The challenge of clinical diagnosis of cardiac amyloidosis: Case report and literature review
Author:
Affiliation:
1. Professor of Faculty of Medicine, Department of Internal Medicine, University of Brasília, Brasília-DF, Brazil
2. Medical Academic, Department of Internal Medicine, University of Brasília, Brasília-DF, Brazil
Abstract
Publisher
Edorium Journals Pvt. Ltd.
Reference13 articles.
1. Gertz MA, Dispenzieri A. Systemic amyloidosis recognition, prognosis, and therapy: A systematic review. JAMA 2020;324(1):79–89.
2. Martinez-Naharro A, Hawkins PN, Fontana M. Cardiac amyloidosis. Clin Med (Lond) 2018;18(Suppl 2):s30–5.
3. Manolis AS, Manolis AA, Manolis TA, Melita H. Cardiac amyloidosis: An underdiagnosed/underappreciated disease. Eur J Intern Med 2019;67:1–13.
4. Quagliato PC, Neto EMVS, Assef JE, et al. What’s new in cardiac amyloidosis? Arq Bras Cardiol: Imagem Cardiovasc 2018;31(3):198–203
5. Dorbala S, Ando Y, Bokhari S, et al. ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: Part 1 of 2-evidence base and standardized methods of imaging. J Nucl Cardiol 2019;26(6):2065–123.
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