A Aimo, M Merlo, A Porcari… - European journal of …, 2022 - Wiley Online Library
Aims An algorithm for non‐invasive diagnosis of amyloid transthyretin cardiac amyloidosis (ATTR‐CA) and novel disease‐modifying therapies have prompted an active search for CA …
C Nitsche, PR Scully, KP Patel… - Journal of the American …, 2021 - jacc.org
Background Older patients with severe aortic stenosis (AS) are increasingly identified as having cardiac amyloidosis (CA). It is unknown whether concomitant AS-CA has worse …
Cardiomyopathy is a manifestation of transthyretin amyloidosis (ATTR), which is an underrecognized systemic disease whereby the transthyretin protein misfolds to form fibrils …
MS Maurer, M Hanna, M Grogan, A Dispenzieri… - Journal of the American …, 2016 - jacc.org
Background: Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan involvement and a genetic or nongenetic basis. Objectives: The goal of this study was to …
E González-López, C Gagliardi… - European heart …, 2017 - academic.oup.com
Aims Wild-type transthyretin amyloidosis (ATTRwt) is mostly considered a disease predominantly of elderly male, characterized by concentric LV hypertrophy, preserved LVEF …
MA Gertz, MD Benson, PJ Dyck, M Grogan… - Journal of the American …, 2015 - jacc.org
Transthyretin amyloidosis is a fatal disorder that is characterized primarily by progressive neuropathy and cardiomyopathy. It occurs in both a mutant form (with autosomal dominant …