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1 s obtained from human subjects, we show that vibratory amplitude is encoded in the strength of the re
6 urticaria, solar urticaria, heat urticaria, vibratory angioedema, cholinergic urticaria, contact urt
11 during which human subjects had to memorize vibratory frequencies in parallel to previous monkey res
13 frequency of cutaneous flutter (10-50 Hz) or vibratory (>200 Hz) stimulation that occur subsequent to
15 ncy tuning and acceleration sensitivity, the vibratory interneurons fall into two groups: the low-fre
16 the data supporting these concepts come from vibratory measurements at cochlear locations tuned to hi
18 to confirm clinical significance, the set of vibratory measures derived in this study may be applicab
19 alysis, a set of three clinically meaningful vibratory measures was extracted from the videos compris
21 nd shapes in a wind tunnel revealed multiple vibratory modes that produce a range of acoustic frequen
22 Sound production always is accompanied by vibratory motions of both labia, indicating that these v
26 ptomatic knee OA underwent evaluation of the vibratory perception threshold (VPT) using a biothesiome
27 examinations, nerve conduction studies, and vibratory perception thresholds determined the presence
29 or the axial wavenumber, fluid pressure, and vibratory relative motions of the cochlear partition as
30 and nerve events (a composite of new loss of vibratory sensation, ankle reflexes, or light touch).
32 s in hip OA and to demonstrate that there is vibratory sense loss at both the upper and lower extremi
33 ioception, joint kinesthesia, and, recently, vibratory sense, have been described in subjects with os
34 384, P=0.033), indicating that the worse the vibratory sense, the higher the knee load during gait.
35 rhaps also in fish where electroreception or vibratory sensing through the lateral line systems plays
36 elucidate the neural mechanisms involved in vibratory signaling, the vibration-sensitive interneuron
37 rception; in touch, the spectral analysis of vibratory signals has been implicated in texture percept
39 nditioned to suppress respiration to a 40-Hz vibratory source and subsequently tested for stimulus ge
41 ter we surgically incapacitated the MTM as a vibratory source, zebra finches and cardinals were not o
43 galaninergic neurons, the ability for penile vibratory stimulation (PVS) to elicit ejaculation when t
44 resonance imaging to study brain activity to vibratory stimulation and voluntary movements of body pa
45 hysterical sensorimotor loss during passive vibratory stimulation of both hands, when their deficit
49 present evidence that pressure, flutter, and vibratory stimuli activate spatially distinct cortical d
50 ponses (hemodynamic response) generated from vibratory stimuli of 35 Hz and 150 Hz with functional MR
57 timulation of one biceps tendon with a 50-Hz vibratory stimulus (a selective stimulus for muscle spin
58 in seven normal volunteers at 1.5 T using a vibratory stimulus applied to the pad of the first finge
60 there was a similar flexion response to the vibratory stimulus in the stimulated arm but movement of
61 alyses of RP status by age, body mass index, vibratory tool use, season of examination, state of resi
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