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Journal of Clinical Medicine|February 15, 2022
Multimodality Imaging in Cardiomyopathies with Hypertrophic PhenotypesEmanuele Monda, Giuseppe Palmiero, Michele Lioncino, et al.Biomolecules|June 2, 2021
Troponin T Mutation as a Cause of Left Ventricular Systolic Dysfunction in a Young Patient with Previous Surgical Correction of Aortic CoarctationMartina Caiazza, Michele Lioncino, Emanuele Monda, et al.International Journal of Molecular Sciences|September 9, 2020
Molecular Basis of Inflammation in the Pathogenesis of CardiomyopathiesEmanuele Monda, Giuseppe Palmiero, Marta Rubino, et al.Heart Failure Clinics|November 15, 2021
Diagnosis and Management of Cardiovascular Involvement in Fabry DiseaseMarta Rubino, Emanuele Monda, Michele Lioncino, et al.Diagnostics (Basel, Switzerland)|February 25, 2023
The Role of Genetic Testing in Patients with Heritable Thoracic Aortic DiseasesEmanuele Monda, Michele Lioncino, Federica Verrillo, et al.International Journal of Molecular Sciences|May 27, 2023
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy PhenotypesEmanuele Monda, Michele Lioncino, Martina Caiazza, et al.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.Heart Failure Clinics|November 15, 2021
The Role of New Imaging Technologies in the Diagnosis of Cardiac AmyloidosisGiuseppe Palmiero, Erica Vetrano, Marta Rubino, 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.Journal of Medical Genetics|January 20, 2023
Effect of Migalastat on cArdiac InvOlvement in FabRry DiseAse: MAIORA studyAntonia Camporeale, Francesco Bandera, Maurizio Pieroni, et al.Pageof 8