Zobrazeno 1 - 10
of 6 153
pro vyhledávání: '"RIGHT-VENTRICULAR CARDIOMYOPATHY"'
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4302-4307 (2024)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare myocardial genetic disease that leads to heart failure and sudden cardiac death. The diagnosis of ARVC remains challenging given its variable presentation. A 66-year-old woman was admit
Externí odkaz:
https://doaj.org/article/3f44c2739a2044b8a10b0c4cb7aab45c
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a family inherited cardiomyopathy associated with ventricular arrhythmias. With the development of molecular biology, histology, imaging, and other diagnostic techniques, the diagnosi
Externí odkaz:
https://doaj.org/article/7587255779ff44f4b1466dd8c07acc23
Autor:
Gergely G. Tamás, Bánfi-Bacsárdi Fanni, Pilecky Dávid, Szűcs Gábor, Hajkó Erik, Hámory Eszter, Som Zoltán, Tóth Attila, Muk Balázs, Borbás Sarolta
Publikováno v:
Cardiologia Hungarica, Vol 54, Iss 3, Pp 217-221 (2024)
Introduction: The 2023 European Society of Cardiology Guidelines for the management of Cardiomyopathies recommends a phenotype-based, multimodal, multidisciplinary, and multiparametric approach to the diagnosis of cardiomyopathies. Case report: We
Externí odkaz:
https://doaj.org/article/371312cc71124297bd9ff9db66fec744
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Introduction Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an infrequent hereditary disorder distinguished by fibrofatty replacement of the myocardium in the right ventricular, which predisposes individuals to life-threatening ar
Externí odkaz:
https://doaj.org/article/2257c29072ee462092b0789091adedac
Publikováno v:
Asian Journal of Surgery, Vol 47, Iss 12, Pp 5169-5170 (2024)
Externí odkaz:
https://doaj.org/article/3a216b86230b42d086e4ea5eaee3ab36
Autor:
Mariana Gomes Tinoco, Margarida Castro, Luísa Pinheiro, Tamara Pereira, Margarida Oliveira, Sílvia Ribeiro, Nuno Ferreira, Olga Azevedo, António Lourenço
Publikováno v:
Monaldi Archives for Chest Disease (2024)
An 18-year-old male presented with syncope during a training break. Post-syncope, he developed effort dyspnea, which he associated with the Pfizer-BioNTech COVID-19 vaccine received a week earlier. Electrocardiogram showed T inversion in V1-V3, III,
Externí odkaz:
https://doaj.org/article/f7471a4aa73349a1b0cc69ae1064f131
Autor:
Anneli Svensson, Henrik Kjaerulf Jensen, Machteld J. Boonstra, Marianne Tétreault‐Langlois, Pia Dahlberg, Henning Bundgaard, Alex Hørby Christensen, Rebecca T. Rylance, Jesper H. Svendsen, Julia Cadrin‐Tourigny, Anneline S. J. M. te Riele, Pyotr G. Platonov
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 16 (2024)
Background Electrocardiographic abnormalities are common in arrhythmogenic right ventricular cardiomyopathy and are included in the 2010 Task Force Criteria. Their time course, however, remains uncertain. In this retrospective observational study, we
Externí odkaz:
https://doaj.org/article/ca5818361a4a4fedb493b9b60c62731c
Sudden Cardiac Death in Athletes: Magnitude, Causes, and Prevention Strategies - A Literature Review
Publikováno v:
Quality in Sport, Vol 19 (2024)
Sudden cardiac death (SCD) in athletes, though rare, is the leading cause of exercise-related mortality and poses significant concern due to the symbolic health and vitality of athletes. This review examines the epidemiology, causes, and prevention s
Externí odkaz:
https://doaj.org/article/f7cb78e121484141a74c413ff9ddc9c6
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-8 (2024)
Abstract Background Arrhythmogenic right ventricular cardiomyopathy (ARVC), or more recently known as arrhythmogenic cardiomyopathy (ACM), is an heritable disorder of the myocardium characterized by progressive fibrofatty replacement the heart muscle
Externí odkaz:
https://doaj.org/article/8bf8240aac8742b98a83797f1ac3a268
Autor:
Jin-Yu Zheng, Bing-Hua Chen, Rui Wu, Dong-Aolei An, Ruo-Yang Shi, Chong-Wen Wu, Lang-Lang Tang, Lei Zhao, Lian-Ming Wu
Publikováno v:
Insights into Imaging, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract Objectives Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by progressive fibrofatty infiltration of atrial and ventricular myocardium resulting in adverse cardiac events. Atrial function h
Externí odkaz:
https://doaj.org/article/fbe339e9aa484623adc8181e3046bfd5