Outcomes of heart transplantation in cardiac amyloidosis: an updated systematic review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10741-022-10252-8.pdf
Reference44 articles.
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2. González-López E, López-Sainz Á, Garcia-Pavia P (2017) Diagnosis and treatment of transthyretin cardiac amyloidosis. Progress and Hope Rev Esp Cardiol (Engl Ed) 70(11):991–1004. https://doi.org/10.1016/j.rec.2017.05.036
3. Tahir UA, Doros G, Kim JS et al (2019) Predictors of mortality in light chain cardiac amyloidosis with heart failure. Sci Rep 9(1):8552. https://doi.org/10.1038/s41598-019-44912-x. (Published 12 Jun 2019)
4. Ruberg FL, Grogan M, Hanna M et al (2019) Transthyretin amyloid cardiomyopathy: JACC State-of-the-Art Review. J Am Coll Cardiol 73(22):2872–2891. https://doi.org/10.1016/j.jacc.2019.04.003.PMID:31171094;PMCID:PMC6724183
5. Kittleson MM, Maurer MS, Ambardekar AV et al (2021) Cardiac amyloidosis: evolving diagnosis and management: a scientific statement from the American Heart Association [published correction appears in Circulation 144(1):e11]. Circulation 142(1):e7-e22. https://doi.org/10.1161/CIR.0000000000000792
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1. Pronóstico del trasplante cardiaco en pacientes con miocardiopatía hipertrófica y restrictiva. Análisis de un registro nacional;Revista Española de Cardiología;2024-04
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