Showing results (111-120 of 142) with videos related to
Sort By:
Pageof 15
Future Cardiology|October 21, 2020
Potential role of imaging markers in predicting future disease expression of arrhythmogenic cardiomyopathyEmanuele Monda, Giulia Frisso, Marta Rubino, et al.European Heart Journal. Digital Health|January 23, 2026
Development of a smartphone-based app to support the differential diagnosis in patients with primary left ventricular hypertrophyNiccolò Maurizi, Emanuele Monda, Maurizio Pieroni, et al.Journal of Clinical Medicine|January 21, 2023
Pathophysiology, Functional Assessment and Prognostic Implications of Nutritional Disorders in Systemic AmyloidosisFrancesca Dongiglio, Emanuele Monda, Giuseppe Palmiero, et al.European Journal of Preventive Cardiology|August 23, 2021
Yield and clinical significance of genetic screening in elite and amateur athletesGiuseppe Limongelli, Marcella Nunziato, Valeria D'Argenio, et al.Plos One|May 20, 2020
Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseasesMaria Paola Belfiore, Francesca Iacobellis, Emma Acampora, et al.JACC. Cardiovascular Interventions|February 19, 2021
Access-Site Crossover in Patients With Acute Coronary Syndrome Undergoing Invasive ManagementFelice Gragnano, Mattia Branca, Enrico Frigoli, et al.International Journal of Cardiology|July 9, 2023
Prevalence and clinical significance of right ventricular pulmonary arterial uncoupling in cardiac amyloidosisGiuseppe Palmiero, Emanuele Monda, Federica Verrillo, et al.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.Journal of Clinical Medicine|February 25, 2023
Multimodality Imaging in Arrhythmogenic Left Ventricular CardiomyopathyEmanuele Monda, Marta Rubino, Giuseppe Palmiero, et al.European Journal of Human Genetics : EJHG|June 1, 2024
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variantAndrea Gazzin, Federico Fornari, Marcello Niceta, et al.Pageof 15