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Titlebook: Electrical Diseases of the Heart; Genetics, Mechanisms Ihor Gussak (Deputy Therapeutic Area Head, Profess Book 20081st edition Springer-Ver

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發(fā)表于 2025-3-21 17:06:17 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Electrical Diseases of the Heart
副標題Genetics, Mechanisms
編輯Ihor Gussak (Deputy Therapeutic Area Head, Profess
視頻videohttp://file.papertrans.cn/306/305716/305716.mp4
概述Provides a perspective on primary (heritable) electrical disease of the heart and sudden cardiac death in cardiology, neurology, nephrology, endocrinology by emphasizing the clinical and basic aspects
圖書封面Titlebook: Electrical Diseases of the Heart; Genetics, Mechanisms Ihor Gussak (Deputy Therapeutic Area Head, Profess Book 20081st edition Springer-Ver
描述."Electrical Diseases of the Heart: Genetics, Mechanisms, Treatment, Prevention" provides a unique contemporary and succinct distillation of the current status of recently delineated electrical diseases of the heart, emphasizing their common and diverse clinical features. The latest developments in the field of experimental and clinical cardiac electrophysiology, genetics, pharmacology and interventional therapies of various clinical arrhythmogenic entities are featured and discussed in terms of recent advances in basic and clinical science. The book is divided into 7 major parts. Each part consists of chapters (total of 64) dealing with related topics. Each chapter is outlined with objectives, key points, current perspectives, and recommendations for future investigations and includes established and evidence-based knowledge, the authors‘ personal opinions, areas of controversy, and future trends..
出版日期Book 20081st edition
關鍵詞Parkinson; electrocardiogram; heart rate; prevention; screening
版次1
doihttps://doi.org/10.1007/978-1-84628-854-8
isbn_ebook978-1-84628-854-8
copyrightSpringer-Verlag London 2008
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 20:53:09 | 只看該作者
Mechanisms of Cardiac Arrhythmiadisturbances may be relatively benign, as in the case of premature ventricular contractions (PVC), whereas others are malignant, as in the case of ventricular fibrillation, capable of leading to sudden death. The most prevalent sustained arrhythmia in the clinic is atrial fibrillation.
板凳
發(fā)表于 2025-3-22 01:12:03 | 只看該作者
K, Channelopathies (,, and ,,) Opening of ion channels allows ions to move along their electrochemical gradient thus either depolarizing the membrane or repolarizing it and creating electrical patterns such as the action potential (see Chapter 9 and Figure 11-1).
地板
發(fā)表于 2025-3-22 06:31:46 | 只看該作者
Comparisons of Substrates Responsible for Atrial Versus Ventricular Fibrillationure 16-1A). can underlie fibrillation. In the latter two cases, although the primary source may be firing regularly, the inability of tissues to follow 1∶1 causes wave breakup and fibrillation. Ironically, these recent ideas echo notions first put forward in the early twentieth century..
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發(fā)表于 2025-3-22 11:09:44 | 只看該作者
https://doi.org/10.1007/978-3-322-91686-0it that stabilizes the closed state of the channel to prevent aberrant calcium (Ca.) leak from the SR.. Direct targeting of several protein kinases and phosphatases to the type 2 cardiac RyR channel (RyR2) allows for rapid and localized modulation of SR Ca. release in response to extracellular signals..
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發(fā)表于 2025-3-22 14:50:21 | 只看該作者
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發(fā)表于 2025-3-22 17:16:26 | 只看該作者
Grundsicherungsarbeit in der Wissenschaft,disturbances may be relatively benign, as in the case of premature ventricular contractions (PVC), whereas others are malignant, as in the case of ventricular fibrillation, capable of leading to sudden death. The most prevalent sustained arrhythmia in the clinic is atrial fibrillation.
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發(fā)表于 2025-3-23 00:43:54 | 只看該作者
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發(fā)表于 2025-3-23 02:27:59 | 只看該作者
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發(fā)表于 2025-3-23 05:56:21 | 只看該作者
Calcium Release Channels (Ryanodine Receptors) and Arrhythmogenesisit that stabilizes the closed state of the channel to prevent aberrant calcium (Ca.) leak from the SR.. Direct targeting of several protein kinases and phosphatases to the type 2 cardiac RyR channel (RyR2) allows for rapid and localized modulation of SR Ca. release in response to extracellular signals..
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