285 related articles for article (PubMed ID: 21831960)
1. Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation.
Barsheshet A; Moss AJ; McNitt S; Polonsky S; Lopes CM; Zareba W; Robinson JL; Ackerman MJ; Benhorin J; Kaufman ES; Towbin JA; Vincent GM; Qi M; Goldenberg I
Circ Cardiovasc Genet; 2011 Oct; 4(5):491-9. PubMed ID: 21831960
[TBL] [Abstract][Full Text] [Related]
2. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
Zareba W; Moss AJ; Locati EH; Lehmann MH; Peterson DR; Hall WJ; Schwartz PJ; Vincent GM; Priori SG; Benhorin J; Towbin JA; Robinson JL; Andrews ML; Napolitano C; Timothy K; Zhang L; Medina A;
J Am Coll Cardiol; 2003 Jul; 42(1):103-9. PubMed ID: 12849668
[TBL] [Abstract][Full Text] [Related]
3. Syncope in genotype-negative long QT syndrome family members.
Olde Nordkamp LR; Ruwald MH; Goldenberg I; Wieling W; McNitt S; Polonsky B; Wilde AA; van Dijk N; Moss AJ
Am J Cardiol; 2014 Oct; 114(8):1223-8. PubMed ID: 25173441
[TBL] [Abstract][Full Text] [Related]
4. Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.
Itoh H; Shimizu W; Hayashi K; Yamagata K; Sakaguchi T; Ohno S; Makiyama T; Akao M; Ai T; Noda T; Miyazaki A; Miyamoto Y; Yamagishi M; Kamakura S; Horie M
Heart Rhythm; 2010 Oct; 7(10):1411-8. PubMed ID: 20541041
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 21308345
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 20071715
[TBL] [Abstract][Full Text] [Related]
7. Atrial Fibrillation in Long QT Syndrome by Genotype.
Platonov PG; McNitt S; Polonsky B; Rosero SZ; Zareba W
Circ Arrhythm Electrophysiol; 2019 Oct; 12(10):e007213. PubMed ID: 31610692
[TBL] [Abstract][Full Text] [Related]
8. Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals.
Goldenberg I; Horr S; Moss AJ; Lopes CM; Barsheshet A; McNitt S; Zareba W; Andrews ML; Robinson JL; Locati EH; Ackerman MJ; Benhorin J; Kaufman ES; Napolitano C; Platonov PG; Priori SG; Qi M; Schwartz PJ; Shimizu W; Towbin JA; Vincent GM; Wilde AA; Zhang L
J Am Coll Cardiol; 2011 Jan; 57(1):51-9. PubMed ID: 21185501
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 21956039
[TBL] [Abstract][Full Text] [Related]
10. Pediatric Cohort With Long QT Syndrome - KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms.
Ozawa J; Ohno S; Hisamatsu T; Itoh H; Makiyama T; Suzuki H; Saitoh A; Horie M
Circ J; 2016; 80(3):696-702. PubMed ID: 26823142
[TBL] [Abstract][Full Text] [Related]
11. Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome.
Migdalovich D; Moss AJ; Lopes CM; Costa J; Ouellet G; Barsheshet A; McNitt S; Polonsky S; Robinson JL; Zareba W; Ackerman MJ; Benhorin J; Kaufman ES; Platonov PG; Shimizu W; Towbin JA; Vincent GM; Wilde AA; Goldenberg I
Heart Rhythm; 2011 Oct; 8(10):1537-43. PubMed ID: 21440677
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 16818214
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 17171344
[TBL] [Abstract][Full Text] [Related]
14. Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.
Hobbs JB; Peterson DR; Moss AJ; McNitt S; Zareba W; Goldenberg I; Qi M; Robinson JL; Sauer AJ; Ackerman MJ; Benhorin J; Kaufman ES; Locati EH; Napolitano C; Priori SG; Towbin JA; Vincent GM; Zhang L
JAMA; 2006 Sep; 296(10):1249-54. PubMed ID: 16968849
[TBL] [Abstract][Full Text] [Related]
15. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
Tester DJ; Will ML; Haglund CM; Ackerman MJ
Heart Rhythm; 2005 May; 2(5):507-17. PubMed ID: 15840476
[TBL] [Abstract][Full Text] [Related]
16. Beta-blocker efficacy in high-risk patients with the congenital long-QT syndrome types 1 and 2: implications for patient management.
Goldenberg I; Bradley J; Moss A; McNitt S; Polonsky S; Robinson JL; Andrews M; Zareba W;
J Cardiovasc Electrophysiol; 2010 Aug; 21(8):893-901. PubMed ID: 20233272
[TBL] [Abstract][Full Text] [Related]
17. Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.
Koponen M; Marjamaa A; Hiippala A; Happonen JM; Havulinna AS; Salomaa V; Lahtinen AM; Hintsa T; Viitasalo M; Toivonen L; Kontula K; Swan H
Circ Arrhythm Electrophysiol; 2015 Aug; 8(4):815-23. PubMed ID: 26063740
[TBL] [Abstract][Full Text] [Related]
18. Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.
Cordeiro JM; Perez GJ; Schmitt N; Pfeiffer R; Nesterenko VV; Burashnikov E; Veltmann C; Borggrefe M; Wolpert C; Schimpf R; Antzelevitch C
Can J Physiol Pharmacol; 2010 Dec; 88(12):1181-90. PubMed ID: 21164565
[TBL] [Abstract][Full Text] [Related]
19. Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.
Tester DJ; Benton AJ; Train L; Deal B; Baudhuin LM; Ackerman MJ
Am J Cardiol; 2010 Oct; 106(8):1124-8. PubMed ID: 20920651
[TBL] [Abstract][Full Text] [Related]
20. Trigger-specific risk factors and response to therapy in long QT syndrome type 2.
Kim JA; Lopes CM; Moss AJ; McNitt S; Barsheshet A; Robinson JL; Zareba W; Ackerman MJ; Kaufman ES; Towbin JA; Vincent M; Goldenberg I
Heart Rhythm; 2010 Dec; 7(12):1797-805. PubMed ID: 20850565
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
