Zobrazeno 1 - 10
of 923
pro vyhledávání: '"Gaetano Thiene"'
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
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 10, p 300 (2024)
The discovery of hypertrophic cardiomyopathy (HCM) dates back to 1958, when the pathologist Donald Teare of the St. George’s Hospital in London performed autopsies in eight cases with asymmetric hypertrophy of the ventricular septum and bizarre dis
Externí odkaz:
https://doaj.org/article/e948ce2905544b21a243c85a0ec96d46
Publikováno v:
Journal of Biological Research (2024)
Sudden Cardiac Death (SCD) may complicate diseases of the heart and great vessels. The cause is easily visible at the naked eye at autopsy in the presence of coronary thrombosis, aortic dissection, pulmonary thromboembolism, or at the microscope with
Externí odkaz:
https://doaj.org/article/a18fa8675f014c0c91101679ef02578e
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
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:
Cristina Vicenzetto, Andrea Silvio Giordani, Caterina Menghi, Anna Baritussio, Maria Grazia Peloso Cattini, Elena Pontara, Elisa Bison, Stefania Rizzo, Monica De Gaspari, Cristina Basso, Gaetano Thiene, Sabino Iliceto, Renzo Marcolongo, Alida Linda Patrizia Caforio
Publikováno v:
Biomedicines, Vol 12, Iss 6, p 1156 (2024)
The role of the immune system in myocarditis onset and progression involves a range of complex cellular and molecular pathways. Both innate and adaptive immunity contribute to myocarditis pathogenesis, regardless of its infectious or non-infectious n
Externí odkaz:
https://doaj.org/article/1f546f361a5e4dbfae88afbc3ad19c38
Publikováno v:
Biology, Vol 13, Iss 4, p 266 (2024)
This review explores the historical development of cardiology knowledge, from ancient Egyptian psychostasis to the modern comprehension of cardiac neuromodulation. In ancient Egyptian religion, psychostasis was the ceremony in which the deceased was
Externí odkaz:
https://doaj.org/article/11c4bc501bc14795807f7ae22a902d2f
Autor:
Gaetano Thiene
Publikováno v:
Biomedicines, Vol 12, Iss 4, p 832 (2024)
In 1900, Fiedler first reported autopsy cases with peculiar inflammation of the myocardium, which he named interstitial myocarditis. He postulated an isolated cardiac inflammation of the myocardium in the absence of multiorgan involvement and with a
Externí odkaz:
https://doaj.org/article/d9069411143e466485b7b9615c95ea10
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 48, Iss , Pp 101261- (2023)
History of cardiology starts scientifically in 1628, when William Harvey (1578–1657) published his revolutionary book Extercitatio anatomica de motu cordis et sanguinis in animalibus, where he described “general” circulation, movements and func
Externí odkaz:
https://doaj.org/article/3c06640e301e4c20a011259177871939
Publikováno v:
Biomedicines, Vol 11, Iss 7, p 2018 (2023)
The history of arrhythmogenic cardiomyopathy (AC) as a genetically determined desmosomal disease started since the original discovery by Lancisi in a four-generation family, published in 1728. Contemporary history at the University of Padua started w
Externí odkaz:
https://doaj.org/article/c3e89dd3036f482784896b98712425ae