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Items: 1 to 20 of 143

1.

Do LQTS gene single nucleotide polymorphisms alter QTc intervals at rest and during exercise stress testing?

Aziz PF, Wieand TS, Ganley J, Henderson J, McBride M, Shah MJ.

Ann Noninvasive Electrocardiol. 2013 May;18(3):288-93. doi: 10.1111/anec.12037. Epub 2013 Jan 20.

2.

Genotype- and mutation site-specific QT adaptation during exercise, recovery, and postural changes in children with long-QT syndrome.

Aziz PF, Wieand TS, Ganley J, Henderson J, Patel AR, Iyer VR, Vogel RL, McBride M, Vetter VL, Shah MJ.

Circ Arrhythm Electrophysiol. 2011 Dec;4(6):867-73. doi: 10.1161/CIRCEP.111.963330. Epub 2011 Sep 28.

3.

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.

4.

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.

Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P; D.E.S.I.R. Study Group.

Eur J Hum Genet. 2005 Nov;13(11):1213-22.

5.

Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.

Jimmy JJ, Chen CY, Yeh HM, Chiu WY, Yu CC, Liu YB, Tsai CT, Lo LW, Yeh SF, Lai LP.

Chin Med J (Engl). 2014;127(8):1482-6.

PMID:
24762593
6.

Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.

Tester DJ, Cronk LB, Carr JL, Schulz V, Salisbury BA, Judson RS, Ackerman MJ.

Heart Rhythm. 2006 Jul;3(7):815-21. Epub 2006 Mar 16.

PMID:
16818214
7.

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.

8.
9.

Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk.

ter Bekke RM, Haugaa KH, van den Wijngaard A, Bos JM, Ackerman MJ, Edvardsen T, Volders PG.

Eur Heart J. 2015 Jan 14;36(3):179-86. doi: 10.1093/eurheartj/ehu370. Epub 2014 Sep 8.

PMID:
25205533
10.

Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications.

Shinwari ZM, Al-Hazzani A, Dzimiri N, Tulbah S, Mallawi Y, Al-Fayyadh M, Al-Hassnan ZN.

Clin Genet. 2013 Apr;83(4):370-4. doi: 10.1111/j.1399-0004.2012.01914.x. Epub 2012 Jul 10.

PMID:
22708720
11.

Long QT and Brugada syndrome gene mutations in New Zealand.

Chung SK, MacCormick JM, McCulley CH, Crawford J, Eddy CA, Mitchell EA, Shelling AN, French JK, Skinner JR, Rees MI.

Heart Rhythm. 2007 Oct;4(10):1306-14. Epub 2007 Jul 14.

PMID:
17905336
12.

Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.

Barc J, Briec F, Schmitt S, Kyndt F, Le Cunff M, Baron E, Vieyres C, Sacher F, Redon R, Le Caignec C, Le Marec H, Probst V, Schott JJ.

J Am Coll Cardiol. 2011 Jan 4;57(1):40-7. doi: 10.1016/j.jacc.2010.08.621.

13.

Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance.

Mints Y, Zipunnikov V, Khurram I, Calkins H, Nazarian S.

Ann Noninvasive Electrocardiol. 2014 Jan;19(1):63-9. doi: 10.1111/anec.12088. Epub 2013 Sep 9.

14.

Single nucleotide polymorphism map of five long-QT genes.

Aydin A, Bähring S, Dahm S, Guenther UP, Uhlmann R, Busjahn A, Luft FC.

J Mol Med (Berl). 2005 Feb;83(2):159-65. Epub 2004 Dec 15.

PMID:
15599693
15.

End-recovery QTc: a useful metric for assessing genetic variants of unknown significance in long-QT syndrome.

Obeyesekere MN, Sy RW, Klein GJ, Gula LJ, Modi S, Conacher S, Leong-Sit P, Skanes AC, Yee R, Krahn AD.

J Cardiovasc Electrophysiol. 2012 Jun;23(6):637-42. doi: 10.1111/j.1540-8167.2011.02265.x. Epub 2012 Mar 19.

PMID:
22429796
16.

Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A.

Seo SH, Kim SY, Cho SI, Park H, Lee S, Choi JM, Kim MJ, Lee JS, Ahn KJ, Song MK, Bae EJ, Park SS, Seong MW.

Ann Lab Med. 2018 Jan;38(1):54-58. doi: 10.3343/alm.2018.38.1.54.

17.

Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.

Trolle C, Mortensen KH, Pedersen LN, Berglund A, Jensen HK, Andersen NH, Gravholt CH.

PLoS One. 2013 Jul 25;8(7):e69614. doi: 10.1371/journal.pone.0069614. Print 2013.

18.

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.

Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ.

Heart Rhythm. 2009 Sep;6(9):1297-303. doi: 10.1016/j.hrthm.2009.05.021. Epub 2009 Jun 23.

19.

[Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].

Liu WL, Hu DY, Li P, Li CL, Qin XG, Li YT, Li L, Li ZM, Dong W, Qi Y, Wang Q.

Zhonghua Nei Ke Za Zhi. 2006 Jun;45(6):463-6. Chinese.

PMID:
16831322
20.

N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome.

Ohno S, Zankov DP, Yoshida H, Tsuji K, Makiyama T, Itoh H, Akao M, Hancox JC, Kita T, Horie M.

Heart Rhythm. 2007 Mar;4(3):332-40. Epub 2006 Nov 10.

PMID:
17341399

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