The genetics of cardiac amyloidosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10741-021-10164-z.pdf
Reference77 articles.
1. Stangou AJ, Banner NR, Hendry BM et al (2010) Hereditary fibrinogen A alpha-chain amyloidosis: phenotypic characterization of a systemic disease and the role of liver transplantation. Blood 115(15):2998–3007. https://doi.org/10.1182/blood-2009-06-223792
2. Coriu D, Dispenzieri A, Stevens FJ et al (2003) Hepatic amyloidosis resulting from deposition of the apolipoprotein A-I variant Leu75Pro. Amyloid Int J Exp Clin Investig Off J Int Soc Amyloidosis 10(4):215–223. https://doi.org/10.3109/13506120309041738
3. Morizane R, Monkawa T, Konishi K et al (2011) Renal amyloidosis caused by apolipoprotein A-II without a genetic mutation in the coding sequence. Clin Exp Nephrol 15(5):774–779. https://doi.org/10.1007/s10157-011-0483-4
4. Schmidt E-K, Mustonen T, Kiuru-Enari S, Kivelä TT, Atula S (2020) Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study. Orphanet J Rare Dis 15(1):19. https://doi.org/10.1186/s13023-020-1300-5
5. Mejia-Vilet JM, Cárdenas-Mastrascusa LR, Palacios-Cebreros EJ et al (2019) LECT2 amyloidosis in kidney transplantation: a report of 5 Cases. Am J Kidney Dis Off J Natl Kidney Found 74(4):563–566. https://doi.org/10.1053/j.ajkd.2018.10.016
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