The long QT syndromes

Progress in Pediatric Cardiology - Tập 6 - Trang 43-51 - 1996
Mark W. Russell1
1Department of Pediatrics, Division of Pediatric Cardiology, C.S. Mott Children's Hospital, University of Michigan Medical Center, Ann Arbor, MI, USA

Tài liệu tham khảo

Romano, 1963, Artimie cardiache rare dell'eta pediatrica, Clin Pediatr, 45, 658 Ward, 1964, New familial cardiac syndrome in children, J Irish Med Assoc, 54, 103 Jervell, 1957, Congenital deaf-mutism, functional heart diseases with prolongation of the QT interval and sudden death, Am Heart J, 54, 59, 10.1016/0002-8703(57)90079-0 Schwartz, 1992, Pathogenesis and therapy of the idiopathic long QT syndrome, Ann NY Acad Sci, 644, 112, 10.1111/j.1749-6632.1992.tb31007.x Garson, 1993, The long QT syndrome in children. An international study of 287 patients, Circulation, 87, 1866, 10.1161/01.CIR.87.6.1866 Moss, 1991, The long QT syndrome. Prospective longitudinal study of 328 families, Circulation, 84, 1136, 10.1161/01.CIR.84.3.1136 Keating, 1991, Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene, Science, 252, 704, 10.1126/science.1673802 Towbin, 1992, Romano-Ward long QT syndrome (RWLQTS): Evidence of genetic heterogeneity, Pediatr Res, 31, 23 Benhorin, 1993, Evidence of genetic heterogeneity in the long QT syndrome, Science, 260, 1960, 10.1126/science.8316839 Curran, 1993, Locus heterogeneity of autosomal dominant long QT syndrome, J Clin Invest, 92, 799, 10.1172/JCI116653 Towbin, 1994, Evidence of genetic heterogeneity in Romano-Ward long QT syndrome: Analysis of 23 families, Circulation, 90, 2635, 10.1161/01.CIR.90.6.2635 Jiang, 1994, Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity, Nature Genet, 8, 141, 10.1038/ng1094-141 Schott, 1995, Mapping of a gene for long QT syndrome to chromosome 4q25–27, Am J Hum Genet, 57, 1114 Wang, 1996, Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias, Nature Genet, 12, 17, 10.1038/ng0196-17 Curran, 1995, A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome, Cell, 80, 795, 10.1016/0092-8674(95)90358-5 Wang, 1995, SCN5A mutations associated with an inherited cardiac arrhythmia, Long QT syndrome, Cell, 80, 805, 10.1016/0092-8674(95)90359-3 Vincent, 1992, The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome, N Engl J Med, 327, 846, 10.1056/NEJM199209173271204 Gellens, 1992, Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage dependent sodium channel, 89, 554 George, 1995, Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel α-subunit gene (SCN5A) to band 3p21, Cytogenet Cell Genet, 68, 67, 10.1159/000133892 Towbin, 1995, New revelations about the long-QT syndrome, N Engl J Med, 333, 384, 10.1056/NEJM199508103330613 Fontaine, 1990, Hyperkalemic periodic paralysis and the skeletal muscle sodium channel gene, Science, 250, 1000, 10.1126/science.2173143 Bennett, 1995, Molecular mechanism for an inherited cardiac arrhythmia, Nature, 376, 683, 10.1038/376683a0 Moss, 1995, ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome, Circulation, 92, 2929, 10.1161/01.CIR.92.10.2929 Wang, 1995, Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia, Hum Mol Genet, 4, 1603, 10.1093/hmg/4.9.1603 Bruggeman, 1993, Ether-a-go-go encodes a voltage-gated channel permeable to k+ and Ca2+ and modulated by cAMP, Nature, 365, 445, 10.1038/365445a0 Warmke, 1994, A family of potassium channel genes related to eag in Drosophlla and mammals, 91, 3438 Jackman, 1988, The long QT syndromes: A critical review, new clinical observations and a unifying hypothesis, Prog Cardiovasc Dis, XXXI, 115, 10.1016/0033-0620(88)90014-X Sanguinetti, 1995, A mechanistic link between an inherited and acquired cardiac arrhythmia: HERG encodes the Ikr potassium channel, Cell, 81, 299, 10.1016/0092-8674(95)90340-2 Shibasaki, 1987, Conductance and kinetics of delayed rectifier potassium channels in nodal cells of the rabbit heart, J Physiol, 387, 227, 10.1113/jphysiol.1987.sp016571 Russell, 1995, Localization of the Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349, Am J Hum Genet, 57, 503 Schwartz, 1995, 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, 3381, 10.1161/01.CIR.92.12.3381 Zareba, 1995, Risk of cardiac events in family members of patients with long QT syndrome, J Am Coll Cardiol, 26, 1685, 10.1016/0735-1097(95)60383-2 Russell, 1996, The molecular genetics of the congenital long QT syndromes, Curr Opin Cardiol, 11, 10.1097/00001573-199601000-00008