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Titlebook: Nisoldipine Coat-Core; Michel F. Rousseau Conference proceedings 1999 Springer-Verlag Berlin Heidelberg 1999 Beta-Blocker.Herzkrankheit.Ko

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書(shū)目名稱(chēng)Nisoldipine Coat-Core
編輯Michel F. Rousseau
視頻videohttp://file.papertrans.cn/667/666617/666617.mp4
概述Includes supplementary material:
圖書(shū)封面Titlebook: Nisoldipine Coat-Core;  Michel F. Rousseau Conference proceedings 1999 Springer-Verlag Berlin Heidelberg 1999 Beta-Blocker.Herzkrankheit.Ko
描述Nisoldipine, a second generation of dihydropyridine derivative, exhibits high vascular and coronary selectivity. This monography focuses on the pharmacologic profile of Nisoldipine Coat-Core, a new galenic form, and its beneficial role in various clinical aspects of myocardial ischemia. The contributors are experts in the field of calcium antagonists.
出版日期Conference proceedings 1999
關(guān)鍵詞Beta-Blocker; Herzkrankheit; Koronare Herzkrankheit; Nisoldipin; Nisoldipine; coronary heart disease; hear
版次1
doihttps://doi.org/10.1007/978-3-642-60220-7
isbn_softcover978-3-540-66049-1
isbn_ebook978-3-642-60220-7
copyrightSpringer-Verlag Berlin Heidelberg 1999
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Michel F. RousseauIncludes supplementary material:
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,The Coronary Selectivity of Calcium Antagonists — Focus on CHD,kers (CCBs), also termed calcium antagonists, calcium entry blockers or more simply calcium blockers (in French, anticalciques), inhibit the inward movement of calcium in depolarised muscles. This calcium influx occurs through L-type (long-lasting, large-current, or slow), voltage-dependent calcium
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,Viable Myocardium — the Place of Calcium Antagonists,ial infarction, may be reversible or permanent [1]. Thrombolytic therapy increases the probability of early reperfusion and may increase the probability of reversible dysfunction [2]. The infarcted segments may show resting hypoperfusion, despite a preserved viability, and functional recovery once p
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Hemodynamic and Cardiac Effects of Nisoldipine in Ischemic Left Ventricular Dysfunction,ohormonal activation and of worsening of congestive heart failure symptoms during their administration [1–5]. However, the negative results observed with some calcium antagonists such as nifedipine or diltiazem [4, 5] are balanced by more promising observations with amlodipine and nisoldipine [6, 7]
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