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1 zolam, ketamine, propofol, pentobarbital, or thiopental.
2                  Anesthesia was induced with thiopental and maintained after intubation using 1% to 1
3                                              Thiopental and propofol may more readily provide adequat
4 the most potent clinically used barbiturate, thiopental, and its general anesthetic EC(50) approaches
5                       Infusion of VEGF165 in thiopental-anesthetized rats dose-dependently increased
6 ia, and that infarct volume was increased in Thiopental-anesthetized rats.
7 letly blocked alpha1G currents with potency [thiopental ( approximately 280 microM), pentobarbital (
8 e quenching experiments showed halothane and thiopental binding at three tryptophan-associated sites
9 halothane binding and intersubunit sites for thiopental binding.
10                             We observed that Thiopental caused a prolonged duration of unconsciousnes
11 iousness with a high rate of mortality, that Thiopental created exaggerated neurological deficits tha
12                                              Thiopental does not interact with specific residues (G29
13               On the basis of our NMR study, thiopental does not oligomerize Abeta40 even at higher c
14                                              Thiopental general anaesthesia did not influence any cha
15 na showed that post-mortem concentrations of thiopental in the blood were lower than that required fo
16 ur findings raise a caution about the use of Thiopental in the setting of ischemic stroke.
17                                              Thiopental is an anesthetic used for controlling high in
18                      These data suggest that Thiopental is detrimental in ischemic stroke.
19    However, it remains controversial whether Thiopental is detrimental or beneficial in ischemic stro
20 ypertensive rats to determine whether or not Thiopental is neuroprotective in the setting of brain is
21 ine EGG (5 pigs in each experimental group): thiopental, isoflurane, nitrous oxide and isoflurane plu
22                          Bath application of thiopental lowered the frequency of gamma oscillations,
23 usually done by sequential administration of thiopental, pancuronium, and potassium chloride.
24 n = 1168) are reported who had therapy with: thiopental, pentobarbital, midazolam, propofol, ketamine
25 metic anesthetic agents--propofol and sodium thiopental--protect against the irreversible neurodegene
26 fluorescence quenching data of halothane and thiopental, respectively.
27                                              Thiopental seems to be the most suitable as it did not c
28  examinations after rectal administration of thiopental sodium injection solution.
29               The solution was prepared from thiopental sodium powder mixed with sterile water to cre
30  with use of a rectal solution prepared from thiopental sodium preparation for intravenous injection,
31                                              Thiopental sodium sedation for pediatric imaging, with u
32                               The regimen of thiopental, succinylcholine (SCh) and unsupplemented nit
33 ic interactions of isoflurane, propofol, and thiopental with uniformly 15N labeled Abeta40 and Abeta4