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Giornale Italiano Di Cardiologia (2006)|August 29, 2017
[Cardiologists and mucopolysaccharidoses. Recommendations of GICEM (Cardiology Experts on Metabolic Disease Italian Group) for diagnosis, follow-up and cardiological management]Pierluigi Russo, Generoso Andria, Alessandra Baldinelli, 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.
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.
Circulation. Genomic and Precision Medicine|February 6, 2026
Cardiovascular Morbidity and Mortality in Fabry DiseaseEmanuele Monda, Athanasios Bakalakos, Annamaria Del Franco, et al.
Journal of Clinical Medicine|February 25, 2023
Multimodality Imaging in Arrhythmogenic Left Ventricular CardiomyopathyEmanuele Monda, Marta Rubino, Giuseppe Palmiero, 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 Public Health (Oxford, England)|May 13, 2021
Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease RegistryGiuseppe Limongelli, Stefano Iucolano, Emanuele Monda, et al.
Pediatric Cardiology|April 17, 2021
Impact of Regular Physical Activity on Aortic Diameter Progression in Paediatric Patients with Bicuspid Aortic ValveEmanuele Monda, Adelaide Fusco, Alessandro Della Corte, et al.
Heart (British Cardiac Society)|February 10, 2021
Standard ECG for differential diagnosis between Anderson-Fabry disease and hypertrophic cardiomyopathyGiovanni Vitale, Raffaello Ditaranto, Francesca Graziani, et al.
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