Cardiologic Manifestation in Amyloidosis
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-17759-0_5
Reference17 articles.
1. Simões MV, Fernandes F, Marcondes-Braga FG, Scheinberg P, Correia EB, Rohde LEP, et al. Position statement on diagnosis and treatment of cardiac Amyloidosis—2021. Arq Bras Cardiol. 2021;117(3):561–98.
2. Ruberg FL, Grogan M, Hanna M, Kelly JW, Maurer MS. Transthyretin amyloid cardiomyopathy: JACC state-of-the-art review. J Am Coll Cardiol. 2019;73(22):2872–91.
3. Maurer MS, Schwartz JH, Gundapaneni B, Elliott PM, Merlini G, Waddington-Cruz M, et al. Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy. N Engl J Med. 2018;379(11):1007–16.
4. Ando Y, Coelho T, Berk JL, Cruz MW, Ericzon B-G, Ikeda S-i, et al. Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet J Rare Dis. 2013;8(1):1–18.
5. Tarasoutchi F, et al. Update of the Brazilian guidelines for valvular heart disease - 2020. Arq Bras Cardiol. 2020;115(4)
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