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1  electromagnetic devices, each integrating a vibratory actuator and a soft strain-sensing sheet, for
2  levels of graded contact and eight distinct vibratory afferents that were not significantly differen
3 s obtained from human subjects, we show that vibratory amplitude is encoded in the strength of the re
4 t that the sensory system operates through a vibratory amplitude modulation/demodulation scheme.
5 , our model accurately predicts observed key vibratory and acoustic performance traits.
6         The QST metrics included measures of vibratory and thermal thresholds and cold and hot pain t
7 nd Tinel signs; thenar atrophy; and 2-point, vibratory, and monofilament sensory testing.
8          Little/no evidence was available on vibratory angioedema and aquagenic and contact urticaria
9  urticaria, solar urticaria, heat urticaria, vibratory angioedema, cholinergic urticaria, contact urt
10 aminomaleonitrile was conducted in 10 min by vibratory ball milling.
11 g an oddball paradigm and consisted of short vibratory bursts applied to hand digits 2 and 3.
12 sects that rely primarily on substrate-borne vibratory communication are still largely unknown.
13  function is discussed with relevance to the vibratory communication of N. viridula.
14 attributed to repetitive tapping (similar to vibratory compaction in geotechnical engineering) used b
15  web, on which interactions are dominated by vibratory cues in a two-dimensional space, simplifies th
16           In this regard, the frequency of a vibratory event can be thought of as a multisensory perc
17 ffectiveness of ionic gelation combined with vibratory extrusion and chitosan hydrochloride coating a
18  during which human subjects had to memorize vibratory frequencies in parallel to previous monkey res
19           We conclude that information about vibratory frequency is not encoded in S1 firing rates bu
20 ultivariate patterns of activity to code the vibratory frequency parametrically during WM.
21 e in frequency coding are confounded because vibratory frequency shapes both the timing and rates of
22 ng that faithfully carries information about vibratory frequency.
23                                              Vibratory grinding (VG-4 and VG-8) improved the bioacces
24 ob pod powder prepared by cryogenic (CG) and vibratory grinding for 4 min (VG-4) and 8 min (VG-8) was
25 ty of phenolic constituents was observed for vibratory ground carob powder.
26 frequency of cutaneous flutter (10-50 Hz) or vibratory (>200 Hz) stimulation that occur subsequent to
27 ensations, flutter (frequencies < 60 Hz) and vibratory hum (frequencies > 60 Hz), subserved by two di
28                             We conclude that vibratory input from muscle can differentially modulate
29 ncy tuning and acceleration sensitivity, the vibratory interneurons fall into two groups: the low-fre
30 the data supporting these concepts come from vibratory measurements at cochlear locations tuned to hi
31                     For over half a century, vibratory measurements to study cochlear traveling waves
32 to confirm clinical significance, the set of vibratory measures derived in this study may be applicab
33 alysis, a set of three clinically meaningful vibratory measures was extracted from the videos compris
34                          A simple monophasic vibratory mode of the basilar membrane is found at both
35 nd shapes in a wind tunnel revealed multiple vibratory modes that produce a range of acoustic frequen
36    Sound production always is accompanied by vibratory motions of both labia, indicating that these v
37 pical of CF, which highlights that different vibratory motions produce SFOAEs and CAPs, and that the
38         This reservoir computer utilizes the vibratory nature of the oscillator, which makes it an id
39 et/loud noise treatments, reflecting natural vibratory noise variation.
40                                   Under loud vibratory noise, rural webs retained more energy in long
41 ica, to influence information reception amid vibratory noise.
42                          Here, we describe a vibratory organ found across a commercially important gr
43 rvised learning (Autoencoder) to reconstruct vibratory patterns elicited by human haptic exploration
44 materials emerges from efficient encoding of vibratory patterns elicited by the interaction with mate
45                                 Knowledge of vibratory patterns in the cochlea is crucial to understa
46 s in Pacinian afferents can readily induce a vibratory percept with the same low frequency attributes
47                                              Vibratory perception threshold (VPT) assesses a distinct
48                                              Vibratory perception threshold (VPT) is a reliable measu
49 ptomatic knee OA underwent evaluation of the vibratory perception threshold (VPT) using a biothesiome
50  examinations, nerve conduction studies, and vibratory perception thresholds determined the presence
51 s with Facioscapulohumeral dystrophy (FSHD), vibratory proprioceptive assistance and neuromuscular el
52 e, subjects were presented with two pairs of vibratory pulses.
53 or the axial wavenumber, fluid pressure, and vibratory relative motions of the cochlear partition as
54 psule, induced precise shifts in the maximal vibratory response of the umbo and neural activation wit
55 epend on prestin, and dominate the cochlea's vibratory response to high-frequency sound.
56                                              Vibratory responses to sound were measured in cochleae f
57 and nerve events (a composite of new loss of vibratory sensation, ankle reflexes, or light touch).
58 , there was no relationship observed between vibratory sense and symptomatic knee OA pain.
59 s in hip OA and to demonstrate that there is vibratory sense loss at both the upper and lower extremi
60 ioception, joint kinesthesia, and, recently, vibratory sense, have been described in subjects with os
61 384, P=0.033), indicating that the worse the vibratory sense, the higher the knee load during gait.
62 rhaps also in fish where electroreception or vibratory sensing through the lateral line systems plays
63 be how each of these substrates modifies the vibratory signal during propagation and affects the fema
64  elucidate the neural mechanisms involved in vibratory signaling, the vibration-sensitive interneuron
65                              Substrate-borne vibratory signals are thought to be one of the most anci
66 rception; in touch, the spectral analysis of vibratory signals has been implicated in texture percept
67         The central processing mechanisms of vibratory signals in small plant-dwelling insects that r
68 sophila female detects these substrate-borne vibratory signals.
69 nditioned to suppress respiration to a 40-Hz vibratory source and subsequently tested for stimulus ge
70 on is not immediately salient in conditioned vibratory source detection.
71 ter we surgically incapacitated the MTM as a vibratory source, zebra finches and cardinals were not o
72 40 Hz) after conditioning with an underwater vibratory source.
73 galaninergic neurons, the ability for penile vibratory stimulation (PVS) to elicit ejaculation when t
74 resonance imaging to study brain activity to vibratory stimulation and voluntary movements of body pa
75  hysterical sensorimotor loss during passive vibratory stimulation of both hands, when their deficit
76               In striking contradistinction, vibratory stimulation of the foot evoked topographically
77                               No response to vibratory stimulation of the hand was observed in the pr
78 dy, we investigated the effect of whole-body vibratory stimulation on postural control strategies emp
79 , an ingestible device that performs luminal vibratory stimulation to activate mechanoreceptors and s
80              The present experiment employed vibratory stimulation to characterize somatosensory ERPs
81 webs retained more energy in longer-distance vibratory stimuli across a narrow frequency range (350-6
82 present evidence that pressure, flutter, and vibratory stimuli activate spatially distinct cortical d
83 ponses (hemodynamic response) generated from vibratory stimuli of 35 Hz and 150 Hz with functional MR
84 In analogous experiments, humans compare two vibratory stimuli on the fingertip.
85                                              Vibratory stimuli on the skin are mediated by two major
86                                   Therefore, vibratory stimuli tend to inactivate rapidly adapting cu
87                       In experiments without vibratory stimuli, dystonic subjects showed normal movem
88                         In experiments using vibratory stimuli, vibration of biceps tendons in normal
89 s lack microphonic potentials in response to vibratory stimuli.
90 timulation of one biceps tendon with a 50-Hz vibratory stimulus (a selective stimulus for muscle spin
91  in seven normal volunteers at 1.5 T using a vibratory stimulus applied to the pad of the first finge
92 ) cortex in awake monkeys while presenting a vibratory stimulus at different amplitudes.
93           Here, we demonstrate that a strong vibratory stimulus evokes tonic immobility in larval zeb
94  there was a similar flexion response to the vibratory stimulus in the stimulated arm but movement of
95 dwidth, not requiring attachment to specific vibratory structures, and potentially reduce acoustic fe
96 alyses of RP status by age, body mass index, vibratory tool use, season of examination, state of resi
97 ion, presents with clinical features such as vibratory urticaria and dysautonomia.
98             Patients with autosomal dominant vibratory urticaria have localized hives and systemic ma
99 nly nonsynonymous variant cosegregating with vibratory urticaria in two large kindreds.
100 nowledge a previously unreported mediator in vibratory urticaria, and extracellular signal-regulated
101 stitution (p.C492Y) associated with familial vibratory urticaria.
102 ential therapeutic targets for patients with vibratory urticaria.

 
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