Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Marianna Cicenia"'
Autor:
Anwar Baban, Giovanni Parlapiano, Marianna Cicenia, Michela Armando, Alessio Franceschini, Concettina Pacifico, Arianna Panfili, Gaetano Zinzanella, Antonino Romanzo, Adelaide Fusco, Martina Caiazza, Gianluigi Perri, Lorenzo Galletti, Maria Cristina Digilio, Paola Sabrina Buonuomo, Andrea Bartuli, Antonio Novelli, Massimiliano Raponi, Giuseppe Limongelli
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 4, p 114 (2024)
Marfan syndrome (MIM: # 154700; MFS) is an autosomal dominant disease representing the most common form of heritable connective tissue disorder. The condition presents variable multiorgan expression, typically involving a triad of cardiovascular, eye
Externí odkaz:
https://doaj.org/article/8b18e6d91e9e4dc8a9270ee3bc6c4306
Autor:
Anwar Baban, Marianna Cicenia, Monia Magliozzi, Giovanni Parlapiano, Marco Cirillo, Giulia Pascolini, Fabiana Fattori, Maria Gnazzo, Pasqualina Bruno, Lorenzo De Luca, Luca Di Chiara, Paola Francalanci, Bjarne Udd, Aurelio Secinaro, Antonio Amodeo, Enrico Silvio Bertini, Marco Savarese, Fabrizio Drago, Antonio Novelli
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundMonoallelic and biallelic TTN truncating variants (TTNtv) may be responsible for a wide spectrum of musculoskeletal and cardiac disorders with different age at onset. Although the prevalence of heterozygous TTNtv is relatively high in the g
Externí odkaz:
https://doaj.org/article/35e0517acfa14006afaeeb4b26218875
Autor:
Nicoletta Cantarutti, Virginia Battista, Nicola Stagnaro, Marianna Eleonora Labate, Marianna Cicenia, Marta Campisi, Valerio Vitali, Aurelio Secinaro, Andrea Campana, Gianluca Trocchio, Fabrizio Drago
Publikováno v:
Biology, Vol 11, Iss 10, p 1474 (2022)
MIS-C is a multisystem inflammatory syndrome that is characterized by multi-organ failure and cardiac involvement. The aim of this study was to describe the long-term cardiovascular outcome in a cohort of MIS-C pediatric patients, who were admitted t
Externí odkaz:
https://doaj.org/article/5bb5ed6b21fc4012992df02b35a095fd
Autor:
Anwar Baban, Viola Alesi, Monia Magliozzi, Giovanni Parlapiano, Silvia Genovese, Marianna Cicenia, Sara Loddo, Valentina Lodato, Luca Di Chiara, Fabiana Fattori, Adele D’Amico, Paola Francalanci, Antonio Amodeo, Antonio Novelli, Fabrizio Drago
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 10, p 332 (2022)
Filamin C is a protein specifically expressed in myocytes and cardiomyocytes and is involved in several biological functions, including sarcomere contractile activity, signaling, cellular adhesion, and repair. FLNC variants are associated with differ
Externí odkaz:
https://doaj.org/article/ef7faa1979664ab1b7f888d2edb197ac
Autor:
Marianna Cicenia, Fabrizio Drago
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 4, p 98 (2022)
Arrhythmogenic cardiomyopathy (ACM) is a cardiomyopathy characterized by the occurrence of a high risk of life-threatening ventricular arrhythmias and sudden cardiac death even at presentation. Diagnosis, evolution and outcomes in adults have been ex
Externí odkaz:
https://doaj.org/article/004d22a0ba194056ae9597c6e2681436
Autor:
Anwar Baban, Marianna Cicenia, Monia Magliozzi, Maria Gnazzo, Nicoletta Cantarutti, Massimo Stefano Silvetti, Rachele Adorisio, Bruno Dallapiccola, Enrico Bertini, Antonio Novelli, Fabrizio Drago
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Lamin A/C (LMNA) encodes for two nuclear intermediate filament proteins. Mutations in LMNA cause a highly heterogeneous group of diseases predominantly leading to muscular or cardiac disease, lipodystrophy syndromes, peripheral neuropathy, and accele
Externí odkaz:
https://doaj.org/article/61ec4489008840aea20313be6c011de2
Autor:
Massimo Stefano Silvetti, Ilaria Tamburri, Marta Campisi, Fabio Anselmo Saputo, Ilaria Cazzoli, Nicoletta Cantarutti, Marianna Cicenia, Rachele Adorisio, Anwar Baban, Lucilla Ravà, Fabrizio Drago
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 9, Iss 2, p 33 (2022)
Background: Pediatric patients with cardiomyopathies are at risk of malignant arrhythmias and sudden cardiac death (SCD). An ICD may prevent SCD. The aim of this study was to evaluate ICD implantation outcomes, and to compare transvenous and subcutan
Externí odkaz:
https://doaj.org/article/2ce374e201984cb2a596152e30ce4c61
Autor:
Massimo S. Silvetti, Ilaria Tamburri, Luigina Porco, Fabio A. Saputo, Corrado Di Mambro, Daniela Righi, Ilaria Cazzoli, Marianna Cicenia, Marta Campisi, Lucilla Ravà, Cecilia Pizzicaroli, Fabrizio Drago
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 23, Iss 1, p 027 (2022)
Background: Remote monitoring-enabled insertable cardiac monitors (ICMs) are useful tools for arrhythmias and symptom management. This study sought to evaluate the outcome of ICM implantation in a large, heterogeneous cohort of pediatric and young ad
Externí odkaz:
https://doaj.org/article/ca7a9fdc89f040849160cc2fced8ecf2
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 8, Iss 12, p 176 (2021)
Premature ventricular contractions (PVCs) are common and generally benign in childhood and tend to resolve spontaneously in most cases. When PVCs occur frequently, an arrhythmia-induced cardiomyopathy may be present requiring medical or catheter abla
Externí odkaz:
https://doaj.org/article/b1fc3f6e853f48c8a1e965b05ee5d821
Autor:
Valentina Lodato, Valeria Orlando, Viola Alesi, Silvia Di Tommaso, Mario Bengala, Giovanni Parlapiano, Elisa Agnolucci, Marianna Cicenia, Federica Calì, Maria Cristina Digilio, Fabrizio Drago, Antonio Novelli, Anwar Baban
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 8, Iss 11, p 159 (2021)
Background: Monosomy 1p36 syndrome is now considered the most common terminal deletion syndrome, with an estimated incidence of 1 in 5000. Cardiac involvement is well described in the literature mainly in terms of congenital heart defects (CHDs) and
Externí odkaz:
https://doaj.org/article/e66cb9230e3c4788851e8444807e9dd6