Search Results - "Tomberli, Alessia"

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    Doctor-patient care relationship in genetic cardiomyopathies: An exploratory study on clinical consultations by Fioretti, Chiara, Magni, Elisa, Barlocco, Fausto, Tomberli, Alessia, Baldini, Katia, Ingles, Jodie, Smorti, Andrea, Olivotto, Iacopo

    Published in PloS one (05-08-2020)
    “…Background The present study aims to explore the setting of consultation and communication between physicians and patients affected by genetic…”
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    Journal Article
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    Prevalence of anxiety and depression symptoms in a sample of outpatients with ATTR cardiac amyloidosis by Smorti, Martina, Ponti, Lucia, Soffio, Francesco, Argirò, Alessia, Perfetto, Federico, Zampieri, Mattia, Mazzoni, Carlotta, Tomberli, Alessia, Allinovi, Marco, Di Mario, Carlo, Olivotto, Iacopo, Cappelli, Francesco

    Published in Frontiers in psychology (18-01-2023)
    “…Patients with ATTR cardiac amyloidosis (ATTR-CA) face rare disease that could negatively influence psychological well-being with consequences on the course of…”
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    Journal Article
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    Arrhythmic Burden in Cardiac Amyloidosis: What We Know and What We Do Not by Argirò, Alessia, Del Franco, Annamaria, Mazzoni, Carlotta, Allinovi, Marco, Tomberli, Alessia, Tarquini, Roberto, Di Mario, Carlo, Perfetto, Federico, Cappelli, Francesco, Zampieri, Mattia

    Published in Biomedicines (01-11-2022)
    “…Cardiac amyloidosis (CA), caused by the deposition of insoluble amyloid fibrils, impairs different cardiac structures, altering not only left ventricle (LV)…”
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    Comprehensive Risk Management in Arrhythmogenic Cardiomyopathy Associated With Autosomal Dominant Carvajal Syndrome by De Gregorio, Maria Grazia, Girolami, Francesca, Tomberli, Benedetta, Rossi, Guendalina, Tomberli, Alessia, Baldini, Katia, Olivotto, Iacopo

    Published in JACC. Case reports (01-06-2020)
    “…In a 37-year-old cardiac arrest survivor with autosomal dominant Carvajal syndrome and arrhythmogenic cardiomyopathy, a desmoplakin mutation was identified…”
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    The evolving paradigm and current perception of hypertrophic cardiomyopathy: Implications for management by Del Franco, Annamaria, Menale, Silvia, Chiti, Chiara, Biagioni, Giulia, Tomberli, Alessia, Zampieri, Mattia, Olivotto, Iacopo

    Published in Progress in cardiovascular diseases (01-09-2023)
    “…Recent evidence from imaging and genetic screening studies has clearly shown that hypertrophic cardiomyopathy (HCM) is more common than initially perceived,…”
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    Mavacamten, a Novel Therapeutic Strategy for Obstructive Hypertrophic Cardiomyopathy by Zampieri, Mattia, Argirò, Alessia, Marchi, Alberto, Berteotti, Martina, Targetti, Mattia, Fornaro, Alessandra, Tomberli, Alessia, Stefàno, Pierluigi, Marchionni, Niccolò, Olivotto, Iacopo

    Published in Current cardiology reports (01-07-2021)
    “…Purpose of review Pharmacological treatment options for hypertrophic cardiomyopathy (HCM) are currently limited and comprise non-disease specific therapies…”
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    686 ASSOCIATION OF PREGNANCY WITH THE NATURAL HISTORY OF WOMEN DIAGNOSED WITH HYPERTROPHIC CARDIOMYOPATHY by Fumagalli, Carlo, Zocchi, Chiara, Cappelli, Francesco, Tassetti, Luigi, Zampieri, Mattia, Maurizi, Niccolo, Tomberli, Alessia, Mecacci, Federico, Favilli, Silvia, Olivotto, Iacopo

    Published in European heart journal supplements (15-12-2022)
    “…Abstract Background Hypertrophic Cardiomyopathy (HCM) is the most common genetic cardiomyopathy. However, few studies have systematically investigated the…”
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    Targeted Medical Therapies for Hypertrophic Cardiomyopathy by Fumagalli, Carlo, De Gregorio, Maria Grazia, Zampieri, Mattia, Fedele, Elisa, Tomberli, Alessia, Chiriatti, Chiara, Marchi, Alberto, Olivotto, Iacopo

    Published in Current cardiology reports (28-01-2020)
    “…Purpose of Review The management of hypertrophic cardiomyopathy (HCM) has changed considerably over the years, although molecular therapies targeting core…”
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    Journal Article
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