Diagnostic delay in wild type transthyretin cardiac amyloidosis – A clinical challenge
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference24 articles.
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3. Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction;Gonzalez-Lopez;Eur. Heart J.,2015
4. Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement;Castano;Eur. Heart J.,2017
5. Predictors of survival stratification in patients with wild-type cardiac amyloidosis;Siepen;Clin. Res. Cardiol.,2018
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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. Tracking the pre-clinical progression of transthyretin amyloid cardiomyopathy using artificial intelligence-enabled electrocardiography and echocardiography;2024-08-26
3. Artificial intelligence-guided detection of under-recognized cardiomyopathies on point-of-care cardiac ultrasound: a multi-center study;2024-03-15
4. Routine 4D Cardiac CT to Identify Concomitant Transthyretin Amyloid Cardiomyopathy in Older Adults with Severe Aortic Stenosis;Radiology;2023-12-01
5. The journey to diagnosis of wild-type transthyretin-mediated (ATTRwt) amyloidosis: a path with multisystem involvement;2023-11-14
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