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1 ng partial neuromuscular blockade (PNB; i.v. cisatracurium).
2 patches by (+)-tubocurarine, pancuronium and cisatracurium.
3 of (+)-tubocurarine and pancuronium but not cisatracurium.
4 ic, 34 +/- 6/s; adult: 13 +/- 5/s) rates for cisatracurium.
5 urium-exposed patients with a negative ST to cisatracurium.
6 inverse ratio ventilation and paralyzed with cisatracurium.
7 imes to 70% recovery of Train-of-Four ratio (cisatracurium 60 mins, atracurium 57 mins), although the
11 Outside-out patches were equilibrated with cisatracurium before application of 300 microM acetylcho
12 ficial binding site for the large antagonist cisatracurium compared to the other ligands, or from a c
15 urium-sensitized patient and negative in all cisatracurium-exposed patients with a negative ST to cis
16 a rapid perfusion system to apply or remove cisatracurium for various times before application of ac
17 e measurements correspond to dissociation of cisatracurium from receptors in the absence of acetylcho
23 20 (9-29), 21 (4-36), and 1.5 (0.3-2.9) for cisatracurium, pancuronium, vecuronium, and rocuronium,
24 vity for four other competitive antagonists: cisatracurium, pancuronium, vecuronium, and rocuronium.
26 in protocol I (FI) matched closely the post-cisatracurium smooth-muscle pressure profile in protocol
28 - 6, 106 +/- 8 and 116 +/- 10 kJ mol(-1) for cisatracurium, (+)-tubocurarine and pancuronium, respect
30 The infusion rate for patients receiving cisatracurium was 3.1 +/- 0.2 microg/kg/min, and for pat
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