Rare Forms of Cardiac Amyloidosis: Diagnostic Clues and Phenotype in Apo AI and AIV Amyloidosis

Apo AI amyloidosis (AApoAI) and Apo AIV amyloidosis (AApoAIV) are rare but increasingly recognized causes of cardiac amyloidosis (CA). We sought to define the cardiac phenotype in AApoAI and AApoAIV using multimodality imaging. METHODS: We identified all patients with AApoAI and AApoAIV assessed at...

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Detalles Bibliográficos
Autores principales: Ioannou, Adam, Porcari, Aldostefano, Patel, Rishi K., Razvi, Yousuf, Sinigiani, Giulio, Martinez-Naharro, Ana, Venneri, Lucia, Moon, James, Rauf, Muhammad U., Lachmann, Helen, Wechelakar, Ashutosh, Hawkins, Philip N., Gillmore, Julian D., Fontana, Marianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351905/
https://www.ncbi.nlm.nih.gov/pubmed/37431665
http://dx.doi.org/10.1161/CIRCIMAGING.123.015259

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351905/
https://www.ncbi.nlm.nih.gov/pubmed/37431665
http://dx.doi.org/10.1161/CIRCIMAGING.123.015259

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