Search Results - "Lioncino, Michele"

Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes by Monda, Emanuele, Lioncino, Michele, Caiazza, Martina, Simonelli, Vincenzo, Nesti, Claudia, Rubino, Marta, Perna, Alessia, Mauriello, Alfredo, Budillon, Alberta, Pota, Vincenzo, Bruno, Giorgia, Varone, Antonio, Nigro, Vincenzo, Santorelli, Filippo Maria, Pacileo, Giuseppe, Russo, Maria Giovanna, Frisso, Giulia, Sampaolo, Simone, Limongelli, Giuseppe

“…Cardiomyopathies are mostly determined by genetic mutations affecting either cardiac muscle cell structure or function. Nevertheless, cardiomyopathies may also…”
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Hypertrophic Cardiomyopathy in Children: Pathophysiology, Diagnosis, and Treatment of Non-sarcomeric Causes by Monda, Emanuele, Rubino, Marta, Lioncino, Michele, Di Fraia, Francesco, Pacileo, Roberta, Verrillo, Federica, Cirillo, Annapaola, Caiazza, Martina, Fusco, Adelaide, Esposito, Augusto, Fimiani, Fabio, Palmiero, Giuseppe, Pacileo, Giuseppe, Calabrò, Paolo, Russo, Maria Giovanna, Limongelli, Giuseppe

“…Hypertrophic cardiomyopathy (HCM) is a myocardial disease characterized by left ventricular hypertrophy not solely explained by abnormal loading conditions…”
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Cognitive Function and Atrial Fibrillation: From the Strength of Relationship to the Dark Side of Prevention. Is There a Contribution from Sinus Rhythm Restoration and Maintenance? by Gallinoro, Emanuele, D'Elia, Saverio, Prozzo, Dario, Lioncino, Michele, Natale, Francesco, Golino, Paolo, Cimmino, Giovanni

“…Atrial fibrillation (AF) is the most common chronic cardiac arrhythmia with an increasing prevalence over time mainly because of population aging. It is well…”
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A complex unit for a complex disease: the HCM-Family Unit by Vriz, Olga, AlSergani, Hani, Elshaer, Ahmed Nahid, Shaik, Abdullah, Mushtaq, Ali Hassan, Lioncino, Michele, Alamro, Bandar, Monda, Emanuele, Caiazza, Martina, Mauro, Ciro, Bossone, Eduardo, Al-Hassnan, Zuhair N, Albert-Brotons, Dimpna, Limongelli, Giuseppe

“…Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease…”
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Thoracic Aortic Dilation: Implications for Physical Activity and Sport Participation by Monda, Emanuele, Verrillo, Federica, Rubino, Marta, Palmiero, Giuseppe, Fusco, Adelaide, Cirillo, Annapaola, Caiazza, Martina, Guarnaccia, Natale, Mauriello, Alfredo, Lioncino, Michele, Perna, Alessia, Diana, Gaetano, D’Andrea, Antonello, Bossone, Eduardo, Calabrò, Paolo, Limongelli, Giuseppe

“…Thoracic aortic dilatation is a progressive condition that results from aging and many pathological conditions (i.e., connective tissue, inflammatory, shear…”
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Double-Outlet Left Ventricle: Case Series and Systematic Review of the Literature by Lioncino, Michele, Calcagni, Giulio, Badolato, Fausto, Antonelli, Giovanni, Leonardi, Benedetta, de Zorzi, Andrea, Secinaro, Aurelio, Brancaccio, Gianluca, Albanese, Sonia, Carotti, Adriano, Drago, Fabrizio, Rinelli, Gabriele

“…Double-outlet left ventricle (DOLV) is an abnormal ventriculo-arterial connection characterized by the origin of both great arteries from the morphological…”
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The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases by Monda, Emanuele, Lioncino, Michele, Verrillo, Federica, Rubino, Marta, Caiazza, Martina, Mauriello, Alfredo, Guarnaccia, Natale, Fusco, Adelaide, Cirillo, Annapaola, Covino, Simona, Altobelli, Ippolita, Diana, Gaetano, Palmiero, Giuseppe, Dongiglio, Francesca, Natale, Francesco, Cesaro, Arturo, Bossone, Eduardo, Russo, Maria Giovanna, Calabrò, Paolo, Limongelli, Giuseppe

“…Heritable thoracic aortic disease (HTAD) is a term used to define a large group of disorders characterized by the occurrence of aortic events, mainly…”
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Multidisciplinary In-Depth Investigation in a Young Athlete Suffering from Syncope Caused by Myocardial Bridge by Brancaccio, Mariarita, Mennitti, Cristina, Cesaro, Arturo, Monda, Emanuele, D’Argenio, Valeria, Casaburi, Giorgio, Mazzaccara, Cristina, Ranieri, Annaluisa, Fimiani, Fabio, Barretta, Ferdinando, Uomo, Fabiana, Caiazza, Martina, Lioncino, Michele, D’Alicandro, Giovanni, Limongelli, Giuseppe, Calabrò, Paolo, Terracciano, Daniela, Lombardo, Barbara, Frisso, Giulia, Scudiero, Olga

“…Laboratory medicine, along with genetic investigations in sports medicine, is taking on an increasingly important role in monitoring athletes’ health…”
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Troponin T Mutation as a Cause of Left Ventricular Systolic Dysfunction in a Young Patient with Previous Surgical Correction of Aortic Coarctation by Caiazza, Martina, Lioncino, Michele, Monda, Emanuele, Di Fraia, Francesco, Verrillo, Federica, Pacileo, Roberta, Amodio, Federica, Rubino, Marta, Cirillo, Annapaola, Fusco, Adelaide, Romeo, Emanuele, Scatteia, Alessandra, Dellegrottaglie, Santo, Calabrò, Paolo, Sarubbi, Berardo, Baban, Anwar, Frisso, Giulia, Russo, Maria Giovanna, Limongelli, Giuseppe

“…Coarctation of the aorta is a leading cause of morbidity and mortality among adults with congenital heart disease (ACHD). Lifelong surveillance is mandatory to…”
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Clinical and Molecular Characteristics of Patients with PLN R14del Cardiomyopathy: State-of-the-Art Review by Monda, Emanuele, Blasi, Ettore, De Pasquale, Antonio, Di Vilio, Alessandro, Amodio, Federica, Caiazza, Martina, Diana, Gaetano, Lioncino, Michele, Perna, Alessia, Verrillo, Federica, Martucci, Maria, Munciguerra, Orlando, Vergara, Andrea, Limongelli, Giuseppe

“…The deletion of the arginine 14 codon (R14del) in the phospholamban (PLN) gene is a rare cause of arrhythmogenic cardiomyopathy (ACM) and is associated with…”
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Diagnosis of Fabry Disease in a Patient with a Surgically Repaired Congenital Heart Defect: When Clinical History and Genetics Make the Difference by Rubino, Marta, Monda, Emanuele, Caiazza, Martina, Palmiero, Giuseppe, Lioncino, Michele, Cirillo, Annapaola, Fusco, Adelaide, Verrillo, Federica, Perna, Alessia, Diana, Gaetano, Amodio, Federica, Cesaro, Arturo, Duro, Giovanni, Sarubbi, Berardo, Russo, Maria, Calabrò, Paolo, Limongelli, Giuseppe

“…Fabry disease (FD) is a multiorgan disease, which can potentially affect any organ or tissue, with the heart, kidneys, and central nervous system representing…”
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Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis by Dongiglio, Francesca, Palmiero, Giuseppe, Monda, Emanuele, Rubino, Marta, Verrillo, Federica, Caiazza, Martina, Cirillo, Annapaola, Fusco, Adelaide, Vetrano, Erica, Lioncino, Michele, Diana, Gaetano, Di Fraia, Francesco, Cerciello, Giuseppe, Manganelli, Fiore, Vriz, Olga, Limongelli, Giuseppe

“…The nutritional assessment is gaining clinical relevance since cardiac cachexia and malnutrition are emerging as novel markers of functional status and…”
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Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis by Lioncino, Michele, Monda, Emanuele, Dellegrottaglie, Santo, Cirillo, Annapaola, Caiazza, Martina, Fusco, Adelaide, Esposito, Francesca, Verrillo, Federica, Ciccarelli, Giovanni, Rubino, Marta, Triggiani, Massimo, Scarpa, Raffaele, Caforio, Alida Linda Patrizia, Marcolongo, Renzo, Rizzo, Stefania, Basso, Cristina, Nigro, Gerardo, Russo, Maria Giovanna, Golino, Paolo, Limongelli, Giuseppe

“…Eosinophilic pancarditis (EP) is a rare, often unrecognized condition caused by endomyocardial infiltration of eosinophil granulocytes (referred as…”
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Sudden cardiac death risk prediction in arrhythmogenic right ventricular cardiomyopathy: the challenge of complex statistical modelling and its impact in clinical practice by Monda, Emanuele, Lioncino, Michele, Limongelli, Giuseppe

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External validation of the increased wall thickness score for the diagnosis of cardiac amyloidosis by Monda, Emanuele, Palmiero, Giuseppe, Lioncino, Michele, Rubino, Marta, Caiazza, Martina, Dongiglio, Francesca, Limongelli, Giuseppe

“…This study aimed to validate the increased wall thickness (IWT) score, a multiparametric echocardiographic score to facilitate diagnosis of cardiac amyloidosis…”
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Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP) by Limongelli, Giuseppe, Adorisio, Rachele, Baggio, Chiara, Bauce, Barbara, Biagini, Elena, Castelletti, Silvia, Favilli, Silvia, Imazio, Massimo, Lioncino, Michele, Merlo, Marco, Monda, Emanuele, Olivotto, Iacopo, Parisi, Vanda, Pelliccia, Francesco, Basso, Cristina, Sinagra, Gianfranco, Indolfi, Ciro, Autore, Camillo

“…Cardiomyopathies (CMPs) are myocardial diseases in which the heart muscle is structurally and functionally abnormal in the absence of coronary artery disease,…”
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Type and dimensions can predict ventricular arrhythmias and cardiac death in primary benign cardiac tumors in children by Placidi, Silvia, Calcagni, Giulio, Lioncino, Michele, Calvieri, Camilla, Maiolo, Stella, Di Mambro, Corrado, Silvetti, Massimo Stefano, Secinaro, Aurelio, Adorisio, Rachele, Albanese, Sonia, Galletti, Lorenzo, Drago, Fabrizio

“…Despite being extremely rare in children, primary benign cardiac tumors can cause malignant ventricular arrhythmias (VA) or even sudden cardiac death. To…”
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Targeted Therapies in Pediatric and Adult Patients With Hypertrophic Heart Disease: From Molecular Pathophysiology to Personalized Medicine by Monda, Emanuele, Bakalakos, Athanasios, Rubino, Marta, Verrillo, Federica, Diana, Gaetano, De Michele, Gianantonio, Altobelli, Ippolita, Lioncino, Michele, Perna, Alessia, Falco, Luigi, Palmiero, Giuseppe, Elliott, Perry M., Limongelli, Giuseppe

“…Hypertrophic cardiomyopathy is a myocardial disease defined by an increased left ventricular wall thickness not solely explained by abnormal loading…”
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Aortic Root Diameter in Highly-Trained Competitive Athletes: Reference Values According to Sport and Prevalence of Aortic Enlargement by Limongelli, Giuseppe, Monda, Emanuele, Lioncino, Michele, Di Paolo, Fernando, Ferrara, Francesco, Vriz, Olga, Calabro, Paolo, Bossone, Eduardo, Pelliccia, Antonio

“…Studies exploring the extent of aortic root dilation across the different types of sport are limited. We aimed to define the physiological limits of aortic…”
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Rare Cardiovascular Diseases: From Genetics to Personalized Medicine by Limongelli, Giuseppe, Monda, Emanuele, Lioncino, Michele, Bossone, Eduardo

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