Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Brugada syndrome (BrS)"'
Publikováno v:
Frontiers in Medicine, Vol 10 (2024)
BackgroundBrugada Syndrome (BrS) is an inherited arrhythmia syndrome in which mutations in the cardiac sodium channel SCN5A (NaV1.5) account for approximately 20% of cases. Mutations in sodium channel-modifying genes may account for additional BrS ca
Externí odkaz:
https://doaj.org/article/82adbee24fd64006912b1ec41b83ec11
Autor:
Valentina Hartwig, Maria Sole Morelli, Nicola Martini, Paolo Seghetti, Davide Tirabasso, Vincenzo Positano, Sara Latrofa, Giacomo Mansi, Andrea Rossi, Alberto Giannoni, Alessandro Tognetti, Nicola Vanello
Publikováno v:
Sensors, Vol 24, Iss 13, p 4342 (2024)
Brugada Syndrome (BrS) is a primary electrical epicardial disease characterized by ST-segment elevation followed by a negative T-wave in the right precordial leads on the surface electrocardiogram (ECG), also known as the ‘type 1’ ECG pattern. Th
Externí odkaz:
https://doaj.org/article/fa5d33846fc142b192da9ea9274c45d4
Autor:
Jun Fan, Shao-hua Wang, Li-li Cao, Wei-jie Li, Shao-xi Sun, Shao-ling Luo, Yi-chao Pan, Wen-liang Tan, Tian-yuan Wu, Zhen Liu, Bing-bo Yu
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundThe Scn3b gene encodes for Navβ3, a pivotal regulatory subunit of the fast sodium channel in cardiomyocytes. However, its mutation status in the Chinese population suffering from Brugada Syndrome (BrS) has not been characterized, and the c
Externí odkaz:
https://doaj.org/article/aa299c982d4549e687353c344cc0a8fc
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Cardiovascular diseases are associated with several morbidities and are the most common cause of worldwide disease-related fatalities. Studies show that treatment and outcome-related differences for cardiovascular diseases disproportionately affect m
Externí odkaz:
https://doaj.org/article/629d5bac4323490d8ad8fad4461a8157
Akademický článek
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Autor:
Dario Melgari, Serena Calamaio, Anthony Frosio, Rachele Prevostini, Luigi Anastasia, Carlo Pappone, Ilaria Rivolta
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 7, p 6687 (2023)
The development of high-throughput automated patch-clamp technology is a recent breakthrough in the field of Brugada syndrome research. Brugada syndrome is a heart disorder marked by abnormal electrocardiographic readings and an elevated risk of sudd
Externí odkaz:
https://doaj.org/article/52d9e53ab9684c32a7bf750d20d4d2c7
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Ajmaline is an anti-arrhythmic drug that is used to unmask the type-1 Brugada syndrome (BrS) electrocardiogram pattern to diagnose the syndrome. Thus, the disease is defined at its core as a particular response to this or other drugs. Ajmaline is usu
Externí odkaz:
https://doaj.org/article/f71a1b1d13834e44bcef1c04b880c37c
Autor:
Sara D'Imperio, Michelle M. Monasky, Emanuele Micaglio, Giuseppe Ciconte, Luigi Anastasia, Carlo Pappone
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Brugada syndrome (BrS) is a hereditary disorder, characterized by a specific electrocardiogram pattern and highly related to an increased risk of sudden cardiac death. BrS has been associated with other cardiac and non-cardiac pathologies, probably b
Externí odkaz:
https://doaj.org/article/b84dfa804dae48bebbbf3e753979754a
Akademický článek
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Akademický článek
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