Zobrazeno 1 - 10
of 4 230
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
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
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
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
Autor:
Adam Kucharski, Konrad Pilarski, Rafał Makuch, Alicja Chrościcka, Kamil Gała, Andrzej Czajka, Paweł Lenard, Sara Michalska, Martyna Dewicka, Alicja Maria Wawrzyniak
Publikováno v:
Quality in Sport, Vol 17 (2024)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a hereditary heart muscle disorder characterized by the progressive replacement of right ventricular myocardium with fibrofatty tissue. This condition predisposes individuals to arrhythmias an
Externí odkaz:
https://doaj.org/article/3021204dc0a0464dbd2651c593b38c2a
Autor:
María Cespón-Fernández, MD, PhD, Luigi Pannone, MD, Domenico Della Rocca, MD, PhD, Mark La Meir, MD, PhD, Alexander Almorad, MD, Gian-Battista Chierchia, MD, PhD, Carlo de Asmundis, MD, PhD, Andrea Sarkozy, MD, PhD
Publikováno v:
JACC: Case Reports, Vol 29, Iss 12, Pp 102356- (2024)
Catheter ablation of septal ventricular tachycardia (VT) is challenging. Pulsed field ablation is a promising technology, potentially reaching deep substrates. We report the first sequential unipolar biventricular pulsed field ablation targeting refr
Externí odkaz:
https://doaj.org/article/33cd1cc936474d10a3b70174a66d218c
Autor:
Elias Noel Andrade-Cuellar, MD, Rogelio Robledo-Nolasco, MD, Ivan Alejandro Elizalde-Uribe, MD
Publikováno v:
JACC: Case Reports, Vol 29, Iss 12, Pp 102362- (2024)
Isolated apical ventricular hypoplasia is an extremely rare congenital heart disease. We describe 2 cases, each affecting a different side, presenting with unique clinical and imaging characteristics not hitherto delineated in the literature.
Externí odkaz:
https://doaj.org/article/fc1d597ff089441f9ce2d98048095a28