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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: keating m. N Engl J Med. 1992 Sep 17;327(12):846-52. doi: 10.1056/NEJM199209173271204. N Engl J Med. 1992. PMID: 1508244
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
Zareba W, Moss AJ, Sheu G, Kaufman ES, Priori S, Vincent GM, Towbin JA, Benhorin J, Schwartz PJ, Napolitano C, Hall WJ, Keating MT, Qi M, Robinson J, Andrews ML; International LQTS Registry, University of Rochester, Rochester, New York. Zareba W, et al. Among authors: keating mt. J Cardiovasc Electrophysiol. 2003 Nov;14(11):1149-53. doi: 10.1046/j.1540-8167.2003.03177.x. J Cardiovasc Electrophysiol. 2003. PMID: 14678125
Compound mutations: a common cause of severe long-QT syndrome.
Westenskow P, Splawski I, Timothy KW, Keating MT, Sanguinetti MC. Westenskow P, et al. Among authors: keating mt. Circulation. 2004 Apr 20;109(15):1834-41. doi: 10.1161/01.CIR.0000125524.34234.13. Epub 2004 Mar 29. Circulation. 2004. PMID: 15051636
An intronic mutation causes long QT syndrome.
Zhang L, Vincent GM, Baralle M, Baralle FE, Anson BD, Benson DW, Whiting B, Timothy KW, Carlquist J, January CT, Keating MT, Splawski I. Zhang L, et al. Among authors: keating mt. J Am Coll Cardiol. 2004 Sep 15;44(6):1283-91. doi: 10.1016/j.jacc.2004.06.045. J Am Coll Cardiol. 2004. PMID: 15364333
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.
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. Moss AJ, et al. Among authors: keating mt. Circulation. 2002 Feb 19;105(7):794-9. doi: 10.1161/hc0702.105124. Circulation. 2002. PMID: 11854117
A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.
Ewart AK, Morris CA, Ensing GJ, Loker J, Moore C, Leppert M, Keating M. Ewart AK, et al. Among authors: keating m. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3226-30. doi: 10.1073/pnas.90.8.3226. Proc Natl Acad Sci U S A. 1993. PMID: 8475063 Free PMC article.
Genetics of the long QT syndrome.
Keating M. Keating M. J Cardiovasc Electrophysiol. 1994 Feb;5(2):146-53. doi: 10.1111/j.1540-8167.1994.tb01155.x. J Cardiovasc Electrophysiol. 1994. PMID: 8186885 Review.
Locus heterogeneity of autosomal dominant long QT syndrome.
Curran M, Atkinson D, Timothy K, Vincent GM, Moss AJ, Leppert M, Keating M. Curran M, et al. Among authors: keating m. J Clin Invest. 1993 Aug;92(2):799-803. doi: 10.1172/JCI116653. J Clin Invest. 1993. PMID: 8102381 Free PMC article.
A new form of long QT syndrome associated with syndactyly.
Marks ML, Whisler SL, Clericuzio C, Keating M. Marks ML, et al. Among authors: keating m. J Am Coll Cardiol. 1995 Jan;25(1):59-64. doi: 10.1016/0735-1097(94)00318-k. J Am Coll Cardiol. 1995. PMID: 7798527 Review.
Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.
Lowery MC, Morris CA, Ewart A, Brothman LJ, Zhu XL, Leonard CO, Carey JC, Keating M, Brothman AR. Lowery MC, et al. Among authors: keating m. Am J Hum Genet. 1995 Jul;57(1):49-53. Am J Hum Genet. 1995. PMID: 7611295 Free PMC article.
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