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Items: 1 to 20 of 193

1.

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.

2.

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
3.

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.

4.

Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.

Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW.

Circ Arrhythm Electrophysiol. 2013 Oct;6(5):946-51. doi: 10.1161/CIRCEP.113.000618. Epub 2013 Aug 30.

5.

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.

6.

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
7.

The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.

Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J.

J Cardiovasc Electrophysiol. 2012 Oct;23(10):1092-8. doi: 10.1111/j.1540-8167.2012.02371.x. Epub 2012 Aug 6.

PMID:
22882672
8.

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.

9.

Cardiac Mechanical Alterations and Genotype Specific Differences in Subjects With Long QT Syndrome.

Leren IS, Hasselberg NE, Saberniak J, Håland TF, Kongsgård E, Smiseth OA, Edvardsen T, Haugaa KH.

JACC Cardiovasc Imaging. 2015 May;8(5):501-10. doi: 10.1016/j.jcmg.2014.12.023. Epub 2015 Apr 15.

10.

Genetics of long QT syndrome.

Tester DJ, Ackerman MJ.

Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):29-33. Review.

11.

Epinephrine bolus test in detecting long QT syndrome mutation carriers with indeterminable electrocardiographic phenotype.

Hekkala AM, Swan H, Viitasalo M, Väänänen H, Toivonen L.

Ann Noninvasive Electrocardiol. 2011 Apr;16(2):172-9. doi: 10.1111/j.1542-474X.2011.00426.x.

PMID:
21496168
12.

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.

13.

Common candidate gene variants are associated with QT interval duration in the general population.

Marjamaa A, Newton-Cheh C, Porthan K, Reunanen A, Lahermo P, Väänänen H, Jula A, Karanko H, Swan H, Toivonen L, Nieminen MS, Viitasalo M, Peltonen L, Oikarinen L, Palotie A, Kontula K, Salomaa V.

J Intern Med. 2009 Apr;265(4):448-58. doi: 10.1111/j.1365-2796.2008.02026.x. Epub 2009 Oct 25.

14.

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.

15.

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.

16.
17.

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.

Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK.

BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31.

18.
19.

"QT clock" to improve detection of QT prolongation in long QT syndrome patients.

Page A, Aktas MK, Soyata T, Zareba W, Couderc JP.

Heart Rhythm. 2016 Jan;13(1):190-8. doi: 10.1016/j.hrthm.2015.08.037. Epub 2015 Aug 31.

20.

Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.

Chang YS, Yang YW, Lin YN, Lin KH, Chang KC, Chang JG.

Int Heart J. 2015;56(4):450-3. doi: 10.1536/ihj.14-428. Epub 2015 Jun 26.

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