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International Journal of Cardiology|January 19, 2024
Clinical characteristics and outcome of end stage hypertrophic cardiomyopathy: Role of age and heart failure phenotypesBeatrice Musumeci, Giacomo Tini, Elena Biagini, et al.
International Journal of Cardiology|August 9, 2026
Pattern of use of conventional medical treatments of heart failure with reduced ejection fraction in end-stage hypertrophic cardiomyopathyGiacomo Tini, Isabella Perlati, Sofia Palma, et al.
ESC Heart Failure|February 19, 2026
Medical treatments at 6 months in hospitalized and ambulatory HFrEF patients in the BRING-UP 3 Heart Failure studyFabrizio Oliva, Francesco Orso, Furio Colivicchi, et al.
European Heart Journal. Cardiovascular Imaging|October 28, 2025
Scar Architecture as a Structural Biomarker of Ventricular Arrhythmias and Sudden Cardiac Death in Patients with Hypertrophic Cardiomyopathy: a Cardiac Magnetic Resonance StudyPietro Francia, Giulio Falasconi, Maria Beatrice Musumeci, et al.
European Journal of Heart Failure|May 5, 2022
Incidence and risk factors for pacemaker implantation in light-chain and transthyretin cardiac amyloidosisAldostefano Porcari, Maddalena Rossi, Francesco Cappelli, et al.
International Journal of Cardiology|September 9, 2023
Incidence and determinants of atrial fibrillation in patients with wild-type transthyretin cardiac amyloidosisCarlo Fumagalli, Mattia Zampieri, Alessia Argirò, et al.
JACC. Cardiooncology|November 29, 2022
Low QRS Voltages in Cardiac Amyloidosis: Clinical Correlates and Prognostic ValueAlberto Cipriani, Laura De Michieli, Aldostefano Porcari, et al.
ESC Heart Failure|November 15, 2024
Exercise limitations in amyloid cardiomyopathy assessed by cardiopulmonary exercise testing-A multicentre studyRobin Willixhofer, Mauro Contini, Michele Emdin, et al.
Circulation. Heart Failure|May 15, 2025
High-Sensitivity Cardiac Troponin I for Risk Stratification in Wild-Type Transthyretin Amyloid CardiomyopathyLaura De Michieli, Giulio Sinigiani, Gianluigi Guida, et al.
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