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The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.
Vincent GM, Timothy KW, Leppert M, Keating M. Vincent GM, et al. Among authors: timothy kw. N Engl J Med. 1992 Sep 17;327(12):846-52. doi: 10.1056/NEJM199209173271204. N Engl J Med. 1992. PMID: 1508244
Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.
Moss AJ, Robinson JL, Gessman L, Gillespie R, Zareba W, Schwartz PJ, Vincent GM, Benhorin J, Heilbron EL, Towbin JA, Priori SG, Napolitano C, Zhang L, Medina A, Andrews ML, Timothy K. Moss AJ, et al. Among authors: timothy k. Am J Cardiol. 1999 Oct 15;84(8):876-9. doi: 10.1016/s0002-9149(99)00458-0. Am J Cardiol. 1999. PMID: 10532503
Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.
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. Moss AJ, et al. Among authors: timothy k. Circulation. 2000 Feb 15;101(6):616-23. doi: 10.1161/01.cir.101.6.616. Circulation. 2000. PMID: 10673253 Clinical Trial.
Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
Allan WC, Timothy K, Vincent GM, Palomaki GE, Neveux LM, Haddow JE. Allan WC, et al. Among authors: timothy k. J Med Screen. 2001;8(4):173-7. doi: 10.1136/jms.8.4.173. J Med Screen. 2001. PMID: 11743032
Long QT syndrome in children: the value of the rate corrected QT interval in children who present with fainting.
Allan WC, Timothy K, Vincent GM, Palomaki GE, Neveux LM, Haddow JE. Allan WC, et al. Among authors: timothy k. J Med Screen. 2001;8(4):178-82. doi: 10.1136/jms.8.4.178. J Med Screen. 2001. PMID: 11743033
Clinical implications for affected parents and siblings of probands with long-QT syndrome.
Kimbrough J, Moss AJ, Zareba W, Robinson JL, Hall WJ, Benhorin J, Locati EH, Medina A, Napolitano C, Priori S, Schwartz PJ, Timothy K, Towbin JA, Vincent GM, Zhang L. Kimbrough J, et al. Among authors: timothy k. Circulation. 2001 Jul 31;104(5):557-62. doi: 10.1161/hc3001.093501. Circulation. 2001. PMID: 11479253
Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome.
Ali RH, Zareba W, Moss AJ, Schwartz PJ, Benhorin J, Vincent GM, Locati EH, Priori S, Napolitano C, Towbin JA, Hall WJ, Robinson JL, Andrews ML, Zhang L, Timothy K, Medina A. Ali RH, et al. Among authors: timothy k. Am J Cardiol. 2000 Feb 15;85(4):457-61. doi: 10.1016/s0002-9149(99)90772-5. Am J Cardiol. 2000. PMID: 10728950
The inherited long QT syndrome: from ion channel to bedside.
Vincent GM, Timothy K, Fox J, Zhang L. Vincent GM, et al. Among authors: timothy k. Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Cardiol Rev. 1999. PMID: 10348966 Review.
Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.
Locati EH, Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Lehmann MH, Towbin JA, Priori SG, Napolitano C, Robinson JL, Andrews M, Timothy K, Hall WJ. Locati EH, et al. Among authors: timothy k. Circulation. 1998 Jun 9;97(22):2237-44. doi: 10.1161/01.cir.97.22.2237. Circulation. 1998. PMID: 9631873
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.
Wang Q, Shen J, Li Z, Timothy K, Vincent GM, Priori SG, Schwartz PJ, Keating MT. Wang Q, et al. Among authors: timothy k. Hum Mol Genet. 1995 Sep;4(9):1603-7. doi: 10.1093/hmg/4.9.1603. Hum Mol Genet. 1995. PMID: 8541846
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