User profiles for "author:Angelo Giuseppe Caponetti"

Angelo Giuseppe Caponetti

Alma Mater studiorum di Bologna
Verified email at unibo.it
Cited by 411

Unmasking the prevalence of amyloid cardiomyopathy in the real world: results from Phase 2 of the AC‐TIVE study, an Italian nationwide survey

M Merlo, L Pagura, A Porcari, M Cameli… - European Journal of …, 2022 - Wiley Online Library
Aim To investigate the prevalence of amyloid cardiomyopathy (AC) and the diagnostic
accuracy of echocardiographic red flags of AC among consecutive adult patients …

Carpal tunnel syndrome in cardiac amyloidosis: implications for early diagnosis and prognostic role across the spectrum of aetiologies

A Milandri, A Farioli, C Gagliardi… - European journal of …, 2020 - Wiley Online Library
Aims We aimed to assess carpal tunnel syndrome (CTS) prevalence in transthyretin (TTR)‐
related and light‐chain amyloidosis (AL), comparing it to the general population, adjusted for …

[HTML][HTML] Pediatric restrictive cardiomyopathies

R Ditaranto, AG Caponetti, V Ferrara, V Parisi… - Frontiers in …, 2022 - frontiersin.org
Restrictive cardiomyopathy (RCM) is the least frequent phenotype among pediatric heart
muscle diseases, representing only 2.5–3% of all cardiomyopathies diagnosed during …

Tc-99m labelled bone scintigraphy in suspected cardiac amyloidosis

MU Rauf, PN Hawkins, F Cappelli… - European Heart …, 2023 - academic.oup.com
Aims To perform evaluation of widely embraced bone scintigraphy-based non-biopsy
diagnostic criteria (NBDC) for ATTR amyloid cardiomyopathy (ATTR-CM) in clinical practice …

Sex-related risk of cardiac involvement in hereditary transthyretin amyloidosis: insights from THAOS

AG Caponetti, C Rapezzi, C Gagliardi, A Milandri… - Heart Failure, 2021 - jacc.org
Abstract Objectives Because patients with ATTRv cardiomyopathy are more likely to be
male, this analysis aimed to increase information on associations between sex and …

A national survey on prevalence of possible echocardiographic red flags of amyloid cardiomyopathy in consecutive patients undergoing routine echocardiography …

M Merlo, A Porcari, L Pagura, M Cameli… - European Journal of …, 2022 - academic.oup.com
* Corresponding author. Tel: þ39 040 399 4477, Fax: þ39 040 399 4878, Email: marco.
merlo79@ gmail. com† The first two authors contributed equally as first authors.‡ The last …

[HTML][HTML] Screening approaches to cardiac amyloidosis in different clinical settings: Current practice and future perspectives

AG Caponetti, A Accietto, G Saturi… - Frontiers in …, 2023 - frontiersin.org
Cardiac amyloidosis is a serious and progressive infiltrative disease caused by the
deposition of amyloid fibrils in the heart. In the last years, a significant increase in the …

Clinical presentations leading to arrhythmogenic left ventricular cardiomyopathy

M Graziosi, R Ditaranto, C Rapezzi, F Pasquale… - Open …, 2022 - openheart.bmj.com
Objectives To describe a cohort of patients with arrhythmogenic left ventricular
cardiomyopathy (ALVC), focusing on the spectrum of the clinical presentations. Methods …

Clinical and prognostic implications of right ventricular uptake on bone scintigraphy in transthyretin amyloid cardiomyopathy

A Porcari, M Fontana, M Canepa, E Biagini, F Cappelli… - Circulation, 2024 - Am Heart Assoc
BACKGROUND: The extent of myocardial bone tracer uptake with technetium
pyrophosphate, hydroxymethylene diphosphonate, and 3, 3-diphosphono-1, 2 …

Standard ECG for differential diagnosis between Anderson-Fabry disease and hypertrophic cardiomyopathy

G Vitale, R Ditaranto, F Graziani, I Tanini… - Heart, 2022 - heart.bmj.com
Objectives To evaluate the role of the ECG in the differential diagnosis between Anderson-
Fabry disease (AFD) and hypertrophic cardiomyopathy (HCM). Methods In this multicentre …