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1 o that only 1 eye at a time had a nonblocked pupil.
2 oked are coupled with brief dilations of the pupil.
3 he increased visual acuity provided by small pupils.
4 y correlated between the songs of tutors and pupils.
6 vel paradigm designed to capture patterns of pupil adaptation during sustained periods of dark and li
8 l status, leading to the design of novel H&H-Pupil-Age score (HHPA) and simplified H&H-Pupil score (s
9 ean values indicated a rising D3MFT count as pupils aged (consistent with new teeth emerging), which
11 while the corresponding fellow eye projected pupil alternated between 0 and 3.0 mm or 0 and 4.0 mm at
17 , we leverage the close relationship between pupil and neural activity to inform our understanding of
19 sions are reported by rapid dilations of the pupil and track a suppression of biases in the accumulat
21 and focal distance to maintain the smallest pupil (and thus the highest visual acuity) that still al
22 ed between a state of rest and a constricted pupil, and one of active locomotion and a dilated pupil,
23 ion, dry mouth, lack of tears, fixed dilated pupils, and diffuse anhidrosis 7 days after a febrile il
24 and larger heart rate, skin conductance, and pupil area responses to loud sounds (multivariate p = .0
25 4.2 and 95.8% of participants showed resting pupil asymmetry of <=0.5 mm and <= 1.0 mm, respectively.
28 and-wide record linkage of education (annual pupil census) and maternity (Scottish Morbidity Record 0
29 hiatric hospitals, maternity records, annual pupil census, examinations, school absences and exclusio
31 e regression model, corneal thickness at the pupil center by the Pentacam and relative increase in ce
32 hich mediates orienting responses, including pupil changes to salient stimuli; and the locus coeruleu
33 tion revealed fully dilated, non-reactive RE pupil, clear lens and tubular remnant of HA containing b
36 0 times less potent in stimulating mouse-eye pupil constriction than muscarinic agonists oxotremorin-
37 ing aspects of light adaptation ranging from pupil constriction to changes in visual circuit performa
38 ral vision over peripheral vision results in pupil constriction, and this likely reflects the fact th
39 ith a bright stimulus results in preparatory pupil constriction, which allows the pupil to respond qu
41 are not explained by convergence responses, pupil constrictions, head movements, or starting eye pos
45 sisted of modifying the transmittance of the pupil corresponding to the fellow eye until the perceive
46 80 school pupils drawn from 564 886 National Pupil Database records of adolescents aged 15 years, liv
49 ork, which has quantified gradual changes in pupil diameter (the so-called "pupil dilation response")
52 baseline catecholamine levels (as indexed by pupil diameter and manipulated pharmacologically) on the
53 nt of vasodilation and vasoconstriction with pupil diameter and measure 3D blood flow at 99 volumes/s
54 so showed a significant relationship between pupil diameter and right amygdala activation after 8IU i
55 sting that the reflex pathways that regulate pupil diameter are under some degree of cognitive contro
56 Functional magnetic resonance imaging, and pupil diameter as a proxy measure for LC-noradrenaline t
60 a measure of women's physiological arousal (pupil diameter change) was correlated with ratings of me
64 effort, and inter-individual variability in pupil diameter during performance of social-cognitive ta
66 ctive attention, we asked whether changes in pupil diameter follow internal shifts of attention to me
70 e further show that both baseline and evoked pupil diameter is modulated by the degree to which indiv
71 ve decision-making task, we show that evoked pupil diameter is more parsimoniously described as signa
72 ng, we tested the hypothesis that changes in pupil diameter reflect inferences humans make about envi
73 by which such cognitive processes influence pupil diameter remain somewhat unclear, although cortica
74 tend previous findings connecting changes in pupil diameter to neural activity under varying cognitiv
77 axial length (AL), accommodation amplitude, pupil diameter, and best-corrected visual acuity were me
78 ented by the ocular wavefront aberration and pupil diameter, both either coming from in vivo measurem
79 show that heightened arousal, as indexed by pupil diameter, broadens frequency-tuned activity of lay
80 oefficient was >0.90 for OCT-derived maximum pupil diameter, minimum pupil diameter, and anisocoria.
81 esbyopic and 42 presbyopic eyes, we measured pupil diameter, radius of corneal curvature values, cent
83 d IV oxytocin on right amygdala activity and pupil diameter, the significant difference between 8IU i
84 bering, assayed by posterior alpha power and pupil diameter, were correlated with reductions in neura
92 ed to capture fundus images before and after pupil dilatation, using a hand-held non-mydriatic (Visus
94 ypan blue (aOR, 1.76; P < 0.001); mechanical pupil dilation (aOR, 1.36; P = 0.024); and iris hooks at
95 ective intensity ratings, tVNS led to robust pupil dilation (peaking 4-5 s after trial onset) that wa
96 ber of factors including poor intraoperative pupil dilation and a higher risk of vision threatening c
97 heir firing during locomotion, whisking, and pupil dilation and are involved in spatially specific to
98 ve healthy male volunteers induced transient pupil dilation and attenuation of occipital alpha oscill
100 the interaction between different causes of pupil dilation and suggest a quantitative approach to ch
102 correlating positively with the magnitude of pupil dilation during a continuous performance task.
103 the superior colliculus (SCi), evoked robust pupil dilation even in the absence of evoked saccades.
108 human movement); and one pupillometry task, pupil dilation in response to viewing affective faces.
113 al changes in pupil diameter (the so-called "pupil dilation response"), here we focus on the occurren
122 ociations of the change in iris volume after pupil dilation with underlying iris surface features in
123 oral (choice probability) and physiological (pupil dilation) signatures of reinforcement learning wit
125 Surprise also positively correlated with pupil dilation, activation in subcortical regions associ
128 In contrast to skin conductance responses or pupil dilation, modulation of the startle reflex is vale
129 ed optimization of input across saccades and pupil dilation, the primate auditory system has fewer me
133 lso related to distinct temporal features of pupil dilations to boundaries as well as to the temporal
134 s activations systematically preceded phasic pupil dilations with a strikingly similar temporal profi
135 h enrolled a random sample of 298 080 school pupils drawn from 564 886 National Pupil Database record
136 metry enables tracking brain state-dependent pupil dynamics and identifying unique cross-scale neuron
141 that provides the parameters of the entrance pupil ellipse for an observer at an arbitrary location.
142 f adherence at baseline (eg, ocular history, pupil examination, and central corneal thickness measure
143 hat, compared to eyes with fully constricted pupils, eyes from A. irradians with fully dilated pupils
144 thermore, the degree to which trial-by-trial pupil fluctuations encoded this nonlinear interaction co
147 ents under conditions that separately assess pupil function driven by different photoreceptor classes
154 brain responses to dilating and constricting pupils in the context of viewing own-race and other-race
155 ong with social network information from all pupils in their year groups (total 5,066 social dyads).
156 g neural temporal fine structure processing, pupil-indexed listening effort, and behavioral FM thresh
162 reflex by the PFC.SIGNIFICANCE STATEMENT The pupil light reflex (PLR) is our brain's first and most f
163 canonical example of a central reflex is the pupil light reflex (PLR): the automatic constriction of
166 ex (expressed as time-series entropy) versus pupil-linked arousal differentially impact perceptual pr
168 reflect a more nuanced relationship between pupil-linked arousal systems and cognitive expectations.
169 h the report of the decision, an increase in pupil-linked arousal, fixational eye movements, and fluc
172 different suboptimalities relate to distinct pupil-linked processes, possibly related to tonic and ph
173 frontal cortex and (ii) predicted by phasic, pupil-linked responses of a number of neuromodulatory br
175 se findings can inform the interpretation of pupil measurements in terms of activation of these neura
176 Collectively, our findings suggest that pupil measures reflect both stability and change in ongo
178 We also investigate the relationship between pupil metrics derived from this novel task and quantitat
180 et simple, paradigm can result in meaningful pupil metrics that correlate with individual differences
182 on reaching its peak (midfilament) near the pupil (n = 3) or midzonal iris (n = 1), before returning
183 dy baseline data, from 12-13 year old school pupils (n = 1656) in Northern Ireland and Bogota (Colomb
184 e, relative dilation and constriction of the pupil occurred dynamically and followed the changing tem
185 ith severe visual loss, nystagmus, amaurotic pupils, oculo-digital sign and markedly reduced or absen
186 that accurate specification of the entrance pupil of a stationary eye requires modeling of corneal r
187 mera at a medical clinic, with dilatation of pupil of those who have ungradable images, provides a va
190 patients without uncomplicated PEX (no small pupils or phacodonesis) all undergoing phacoemulsificati
191 eyes without shallow anterior chamber, small pupils, or apparent zonulopathy may represent eyes with
192 1 had a higher proportion of poorly reactive pupils (P < 0.001) and abnormal ocular movements (P = 0.
195 g photon catch, either optically, with large pupils, photoreceptors, and ever larger eyes [2], or neu
196 spectrum disorder (ASD), some work has used pupil physiology to successfully classify patients with
198 required incident field distribution at the pupil plane to create the multi-segmented optical needle
199 e (less than $10) phase mask inserted in the pupil plane to encode the light field and enhance the de
200 microlenses to capture 12-bit images of the pupil plane, and a superluminescent diode of 830 nm wave
201 puter-randomised, stratified by school-level pupil premium funding (below/above county-specific media
202 voking corollary to our findings is that the pupils provide a reliable measure of what is in the focu
203 s, eyes from A. irradians with fully dilated pupils provide approximately three times the sensitivity
204 in multiple PLR parameters including resting pupil radius, minimal pupil radius, relative constrictio
205 ters including resting pupil radius, minimal pupil radius, relative constriction, latency, and respon
206 muscle, whereas another is triggered by the pupil reaction when shifting focus from far to near.
214 l signal, with the individual differences in pupil response associated with individual differences in
215 a strong test of top-down modulation of the pupil response by selective attention, we asked whether
217 kernel, while trial-by-trial fluctuations in pupil response were associated with trial-by-trial fluct
218 ation in the amplification of discomfort vs. pupil response, our findings suggest a postretinal alter
224 vide surprising and consistent evidence that pupil responses are under top-down control by cognitive
228 snippets from familiar and unfamiliar songs: Pupil responses showed greater dilation rate to familiar
230 visual discomfort, in that an enhancement of pupil responses was not seen in the migraine group, nor
234 r tightly controlled conditions, task-evoked pupil responses, an LC activity proxy, are lower in indi
235 In this review, I propose that cognitive pupil responses, like their reflexive counterparts, serv
238 predictors at admission were acquired (age, pupil responsiveness, admission Glasgow Coma Scale, gluc
239 ately polygenic scores predict an individual pupil's educational performance conditional on other phe
241 ies were related to different aspects of the pupil signal, with the individual differences in pupil r
242 the ICMA Group had a significant decrease in pupil size (>=3 mm) intraoperatively compared to 4 (16.0
243 SA, coma, and Q value (P < .05), and smaller pupil size (P = .05) than normal eyes implanted with abe
244 mined automatically: percentage of change of pupil size (PPC), maximum contraction velocity (MCV; in
245 response follows dynamics similar to that of pupil size and heart rate, suggesting that task-related
246 During this session, we also recorded ocular pupil size as an implicit measure of listeners' arousal.
247 nd information processing and indicates that pupil size can be used to track the progression of impli
252 of implicit learning.SIGNIFICANCE STATEMENT Pupil size dilates following increase in mental effort,
256 bout environmental conditions were linked to pupil size in the ASD group, thus suggesting heightened
257 During mesopic and scotopic conditions the pupil size increases, increasing the effects on visual p
259 f focus [EROF], sphere shift [SS], EROF-SS), pupil size measurements at far and near, and ocular and
260 o evaluate the intrasession repeatability of pupil size measurements provided by a multidiagnostic pl
262 de of more than 4 (P = 0.001), and to have a pupil size of less than 6 mm (P < 0.001) when compared w
268 ystem can provide consistent measurements of pupil size under scotopic, low mesopic and photopic cond
270 no statistically significant differences in pupil size were found between right and left eyes in any
271 egards stimulus category and correlates with pupil size, and a specific process, which facilitates ca
272 ffects of prediction error and volatility on pupil size, consistent with slower belief updating.
276 sing marker of cognitive states in humans is pupil size, which reflects the activity of an 'arousal'
277 fy a global brain network that covaried with pupil size, which served to generate an index indicative
278 than expected considering the difference in pupil sizes and the Stiles-Crawford effect, showing an e
282 e found that, under semi-natural conditions, pupils (sons) significantly reproduced the sequence stat
283 ion models included Hunt & Hess scale (H&H), pupil status and age or in a simplified variation only H
284 This study aims to evaluate the role of pupil status for mortality prediction and provide improv
285 Accordingly, including information about pupil status improves the predictive performance of prog
286 ge or in a simplified variation only H&H and pupil status, leading to the design of novel H&H-Pupil-A
289 he sea scallop Placopecten magellanicus have pupils that constrict to ~60% of their fully dilated are
290 aratory pupil constriction, which allows the pupil to respond quickly when that bright stimulus is su
294 of sequence similarities between tutors and pupils were significantly predicted by the prevalence of
295 higher-order aberrations (HOAs) over a 6 mm pupil, were assessed before and 6 months, postoperativel
296 Across 3 studies, we reveal dilation of the pupil when participants orient attention to the memorand
299 95% confidence interval, 3.90-5.16) in those pupils with caries in their primary dentition than in th