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Biopharmaceutics & Drug Disposition|September 11, 2015
A physiologically based pharmacokinetic modeling approach to predict drug-drug interactions between domperidone and inhibitors of CYP3A4Ian Templeton, Paulien Ravenstijn, Carlo Sensenhauser, et al.
Biopharmaceutics & Drug Disposition|September 30, 2014
Effects of the inhibition of intestinal P-glycoprotein on aliskiren pharmacokinetics in cynomolgus monkeysMikiko Tsukimoto, Rikiya Ohashi, Nao Torimoto, et al.
Biopharmaceutics & Drug Disposition|March 1, 1989
The absorption of sustained-release methylphenidate formulations compared to an immediate-release formulationK S Patrick, A B Straughn, E J Jarvi, et al.
Biopharmaceutics & Drug Disposition|March 1, 1989
Removal of sulfonamides by hemofiltrationS S Yu, D H Waters, S H Shen, et al.
Biopharmaceutics & Drug Disposition|March 1, 1989
Bioequivalency of oral suspension formulations of cefiximeR D Faulkner, L L Sia, J S Barone, et al.
Biopharmaceutics & Drug Disposition|April 11, 2016
Expression of UGT1A subfamily in rat brainYukiko Sakakibara, Miki Katoh, Kuniyuki Imai, et al.
Biopharmaceutics & Drug Disposition|March 1, 1986
The pharmacokinetics of exaprolol and propranolol in rats with interrupted enterohepatic circulationO Motheová, S Bezek, M Durisová, et al.
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