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Wild-type TTR amyloidosis among patients with unexplained heart failure and systolic LV dysfunction
AIM: Transthyretin cardiac amyloidosis (ATTR-CA) is an increasingly recognized cause of heart failure (HF) with preserved left ventricular ejection fraction (LVEF), typically presenting as restrictive cardiomyopathy. The potential co-existence of ATTR-CA with systolic heart failure has not been stud...
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| Publicado en: | PLoS One |
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| Autores principales: | , , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Public Library of Science
2021
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8270434/ https://ncbi.nlm.nih.gov/pubmed/34242301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0254104 |
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