Noninvasive diagnosis of hereditary transthyretin-related cardiac amyloidosis: A case report

RATIONALE: Cardiac transthyretin amyloidosis is a progressive and fatal cardiomyopathy for which several promising therapies are in development. The diagnosis is frequently delayed or missed because of the limited specificity of clinical manifestations, routine electrocardiogram, echocardiography an...

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Detalles Bibliográficos
Autores principales: Qin, Jin, Zhan, Chenao, Li, Haojie, Han, Yunfeng, Wang, Hong, Li, Rui, Ma, Fei, Yan, Jiangtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709038/
https://www.ncbi.nlm.nih.gov/pubmed/31348283
http://dx.doi.org/10.1097/MD.0000000000016566

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709038/
https://www.ncbi.nlm.nih.gov/pubmed/31348283
http://dx.doi.org/10.1097/MD.0000000000016566

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