Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Federica Amodio"'
Autor:
Emanuele Monda, Gianantonio De Michele, Gaetano Diana, Federica Verrillo, Marta Rubino, Annapaola Cirillo, Adelaide Fusco, Federica Amodio, Martina Caiazza, Francesca Dongiglio, Giuseppe Palmiero, Pietro Buono, Maria Giovanna Russo, Giuseppe Limongelli
Publikováno v:
Diagnostics, Vol 14, Iss 23, p 2626 (2024)
The journal retracts the article, titled “Left Ventricular Non-Compaction in Children: Aetiology and Diagnostic Criteria” [...]
Externí odkaz:
https://doaj.org/article/98de65083ee542a682089076a2839953
Autor:
Emanuele Monda, Gianantonio De Michele, Gaetano Diana, Federica Verrillo, Marta Rubino, Annapaola Cirillo, Adelaide Fusco, Federica Amodio, Martina Caiazza, Francesca Dongiglio, Giuseppe Palmiero, Pietro Buono, Maria Giovanna Russo, Giuseppe Limongelli
Publikováno v:
Diagnostics, Vol 14, Iss 1, p 115 (2024)
Left ventricular non-compaction (LVNC) is a heterogeneous myocardial disorder characterized by prominent trabeculae protruding into the left ventricular lumen and deep intertrabecular recesses. LVNC can manifest in isolation or alongside other heart
Externí odkaz:
https://doaj.org/article/b1b508a37074461698d86573ac42bb22
Autor:
Emanuele Monda, Ettore Blasi, Antonio De Pasquale, Alessandro Di Vilio, Federica Amodio, Martina Caiazza, Gaetano Diana, Michele Lioncino, Alessia Perna, Federica Verrillo, Maria Luigia Martucci, Orlando Munciguerra, Andrea Vergara, Giuseppe Limongelli
Publikováno v:
Cardiogenetics, Vol 12, Iss 1, Pp 112-121 (2022)
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 prevalent ventricular arrhythmias, heart failure, and sudden cardiac death. The pathophysiolo
Externí odkaz:
https://doaj.org/article/1614399154564dd2851a5a04fdb54bbe
Autor:
Marta Rubino, Emanuele Monda, Martina Caiazza, Giuseppe Palmiero, Michele Lioncino, Annapaola Cirillo, Adelaide Fusco, Federica Verrillo, Alessia Perna, Gaetano Diana, Federica Amodio, Arturo Cesaro, Giovanni Duro, Berardo Sarubbi, Maria Giovanna Russo, Paolo Calabrò, Giuseppe Limongelli
Publikováno v:
Cardiogenetics, Vol 12, Iss 1, Pp 102-108 (2022)
Fabry disease (FD) is a multiorgan disease, which can potentially affect any organ or tissue, with the heart, kidneys, and central nervous system representing the major disease targets. FD can be suspected based on the presence of specific red flags,
Externí odkaz:
https://doaj.org/article/722da436dbbc46d597aea335bfd20a1e
Publikováno v:
Cardiogenetics, Vol 11, Iss 4, Pp 230-254 (2021)
MicroRNAs (miRNAs) are single-stranded small non-coding RNA (18–25 nucleotides) that until a few years ago were considered junk RNA. In the last twenty years, they have acquired more importance thanks to the understanding of their influence on gene
Externí odkaz:
https://doaj.org/article/3e9ff9072351463eb9ad01aba65e692f
Publikováno v:
Cardiogenetics, Vol 11, Iss 1, Pp 28-30 (2021)
Since late 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its associated coronavirus disease 2019 (COVID-19) have become a worldwide threat to public health [...]
Externí odkaz:
https://doaj.org/article/7f181def70b845488bf14e679a86d3f1
Autor:
Federica Amodio, Martina Caiazza, Emanuele Monda, Marta Rubino, Laura Capodicasa, Flavia Chiosi, Vincenzo Simonelli, Francesca Dongiglio, Fabio Fimiani, Nicola Pepe, Cristina Chimenti, Paolo Calabrò, Giuseppe Limongelli
Publikováno v:
Biomolecules, Vol 12, Iss 10, p 1460 (2022)
Fabry disease (FD) (OMIM #301500) is a rare genetic lysosomal storage disorder (LSD). LSDs are characterized by inappropriate lipid accumulation in lysosomes due to specific enzyme deficiencies. In FD, the defective enzyme is α-galactosidase A (α-G
Externí odkaz:
https://doaj.org/article/3cdddb2ea6214dfe8b735cfc2b099519
Autor:
Martina Caiazza, Michele Lioncino, Emanuele Monda, Francesco Di Fraia, Federica Verrillo, Roberta Pacileo, Federica Amodio, Marta Rubino, Annapaola Cirillo, Adelaide Fusco, Emanuele Romeo, Alessandra Scatteia, Santo Dellegrottaglie, Paolo Calabrò, Berardo Sarubbi, Anwar Baban, Giulia Frisso, Maria Giovanna Russo, Giuseppe Limongelli
Publikováno v:
Biomolecules, Vol 11, Iss 5, p 696 (2021)
Coarctation of the aorta is a leading cause of morbidity and mortality among adults with congenital heart disease (ACHD). Lifelong surveillance is mandatory to screen for possible long-term cardiovascular events. Left ventricular systolic dysfunction
Externí odkaz:
https://doaj.org/article/df3d72acd21a4a64a84ce73c58187c6e
Autor:
Michele Iavarone, Emanuele Monda, Olga Vritz, Dimpna Calila Albert, Marta Rubino, Federica Verrillo, Martina Caiazza, Michele Lioncino, Federica Amodio, Natale Guarnaccia, Felice Gragnano, Raffaella Lombardi, Giovanni Esposito, Eduardo Bossone, Paolo Calabrò, Maria Angela Losi, Giuseppe Limongelli
Publikováno v:
Archives of Cardiovascular Diseases. 115:529-537
Several treatments have demonstrated safety and effectiveness in the treatment of patients with hypertrophic cardiomyopathy; however, no drug has been shown to modify the natural history of the disease or to decrease maximal wall thickness. Improveme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eef88cd815045dc437323c19de3ee247
https://doi.org/10.1016/j.acvd.2022.06.003
https://doi.org/10.1016/j.acvd.2022.06.003
Autor:
Michele Lioncino, Martina Caiazza, Annapaola Cirillo, Federica Amodio, Maria Giovanna Russo, Giulia Frisso, Marta Rubino, Adelaide Fusco, Nunzia Borrelli, Giuseppe Limongelli, Silvia Castelletti, Fabio Fimiani, Barbara D'Onofrio, Fabrizio Drago, Paolo Calabrò, Roberta Pacileo, Emanuele Monda, Berardo Sarubbi, Diego Colonna
Publikováno v:
Heart Failure Clinics. 18:115-123
"Sudden unexplained death (SUD) is a tragic event for both the family and community, particularly when it occurs in young individuals. Sudden cardiac death (SCD) represents the leading form of SUD and is defined as an unexpected event without an obvi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a219e425db0fde63d88c268000ea698
https://doi.org/10.1016/j.hfc.2021.07.002
https://doi.org/10.1016/j.hfc.2021.07.002