Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Federico, Perfetto"'
Autor:
Giacomo Tini, MD, Ernesto Cristiano, MD, Mattia Zampieri, MD, Alberto Ponziani, MD, Aldostefano Porcari, MD, Margherita Zanoletti, MD, Carlotta Mazzoni, MD, Matteo Sclafani, MD, Giulia Saturi, MD, Andrea Lalario, MD, Marianna Eleonora Labate, MD, Camillo Autore, MD, Emanuele Barbato, MD, Federico Perfetto, MD, Elena Biagini, MD, Gianfranco Sinagra, MD, Marco Canepa, MD, Marco Merlo, MD, Simone Longhi, MD, Francesco Cappelli, MD, Beatrice Musumeci, MD
Publikováno v:
JACC: Advances, Vol 3, Iss 10, Pp 101232- (2024)
Background: The introduction of a noninvasive diagnostic algorithm in 2016 led to increased awareness and recognition of cardiac amyloidosis (CA). Objectives: The purpose of this study was to analyze the impact of the introduction of the noninvasive
Externí odkaz:
https://doaj.org/article/6524464884ae41d399c2bb9b3df16316
Autor:
Giulia Grazzini, Silvia Pradella, Rossella Bani, Chiara Fornaciari, Francesco Cappelli, Federico Perfetto, Diletta Cozzi, Simona Giovannelli, Giacomo Sica, Vittorio Miele
Publikováno v:
Diagnostics, Vol 14, Iss 10, p 1048 (2024)
Cardiac amyloidosis (CA) is an infiltrative cardiomyopathy divided into two types: light-chain (LA) and transthyretin (ATTR) CA. Cardiac magnetic resonance (CMR) has emerged as an important diagnostic tool in CA. While late gadolinium enhancement (LG
Externí odkaz:
https://doaj.org/article/8ae57be927e44808aa5afb00dddd1a2a
Autor:
Samantha Innocenti, Beatrice Bacchi, Marco Allinovi, Federico Perfetto, Elisabetta Antonioli, Niccolo’ Marchionni, Carlo Di Mario, Leonardo Caroti, Francesco Cappelli, Pierluigi Stefàno
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-8 (2022)
Abstract Background Multiple myeloma (MM) is a malignant neoplasm associated with kidney involvement in nearly half of the patients. Cast nephropathy, monoclonal immunoglobulin deposition disease (MIDD), and light chain (AL) amyloidosis are the most
Externí odkaz:
https://doaj.org/article/083f2131320c4286a00b6cc0e1b781b2
Autor:
Martina Smorti, Lucia Ponti, Francesco Soffio, Alessia Argirò, Federico Perfetto, Mattia Zampieri, Carlotta Mazzoni, Alessia Tomberli, Marco Allinovi, Carlo Di Mario, Iacopo Olivotto, Francesco Cappelli
Publikováno v:
Frontiers in Psychology, Vol 13 (2023)
Patients with ATTR cardiac amyloidosis (ATTR-CA) face rare disease that could negatively influence psychological well-being with consequences on the course of the disease and quality of life. However, to date, no study analyzed the prevalence of anxi
Externí odkaz:
https://doaj.org/article/1a3b49f23e8148a9aac73beed2c5e249
Autor:
Giacomo Tini, Francesco Cappelli, Elena Biagini, Beatrice Musumeci, Marco Merlo, Lia Crotti, Matteo Cameli, Gianluca Di Bella, Alberto Cipriani, Francesca Marzo, Federico Guerra, Cinzia Forleo, Christian Gagliardi, Mattia Zampieri, Samuela Carigi, Pier Filippo Vianello, Giulia Elena Mandoli, Giuseppe Ciliberti, Luca Lichelli, Davide Mariani, Aldostefano Porcari, Domitilla Russo, Roberto Licordari, Alberto Ponziani, Italo Porto, Federico Perfetto, Camillo Autore, Claudio Rapezzi, Giafranco Sinagra, Marco Canepa
Publikováno v:
ESC Heart Failure, Vol 8, Iss 4, Pp 3369-3374 (2021)
Abstract Aims The use of beta‐blocker therapy in cardiac amyloidosis (CA) is debated. We aimed at describing patterns of beta‐blocker prescription through a nationwide survey. Methods and results From 11 referral centres, we retrospectively colle
Externí odkaz:
https://doaj.org/article/e17354fbab234649bb0aa43c9fa75769
Autor:
Lorenza Magliano, Laura Obici, Claudia Sforzini, Anna Mazzeo, Massimo Russo, Francesco Cappelli, Silvia Fenu, Marco Luigetti, Matteo Tagliapietra, Chiara Gemelli, Luca Leonardi, Stefano Tozza, Luca Guglielmo Pradotto, Giulia Citarelli, Alessandro Mauro, Fiore Manganelli, Giovanni Antonini, Marina Grandis, Gian Maria Fabrizi, Mario Sabatelli, Davide Pareyson, Federico Perfetto, Giampaolo Merlini, Giuseppe Vita, ATTRv Collaborators
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Background Hereditary transthyretin amyloidosis (hATTR), alias ATTR variant (ATTRv) is a severe and disabling disease causing sensory and motor neuropathy, autonomic dysfunction, and cardiomyopathy. The progressive decline of patient’s fun
Externí odkaz:
https://doaj.org/article/ec614e801b3a4556b8a4dca986e3adab
Autor:
Federico Perfetto, Mattia Zampieri, Giulia Bandini, Roberto Fedi, Roberto Tarquini, Raffaella Santi, Luca Novelli, Marco Allinovi, Alessia Argirò, Francesco Cappelli
Publikováno v:
Biomedicines, Vol 10, Iss 12, p 3226 (2022)
Orthopaedic manifestations of wild-type transthyretin amyloidosis are frequent and characteristic, including idiopathic bilateral carpal tunnel syndrome, idiopathic lumbar canal stenosis, atraumatic rupture of the brachial biceps tendon, and, more ra
Externí odkaz:
https://doaj.org/article/e0c5d13ea9194b8b8b8cebc0e3c772d3
Autor:
Alessia Argirò, Annamaria Del Franco, Carlotta Mazzoni, Marco Allinovi, Alessia Tomberli, Roberto Tarquini, Carlo Di Mario, Federico Perfetto, Francesco Cappelli, Mattia Zampieri
Publikováno v:
Biomedicines, Vol 10, Iss 11, p 2888 (2022)
Cardiac amyloidosis (CA), caused by the deposition of insoluble amyloid fibrils, impairs different cardiac structures, altering not only left ventricle (LV) systo-diastolic function but also atrial function and the conduction system. The consequences
Externí odkaz:
https://doaj.org/article/f2d8bcea9d6e4cf592f6dfb16c0f0cf8
Autor:
Carlo Fumagalli, Martina Smorti, Lucia Ponti, Francesca Pozza, Alessia Argirò, Giacomo Credi, Carlo Di Mario, Raffaele Marfella, Niccolò Marchionni, Iacopo Olivotto, Federico Perfetto, Andrea Ungar, Francesco Cappelli
Publikováno v:
Aging Clinical and Experimental Research. 35:1363-1367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44ca390b45526169c7023af8e8df9d1f
https://doi.org/10.1007/s40520-023-02419-6
https://doi.org/10.1007/s40520-023-02419-6
Autor:
Giovanni Donato Aquaro, Sofia Morini, Chrysanthos Grigoratos, Giulia Taborchi, Gianluca Di Bella, Raffaele Martone, Elisa Vignini, Michele Emdin, Iacopo Olivotto, Federico Perfetto, Francesco Cappelli
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 31, Iss , Pp 100633- (2020)
Objectives: Left atrial (LA) function is an important marker of hemodynamic status in cardiac amyloidosis (CA), and its characterization may provide relevant prognostic information. We sought to assess the prevalence and prognostic impact of LA dysfu
Externí odkaz:
https://doaj.org/article/159b1864b3854256902f07958c358578