Cardiac and renal AL amyloidosis controlled by autologous stem cell transplantation for 17 years accompanying late onset atrial fibrillation and complete atrioventricular block
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
https://link.springer.com/content/pdf/10.1007/s13730-023-00777-8.pdf
Reference18 articles.
1. Hwa YL, et al. Immunoglobulin light-chain amyloidosis: clinical presentations and diagnostic approach. J Adv Pract Oncol. 2019;10(5):470–81.
2. Grogan M, Dispenzieri A. Natural history and therapy of AL cardiac amyloidosis. Heart Fail Rev. 2015;20(2):155–62.
3. Ohara T, et al. Long-term electrocardiographic follow-up of a patient with light-chain Cardiac amyloidosis. J Nippon Med Sch. 2022;89(1):119–25.
4. Escher F, et al. When and how do patients with cardiac amyloidosis die? Clin Res Cardiol. 2020;109(1):78–88.
5. Garofalo M, et al. Machine learning analyses of antibody somatic mutations predict immunoglobulin light chain toxicity. Nat Commun. 2021;12(1):3532.
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