Potassium channel openers: pharmacological and clinical aspects
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1472-8206.1992.tb00122.x/fullpdf
Reference90 articles.
1. 2-(3-pyridyl)-tetrahydrothiopyran-2-carbothioamide derivatives and analogues: a novel family of potent potassium channel openers;Aloup;Drugs Future,1990
2. Effects of cromakalim (BRL 34915) on potassium conductances in CA3 neurons of the guinea-pig hippocampus in vitro;Alzheimer;Naunyn-Schmiedeberg's Arch Pharmacol,1989
3. Clinical pharmacology of potassium channel openers;Andersson;Pharmacol Toxicol,1992
4. Enhancement of muscle blood cell flux and pO2 by cromakalim (BRL 34915) and other compounds enhancing membrane K+ conductance, but not by Ca2+ antagonists or hydralazine, in an animal model of occlusive arterial disease;Angersbach;Naunyn-Schmiedeberg's Arch Pharmacol,1988
5. Properties and functions of ATP-sensitive K-channels;Aschcroft;Cell Sig,1990
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