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pro vyhledávání: '"Lea Philine Hoffmann"'
Autor:
Florian Doldi, Lucas Plagwitz, Lea Philine Hoffmann, Benjamin Rath, Gerrit Frommeyer, Florian Reinke, Patrick Leitz, Antonius Büscher, Fatih Güner, Tobias Brix, Felix Konrad Wegner, Kevin Willy, Yvonne Hanel, Sven Dittmann, Wilhelm Haverkamp, Eric Schulze-Bahr, Julian Varghese, Lars Eckardt
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 7, p 1135 (2022)
Introduction: The long-QT syndrome (LQTS) is the most common ion channelopathy, typically presenting with a prolonged QT interval and clinical symptoms such as syncope or sudden cardiac death. Patients may present with a concealed phenotype making th
Externí odkaz:
https://doaj.org/article/482e6fadfcf542ee9aeee0e8a9e84670
Autor:
Eckardt, Florian Doldi, Lucas Plagwitz, Lea Philine Hoffmann, Benjamin Rath, Gerrit Frommeyer, Florian Reinke, Patrick Leitz, Antonius Büscher, Fatih Güner, Tobias Brix, Felix Konrad Wegner, Kevin Willy, Yvonne Hanel, Sven Dittmann, Wilhelm Haverkamp, Eric Schulze-Bahr, Julian Varghese, Lars
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 7; Pages: 1135
Introduction: The long-QT syndrome (LQTS) is the most common ion channelopathy, typically presenting with a prolonged QT interval and clinical symptoms such as syncope or sudden cardiac death. Patients may present with a concealed phenotype making th