Stratifying Disease Progression in Patients With Cardiac ATTR Amyloidosis

Author:

Ioannou AdamORCID,Cappelli Francesco,Emdin Michele,Nitsche Christian,Longhi Simone,Masri Ahmad,Cipriani Alberto,Zampieri Mattia,Colio Federica,Poledniczek Michael,Porcari Aldostefano,Razvi Yousuf,Aimo Alberto,Vergaro Giuseppe,De Michieli Laura,Rauf Muhammad U.,Patel Rishi K.ORCID,Villanueva Eugenia,Lustig Yael,Venneri Lucia,Martinez-Naharro Ana,Lachmann Helen,Wechalekar Ashutosh,Whelan Carol,Petrie Aviva,Hawkins Philip N.,Solomon Scott,Gillmore Julian D.,Fontana Marianna

Funder

British Heart Foundation

Publisher

Elsevier BV

Reference22 articles.

1. Multi-imaging characterization of cardiac phenotype in different types of amyloidosis;Ioannou;J Am Coll Cardiol Img,2022

2. Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review;Ruberg;J Am Coll Cardiol,2019

3. Prevalence, characteristics and outcomes of older patients with hereditary versus wild-type transthyretin amyloid cardiomyopathy;Porcari;Eur J Heart Fail,2023

4. Sex differences among patients with transthyretin amyloid cardiomyopathy – from diagnosis to prognosis;Patel;Eur J Heart Fail,2022

5. Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy;Maurer;N Engl J Med,2018

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