Light chain and transthyretin cardiac amyloidosis: Clinical characteristics, natural history and prognostic factors-Reference-Cited by-同舟云学术

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Light chain and transthyretin cardiac amyloidosis: Clinical characteristics, natural history and prognostic factors

Published:2021-04 Issue:8 Volume:156 Page:369-378
ISSN:2387-0206
Container-title:Medicina Clínica (English Edition)
language:en
Short-container-title:Medicina Clínica (English Edition)

Author:

Barge-Caballero Gonzalo,Vázquez-García Raquel,Barge-Caballero Eduardo,Couto-Mallón David,Paniagua-Martín María J.,Barriales-Villa Roberto,Piñón-Esteban Pablo,Bouzas-Mosquera Alberto,Pombo-Otero Jorge,Debén-Ariznavarreta Guillermo,Vázquez-Rodríguez José M.,Crespo-Leiro María G.

Funder

Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares

Instituto de Salud Carlos III

Publisher

Elsevier BV

Subject

General Medicine

Reference23 articles.

1. Incidence and natural history of primary systemic amyloidosis in Olmsted County, Minnesota, 1950 through 1989;Kyle;Blood,1992

2. Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths;González-López;Eur Heart J.,2017

3. Natural history, quality of life, and outcome in cardiac transthyretin amyloidosis;Lane;Circulation.,2019

4. How to face a clinical suspicion of cardiac amyloidosis? A practical approach to the diagnosis;Barge-Caballero;Cardiocore.,2017

5. Non-biopsy diagnosis of cardiac transthyretin amyloidosis;Gillmore;Circulation.,2016

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