These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Arrhythmogenic right ventricular dysplasia/cardiomyopathy according to revised 2010 task force criteria with inclusion of non-desmosomal phospholamban mutation carriers. Groeneweg JA; van der Zwaag PA; Olde Nordkamp LR; Bikker H; Jongbloed JD; Jongbloed R; Wiesfeld AC; Cox MG; van der Heijden JF; Atsma DE; de Boer K; Doevendans PA; Vink A; van Veen TA; Dooijes D; van den Berg MP; Wilde AA; van Tintelen JP; Hauer RN Am J Cardiol; 2013 Oct; 112(8):1197-206. PubMed ID: 23871674 [TBL] [Abstract][Full Text] [Related]
24. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. Millat G; Bouvagnet P; Chevalier P; Sebbag L; Dulac A; Dauphin C; Jouk PS; Delrue MA; Thambo JB; Le Metayer P; Seronde MF; Faivre L; Eicher JC; Rousson R Eur J Med Genet; 2011; 54(6):e570-5. PubMed ID: 21846512 [TBL] [Abstract][Full Text] [Related]
25. Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. Chami N; Tadros R; Lemarbre F; Lo KS; Beaudoin M; Robb L; Labuda D; Tardif JC; Racine N; Talajic M; Lettre G Can J Cardiol; 2014 Dec; 30(12):1655-61. PubMed ID: 25448463 [TBL] [Abstract][Full Text] [Related]
26. Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis. Antoniades L; Tsatsopoulou A; Anastasakis A; Syrris P; Asimaki A; Panagiotakos D; Zambartas C; Stefanadis C; McKenna WJ; Protonotarios N Eur Heart J; 2006 Sep; 27(18):2208-16. PubMed ID: 16893920 [TBL] [Abstract][Full Text] [Related]
27. DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy. Heliö K; Kangas-Kontio T; Weckström S; Vanninen SUM; Aalto-Setälä K; Alastalo TP; Myllykangas S; Heliö TM; Koskenvuo JW BMC Med Genet; 2020 Jan; 21(1):19. PubMed ID: 32005173 [TBL] [Abstract][Full Text] [Related]
28. Familial dilated cardiomyopathy with troponin T K210del mutation. Martins E; Silva-Cardoso J; Alves C; Pereira H; Soares B; Damasceno A; Abreu-Lima C; Amorim A; Rocha-Gonçalves F Rev Port Cardiol; 2006 Mar; 25(3):295-300. PubMed ID: 16789403 [TBL] [Abstract][Full Text] [Related]