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Titlebook: Electrocardiography of Inherited Arrhythmias and Cardiomyopathies; From Basic Science t Martin Green,Andrew Krahn,Wael Alqarawi Book 2020 S

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书目名称Electrocardiography of Inherited Arrhythmias and Cardiomyopathies
副标题From Basic Science t
编辑Martin Green,Andrew Krahn,Wael Alqarawi
视频video
概述Focuses on ECG recognition and pathophysiologic explanation of inherited arrhythmias and cardiomyopathies.Each chapter covers a specific condition and highlights typical or critically important ECG fi
图书封面Titlebook: Electrocardiography of Inherited Arrhythmias and Cardiomyopathies; From Basic Science t Martin Green,Andrew Krahn,Wael Alqarawi Book 2020 S
描述This book provides a comprehensive review of the ECG findings of inherited arrhythmias and cardiomyopathies. Despite new forms of medical imaging, electrocardiography (ECG) remains the cornerstone of diagnosis, risk-stratification, and prognosis for these conditions. It is extremely important for clinicians to develop the skills required to interpret the ECG correctly as both overdiagnosis and underdiagnosis of these conditions can have a deleterious effect on patients and their families.. .Each chapter covers a specific condition and highlights typical or critically important ECG findings. Chapters include detailed descriptions of these findings along with pathophysiological mechanisms and clinical vignettes. In addition, the book reviews some normal ECG findings in athletes in order to differentiate some ECG findings from those which may be found in inherited arrhythmia or cardiomyopathy conditions. . .Electrocardiographyof Inherited Arrhythmias and Cardiomyopathies: From Basic Science to Clinical Practice. is an essential resource for physicians, residents, fellows, and medical students in cardiology, cardiac electrophysiology, emergency medicine, sports medicine, and primary ca
出版日期Book 2020
关键词ECG and EKG; ECG of arrhythmogenic right ventricular cardiomyopathy; ECG of early repolarization syndr
版次1
doihttps://doi.org/10.1007/978-3-030-52173-8
isbn_softcover978-3-030-52175-2
isbn_ebook978-3-030-52173-8
copyrightSpringer Nature Switzerland AG 2020
The information of publication is updating

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Brugada Syndrome an increased risk of sudden cardiac death (SCD) due to ventricular arrhythmias in young adults with no apparent structural heart disease. Genetically mediated dysfunction of the cardiac sodium channel responsible for the inward sodium currents is thought to be responsible for the ECG phenotype and
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Early Repolarization Syndromerdiac death due to polymorphic ventricular tachycardia or ventricular fibrillation. Because of the high prevalence of JPE in the general population, the diagnosis of ERS in presymptomatic patients and the subsequent implementation of primary prevention strategies (e.g., implantable cardioverter-defi
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Arrhythmogenic Cardiomyopathyc cardiomyopathies. In some specific arrhythmogenic cardiomyopathies, the ECG is to some extent diagnostic, e.g. QRS microvoltages in the extremity leads to PLN-associated cardiomyopathy and prolonged PQ interval with a narrow QRS in laminopathies. In others, it contributes to the diagnosis, e.g. an
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