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1 yl = oxymorphine > butorphanol = oxycodone = nalbuphine.
2 ent study, rats were trained to discriminate nalbuphine (3.2 mg/kg, s.c.) from saline in an operant c
3 imaging sessions subjects were administered nalbuphine (5 mg/70 kg) preceded by either saline (Sal-N
6 other predominantly kappa-opioid analgesics, nalbuphine and butorphanol; was compared in males and fe
7 dopa levels were determined with and without nalbuphine, and postmortem brain samples were subjected
11 nation, subjects were injected with a single nalbuphine dose (0.1-3.2 mg/kg) and given 30-min access
12 ism and reproducible LID received a range of nalbuphine doses or saline subcutaneously as: (1) monoth
14 using the mixed agonist/antagonist analgesic nalbuphine in reducing LID and its molecular markers in
15 of clonidine, dexmedetomidine, ketamine and nalbuphine in the treatment of emergence delirium after
27 sucrose consumption increased the potency of nalbuphine to produce its discriminative stimulus effect
28 -efficacy partial agonists buprenorphine and nalbuphine was increased in cells expressing RGS-insensi
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