Sfoglia per Autore
Is There a Role for Genetic Testing in Patients With Myocarditis?
2022 Monda, Emanuele; Limongelli, Giuseppe
An Overview of Molecular Mechanisms in Fabry Disease
2022 Amodio, Federica; Caiazza, Martina; Monda, Emanuele; Rubino, Marta; Capodicasa, Laura; Chiosi, Flavia; Simonelli, Vincenzo; Dongiglio, Francesca; Fimiani, Fabio; Pepe, Nicola; Chimenti, Cristina; Calabrò, Paolo; Limongelli, Giuseppe
Rare Cardiovascular Diseases: From Genetics to Personalized Medicine
2022 Limongelli, G.; Monda, E.; Lioncino, M.; Bossone, E.
Thoracic Aortic Dilation: Implications for Physical Activity and Sport Participation
2022 Monda, E.; Verrillo, F.; Rubino, M.; Palmiero, G.; Fusco, A.; Cirillo, A.; Caiazza, M.; Guarnaccia, N.; Mauriello, A.; Lioncino, M.; Perna, A.; Diana, G.; D'Andrea, A.; Bossone, E.; Calabro, P.; Limongelli, G.
Clinical pathway on pediatric cardiomyopathies: A genetic testing strategy proposed by the Italian Society of Pediatric Cardiology
2022 Girolami, F.; Iascone, M.; Pezzoli, L.; Passantino, S.; Limongelli, G.; Monda, E.; Rubino, M.; Adorisio, R.; Lombardi, M.; Ragni, L.; Olivotto, I.; Favilli, S.
Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes
2022 Mazzaccara, Cristina; Lombardi, Raffaella; Mirra, Bruno; Barretta, Ferdinando; Esposito, Maria Valeria; Uomo, Fabiana; Caiazza, Martina; Monda, Emanuele; Losi, Maria Angela; Limongelli, Giuseppe; D'Argenio, Valeria; Frisso, Giulia
Sudden cardiac death risk prediction in arrhythmogenic right ventricular cardiomyopathy: the challenge of complex statistical modelling and its impact in clinical practice
2022 Monda, Emanuele; Lioncino, Michele; Limongelli, Giuseppe
A complex unit for a complex disease: The HCM-Family Unit
2022 Vriz, O.; Alsergani, H.; Elshaer, A. N.; Shaik, A.; Mushtaq, A. H.; Lioncino, M.; Alamro, B.; Monda, E.; Caiazza, M.; Russo, G.; Mauro, C.; Bossone, E.; Al-Hassnan, Z. N.; Albert-Brotons, D.; Limongelli, G.
Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation
2022 Lioncino, M.; Fusco, A.; Monda, E.; Colonna, D.; Sibilio, M.; Caiazza, M.; Magri, D.; Borrelli, A. C.; D'Onofrio, B.; Mazzella, M. L.; Colantuono, R.; Arienzo, M. R.; Sarubbi, B.; Russo, M. G.; Chello, G.; Limongelli, G.
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)
2022 Limongelli, G.; Adorisio, R.; Baggio, C.; Bauce, B.; Biagini, E.; Castelletti, S.; Favilli, S.; Imazio, M.; Lioncino, M.; Merlo, M.; Monda, E.; Olivotto, I.; Parisi, V.; Pelliccia, F.; Basso, C.; Sinagra, G.; Indolfi, C.; Autore, C.
Implantable cardioverter defibrillator in hypertrophic cardiomyopathy: Time to avoid unnecessary procedure
2022 Limongelli, G.; Monda, E.
Cardiovascular Involvement in Transthyretin Cardiac Amyloidosis
2022 Lioncino, M.; Monda, E.; Palmiero, G.; Caiazza, M.; Vetrano, E.; Rubino, M.; Esposito, A.; Salerno, G.; Dongiglio, F.; D'Onofrio, B.; Verrillo, F.; Cerciello, G.; Manganelli, F.; Pacileo, G.; Bossone, E.; Golino, P.; Calabro, P.; Limongelli, G.
Multimodality Imaging in Cardiomyopathies with Hypertrophic Phenotypes
2022 Monda, E.; Palmiero, G.; Lioncino, M.; Rubino, M.; Cirillo, A.; Fusco, A.; Caiazza, M.; Verrillo, F.; Diana, G.; Mauriello, A.; Iavarone, M.; Losi, M. A.; De Rimini, M. L.; Dellegrottaglie, S.; D'Andrea, A.; Bossone, E.; Pacileo, G.; Limongelli, G.
Medical treatment of patients with hypertrophic cardiomyopathy: An overview of current and emerging therapy
2022 Iavarone, Michele; Monda, Emanuele; Vritz, Olga; Calila Albert, Dimpna; Rubino, Marta; Verrillo, Federica; Caiazza, Martina; Lioncino, Michele; Amodio, Federica; Guarnaccia, Natale; Gragnano, Felice; Lombardi, Raffaella; Esposito, Giovanni; Bossone, Eduardo; Calabro, Paolo; Losi, Maria Angela; Limongelli, Giuseppe
Bisoprolol for treatment of symptomatic patients with obstructive hypertrophic cardiomyopathy. The BASIC (bisoprolol AS therapy in hypertrophic cardiomyopathy) study
2022 Monda, E.; Lioncino, M.; Palmiero, G.; Franco, F.; Rubino, M.; Cirillo, A.; Verrillo, F.; Fusco, A.; Caiazza, M.; Mazzella, M.; Moscarella, E.; Dongiglio, F.; Sepe, J.; Pacileo, G.; Calabro, P.; Limongelli, G.
Effectiveness in the short-term of a novel nutraceutical for the management of hypercholesterolemia: an observational multicenter primary care experience
2022 Natale, Francesco; Molinari, Riccardo; Covino, Simona; Piccinocchi, Gaetano; Salvetti, Andrea; Monda, Emanuele; Limongelli, Giuseppe; Cimmino, Giovanni
Clinical manifestation of patients with Fabry disease and R356W GLA variant
2023 Monda, Emanuele; Rubino, Marta; Riccio, Eleonora; Caiazza, Martina; Iaccarino, Guido; Dongiglio, Francesca; Graziani, Francesca; Pisani, Antonio; Limongelli, Giuseppe
Impact of GLA Variant Classification on the Estimated Prevalence of Fabry Disease: A Systematic Review and Meta-Analysis of Screening Studies
2023 Monda, Emanuele; Diana, Gaetano; Graziani, Francesca; Rubino, Marta; Bakalakos, Athanasios; Linhart, Ales; Germain, Dominique P; Scarpa, Maurizio; Biagini, Elena; Pieroni, Maurizio; Elliott, Perry Mark; Limongelli, Giuseppe
Hypertrophic Cardiomyopathy-Current Challenges and Future Perspectives
2023 Monda, Emanuele; Limongelli, Giuseppe; Pelliccia, Francesco
Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy
2023 Monda, Emanuele; Kaski, Juan Pablo; Limongelli, Giuseppe
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Is There a Role for Genetic Testing in Patients With Myocarditis? | 1-gen-2022 | Monda, Emanuele; Limongelli, Giuseppe | |
An Overview of Molecular Mechanisms in Fabry Disease | 1-gen-2022 | Amodio, Federica; Caiazza, Martina; Monda, Emanuele; Rubino, Marta; Capodicasa, Laura; Chiosi, Flavia; Simonelli, Vincenzo; Dongiglio, Francesca; Fimiani, Fabio; Pepe, Nicola; Chimenti, Cristina; Calabrò, Paolo; Limongelli, Giuseppe | |
Rare Cardiovascular Diseases: From Genetics to Personalized Medicine | 1-gen-2022 | Limongelli, G.; Monda, E.; Lioncino, M.; Bossone, E. | |
Thoracic Aortic Dilation: Implications for Physical Activity and Sport Participation | 1-gen-2022 | Monda, E.; Verrillo, F.; Rubino, M.; Palmiero, G.; Fusco, A.; Cirillo, A.; Caiazza, M.; Guarnaccia, N.; Mauriello, A.; Lioncino, M.; Perna, A.; Diana, G.; D'Andrea, A.; Bossone, E.; Calabro, P.; Limongelli, G. | |
Clinical pathway on pediatric cardiomyopathies: A genetic testing strategy proposed by the Italian Society of Pediatric Cardiology | 1-gen-2022 | Girolami, F.; Iascone, M.; Pezzoli, L.; Passantino, S.; Limongelli, G.; Monda, E.; Rubino, M.; Adorisio, R.; Lombardi, M.; Ragni, L.; Olivotto, I.; Favilli, S. | |
Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes | 1-gen-2022 | Mazzaccara, Cristina; Lombardi, Raffaella; Mirra, Bruno; Barretta, Ferdinando; Esposito, Maria Valeria; Uomo, Fabiana; Caiazza, Martina; Monda, Emanuele; Losi, Maria Angela; Limongelli, Giuseppe; D'Argenio, Valeria; Frisso, Giulia | |
Sudden cardiac death risk prediction in arrhythmogenic right ventricular cardiomyopathy: the challenge of complex statistical modelling and its impact in clinical practice | 1-gen-2022 | Monda, Emanuele; Lioncino, Michele; Limongelli, Giuseppe | |
A complex unit for a complex disease: The HCM-Family Unit | 1-gen-2022 | Vriz, O.; Alsergani, H.; Elshaer, A. N.; Shaik, A.; Mushtaq, A. H.; Lioncino, M.; Alamro, B.; Monda, E.; Caiazza, M.; Russo, G.; Mauro, C.; Bossone, E.; Al-Hassnan, Z. N.; Albert-Brotons, D.; Limongelli, G. | |
Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation | 1-gen-2022 | Lioncino, M.; Fusco, A.; Monda, E.; Colonna, D.; Sibilio, M.; Caiazza, M.; Magri, D.; Borrelli, A. C.; D'Onofrio, B.; Mazzella, M. L.; Colantuono, R.; Arienzo, M. R.; Sarubbi, B.; Russo, M. G.; Chello, G.; Limongelli, G. | |
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) | 1-gen-2022 | Limongelli, G.; Adorisio, R.; Baggio, C.; Bauce, B.; Biagini, E.; Castelletti, S.; Favilli, S.; Imazio, M.; Lioncino, M.; Merlo, M.; Monda, E.; Olivotto, I.; Parisi, V.; Pelliccia, F.; Basso, C.; Sinagra, G.; Indolfi, C.; Autore, C. | |
Implantable cardioverter defibrillator in hypertrophic cardiomyopathy: Time to avoid unnecessary procedure | 1-gen-2022 | Limongelli, G.; Monda, E. | |
Cardiovascular Involvement in Transthyretin Cardiac Amyloidosis | 1-gen-2022 | Lioncino, M.; Monda, E.; Palmiero, G.; Caiazza, M.; Vetrano, E.; Rubino, M.; Esposito, A.; Salerno, G.; Dongiglio, F.; D'Onofrio, B.; Verrillo, F.; Cerciello, G.; Manganelli, F.; Pacileo, G.; Bossone, E.; Golino, P.; Calabro, P.; Limongelli, G. | |
Multimodality Imaging in Cardiomyopathies with Hypertrophic Phenotypes | 1-gen-2022 | Monda, E.; Palmiero, G.; Lioncino, M.; Rubino, M.; Cirillo, A.; Fusco, A.; Caiazza, M.; Verrillo, F.; Diana, G.; Mauriello, A.; Iavarone, M.; Losi, M. A.; De Rimini, M. L.; Dellegrottaglie, S.; D'Andrea, A.; Bossone, E.; Pacileo, G.; Limongelli, G. | |
Medical treatment of patients with hypertrophic cardiomyopathy: An overview of current and emerging therapy | 1-gen-2022 | Iavarone, Michele; Monda, Emanuele; Vritz, Olga; Calila Albert, Dimpna; Rubino, Marta; Verrillo, Federica; Caiazza, Martina; Lioncino, Michele; Amodio, Federica; Guarnaccia, Natale; Gragnano, Felice; Lombardi, Raffaella; Esposito, Giovanni; Bossone, Eduardo; Calabro, Paolo; Losi, Maria Angela; Limongelli, Giuseppe | |
Bisoprolol for treatment of symptomatic patients with obstructive hypertrophic cardiomyopathy. The BASIC (bisoprolol AS therapy in hypertrophic cardiomyopathy) study | 1-gen-2022 | Monda, E.; Lioncino, M.; Palmiero, G.; Franco, F.; Rubino, M.; Cirillo, A.; Verrillo, F.; Fusco, A.; Caiazza, M.; Mazzella, M.; Moscarella, E.; Dongiglio, F.; Sepe, J.; Pacileo, G.; Calabro, P.; Limongelli, G. | |
Effectiveness in the short-term of a novel nutraceutical for the management of hypercholesterolemia: an observational multicenter primary care experience | 1-gen-2022 | Natale, Francesco; Molinari, Riccardo; Covino, Simona; Piccinocchi, Gaetano; Salvetti, Andrea; Monda, Emanuele; Limongelli, Giuseppe; Cimmino, Giovanni | |
Clinical manifestation of patients with Fabry disease and R356W GLA variant | 1-gen-2023 | Monda, Emanuele; Rubino, Marta; Riccio, Eleonora; Caiazza, Martina; Iaccarino, Guido; Dongiglio, Francesca; Graziani, Francesca; Pisani, Antonio; Limongelli, Giuseppe | |
Impact of GLA Variant Classification on the Estimated Prevalence of Fabry Disease: A Systematic Review and Meta-Analysis of Screening Studies | 1-gen-2023 | Monda, Emanuele; Diana, Gaetano; Graziani, Francesca; Rubino, Marta; Bakalakos, Athanasios; Linhart, Ales; Germain, Dominique P; Scarpa, Maurizio; Biagini, Elena; Pieroni, Maurizio; Elliott, Perry Mark; Limongelli, Giuseppe | |
Hypertrophic Cardiomyopathy-Current Challenges and Future Perspectives | 1-gen-2023 | Monda, Emanuele; Limongelli, Giuseppe; Pelliccia, Francesco | |
Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy | 1-gen-2023 | Monda, Emanuele; Kaski, Juan Pablo; Limongelli, Giuseppe |
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