Diagnostic and therapeutic advances have led to much greater awareness of transthyretin cardiac amyloidosis (ATTR-CA). We aimed to characterize changes in the clinical phenotype of patients diagnosed with ATTR-CA over the past 20 years.

Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years / Ioannou, A., Patel, R.K., Razvi, Y., Porcari, A., Sinagra, G., Venneri, L., Bandera, F., Masi, A., Williams, G.E., O'Beara, S., Ganesananthan, S., Massa, P., Knight, D., Martinez-Naharro, A., Kotecha, T., Chacko, L., Brown, J., Rauf, M.U., Manisty, C., Moon, J., et al.. - In: CIRCULATION. - ISSN 0009-7322. - ELETTRONICO. - 146:22(2022), pp. 1657-1670. [10.1161/CIRCULATIONAHA.122.060852]

Impact of Earlier Diagnosis in Cardiac ATTR Amyloidosis Over the Course of 20 Years

Porcari, Aldostefano;Sinagra, Gianfranco;
2022-01-01

Abstract

Diagnostic and therapeutic advances have led to much greater awareness of transthyretin cardiac amyloidosis (ATTR-CA). We aimed to characterize changes in the clinical phenotype of patients diagnosed with ATTR-CA over the past 20 years.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3033098
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