Amyloid Cardiomyopathy in Older Adults
Author:
Publisher
Springer Science and Business Media LLC
Subject
Geriatrics and Gerontology
Link
https://link.springer.com/content/pdf/10.1007/s13670-022-00374-0.pdf
Reference72 articles.
1. Kittleson MM, et al. Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association. Circulation. 2020;142(1):e7–22.
2. Gillmore JD, et al. Guidelines on the diagnosis and investigation of AL amyloidosis. Br J Haematol. 2015;168(2):207–18.
3. Dubrey SW, Hawkins PN, Falk RH. Amyloid diseases of the heart: assessment, diagnosis, and referral. Heart. 2011;97(1):75–84.
4. Grogan M, Dispenzieri A. Natural history and therapy of AL cardiac amyloidosis. Heart Fail Rev. 2015;20(2):155–62.
5. González-López E, et al. Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction. Eur Heart J. 2015;36(38):2585–94.
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