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Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations.
Bauce B, Rampazzo A, Basso C, Mazzotti E, Rigato I, Steriotis A, Beffagna G, Lorenzon A, De Bortoli M, Pilichou K, Marra MP, Corbetti F, Daliento L, Iliceto S, Corrado D, Thiene G, Nava A. Bauce B, et al. Among authors: rampazzo a. Heart Rhythm. 2011 Nov;8(11):1686-95. doi: 10.1016/j.hrthm.2011.06.026. Epub 2011 Jun 30. Heart Rhythm. 2011. PMID: 21723241 Free PMC article.
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.
Bauce B, Rampazzo A, Basso C, Bagattin A, Daliento L, Tiso N, Turrini P, Thiene G, Danieli GA, Nava A. Bauce B, et al. Among authors: rampazzo a. J Am Coll Cardiol. 2002 Jul 17;40(2):341-9. doi: 10.1016/s0735-1097(02)01946-0. J Am Coll Cardiol. 2002. PMID: 12106942 Free article.
249 results