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Journal of Cardiovascular Medicine (Hagerstown, Md.)|January 3, 2020
Bridging the gap between hypertrabeculation phenotype, noncompaction phenotype and left ventricular noncompaction cardiomyopathyVittoria Vergani, Davide Lazzeroni, Giovanni PerettoInternational Journal of Molecular Sciences|December 23, 2022
The Aging Heart: A Molecular and Clinical ChallengeDavide Lazzeroni, Andrea Villatore, Gaia Souryal, et al.Frontiers in Bioscience (Landmark Edition)|April 15, 2017
Cardiotoxicity in oncology and coronary microcirculation: future challenges in theranosticsGiovanni Peretto, Davide Lazzeroni, Carmem L Sartorio, et al.Journal of Clinical Medicine|March 28, 2024
Cardiac Wolframinopathies: A Case Report of Myocarditis and a Literature Review of Cardiac Involvement in Wolfram Syndrome 1Andrea Villatore, Giulio Frontino, Maria Lucia Cascavilla, et al.International Journal of Cardiology|May 7, 2017
Serum uric acid on admission predicts in-hospital mortality in patients with acute coronary syndromeMarco Magnoni, Martina Berteotti, Ferruccio Ceriotti, et al.Biomolecules|May 16, 2023
Myocardial Inflammation as a Manifestation of Genetic Cardiomyopathies: From Bedside to the BenchGiovanni Peretto, Elena Sommariva, Chiara Di Resta, et al.Journal of Personalized Medicine|May 27, 2023
Personalized Management of Sudden Death Risk in Primary Cardiomyopathies: From Clinical Evaluation and Multimodality Imaging to Ablation and Cardioverter-Defibrillator ImplantDavide Lazzeroni, Antonio Crocamo, Valentina Ziveri, et al.Minerva Cardioangiologica|February 21, 2018
Risk stratification in secondary cardiovascular preventionDavide Lazzeroni, Paolo CoruzziHeart, Lung & Circulation|April 18, 2020
Septal Late Gadolinium Enhancement and Arrhythmic Risk in Genetic and Acquired Non-Ischaemic CardiomyopathiesGiovanni Peretto, Simone Sala, Davide Lazzeroni, et al.Journal of Personalized Medicine|August 26, 2022
Arrhythmogenic Cardiomyopathy: One, None and a Hundred Thousand DiseasesGiovanni Peretto, Patrizio MazzonePageof 18