Zobrazeno 1 - 10
of 185
pro vyhledávání: '"Barbara Bauce"'
Publikováno v:
Biomolecules, Vol 14, Iss 6, p 702 (2024)
Dilated cardiomyopathy (DCM) is a common cause of heart failure (HF) and heart transplantation (HTx), with genetic factors playing a significant role. In recent years, the RNA-binding protein motif 20 (RBM20), which affects the gene splicing of vario
Externí odkaz:
https://doaj.org/article/7bd8eedcb4c745d7a17bf34ef482a408
Autor:
Maria Bueno Marinas, Marco Cason, Riccardo Bariani, Rudy Celeghin, Monica De Gaspari, Serena Pinci, Alberto Cipriani, Ilaria Rigato, Alessandro Zorzi, Stefania Rizzo, Gaetano Thiene, Martina Perazzolo Marra, Domenico Corrado, Cristina Basso, Barbara Bauce, Kalliopi Pilichou
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 6267 (2024)
Arrhythmogenic cardiomyopathy (ACM) is an inherited myocardial disease at risk of sudden death. Genetic testing impacts greatly in ACM diagnosis, but gene-disease associations have yet to be determined for the increasing number of genes included in c
Externí odkaz:
https://doaj.org/article/badb83bf459843c59f337e7750b124c3
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 7, p 2660 (2023)
Desmoplakin (DSP) is a desmosomal protein that plays an essential role for cell-to-cell adhesion within the cardiomyocytes. The first association between DSP genetic variants and the presence of a myocardial disease referred to patients with Carvajal
Externí odkaz:
https://doaj.org/article/e2d1757e17a6406abc70587b0d5a2957
Autor:
Giulia Mattesi, Sara Di Michele, Donato Mele, Ilaria Rigato, Riccardo Bariani, Andrea Fiorencis, Marco Previtero, Abdullah Al Sergani, Loira Leoni, Barbara Bauce, Valeria Pergola
Publikováno v:
Monaldi Archives for Chest Disease (2022)
Thyroid hormones have a considerable influence on cardiac function and structure. There are direct and indirect effects of thyroid hormone on the cardiovascular system, which are prominent in both hypothyroidism and hyperthyroidism. In this review, w
Externí odkaz:
https://doaj.org/article/c2e68388968b4b1b8c00a6fe3277bd0b
Autor:
Emanuele Monda, Marta Rubino, Giuseppe Palmiero, Federica Verrillo, Michele Lioncino, Gaetano Diana, Annapaola Cirillo, Adelaide Fusco, Francesca Dongiglio, Martina Caiazza, Ippolita Altobelli, Alfredo Mauriello, Natale Guarnaccia, Alessandra Scatteia, Arturo Cesaro, Giuseppe Pacileo, Berardo Sarubbi, Giulia Frisso, Barbara Bauce, Antonello D’Andrea, Santo Dellegrottaglie, Maria Giovanna Russo, Paolo Calabrò, Giuseppe Limongelli
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 4, p 1568 (2023)
The term arrhythmogenic cardiomyopathy (ACM) describes a large spectrum of myocardial diseases characterized by progressive fibrotic or fibrofatty replacement, which gives the substrate for the occurrence of ventricular tachyarrhythmias and the devel
Externí odkaz:
https://doaj.org/article/3a706434577442e6909446fbfefe0574
Autor:
Domenico Corrado, Alessandro Zorzi, Alberto Cipriani, Barbara Bauce, Riccardo Bariani, Giorgia Beffagna, Manuel De Lazzari, Federico Migliore, Kalliopi Pilichou, Alessandra Rampazzo, Ilaria Rigato, Stefania Rizzo, Gaetano Thiene, Martina Perazzolo Marra, Cristina Basso
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 18 (2021)
Criteria for diagnosis of arrhythmogenic cardiomyopathy (ACM) were first proposed in 1994 and revised in 2010 by a Task Force. Although the Task Force criteria demonstrated a good accuracy for diagnosis of the original right ventricular phenotype (ar
Externí odkaz:
https://doaj.org/article/37bbe4398dd24249a34002d7ee2e8e2f
Autor:
Riccardo Bariani, Maria Bueno Marinas, Ilaria Rigato, Paola Veronese, Rudy Celeghin, Alberto Cipriani, Marco Cason, Valeria Pergola, Giulia Mattesi, Petra Deola, Alessandro Zorzi, Giuseppe Limongelli, Sabino Iliceto, Domenico Corrado, Cristina Basso, Kalliopi Pilichou, Barbara Bauce
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 22, p 6735 (2022)
Background: In the last few years, a phenotypic variant of arrhythmogenic cardiomyopathy (ACM) labeled arrhythmogenic left ventricular cardiomyopathy (ALVC) has been defined and researched. This type of cardiomyopathy is characterized by a predominan
Externí odkaz:
https://doaj.org/article/cd9fa769548243c5a42f23de24e4750d
Autor:
Francesca Graziano, Alessandro Zorzi, Alberto Cipriani, Manuel De Lazzari, Barbara Bauce, Ilaria Rigato, Giulia Brunetti, Kalliopi Pilichou, Cristina Basso, Martina Perazzolo Marra, Domenico Corrado
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 23, Iss 10, p 335 (2022)
Arrhythmogenic cardiomyopathy (ACM) is a rare heart muscle disease characterized by a progressive fibro-fatty myocardial replacement, ventricular arrhythmias, and increased risk of sudden cardiac death. The first diagnostic criteria were proposed by
Externí odkaz:
https://doaj.org/article/03dbe7abcb5a4384907baa213fa4e778
Autor:
Riccardo Bariani, Ilaria Rigato, Alberto Cipriani, Maria Bueno Marinas, Rudy Celeghin, Cristina Basso, Domenico Corrado, Kalliopi Pilichou, Barbara Bauce
Publikováno v:
Biomolecules, Vol 12, Iss 9, p 1324 (2022)
Arrhythmogenic cardiomyopathy (ACM) is a genetically determined myocardial disease, characterized by myocytes necrosis with fibrofatty substitution and ventricular arrhythmias that can even lead to sudden cardiac death. The presence of inflammatory c
Externí odkaz:
https://doaj.org/article/5d5a684bce2b41ee92caa644f1b4aafe
Autor:
Nicola Moro, Lolita Dokshokova, Induja Perumal Vanaja, Valentina Prando, Sophie Julie A Cnudde, Anna Di Bona, Riccardo Bariani, Leonardo Schirone, Barbara Bauce, Annalisa Angelini, Sebastiano Sciarretta, Alessandra Ghigo, Marco Mongillo, Tania Zaglia
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11098 (2022)
Doxorubicin (DOXO) remains amongst the most commonly used anti-cancer agents for the treatment of solid tumors, lymphomas, and leukemias. However, its clinical use is hampered by cardiotoxicity, characterized by heart failure and arrhythmias, which m
Externí odkaz:
https://doaj.org/article/57ba9546e8014019a73f5b9400dbb6e8