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Titlebook: Cardiac Arrhythmias: The Management of Atrial Fibrillation; Ronald W. F. Campbell,Michiel J. Janse Conference proceedings 1992 Springer-Ve

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書目名稱Cardiac Arrhythmias: The Management of Atrial Fibrillation
編輯Ronald W. F. Campbell,Michiel J. Janse
視頻videohttp://file.papertrans.cn/222/221730/221730.mp4
圖書封面Titlebook: Cardiac Arrhythmias: The Management of Atrial Fibrillation;  Ronald W. F. Campbell,Michiel J. Janse Conference proceedings 1992 Springer-Ve
描述This publication contains the papers presented at a specialSymposium onAtrial Fibrillation during the European Societyof Cardiology 1991 meetingin Amsterdam, Holland. Thecontributors offer the current state of the artof themanagement of the most difficult cardiac arrhythmias atrialfibrillation.
出版日期Conference proceedings 1992
關(guān)鍵詞Atrial Fibrillation; Class IC-drugs; Electrophysiology; QT-Syndrome; arrhythmia; atrial fibrillation; card
版次1
doihttps://doi.org/10.1007/978-3-662-30492-1
isbn_ebook978-3-662-30492-1
copyrightSpringer-Verlag Berlin Heidelberg 1992
The information of publication is updating

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Atrial Fibrillation: Is Our Electrophysiological Understanding on the Right Wavelength?,a is due to a focus that discharges so rapidly that uniform excitation of the atrium is no longer possible. This kind of fibrillation is best described as “fibrillatory conduction” where at multiple and varying sites rate-dependent arcs of conduction block develop (Allessie et al. 1985). To explain
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Class I Antiarrhythmic Drug Effects: What Is the Basis for Subgroups Ia, Ib and Ic in Human Heart Mtransmembrane potentials using conventional microelectrode techniques. Class I drugs, such as quinidine, share the property of depressing phase zero of the action potential by their ability to decrease the membrane conductance for Na.. Class II agents, such as propranolol, are characterized by their
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https://doi.org/10.1007/978-3-0348-8895-0a is due to a focus that discharges so rapidly that uniform excitation of the atrium is no longer possible. This kind of fibrillation is best described as “fibrillatory conduction” where at multiple and varying sites rate-dependent arcs of conduction block develop (Allessie et al. 1985). To explain
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Pseudomonotone or weakly continuous mappingstransmembrane potentials using conventional microelectrode techniques. Class I drugs, such as quinidine, share the property of depressing phase zero of the action potential by their ability to decrease the membrane conductance for Na.. Class II agents, such as propranolol, are characterized by their
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