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Titlebook: Cardiac Glycosides; Part II: Pharmacokin Kurt Greeff (Direktor) Book 1981 Springer-Verlag Berlin Heidelberg 1981 absorption.kinetics.pharma

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樓主: invoke
11#
發(fā)表于 2025-3-23 10:40:06 | 只看該作者
0171-2004 . Research on glycoside kinetics has progressed at a rapid pace, requiring continuing reevaluation of the state of our understanding of this problem. The present article focuses on the effect of disease states (renal, gastrointestinal, thyroid, and cardiac) on the absorption, distribution, and clear
12#
發(fā)表于 2025-3-23 16:41:20 | 只看該作者
13#
發(fā)表于 2025-3-23 20:02:49 | 只看該作者
Hugo H. Rabbia,Juan Marco Vaggioneto be defined: a description of the substance, solubility, tests for identity, assay, foreign substances, related cardiac glycosides, specific optical rotation, loss on drying, and ash. Tests for absence of microbial pathogens are carried out where appropriate.
14#
發(fā)表于 2025-3-23 22:26:00 | 只看該作者
Michael Weinhardt,Stefan Liebigamic properties of the glycosides and their application in patients (. and ., 1979). This chapter focuses attention on the cardiac action of digitalis on the failing and nonfailing heart. Finally, these observations are integrated to provide a unified concept of the actions of the glycosides on the cardiocirculation.
15#
發(fā)表于 2025-3-24 02:29:24 | 只看該作者
https://doi.org/10.1007/978-3-658-10459-7ion pharmacokinetics, and severity of the heart disease. In addition, interactions with other substances have been found to explain observations of resistance or increased sensitivity to treatment with cardiac glycosides.
16#
發(fā)表于 2025-3-24 08:10:50 | 只看該作者
Pharmacokinetics of Squill Glycosidesd on clinical parameters and by measurements in plasma and other body fluids by use of .Rb uptake inhibition assay or by ..-labeled glycosides. Generally, there is agreement between the results from the two approaches.
17#
發(fā)表于 2025-3-24 10:54:24 | 只看該作者
18#
發(fā)表于 2025-3-24 16:02:09 | 只看該作者
19#
發(fā)表于 2025-3-24 21:02:16 | 只看該作者
20#
發(fā)表于 2025-3-25 02:43:07 | 只看該作者
Book 1981 on glycoside kinetics has progressed at a rapid pace, requiring continuing reevaluation of the state of our understanding of this problem. The present article focuses on the effect of disease states (renal, gastrointestinal, thyroid, and cardiac) on the absorption, distribution, and clearance of a
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