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1  We found that local application of an inert nocebo cream on the forearm increased pain ratings compa
2                                          The nocebo effect in motor performance consists in a reducti
3 ctivation of the main effect of pain and the nocebo effect spatially overlapped.
4 ION: These analyses illustrate the so-called nocebo effect, with an excess rate of muscle-related AE
5  nonconscious conditioned stimuli on placebo/nocebo effects and the results challenge the exclusive r
6                                  Placebo and nocebo effects are associated with opposite responses of
7 n increased understanding of how placebo and nocebo effects are produced and what biological and psyc
8 t the mechanisms responsible for placebo and nocebo effects can operate without conscious awareness o
9 puncture produced larger placebo and smaller nocebo effects than did pills for the treatment of hot f
10                      Significant placebo and nocebo effects were found in both experiment 1 (using cl
11                Previous studies suggest that nocebo effects, sometimes termed "negative placebo effec
12                                  Placebo and nocebo effects, the therapeutic and adverse effects, res
13 er, with a specific focus on the placebo and nocebo effects.
14 his is particularly relevant for placebo and nocebo effects.
15 the role of indirect exposure in placebo and nocebo effects.
16 orsal horn of the spinal cord, we combined a nocebo heat pain paradigm with spinal functional magneti
17                                              Nocebo hyperalgesia is an increase in subjective pain pe
18        In conclusion, we found evidence that nocebo hyperalgesia may be predominantly produced throug
19 ment as expensive medication led to stronger nocebo hyperalgesia than labeling it as cheap medication
20 odel to investigate the neural substrates of nocebo hyperalgesia using heat pain on the right forearm
21 ontal cortex mediated the effect of value on nocebo hyperalgesia.
22 with greater dlPFC and caudate activation to nocebo-induced itch also demonstrated greater dlPFC and
23                   Subjects reporting greater nocebo-induced itch also demonstrated greater placebo re
24 n insight to the brain mechanisms supporting nocebo-induced itch in AD, thus aiding our understanding
25               Brain activity likely supports nocebo-induced itch, but is currently unknown.
26 s related to dispositional traits and to the nocebo-induced reduction of force.
27                                  Placebo and nocebo mechanisms, not well understood, are likely multi
28  also highly susceptible to both placebo and nocebo (negative placebo) effects.
29 ch relies mostly on the study of placebo and nocebo phenomena which influence physiological and patho
30 actors that appear to be associated with the nocebo phenomenon and/or reporting of nonspecific side e
31                                          The nocebo phenomenon, in which placebos produce adverse sid
32 sity ratings increased significantly more on nocebo regions compared with the control regions in whic
33                The findings from placebo and nocebo research have important implications for the desi
34  personality traits and the magnitude of the nocebo response in motor performance.
35 strong placebo response while mitigating any nocebo response.
36                                              Nocebo responses can explain some adverse clinical outco
37 ts, assessed whether conditioned placebo and nocebo responses could be triggered in response to nonco
38                fMRI analysis of hyperalgesic nocebo responses to identical calibrated noxious stimuli
39                                              Nocebo responses were associated with a deactivation of
40  high and low pain, could induce placebo and nocebo responses.
41 y be an unwitting contributor to placebo and nocebo responses.
42                     Compared to open saline, nocebo saline demonstrated greater fMRI response in caud
43                                              Nocebo saline produced greater itch than open saline con
44       Our study demonstrates the capacity of nocebo saline to mimic both the sensory and neural effec
45 bject design, and contrast brain response to nocebo saline understood to be allergen vs open-label sa
46             Comparing pain stimulation under nocebo to a control pain stimulation of the same physica
47 eam, and also reduced pain thresholds on the nocebo-treated skin patch.
48 activated by cognitive manipulations such as nocebo treatments.
49                                  Placebo and nocebo use is common in practice.

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