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Related Citations for PubMed (Select 21315844)


T-wave morphology abnormalities in benign, potent, and arrhythmogenic I(kr) inhibition.

Couderc JP, Xia X, Peterson DR, McNitt S, Zhao H, Polonsky S, Moss AJ, Zareba W.

Heart Rhythm. 2011 Jul;8(7):1036-43. doi: 10.1016/j.hrthm.2011.02.005. Epub 2011 Feb 9.


Improving the detection of subtle I(Kr)-inhibition: assessing electrocardiographic abnormalities of repolarization induced by moxifloxacin.

Couderc JP, McNitt S, Hyrien O, Vaglio M, Xia X, Polonsky S, Moss AJ, Zareba W.

Drug Saf. 2008;31(3):249-60.


Impaired T-amplitude adaptation to heart rate characterizes I(Kr) inhibition in the congenital and acquired forms of the long QT syndrome.

Couderc JP, Vaglio M, Xia X, McNitt S, Wicker P, Sarapa N, Moss AJ, Zareba W.

J Cardiovasc Electrophysiol. 2007 Dec;18(12):1299-305. Epub 2007 Oct 4.


Repolarization morphology in adult LQT2 carriers with borderline prolonged QTc interval.

Couderc JP, McNitt S, Xia J, Zareba W, Moss AJ.

Heart Rhythm. 2006 Dec;3(12):1460-6. Epub 2006 Aug 10.


The phenotype characteristics of type 13 long QT syndrome with mutation in KCNJ5 (Kir3.4-G387R).

Wang F, Liu J, Hong L, Liang B, Graff C, Yang Y, Christiansen M, Olesen SP, Zhang L, Kanters JK.

Heart Rhythm. 2013 Oct;10(10):1500-6. doi: 10.1016/j.hrthm.2013.07.022. Epub 2013 Jul 18.


A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death.

Zhang Y, Zhou N, Jiang W, Peng J, Wan H, Huang C, Xie Z, Huang CL, Grace AA, Ma A.

Eur J Pediatr. 2007 Sep;166(9):927-33. Epub 2006 Dec 14.


Effect of nalmefene 20 and 80 mg on the corrected QT interval and T-wave morphology: a randomized, double-blind, parallel-group, placebo- and moxifloxacin-controlled, single-centre study.

Matz J, Graff C, Vainio PJ, Kallio A, Højer AM, Struijk JJ, Kanters JK, Andersen MP, Toft E.

Clin Drug Investig. 2011 Nov 1;31(11):799-811. doi: 10.2165/11592950-000000000-00000.


Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.

Wong JA, Gula LJ, Klein GJ, Yee R, Skanes AC, Krahn AD.

Circ Arrhythm Electrophysiol. 2010 Apr;3(2):120-5. doi: 10.1161/CIRCEP.109.907865. Epub 2010 Jan 9.


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.

J Am Coll Cardiol. 2004 Sep 15;44(6):1283-91.


QT prolongation and proarrhythmia by moxifloxacin: concordance of preclinical models in relation to clinical outcome.

Chen X, Cass JD, Bradley JA, Dahm CM, Sun Z, Kadyszewski E, Engwall MJ, Zhou J.

Br J Pharmacol. 2005 Nov;146(6):792-9.


Investigation of ion channel gene variants in patients with long QT syndrome.

Ernesto C, Cruz FE, Lima FS, Coutinho JL, Silva R, Urményi TP, Carvalho AC, Rondinelli E.

Arq Bras Cardiol. 2011 Mar;96(3):172-8. Epub 2011 Feb 4. English, Portuguese, Spanish.


Multi-undulant T-U-wave, sinus bradycardia and long QT syndrome: a possible phenotype of mutant genes controlling the inward potassium rectifiers.

Shen CT, Wu YC, Yu SS, Wang NK.

Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 Jul-Aug;38(4):267-75.


Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.

Lupoglazoff JM, Denjoy I, Berthet M, Neyroud N, Demay L, Richard P, Hainque B, Vaksmann G, Klug D, Leenhardt A, Maillard G, Coumel P, Guicheney P.

Circulation. 2001 Feb 27;103(8):1095-101.


A quantitative assessment of T-wave morphology in LQT1, LQT2, and healthy individuals based on Holter recording technology.

Vaglio M, Couderc JP, McNitt S, Xia X, Moss AJ, Zareba W.

Heart Rhythm. 2008 Jan;5(1):11-8. doi: 10.1016/j.hrthm.2007.08.026. Epub 2007 Aug 28.


KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.

Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ.

Circulation. 2005 Aug 30;112(9):1251-8. Epub 2005 Aug 22. Erratum in: Circulation. 2005 Oct 25;112(17):e294.


Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.

Zhang X, Chen S, Zhang L, Liu M, Redfearn S, Bryant RM, Oberti C, Vincent GM, Wang QK.

BMC Med Genet. 2008 Sep 23;9:87. doi: 10.1186/1471-2350-9-87.


Pharmacogenomics of anesthetic drugs in transgenic LQT1 and LQT2 rabbits reveal genotype-specific differential effects on cardiac repolarization.

Odening KE, Hyder O, Chaves L, Schofield L, Brunner M, Kirk M, Zehender M, Peng X, Koren G.

Am J Physiol Heart Circ Physiol. 2008 Dec;295(6):H2264-72. doi: 10.1152/ajpheart.00680.2008. Epub 2008 Oct 3.


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.

Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantù F, Towbin JA, Keating MT, Hammoude H, Brown AM, Chen LS.

Circulation. 1995 Dec 15;92(12):3381-6.


KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.

Liu W, Yang J, Hu D, Kang C, Li C, Zhang S, Li P, Chen Z, Qin X, Ying K, Li Y, Li Y, Li Z, Cheng X, Li L, Qi Y, Chen S, Wang Q.

Hum Mutat. 2002 Dec;20(6):475-6.

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