Incidence and predictors of worsening heart failure in patients with wild‐type transthyretin cardiac amyloidosis
Author:
Affiliation:
1. The Department of Cardiology Aarhus University Hospital Aarhus Denmark
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ehf2.14000
Reference19 articles.
1. Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis
2. Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths
3. Diagnostic delay in wild type transthyretin cardiac amyloidosis – A clinical challenge
4. Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosis
5. Native T1 Mapping, Extracellular Volume Mapping, and Late Gadolinium Enhancement in Cardiac Amyloidosis
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1. Changes of clinical characteristics, distribution of red flags and prognosis in contemporary patients with wild-type transthyretin amyloidosis cardiomyopathy;Annals of Medicine;2024-09-09
2. Myocardial Mechanics and Valvular and Vascular Abnormalities in Cardiac Amyloidosis;Journal of Clinical Medicine;2024-07-25
3. Exercise Hemodynamics and Mitochondrial Oxidative Capacity in Disease Stages of Wild‐Type Transthyretin Amyloid Cardiomyopathy;Journal of the American Heart Association;2024-07-02
4. Prevalence of transthyretin cardiac amyloidosis in patients with high-degree AV block;Open Heart;2024-03
5. Arrhythmias and Device Therapies in Cardiac Amyloidosis;Journal of Clinical Medicine;2024-02-25
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