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Journal Abstract Search

289 related items for 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
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  • 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 15; 114(8):1223-8. PubMed ID: 25173441
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  • 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 15; 7(10):1411-8. PubMed ID: 20541041
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  • 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 15; 96(3):172-8. PubMed ID: 21308345
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  • 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 15; 3(2):120-5. PubMed ID: 20071715
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  • 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 04; 57(1):51-9. PubMed ID: 21185501
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  • 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 04; 4(6):867-73. PubMed ID: 21956039
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  • 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 Dec 04; 80(3):696-702. PubMed ID: 26823142
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  • 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 04; 3(7):815-21. PubMed ID: 16818214
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  • 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 04; 166(9):927-33. PubMed ID: 17171344
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  • 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 13; 296(10):1249-54. PubMed ID: 16968849
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  • 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 13; 2(5):507-17. PubMed ID: 15840476
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  • 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, International LQTS Registry Investigators.
    J Cardiovasc Electrophysiol; 2010 Aug 01; 21(8):893-901. PubMed ID: 20233272
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  • 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 01; 8(4):815-23. PubMed ID: 26063740
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  • 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 01; 88(12):1181-90. PubMed ID: 21164565
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  • 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 15; 106(8):1124-8. PubMed ID: 20920651
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  • 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 15; 7(12):1797-805. PubMed ID: 20850565
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