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Journal Abstract Search

368 related items for PubMed ID: 10588221

  • 21. A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22.
    Bhuiyan ZA, Hamdan MA, Shamsi ET, Postma AV, Mannens MM, Wilde AA, Al-Gazali L.
    J Cardiovasc Electrophysiol; 2007 Sep; 18(10):1060-6. PubMed ID: 17666061
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  • 22. Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
    Protonotarios A, Anastasakis A, Panagiotakos DB, Antoniades L, Syrris P, Vouliotis A, Stefanadis C, Tsatsopoulou A, McKenna WJ, Protonotarios N.
    Europace; 2016 Apr; 18(4):610-6. PubMed ID: 25825460
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  • 25. Exercise-induced bidirectional ventricular tachycardia with alternating right and left bundle branch block-type patterns--a case report.
    Khan IA.
    Angiology; 2002 Apr; 53(5):593-8. PubMed ID: 12365869
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  • 26. [Arrhythmogenic right ventricular disease].
    Brachmann J, Hilbel T, Schöls W, Beyer T, Wiest G, Mall G, Kübler W.
    Z Kardiol; 1994 Apr; 83 Suppl 6():175-80. PubMed ID: 7863692
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  • 27. Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.
    Bhuiyan ZA, van den Berg MP, van Tintelen JP, Bink-Boelkens MT, Wiesfeld AC, Alders M, Postma AV, van Langen I, Mannens MM, Wilde AA.
    Circulation; 2007 Oct 02; 116(14):1569-76. PubMed ID: 17875969
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  • 28. Epinephrine infusion in the evaluation of unexplained cardiac arrest and familial sudden death: from the cardiac arrest survivors with preserved Ejection Fraction Registry.
    Krahn AD, Healey JS, Chauhan VS, Birnie DH, Champagne J, Sanatani S, Ahmad K, Ballantyne E, Gerull B, Yee R, Skanes AC, Gula LJ, Leong-Sit P, Klein GJ, Gollob MH, Simpson CS, Talajic M, Gardner M.
    Circ Arrhythm Electrophysiol; 2012 Oct 02; 5(5):933-40. PubMed ID: 22944906
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  • 29. Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia: A Randomized Clinical Trial.
    Kannankeril PJ, Moore JP, Cerrone M, Priori SG, Kertesz NJ, Ro PS, Batra AS, Kaufman ES, Fairbrother DL, Saarel EV, Etheridge SP, Kanter RJ, Carboni MP, Dzurik MV, Fountain D, Chen H, Ely EW, Roden DM, Knollmann BC.
    JAMA Cardiol; 2017 Jul 01; 2(7):759-766. PubMed ID: 28492868
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  • 34. Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.
    Kumar S, Peters S, Thompson T, Morgan N, Maccicoca I, Trainer A, Zentner D, Kalman JM, Winship I, Vohra JK.
    Heart Rhythm; 2013 Nov 01; 10(11):1653-60. PubMed ID: 23973953
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  • 35. [Catecholaminergic polymorphic ventricular tachycardia; possible diagnosis in cases of syncope and sudden death of family members].
    Lieve KV, Wilde AA, van der Werf C.
    Ned Tijdschr Geneeskd; 2015 Nov 01; 159():A8205. PubMed ID: 25650029
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  • 36. Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death.
    Corrado D, Nava A, Buja G, Martini B, Fasoli G, Oselladore L, Turrini P, Thiene G.
    J Am Coll Cardiol; 1996 Feb 01; 27(2):443-8. PubMed ID: 8557918
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  • 37. Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives.
    van der Werf C, Nederend I, Hofman N, van Geloven N, Ebink C, Frohn-Mulder IM, Alings AM, Bosker HA, Bracke FA, van den Heuvel F, Waalewijn RA, Bikker H, van Tintelen JP, Bhuiyan ZA, van den Berg MP, Wilde AA.
    Circ Arrhythm Electrophysiol; 2012 Aug 01; 5(4):748-56. PubMed ID: 22787013
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