Zobrazeno 1 - 10
of 608
pro vyhledávání: '"Pilichou, A."'
Autor:
Corrado, Domenico, Thiene, Gaetano, Bauce, Barbara, Calore, Chiara, Cipriani, Alberto, De Lazzari, Manuel, Migliore, Federico, Perazzolo Marra, Martina, Pilichou, Kalliopi, Rigato, Ilaria, Rizzo, Stefania, Zorzi, Alessandro, Basso, Cristina
Publikováno v:
In International Journal of Cardiology 1 January 2025 418
Publikováno v:
The Application of Clinical Genetics, Vol Volume 16, Pp 233-239 (2023)
Hubertus von Korn,1 Cristina Basso,2 Kalliopi Pilichou,2 Victor Stefan,1 Patrick Swojanowsky1 1Department of Cardiology, Marienhaus Klinikum Hetzelstift, Neustadt, Weinstraße, 67434, Germany; 2Department of Cardiac, Thoracic and Vascular Sciences an
Externí odkaz:
https://doaj.org/article/f38816f5be3943a1ac51d8c49d1bfc0c
Autor:
Rudy Celeghin, Giovanni Risato, Giorgia Beffagna, Marco Cason, Maria Bueno Marinas, Mila Della Barbera, Nicola Facchinello, Alice Giuliodori, Raquel Brañas Casas, Micol Caichiolo, Andrea Vettori, Enrico Grisan, Stefania Rizzo, Luisa Dalla Valle, Francesco Argenton, Gaetano Thiene, Natascia Tiso, Kalliopi Pilichou, Cristina Basso
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-14 (2023)
Abstract Arrhythmogenic cardiomyopathy (AC) is an inherited disorder characterized by progressive loss of the ventricular myocardium causing life-threatening ventricular arrhythmias, syncope and sudden cardiac death in young and athletes. About 40% o
Externí odkaz:
https://doaj.org/article/19472e78aa4e4bbcaaac30f07520d4e5
Autor:
Francesca Graziano, Alessandro Zorzi, Simone Ungaro, Barbara Bauce, Ilaria Rigato, Alberto Cipriani, Martina Perazzolo Marra, Kalliopi Pilichou, Cristina Basso, Domenico Corrado
Publikováno v:
Reviews in Cardiovascular Medicine, Vol 25, Iss 9, p 348 (2024)
Arrhythmogenic cardiomyopathy (ACM) is a cardiac disease featured by non-ischemic myocardial scarring linked to ventricular electrical instability. As there is no single gold-standard test, diagnosing ACM remains challenging and a combination of spec
Externí odkaz:
https://doaj.org/article/be468e0f05f24706b9999f8f355e5720
Autor:
Bermudez-Jimenez, Francisco J., Protonotarios, Alexandros, García-Hernández, Soledad, Pérez Asensio, Ana, Rampazzo, Alessandra, Zorio, Esther, Brodehl, Andreas, Arias, Miguel A., Macías-Ruiz, Rosa, Fernández-Armenta, Juan, Remior Perez, Paloma, Muñoz-Esparza, Carmen, Pilichou, Kalliopi, Bauce, Barbara, Merino, Jose L., Moliner-Abós, Carlos, Ochoa, Juan P., Barriales-Villa, Roberto, Garcia-Pavia, Pablo, Lopes, Luis R., Syrris, Petros, Corrado, Domenico, Elliott, Perry M., McKenna, William J., Jimenez-Jaimez, Juan
Publikováno v:
In JACC: Clinical Electrophysiology June 2024 10(6):1178-1190
Autor:
Giovanni Risato, Raquel Brañas Casas, Marco Cason, Maria Bueno Marinas, Serena Pinci, Monica De Gaspari, Silvia Visentin, Stefania Rizzo, Gaetano Thiene, Cristina Basso, Kalliopi Pilichou, Natascia Tiso, Rudy Celeghin
Publikováno v:
Cells, Vol 13, Iss 15, p 1264 (2024)
Arrhythmogenic cardiomyopathy (AC) is a hereditary cardiac disorder characterized by the gradual replacement of cardiomyocytes with fibrous and adipose tissue, leading to ventricular wall thinning, chamber dilation, arrhythmias, and sudden cardiac de
Externí odkaz:
https://doaj.org/article/ee3cf922c2ed4a989dfe6e3be29f26d0
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
Autor:
Graziano, Francesca, Zorzi, Alessandro, Cipriani, Alberto, Bauce, Barbara, Rigato, Ilaria, Perazzolo Marra, Martina, Vago, Hajnalka, Merkely, Bela, Pilichou, Kalliopi, Basso, Cristina, Corrado, Domenico
Publikováno v:
In Trends in Cardiovascular Medicine
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