996 833 836
    • (1996) Nature , vol.379 , pp. 833-836
    • Smith, P.L.1    Baukrowitz, T.2    Yellen, G.3
  • 61
    • 17344389134 scopus 로고    scopus 로고
    • Genomic structure of three long QT syndrome genes: KVLQT1, HERG and KCNE1
    • I. Splawski J. Shen K.W. Timothy Genomic structure of three long QT syndrome genes: KVLQT1, HERG and KCNE1 Genomics 51 1998 86 97
    • (1998) Genomics , vol.51 , pp. 86-97
    • Splawski, I.1    Shen, J.2    Timothy, K.W.3
  • 62
    • 0031230388 scopus 로고    scopus 로고
    • Molecular basis of the long-QT syndrome associated with deafness
    • I. Splawski K.W. Timothy G.M. Vincent Molecular basis of the long-QT syndrome associated with deafness Proc Assoc Am Physicians 109 1997 504 511
    • (1997) Proc Assoc Am Physicians , vol.109 , pp. 504-511
    • Splawski, I.1    Timothy, K.W.2    Vincent, G.M.3
  • 63
    • 0030918946 scopus 로고    scopus 로고
    • Molecular basis of the long-QT syndrome associated with deafness
    • I. Splawski K.W. Timothy G.M. Vincent Molecular basis of the long-QT syndrome associated with deafness N Engl J Med 336 1997 1562 1567
    • (1997) N Engl J Med , vol.336 , pp. 1562-1567
    • Splawski, I.1    Timothy, K.W.2    Vincent, G.M.3
  • 64
    • 0032616508 scopus 로고    scopus 로고
    • The IKs channel: Coassembly of IsK (minK) and KvLQT1 proteins. [Review]
    • H. Suessbrich A.E. Busch The IKs channel: Coassembly of IsK (minK) and KvLQT1 proteins. [Review] Rev Physiol Biochem Pharmacol 137 1999 191 226
    • (1999) Rev Physiol Biochem Pharmacol , vol.137 , pp. 191-226
    • Suessbrich, H.1    Busch, A.E.2
  • 65
    • 0032030673 scopus 로고    scopus 로고
    • Rate adaptation of QT intervals during and after exercise in children with congenital long QT syndrome
    • H. Swan L. Toivonen M. Viitasalo Rate adaptation of QT intervals during and after exercise in children with congenital long QT syndrome Eur Heart J 19 1998 508 513
    • (1998) Eur Heart J , vol.19 , pp. 508-513
    • Swan, H.1    Toivonen, L.2    Viitasalo, M.3
  • 66
    • 0023734276 scopus 로고    scopus 로고
    • Cloning of a membrane protein that induces a slow voltage-gated potassium current
    • T. Takumi H. Ohkubo S. Nakanishi Cloning of a membrane protein that induces a slow voltage-gated potassium current Science 242 1998 1042 1045
    • (1998) Science , vol.242 , pp. 1042-1045
    • Takumi, T.1    Ohkubo, H.2    Nakanishi, S.3
  • 67
    • 0032967864 scopus 로고    scopus 로고
    • Long-term (subacute) potassium treatment in congenital HERG-related long QT syndrome (LQTS2)
    • H.L. Tan M. Alings R.W. VanOlden Long-term (subacute) potassium treatment in congenital HERG-related long QT syndrome (LQTS2) J Cardiovasc Electrophysiol 10 1999 229 233
    • (1999) J Cardiovasc Electrophysiol , vol.10 , pp. 229-233
    • Tan, H.L.1    Alings, M.2    VanOlden, R.W.3
  • 68
    • 0028898211 scopus 로고
    • Electrophysiologic mechanisms of the long QT interval syndromes and torsades de pointes
    • H.L. Tan C.J. Hou M.R. Lauer Electrophysiologic mechanisms of the long QT interval syndromes and torsades de pointes Ann Intern Med 122 1995 701 714
    • (1995) Ann Intern Med , vol.122 , pp. 701-714
    • Tan, H.L.1    Hou, C.J.2    Lauer, M.R.3
  • 69
    • 0013516545 scopus 로고    scopus 로고
    • Differences in precipitators of cardiac arrest and sudden death in chromosome 11 versus 7 genotype long QT syndrome patients
    • K.W. Timothy L. Zhang K.J. Meyer Differences in precipitators of cardiac arrest and sudden death in chromosome 11 versus 7 genotype long QT syndrome patients Circulation 94 1996 I-204
    • (1996) Circulation , vol.94 , pp. I-204
    • Timothy, K.W.1    Zhang, L.2    Meyer, K.J.3
  • 70
    • 9844261701 scopus 로고    scopus 로고
    • IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome
    • J. Tyson L. Tranebjaerg S. Bellman IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome Hum Mol Genet 6 1997 2179 2185
    • (1997) Hum Mol Genet , vol.6 , pp. 2179-2185
    • Tyson, J.1    Tranebjaerg, L.2    Bellman, S.3
  • 71
    • 0030461289 scopus 로고    scopus 로고
    • Inner ear defects induced by null mutation of the IsK gene
    • D.E. Vetter J.R. Mann P. Wangemann Inner ear defects induced by null mutation of the IsK gene Neuron 17 1996 1251 1264
    • (1996) Neuron , vol.17 , pp. 1251-1264
    • Vetter, D.E.1    Mann, J.R.2    Wangemann, P.3
  • 72
    • 0028912846 scopus 로고
    • Heterogeneity in the inherited long QT syndrome
    • G.M. Vincent Heterogeneity in the inherited long QT syndrome J Cardiovasc Electrophysiol 6 1995 137 146
    • (1995) J Cardiovasc Electrophysiol , vol.6 , pp. 137-146
    • Vincent, G.M.1
  • 73
    • 68249154224 scopus 로고
    • Long-term follow-up of a family with Romano-Ward prolonged QT interval syndrome
    • G.M. Vincent Long-term follow-up of a family with Romano-Ward prolonged QT interval syndrome Butrous G.S. Schwartz P.J. Clinical Aspects of Ventricular Repolarization 1989 Farrand Press London 411 413
    • (1989) , pp. 411-413
    • Vincent, G.M.1
  • 74
    • 25044450042 scopus 로고    scopus 로고
    • Effects of a potassium channel opener in KVLQT1 long QT gene carriers [abstract]
    • G.M. Vincent J. Fox L. Zhang Effects of a potassium channel opener in KVLQT1 long QT gene carriers [abstract] J Am Coll Cardiol 29 1997 183A
    • (1997) J Am Coll Cardiol , vol.29 , pp. 183A
    • Vincent, G.M.1    Fox, J.2    Zhang, L.3
  • 75
    • 85120115297 scopus 로고
    • Abnormal QT/QS2 ratio at rest and exercise in Romano-Ward long QT patients, normalized by β-blocker therapy [abstract]
    • G.M. Vincent D. Jaiswal K.W. Timothy Abnormal QT/QS2 ratio at rest and exercise in Romano-Ward long QT patients, normalized by β-blocker therapy [abstract] J Am Coll Cardiol 13 1989 11A
    • (1989) J Am Coll Cardiol , vol.13 , pp. 11A
    • Vincent, G.M.1    Jaiswal, D.2    Timothy, K.W.3
  • 76
    • 0025883918 scopus 로고
    • Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome
    • G.M. Vincent D. Jaiswal K.W. Timothy Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome Am J Cardiol 68 1991 498 503
    • (1991) Am J Cardiol , vol.68 , pp. 498-503
    • Vincent, G.M.1    Jaiswal, D.2    Timothy, K.W.3
  • 77
    • 84958841034 scopus 로고
    • Seventeen year study of a Romano-Ward long QT family
    • G.M. Vincent K.W. Timothy D. Jaiswal Seventeen year study of a Romano-Ward long QT family Circulation 80 1989 II-654
    • (1989) Circulation , vol.80 , pp. II-654
    • Vincent, G.M.1    Timothy, K.W.2    Jaiswal, D.3
  • 79
    • 0000392371 scopus 로고    scopus 로고
    • Beta-blockers markedly reduce risk and syncope in KVLQT1 long QT patients [abstract]
    • G.M. Vincent L. Zhang K.W. Timothy Beta-blockers markedly reduce risk and syncope in KVLQT1 long QT patients [abstract] Circulation 94 1996 I-204
    • (1996) Circulation , vol.94 , pp. I-204
    • Vincent, G.M.1    Zhang, L.2    Timothy, K.W.3
  • 80
    • 1842273160 scopus 로고
    • In LQTS, β-blockers reduce QT, QTc, and T morphology abnormalities during exercise: This may be the mechanism of therapeutic benefit
    • G.M. Vincent K.W. Timothy C.Z. Cui In LQTS, β-blockers reduce QT, QTc, and T morphology abnormalities during exercise: This may be the mechanism of therapeutic benefit Circulation 86 1992 I-393
    • (1992) Circulation , vol.86 , pp. I-393
    • Vincent, G.M.1    Timothy, K.W.2    Cui, C.Z.3
  • 81
    • 85120102634 scopus 로고
    • The spectrum of symptoms and QT intervals in long QT syndrome gene carriers
    • G.M. Vincent K.W. Timothy M. Leppert The spectrum of symptoms and QT intervals in long QT syndrome gene carriers Clin Res 40 1992 324A
    • (1992) Clin Res , vol.40 , pp. 324A
    • Vincent, G.M.1    Timothy, K.W.2    Leppert, M.3
  • 82
    • 0026759352 scopus 로고
    • The spectrum of symptoms and QT intervals in the carriers of the gene for the long-QT syndrome
    • G.M. Vincent K.W. Timothy M. Leppert The spectrum of symptoms and QT intervals in the 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
  • 83
    • 17344371959 scopus 로고    scopus 로고
    • High prevalence of normal QT interval in patients with the inherited long QT syndrome: Important implications for diagnosis [abstract]
    • G.M. Vincent K.W. Timothy L. Zhang High prevalence of normal QT interval in patients with the inherited long QT syndrome: Important implications for diagnosis [abstract] Pacing Clin Electrophysiol 19 1996 588
    • (1996) Pacing Clin Electrophysiol , vol.19 , pp. 588
    • Vincent, G.M.1    Timothy, K.W.2    Zhang, L.3
  • 84
    • 0005037870 scopus 로고    scopus 로고
    • Intragenic, intramutational and intrafamilial heterogeneity of the QT phenotype in the long QT syndrome [abstract]
    • G.M. Vincent L. Zhang K.W. Timothy Intragenic, intramutational and intrafamilial heterogeneity of the QT phenotype in the long QT syndrome [abstract] Pacing Clin Electrophysiol 21 1998 850
    • (1998) Pacing Clin Electrophysiol , vol.21 , pp. 850
    • Vincent, G.M.1    Zhang, L.2    Timothy, K.W.3
  • 85
    • 0030298484 scopus 로고    scopus 로고
    • Mode of onset of torsades de pointes in congenital long QT syndrome
    • S. Viskin S.R. Alla H.V. Barron 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
  • 86
    • 0031959366 scopus 로고    scopus 로고
    • Prevention of torsades de pointes in the congenital long QT syndrome: Use of a pause prevention pacing algorithm
    • S. Viskin R. Fish A. Roth Prevention of torsades de pointes in the congenital long QT syndrome: Use of a pause prevention pacing algorithm Heart 79 1998 417 419
    • (1998) Heart , vol.79 , pp. 417-419
    • Viskin, S.1    Fish, R.2    Roth, A.3
  • 87
    • 0024280882 scopus 로고
    • Regulation of a heart potassium channel by protein kinase A and C
    • K.B. Walsh R.S. Kass Regulation of a heart potassium channel by protein kinase A and C Science 242 1988 67 69
    • (1988) Science , vol.242 , pp. 67-69
    • Walsh, K.B.1    Kass, R.S.2
  • 88
    • 0025874842 scopus 로고
    • Delayed rectifier potassium channel activity in isolated membrane patches of guinea pig ventricular myocytes
    • K.B. Walsh J.P. Arena W.M. Kwok Delayed rectifier potassium channel activity in isolated membrane patches of guinea pig ventricular myocytes Am J Physiol 260 1991 H1390 H1393
    • (1991) Am J Physiol , vol.260 , pp. H1390-H1393
    • Walsh, K.B.1    Arena, J.P.2    Kwok, W.M.3
  • 89
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • Q. Wang M.E. Curran I. Splawski 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
  • 90
    • 0029992905 scopus 로고    scopus 로고
    • Genomic organization of the human SCN5A gene encoding the cardiac sodium channel
    • Q. Wang Z. Li J. Shen Genomic organization of the human SCN5A gene encoding the cardiac sodium channel Genomics 34 1996 9 16
    • (1996) Genomics , vol.34 , pp. 9-16
    • Wang, Q.1    Li, Z.2    Shen, J.3
  • 91
    • 0029116230 scopus 로고
    • Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia
    • Q. Wang J. Shen Z. Li Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia Hum Mol Genet 4 1995 1603 1607
    • (1995) Hum Mol Genet , vol.4 , pp. 1603-1607
    • Wang, Q.1    Shen, J.2    Li, Z.3
  • 92
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Q. Wang J. Shen I. Splawski 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
  • 94
    • 0033081030 scopus 로고    scopus 로고
    • Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)
    • A.A. Wilde R.J. Jongbloed P.A. Doevendans Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) J Am Coll Cardiol 33 1999 327 332
    • (1999) J Am Coll Cardiol , vol.33 , pp. 327-332
    • Wilde, A.A.1    Jongbloed, R.J.2    Doevendans, P.A.3
  • 95
    • 0013893665 scopus 로고    scopus 로고
    • Functional distribution of right and left stellate innervation to the ventricles: Production of neurogenic electrocardiographic changes by unilateral alterations of sympathetic tone
    • F. Yanowitz J.B. Preston J.A. Abildskov Functional distribution of right and left stellate innervation to the ventricles: Production of neurogenic electrocardiographic changes by unilateral alterations of sympathetic tone Circ Res 18 1996 416
    • (1996) Circ Res , vol.18 , pp. 416
    • Yanowitz, F.1    Preston, J.B.2    Abildskov, J.A.3
  • 96
    • 0032922888 scopus 로고    scopus 로고
    • Potassium channels: Basic aspects, functional roles, and medical significance
    • C.S. Yost Potassium channels: Basic aspects, functional roles, and medical significance Anesthesiology 90 1999 1186 1203
    • (1999) Anesthesiology , vol.90 , pp. 1186-1203
    • Yost, C.S.1
  • 97
    • 33847461169 scopus 로고    scopus 로고
    • The influence of β-blockers on QT interval in patients with long QT syndrome [abstract]
    • W. Zareba A.J. Moss J. Benhorin The influence of β-blockers on QT interval in patients with long QT syndrome [abstract] J Am Coll Cardiol 27 1996 121A
    • (1996) J Am Coll Cardiol , vol.27 , pp. 121A
    • Zareba, W.1    Moss, A.J.2    Benhorin, J.3
  • 98
    • 0032189139 scopus 로고    scopus 로고
    • Influence of genotype on the clinical course of the long-QT syndrome: International Long-QT Syndrome Registry Research Group
    • W. Zareba A.J. Moss P.J. Schwartz Influence of genotype on the clinical course of the long-QT syndrome: International Long-QT Syndrome Registry Research Group N Engl J Med 339 1998 960 965
    • (1998) N Engl J Med , vol.339 , pp. 960-965
    • Zareba, W.1    Moss, A.J.2    Schwartz, P.J.3
  • 99
    • 0026564187 scopus 로고
    • Role of early afterdepolarization in familial long QTU syndromes and torsade de pointes
    • J.T. Zhou L.R. Zheng W.Y. Liu Role of early afterdepolarization in familial long QTU syndromes and torsade de pointes Pacing Clin Electrophysiol 1992 2164 2168
    • (1992) Pacing Clin Electrophysiol , pp. 2164-2168
    • Zhou, J.T.1    Zheng, L.R.2    Liu, W.Y.3
  • 100


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