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Items: 1 to 20 of 47

1.

Effectiveness of beta-blockers depending on the genotype of congenital long-QT syndrome: A meta-analysis.

Ahn J, Kim HJ, Choi JI, Lee KN, Shim J, Ahn HS, Kim YH.

PLoS One. 2017 Oct 23;12(10):e0185680. doi: 10.1371/journal.pone.0185680. eCollection 2017.

2.

Syncope and risk of sudden cardiac arrest in coronary artery disease.

Aro AL, Rusinaru C, Uy-Evanado A, Reinier K, Phan D, Gunson K, Jui J, Chugh SS.

Int J Cardiol. 2017 Mar 15;231:26-30. doi: 10.1016/j.ijcard.2016.12.021. Epub 2016 Dec 12.

3.

Catheter ablation for ventricular tachyarrhythmia in patients with channelopathies.

Murakoshi N, Aonuma K.

J Arrhythm. 2016 Oct;32(5):404-410. Epub 2016 Jun 10. Review.

4.

Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study.

Wilde AA, Moss AJ, Kaufman ES, Shimizu W, Peterson DR, Benhorin J, Lopes C, Towbin JA, Spazzolini C, Crotti L, Zareba W, Goldenberg I, Kanters JK, Robinson JL, Qi M, Hofman N, Tester DJ, Bezzina CR, Alders M, Aiba T, Kamakura S, Miyamoto Y, Andrews ML, McNitt S, Polonsky B, Schwartz PJ, Ackerman MJ.

Circulation. 2016 Sep 20;134(12):872-82. doi: 10.1161/CIRCULATIONAHA.116.021823. Epub 2016 Aug 26.

5.

Evaluation and Management of Athletes With Long QT Syndrome.

Gomez AT, Prutkin JM, Rao AL.

Sports Health. 2016 Nov/Dec;8(6):527-535. doi: 10.1177/1941738116660294. Epub 2016 Aug 6. Review.

6.

Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs.

Samol A, Gönes M, Zumhagen S, Bruns HJ, Paul M, Vahlhaus C, Waltenberger J, Schulze-Bahr E, Eckardt L, Mönnig G.

PLoS One. 2016 Jul 5;11(7):e0158085. doi: 10.1371/journal.pone.0158085. eCollection 2016.

7.

Anaesthesia Application for Cardiac Denervation in a Patient with Long QT Syndrome and Cardiomyopathy.

Karadeniz Ü, Demir A, Koçulu R.

Turk J Anaesthesiol Reanim. 2016 Feb;44(1):50-3. doi: 10.5152/TJAR.2016.91249. Epub 2016 Feb 1.

8.

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3.

Mazzanti A, Maragna R, Faragli A, Monteforte N, Bloise R, Memmi M, Novelli V, Baiardi P, Bagnardi V, Etheridge SP, Napolitano C, Priori SG.

J Am Coll Cardiol. 2016 Mar 8;67(9):1053-8. doi: 10.1016/j.jacc.2015.12.033.

9.

Clinical presentation and course of long QT syndrome in Thai children.

Saprungruang A, Vithessonthi K, La-Orkhun V, Lertsapcharoen P, Khongphatthanayothin A.

J Arrhythm. 2015 Oct;31(5):296-301. doi: 10.1016/j.joa.2015.03.009. Epub 2015 May 28.

10.

Stop-codon and C-terminal nonsense mutations are associated with a lower risk of cardiac events in patients with long QT syndrome type 1.

Ruwald MH, Xu Parks X, Moss AJ, Zareba W, Baman J, McNitt S, Kanters JK, Shimizu W, Wilde AA, Jons C, Lopes CM.

Heart Rhythm. 2016 Jan;13(1):122-31. doi: 10.1016/j.hrthm.2015.08.033. Epub 2015 Aug 28.

11.

Long QT syndrome: how effective therapy in a single patient favorably influenced the long-term clinical course and genetic understanding of this hereditary disorder.

Lowengrub KM, Moss DR, Moss DA, Moss AJ.

Prog Cardiovasc Dis. 2015 Sep-Oct;58(2):221-6. doi: 10.1016/j.pcad.2015.08.002. Epub 2015 Aug 4.

12.

Long-QT Syndrome and Therapy for Attention Deficit/Hyperactivity Disorder.

Zhang C, Kutyifa V, Moss AJ, McNitt S, Zareba W, Kaufman ES.

J Cardiovasc Electrophysiol. 2015 Oct;26(10):1039-44. doi: 10.1111/jce.12739. Epub 2015 Aug 6.

13.

Obstructive Sleep Apnea in Patients with Congenital Long QT Syndrome: Implications for Increased Risk of Sudden Cardiac Death.

Shamsuzzaman AS, Somers VK, Knilans TK, Ackerman MJ, Wang Y, Amin RS.

Sleep. 2015 Jul 1;38(7):1113-9. doi: 10.5665/sleep.4824.

14.

High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance.

Steffensen AB, Refaat MM, David JP, Mujezinovic A, Calloe K, Wojciak J, Nussbaum RL, Scheinman MM, Schmitt N.

Sci Rep. 2015 Jun 12;5:10009. doi: 10.1038/srep10009.

15.

Novel calmodulin mutations associated with congenital arrhythmia susceptibility.

Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, Theisen D, Tsunoda T, Satake W, Toda T, Nakagawa H, Tsuji Y, Tsuchiya T, Yamamoto H, Miyamoto Y, Endo N, Kimura A, Ozaki K, Motomura H, Suda K, Tanaka T, Schwartz PJ, Meitinger T, Kääb S, Guicheney P, Shimizu W, Bhuiyan ZA, Watanabe H, Chazin WJ, George AL Jr.

Circ Cardiovasc Genet. 2014 Aug;7(4):466-74. doi: 10.1161/CIRCGENETICS.113.000459. Epub 2014 Jun 10.

16.

Long QT syndrome: a Korean single center study.

Lee YS, Kwon BS, Kim GB, Oh SI, Bae EJ, Park SS, Noh CI.

J Korean Med Sci. 2013 Oct;28(10):1454-60. doi: 10.3346/jkms.2013.28.10.1454. Epub 2013 Sep 25.

17.

Implantable cardioverter defibrillator therapy in pediatric and congenital heart disease patients: a single tertiary center experience in Korea.

Jin BK, Bang JS, Choi EY, Kim GB, Kwon BS, Bae EJ, Noh CI, Choi JY, Kim WH.

Korean J Pediatr. 2013 Mar;56(3):125-9. doi: 10.3345/kjp.2013.56.3.125. Epub 2013 Mar 18.

18.

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation.

Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP.

J Cardiovasc Electrophysiol. 2013 May;24(5):562-9. doi: 10.1111/jce.12068. Epub 2013 Jan 25.

19.

Left cardiac sympathetic denervation for the management of life-threatening ventricular tachyarrhythmias in young patients with catecholaminergic polymorphic ventricular tachycardia and long QT syndrome.

Schneider HE, Steinmetz M, Krause U, Kriebel T, Ruschewski W, Paul T.

Clin Res Cardiol. 2013 Jan;102(1):33-42. doi: 10.1007/s00392-012-0492-7. Epub 2012 Jul 21.

20.

The molecular autopsy: should the evaluation continue after the funeral?

Tester DJ, Ackerman MJ.

Pediatr Cardiol. 2012 Mar;33(3):461-70. doi: 10.1007/s00246-012-0160-8. Epub 2012 Feb 4. Review.

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