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Journal Abstract Search

245 related items for PubMed ID: 16769042

  • 21. Genetic testing of candidate genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Campuzano O, Alcalde M, Berne P, Castro V, Guzzo G, Iglesias A, Alonso-Pulpon L, Garcia-Pavia P, Brugada J, Brugada R.
    Eur J Med Genet; 2012 Apr; 55(4):225-34. PubMed ID: 22421524
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  • 22. 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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  • 24. Age- and training-dependent development of arrhythmogenic right ventricular cardiomyopathy in heterozygous plakoglobin-deficient mice.
    Kirchhof P, Fabritz L, Zwiener M, Witt H, Schäfers M, Zellerhoff S, Paul M, Athai T, Hiller KH, Baba HA, Breithardt G, Ruiz P, Wichter T, Levkau B.
    Circulation; 2006 Oct 24; 114(17):1799-806. PubMed ID: 17030684
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  • 27. ARVC-related mutations in divergent region 3 alter functional properties of the cardiac ryanodine receptor.
    Koop A, Goldmann P, Chen SR, Thieleczek R, Varsányi M.
    Biophys J; 2008 Jun 24; 94(12):4668-77. PubMed ID: 18326664
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  • 29. Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy.
    Christensen AH, Andersen CB, Tybjaerg-Hansen A, Haunso S, Svendsen JH.
    Clin Genet; 2011 Sep 24; 80(3):256-64. PubMed ID: 21214875
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  • 31. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).
    Tiso N, Stephan DA, Nava A, Bagattin A, Devaney JM, Stanchi F, Larderet G, Brahmbhatt B, Brown K, Bauce B, Muriago M, Basso C, Thiene G, Danieli GA, Rampazzo A.
    Hum Mol Genet; 2001 Feb 01; 10(3):189-94. PubMed ID: 11159936
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  • 33. Sarcoplasmic reticulum calcium leak and cardiac arrhythmias.
    Chelu MG, Wehrens XH.
    Biochem Soc Trans; 2007 Nov 01; 35(Pt 5):952-6. PubMed ID: 17956253
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  • 35. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
    Postma AV, Denjoy I, Kamblock J, Alders M, Lupoglazoff JM, Vaksmann G, Dubosq-Bidot L, Sebillon P, Mannens MM, Guicheney P, Wilde AA.
    J Med Genet; 2005 Nov 01; 42(11):863-70. PubMed ID: 16272262
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  • 37. A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy.
    Djouadi F, Lecarpentier Y, Hébert JL, Charron P, Bastin J, Coirault C.
    Cardiovasc Res; 2009 Oct 01; 84(1):83-90. PubMed ID: 19497962
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  • 40. Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.
    Chen J, Ma Y, Li H, Lin Z, Yang Z, Zhang Q, Wang F, Lin Y, Ye Z, Lin Y.
    Orphanet J Rare Dis; 2022 May 07; 17(1):183. PubMed ID: 35526016
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