REFERENCES
1. Porcari A, Pagura L, Rossi M, et al. Light-chain cardiac amyloidosis: a case report of extraordinary sustained pathological response to cyclophosphamide, bortezomib, and dexamethasone combined therapy. Eur Heart J Case Rep 2022;6:ytac130.
2. Porcari A, Merlo M, Rapezzi C, Sinagra G. Transthyretin amyloid cardiomyopathy: an uncharted territory awaiting discovery. Eur J Intern Med 2020;82:7-15.
3. Porcari A, Bussani R, Merlo M, et al. Incidence and characterization of concealed cardiac amyloidosis among unselected elderly patients undergoing post-mortem examination. Front Cardiovasc Med 2021;8:749523.
4. De Gaspari M, Finato N, Basso C, et al. Cardiac amyloidosis: the pathologist’s point of view. Vessel Plus 2022;5:[Accept].
5. Aimo A, Merlo M, Porcari A, et al. Redefining the epidemiology of cardiac amyloidosis. A systematic review and meta-analysis of screening studies. Eur J Heart Fail 2022;Online ahead of print.
6. Canepa M, Vianello PF, Porcari A, Merlo M, Scarpa M. Cardiac amyloidosis: a changing epidemiology with open challenges. Vessel Plus 2022;6:30.
7. Merlo M, Pagura L, Porcari A, et al. Unmasking the prevalence of amyloid cardiomyopathy in the real world: results from Phase 2 of the AC-TIVE study, an Italian nationwide survey. Eur J Heart Fail 2022;Online ahead of print.
8. Porcari A, Pagura L, Longo F, et al. Prognostic significance of unexplained left ventricular hypertrophy in patients undergoing carpal tunnel surgery. ESC Heart Fail 2022;9:751-60.
9. Gillmore JD, Maurer MS, Falk RH, et al. Nonbiopsy diagnosis of cardiac transthyretin amyloidosis. Circulation 2016;133:2404-12.
10. Porcari A, Rossi M, Dore F, et al. Ten questions for the cardiologist about cardiac scintigraphy with bone tracers, amyloidosis and the heart. G Ital Cardiol (Rome) 2022;23:424-32.
11. Mattana F, Muraglia L, Girardi F, et al. Clinical application of cardiac scintigraphy with bone tracers: controversies and pitfalls in cardiac amyloidosis. Vessel Plus 2022;6:13.
12. Bishop E, Brown EE, Fajardo J, Barouch LA, Judge DP, Halushka MK. Seven factors predict a delayed diagnosis of cardiac amyloidosis. Amyloid 2018;25:174-9.
13. Pica S, Lombardi M. Disclosing the cardiomyopathic substrate within the heart muscles in amyloidosis by cardiac magnetic resonance: diagnostic and prognostic implications. Vessel Plus 2022;6:10.
14. Genovesi D, Giorgetti A. Nuclear medicine techniques for the diagnosis of cardiac amyloidosis: the state of the art. Vessel Plus 2021;5:50.
15. Porcari A, Rossi M, Cappelli F, et al. Incidence and risk factors for pacemaker implantation in light-chain and transthyretin cardiac amyloidosis. Eur J Heart Fail 2022;24:1227-36.
16. Porcari A, Pagura L, Varrà GG, et al. Grey zones in the supportive treatments of cardiac amyloidosis. Vessel Plus 2022;6:33.
17. Scirpa R, Russo D, Tini G, et al. Clinical translation of genetic testing in TTR amyloidosis: genotype-phenotype correlations, management of asymptomatic carriers and familial screening. Vessel Plus 2022;6:[Accept].
18. Camerini L, Aimo A, Pucci A, et al. Serum and tissue light-chains as disease biomarkers and targets for treatment in AL amyloidosis. Vessel Plus 2022;6:[Accept].
19. Licordari R, Minutoli F, Cappelli F, et al. Mid-basal left ventricular longitudinal dysfunction as a prognostic marker in mutated transthyretin-related cardiac amyloidosis. Vessel Plus 2022;6:12.
20. Zhang KW, Stockerl-Goldstein KE, Lenihan DJ. Emerging therapeutics for the treatment of light chain and transthyretin amyloidosis. JACC Basic Transl Sci 2019;4:438-48.
21. Di Nora C, Sponga S, Nalli C, et al. Heart transplantation in cardiac amyloidosis. Vessel Plus 2022;6:[Accept].