Therapy of ATTR Cardiac Amyloidosis: Current Indications
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Reference24 articles.
1. Transthyretin amyloid cardiomyopathy: JACC state-of-the-art review;Ruberg;J Am Coll Cardiol,2019
2. Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases;Garcia-Pavia;Eur J Heart Fail,2021
3. RNA-targeting and gene editing therapies for transthyretin amyloidosis;Aimo;Nat Rev Cardiol,2022
4. Management of complications of cardiac amyloidosis: 10 questions and answers;Aimo;Eur J Prev Cardiol,2021
5. Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner;Gertz;BMC Fam Pract,2020
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2. Multi-view feature fusion and density-based minority over-sampling technique for amyloid protein prediction under imbalanced data;Applied Soft Computing;2024-01
3. Hereditary Transthyretin Amyloidosis: How to Differentiate Carriers and Patients Using Speckle-Tracking Echocardiography;Diagnostics;2023-12-09
4. Dapagliflozin treatment and cardiovascular outcome in RBP4/TTRVal30Met (transthyretin cardiac amyloidosis) mice;ESC Heart Failure;2023-10-25
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