Page 113 - Read Online
P. 113
Page 4 of 4 Sinagra et al. Vessel Plus 2022;6:44 https://dx.doi.org/10.20517/2574-1209.2021.143
Ethical approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Copyright
© The Author(s) 2022.
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. DOI PubMed PMC
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. DOI PubMed PMC
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. DOI PubMed PMC
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. DOI PubMed
6. Canepa M, Vianello PF, Porcari A, Merlo M, Scarpa M. Cardiac amyloidosis: a changing epidemiology with open challenges. Vessel
Plus 2022;6:30. DOI
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. DOI PubMed
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. DOI PubMed PMC
9. Gillmore JD, Maurer MS, Falk RH, et al. Nonbiopsy diagnosis of cardiac transthyretin amyloidosis. Circulation 2016;133:2404-12.
DOI PubMed
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. DOI PubMed
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. DOI
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. DOI PubMed
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. DOI
14. Genovesi D, Giorgetti A. Nuclear medicine techniques for the diagnosis of cardiac amyloidosis: the state of the art. Vessel Plus
2021;5:50. DOI
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. DOI PubMed
16. Porcari A, Pagura L, Varrà GG, et al. Grey zones in the supportive treatments of cardiac amyloidosis. Vessel Plus 2022;6:33. DOI
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. DOI
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. DOI PubMed PMC
21. Di Nora C, Sponga S, Nalli C, et al. Heart transplantation in cardiac amyloidosis. Vessel Plus 2022;6:[Accept].
22. Di Nora C, Sponga S, Ferrara V, et al. Emerging therapy in light-chain and acquired transthyretin-related amyloidosis: an Italian
single-centre experience in heart transplantation. J Cardiovasc Med (Hagerstown) 2021;22:261-7. DOI PubMed