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1 ses of human subjects to both mechanical and thermal stimulation.
2 horn neurones to electrical, mechanical and thermal stimulation.
3 atter correlating only to pain intensity for thermal stimulation.
4 tinued sensitivity to auditory, tactile, and thermal stimulation.
5 nd 18 healthy individuals exposed to noxious thermal stimulations administered in a functional magnet
7 ver, these neurons were activated by noxious thermal stimulation and menthol applied to the corneal s
8 ulomb, Lorentz and Ampere forces, as well as thermal stimulation and optical signals, can be engaged
9 e tail-flick reflex restored vocalization to thermal stimulation and revealed a concurrent sensitizat
10 tations for barely painful or highly painful thermal stimulation, and we assessed how cues influenced
12 rmal sensitivity to cutaneous mechanical and thermal stimulation compared with wild-type mice, the de
16 line reflex nocifensive responses to noxious thermal stimulation (hotplate, tail flick) and to persis
17 n psychophysical responses to mechanical and thermal stimulation in a model of UVB irradiation and in
18 suppression of withdrawals evoked by noxious thermal stimulation in either lumbar or cervical dermato
19 s mechanical was more effective than noxious thermal stimulation in inducing NK-1 receptor internaliz
20 re we compared the effects of mechanical and thermal stimulation in normal rats and in rats with pers
21 ensations of taste, it has been assumed that thermal stimulation in the gustatory system is somehow n
22 increased sensitivity to both mechanical and thermal stimulation in wild-type mice but not in PAF-R K
23 nsitivity of hindpaws to mechanical, but not thermal, stimulation, indicating that mechanical sensiti
24 lity of CPu and GP neurons to encode noxious thermal stimulation intensity and respond during the dyn
25 in imaging to record responses to concurrent thermal stimulation (left forearm) and visual attention
26 er, no study has investigated whether purely thermal stimulation might induce TR, without any tactile
27 ease of specific virus proteins initiated by thermal stimulation, mimicking the early stage of HAdV d
29 al lobe by using PET scanning during painful thermal stimulation of normal and capsaicin-treated skin
31 behavioral responsiveness to mechanical and thermal stimulation of sites below and above the injury
32 on of the face and hyperalgesic responses to thermal stimulation of the hind paw without alterations
33 , rats performed learned escape responses to thermal stimulation of the paws by 44.0. 47.0. or 0.3 de
34 reduced neuronal responses evoked by noxious thermal stimulation of the skin, an effect that was reve
35 owing electrical and natural (mechanical and thermal) stimulation of peripheral receptive fields.
36 ies have examined the effects of non-noxious thermal stimulation on tactile discriminative capacity.
38 enuated antinociceptive responses to noxious thermal stimulation (tail-flick test) by both types of a
40 d from dental pulp upon dentin mechanical or thermal stimulation that induces dentin hypersensitivity
41 stress, produces hyperalgesia for a level of thermal stimulation that preferentially activates C noci
46 ly on the nanofibrous substrate for applying thermal stimulation to release antibiotics on-demand.
49 en spontaneous pain of CBP was contrasted to thermal stimulation, we observe a double-dissociation be
51 ape and lick/guard (L/G) reflex responses to thermal stimulation were evaluated before and for 13-15
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