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Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus.
Grandis M, Obici L, Luigetti M, Briani C, Benedicenti F, Bisogni G, Canepa M, Cappelli F, Danesino C, Fabrizi GM, Fenu S, Ferrandes G, Gemelli C, Manganelli F, Mazzeo A, Melchiorri L, Perfetto F, Pradotto LG, Rimessi P, Tini G, Tozza S, Trevisan L, Pareyson D, Mandich P. Grandis M, et al. Among authors: perfetto f. Orphanet J Rare Dis. 2020 Dec 14;15(1):348. doi: 10.1186/s13023-020-01633-z. Orphanet J Rare Dis. 2020. PMID: 33317601 Free PMC article.
Cardiac amyloidosis: the heart of the matter.
Perfetto F, Cappelli F, Bergesio F, Ciuti G, Porciani MC, Padeletti L, Moggi Pignone A. Perfetto F, et al. Intern Emerg Med. 2013 Apr;8(3):191-203. doi: 10.1007/s11739-011-0647-y. Epub 2011 Jul 8. Intern Emerg Med. 2013. PMID: 21739229 Review.
Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.
Rapezzi C, Quarta CC, Obici L, Perfetto F, Longhi S, Salvi F, Biagini E, Lorenzini M, Grigioni F, Leone O, Cappelli F, Palladini G, Rimessi P, Ferlini A, Arpesella G, Pinna AD, Merlini G, Perlini S. Rapezzi C, et al. Among authors: perfetto f. Eur Heart J. 2013 Feb;34(7):520-8. doi: 10.1093/eurheartj/ehs123. Epub 2012 Jun 28. Eur Heart J. 2013. PMID: 22745357
Troponins in cardiac amyloidosis: multipurpose markers.
Perfetto F, Bergesio F, Emdin M, Cappelli F. Perfetto F, et al. Nat Rev Cardiol. 2014 Mar;11(3):179. doi: 10.1038/nrcardio.2013.129-c1. Epub 2014 Jan 28. Nat Rev Cardiol. 2014. PMID: 24469674 No abstract available.
192 results