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1 g to nasal, inferonasal, inferotemporal, and temporal regions).
2 = 0.73), with tensile strains largest in the temporal region.
3 right hemisphere activation in the posterior temporal region.
4 early development of sclerosis in the medial temporal region.
5 ced activation in a right posterior superior temporal region.
6 nal anisotropy of lower frontal regions or a temporal region.
7 resection, the majority (12 patients) in the temporal region.
8 izure onset exclusively in the contralateral temporal region.
9 odal efficiency mainly in bilateral superior temporal regions.
10 ionally many higher-order frontoparietal and temporal regions.
11 ic asymmetries that are maximal in posterior temporal regions.
12  superior and inferior than in the nasal and temporal regions.
13  left inferior frontal and anterior superior temporal regions.
14  superior and inferior than in the nasal and temporal regions.
15 ased brain atrophy rates in the right medial temporal regions.
16 ll networks of neurons) in anterior superior temporal regions.
17 tently shown reduced activity in frontal and temporal regions.
18 ivity in the prefrontal, centroparietal, and temporal regions.
19 tical areas spanning occipital, parietal and temporal regions.
20  frontal gyrus (IFG) as well as in bilateral temporal regions.
21 s localized areas in posterior occipital and temporal regions.
22 ) it projects to lateral and medial anterior temporal regions.
23 creased cortical surface area in frontal and temporal regions.
24 were in the prefrontal and anterior superior temporal regions.
25 ates of others, namely medial prefrontal and temporal regions.
26 d activation of left prefrontal and superior temporal regions.
27 with decreased rCBF in prefrontal and medial temporal regions.
28 mpal ReHo and greater tau burden in anterior-temporal regions.
29 to the memory functions attributed to medial temporal regions.
30 gram tasks increased activity in frontal and temporal regions.
31 ctivity most prominently in left frontal and temporal regions.
32 rom the control group, mostly in frontal and temporal regions.
33 al and functional alterations in frontal and temporal regions.
34 phere language representation in frontal and temporal regions.
35 ctivation of cingulate and ventral limbic or temporal regions.
36 concomitant to reduced auditory responses in temporal regions.
37  we observed sex differences in parietal and temporal regions.
38 l binding impacted quantitative estimates in temporal regions.
39 from 0.86 for midfrontal regions to 0.98 for temporal regions.
40 gages a cortical network of left frontal and temporal regions.
41 LD compared to HC in the prefrontal and left temporal regions.
42 esting less desynchrony, within the cortical temporal regions.
43 althy controls (HC) in the prefrontal and bi-temporal regions.
44 al frontal, Intraparietal, and ventrolateral temporal regions.
45 ), as well as greater gray matter volumes in temporal regions.
46 [11C]DPA-713 standardized uptake values from temporal regions.
47 ith activation in the amygdala and posterior temporal regions.
48 ogressors and hypometabolism in AD in medial temporal regions.
49 nd whether they are common across all medial temporal regions.
50 decreased activity in occipital and superior temporal regions.
51 ral frontal, superior parietal, and superior temporal regions.
52 lso activates epileptic activities in medial temporal regions.
53 d between the posterior cingulate and medial temporal regions.
54 al regions and visual sensory (occipital and temporal) regions.
55 ntic processing likely require more anterior temporal regions.10.1093/brain/awx169_video1awx169media1
56 SAL, most severely in posterior parietal and temporal regions (24-40% decrease from PBS+saline).
57 ith TLE than in controls for all ipsilateral temporal regions (27%-42%; P < .05) and in contralateral
58  nerve fiber layer (RNFL), especially in the temporal region (32 mum vs. 56 mum, p < 0.0001), but not
59 central region and/or enhancing the anterior temporal region), aiming to encourage recovery or arrest
60 rographical seizure activity recorded in the temporal region and another had a choroid fissure cyst d
61  matter network including the left posterior temporal region and its connections to the middle tempor
62 28 uptake localized to a more posterior, mid-temporal region and left insula and orbitofrontal cortex
63        Young's modulus trended higher in the temporal region and mediolateral direction.
64  identify a link between the affected medial temporal region and memory performance (as measured by a
65 reased correlation between the epileptogenic temporal region and remaining cortex during the interict
66 fficient in the ipsilateral insula, superior temporal region and thalamus.
67  increased its interaction with the auditory temporal region and the inferior parietal lobule in the
68            A tau PET cut point in the medial temporal region and two cut points in the temporoparieta
69 g cost were predominantly observed in fronto-temporal regions and also significantly predicted the se
70 different entities that are localized to the temporal regions and are not clearly differentiated from
71 erior lateral frontal and posterior superior temporal regions and assessed post hoc in all regions to
72  cortex, which has been shown to link medial temporal regions and cortical regions of the DMN.
73      HDBR resulted in FW increases in fronto-temporal regions and decreases in posterior-parietal reg
74 additional input from posterior parietal and temporal regions and from M1 and MMA.
75 bserved also in right-hemisphere frontal and temporal regions and in the anterior cingulate gyrus.
76  fast transfer of visual signals to anterior temporal regions and neuromodulatory back-projections fr
77 disease characterized by atrophy of anterior temporal regions and progressive loss of semantic memory
78 d a thinner cortex in bilateral, frontal and temporal regions and some thinning in inferior parietal
79 evere hypometabolism was found in the mesial temporal regions and thalami, accentuating a relative si
80 mporary neuroscience indicates that anterior temporal regions and the "ventral" language pathway also
81 l volume (CV); greater cortical thickness in temporal regions and the insula; lower thickness in the
82 rentially increased, maximally over superior temporal regions and the left inferior parietal region.
83 ickness in right inferior frontal and middle temporal regions and with radial and mean diffusivity in
84 long the inferior frontal gyrus and inferior temporal regions and, to a lesser degree, in specific ea
85 rcations were placed on the midbrain, medial temporal region, and basal ganglia region.
86 < 0.01), with highest rates occurring in the temporal region, and the lowest rates occurring in the n
87 r the midbrain, 1.27 +/- 0.10 for the medial temporal regions, and 1.11 +/- 0.07 for the striatum.
88  bilateral medial temporal and right lateral temporal regions, and ApoE4- patients showed greater hyp
89 ateral prefrontal brain regions, in inferior temporal regions, and at the left temporoparietal juncti
90 gressive aphasia compared to controls in the temporal regions, and both semantic variant primary prog
91 , continuing with sensory fusion in parietal-temporal regions, and culminating as causal inference in
92 ral prefrontal, lateral parietal, and medial temporal regions, and negative activation (FE>NE) in the
93 ith activation in the right lateral superior temporal region, anterior to primary auditory cortex.
94 parietal cortical integrity while effects in temporal regions appear later and accelerate, leading to
95 Furthermore, posterior perisylvian and basal temporal regions appear to play an integral role in spon
96 gest that the posterior lateral and inferior temporal regions are crucial for word comprehension, ser
97                               These inferior temporal regions are involved in visual face processing.
98  network and additional recruitment of right temporal regions are significant mediators of aberrant s
99 ter anisotropy in the frontal, parietal, and temporal regions as well as in tracts connecting the fro
100 cularly cortical thickness in prefrontal and temporal regions as well as volume and microstructural i
101  dependent on anterolateral and ventral left temporal regions, as suggested by observations on patien
102 tosensory, retrosplenial, visual, motor, and temporal regions, as well as in several subregions.
103 e values in several prefrontal, premotor and temporal regions, as well as stronger intra PFC connecti
104 l blood flow was measured over both parietal-temporal regions at three PaCO2 values using xenon-133 c
105 ed the critical role of the thalamus, mesial temporal region, basal ganglia and cerebellum, along wit
106 erally (including Broca's area) and superior temporal regions bilaterally (including Wernicke's area)
107 d thicker cortex than those with X(m) in the temporal regions bilaterally, while X(m) individuals sho
108 ontal, anterior/middle cingulate cortex, and temporal regions; Biotype2, intermediate and more locali
109 uronal loss found that anterior and inferior temporal regions bore the brunt of disease across all hi
110 frontal-parietal regions and reading frontal-temporal regions, both domains rely on shared cognitive
111  (CFS), which obliterates input into ventral temporal regions, but leaves dorsal stream processes lar
112  ADHD were more prominent in the frontal and temporal regions, but rCBF changes in men with ADHD were
113 ing reduced activity in inferior frontal and temporal regions, but some also finding increased activi
114 ions with altered functional connectivity to temporal regions can improve understanding of the involv
115        These results suggest that a superior temporal region centered in the STS is preferentially in
116 bserved during the ictal state in the medial temporal region, cerebellum, thalamus, insula and putame
117  hyperintensities in the bilateral posterior temporal region compared to SVCI patients (p < 0.001, un
118 a higher percentage of infranormal values in temporal regions compared with those who did not convert
119 mes (P < .05 for medial temporal and lateral temporal regions) compared with the A-N+ group (n = 22).
120                  At the same time, posterior temporal regions connect more strongly to the ventral wh
121 sponses were identified in anterior superior temporal regions, consisting of clusters selective for m
122 ppears that both the left temporal and right temporal regions contribute in different proportions to
123 fferences were maximal in ipsilateral mesial temporal regions (corrected P < 0.05).
124  observed, and inferior parietal and lateral temporal regions demonstrated the greatest magnitude (5%
125  imaging, we investigated the role of medial temporal regions during active maintenance of informatio
126 eories positing roles for frontal and medial temporal regions during episodic retrieval and suggest a
127 The involvement of dorsal frontal and medial temporal regions during the encoding of words, namable l
128 ger right than left responses, the posterior temporal region escaped this general pattern, showing fa
129 ed by filter paper-stripping from the bulbar temporal region for mRNA isolation.
130 role of backward projections to the occipito-temporal region for understanding conceptual object prop
131 ortex, particularly in frontal, parietal and temporal regions, for individuals with autism spectrum d
132 sities revealed the sequential activation of temporal regions, from the occipital-temporal junction t
133 ft assays were used to begin to characterize temporal region function at the molecular level.
134                                           In temporal regions, gray matter loss was completely absent
135                                  Outside the temporal region, Group Novel showed relatively increased
136 similar but attenuated associations, and non-temporal regions had negligible associations between mem
137 poralis muscle, the STG, like other inferior temporal regions, has been a challenging target for phys
138 tions of these multiple maps in the superior temporal region have not been determined.
139 nd gray matter volume differences in various temporal regions have been reported in dyslexic subjects
140 ation of the ictal onset zone to the lateral temporal region, highlighting the need for accurate char
141 e of the hippocampus, amygdala, and inferior temporal region (hippocampus: betaTL [SE], 0.08 [0.02],
142              In humans, the occipital middle-temporal region (hMT(+)/V5) specializes in the processin
143                 In contrast, in the superior temporal region, hyperoxia failed to reduce blood volume
144 ifically, we found that the volume in medial temporal regions (i.e. amygdala, entorhinal cortex, hipp
145 e neural computations that these frontal and temporal regions implement remains limited.
146 show differential connectivity with anterior temporal regions implicated in the processing of invaria
147 dings reinforce the importance of the medial temporal region in schizophrenia and are consistent with
148 6 bilaterally symmetric pairs plus a lateral temporal region in the right hemisphere.
149 , striatum, right amygdala, hippocampus, and temporal regions in all 75 participants (p<0.05, whole-b
150 tly correlated with metabolic decline in the temporal regions in APOE4 carriers but not in noncarrier
151  parietal regions and in middle and superior temporal regions in comparison with the healthy subjects
152 ptal CA3 rhythm preceded the oscillations in temporal regions in control conditions, this was reverse
153 ed the relationship between acetylcholine in temporal regions in memory.
154 Tau burden was relatively higher in anterior-temporal regions in normal ageing and this difference wa
155          Besides the involvement of superior temporal regions in processing complex speech sounds, ev
156 al cortex (PFC), the frontopolar cortex, and temporal regions in subjects with schizophrenia compared
157 nd Abeta-positive groups and in amygdala and temporal regions in the Abeta-positive group.
158 l and in the posterior cingulate and lateral temporal regions in the MDD group.
159 al regions would exert a top-down control on temporal regions in the recruitment of the anterior temp
160  direct support for the role of human medial temporal regions in the representation of different cate
161 stering and path length in orbitofrontal and temporal regions in TLE, suggesting a shift towards netw
162 ed network of inferior frontal and posterior temporal regions in which symbolic gestures and spoken w
163 ons within the insula, amygdala, frontal and temporal regions in youths with CP as well as inconsiste
164 age areas (inferior frontal gyrus, posterior temporal regions) in such basic composition.
165                Domain-specific activation of temporal regions, in contrast, did not differ between th
166  reduction, predominantly in the frontal and temporal regions, in the schizophrenic patients when com
167 as showed predominant connectivity to medial temporal regions including amygdala and hippocampus.
168 ociated with reductions of FA in frontal and temporal regions including the anterior corpus callosum
169 ode network (DMN) and activation of inferior temporal regions including the fusiform gyrus.
170 llidum, anterior cingulate gyrus, and medial temporal regions, including amygdala and hippocampus (cl
171 -150Hz) activity in specific mesial or basal temporal regions, including amygdala, hippocampus, and f
172 uctions within the left frontal and inferior temporal regions, indicating that these activity reducti
173 med that BPND was significantly increased in temporal regions, insula and fusiform gyrus, consistent
174 his region could be distinguished from other temporal regions involved in face processing.
175 es, which may indicate a dysfunction of left temporal regions involved in phonetic classification.
176                 We find frontal and anterior temporal regions involved in social and motivational beh
177              We suggest that the left medial temporal region is not only activated by novel, to-be-le
178 es suggest that activation of these inferior temporal regions is maintained via frontal- and posterio
179 ide direct evidence that left prefrontal and temporal regions jointly promote memory formation for ve
180 or objects enhanced the activity of inferior temporal regions known to be involved in face and object
181 ngular gyrus; semantic memory: left anterior temporal regions; language: left posterior superior temp
182    Combined DTI/MTI deficits in the occipito-temporal region may be an important variable when consid
183 ere damage, we suggest that the right middle temporal regions may be especially important for integra
184  dementia; (iii) the right and left anterior temporal regions may mediate different behavioural funct
185 al networks, with compensatory activation in temporal regions, may thus contribute to deficient old-n
186 torage taking place in higher frequencies in temporal regions might be effectively coordinated by dis
187 al connectivity between occipital and fronto-temporal regions mirror the changes in visuo-cortical re
188 (n = 6), eyelid and orbit (n = 7), orbit and temporal region (n = 7), or diffuse orbit (n = 1).
189 , cingulate, frontal, parietal, insular, and temporal regions), nucleus accumbens core, amygdalohippo
190 lor-selective area in the inferior occipital-temporal region of human visual cortex.
191  0.80), but was less predictive of a tau PET temporal region of interest (AUROC < 0.70).
192 : t = 2.90, P = 0.004), younger individuals (temporal region of interest: t = -2.49, P = 0.013), and
193   Tau-PET uptake was accelerated in females (temporal region of interest: t = 2.86, P = 0.005; neocor
194 viduals with higher baseline tau-PET signal (temporal region of interest: t = 3.83, P < 0.001; neocor
195 of global amyloid burden (A) and a composite temporal region of tau PET uptake (T), participants were
196 epth specificity are prevalent in the medial temporal region of the cerebral cortex.
197  is off the retinal center towards the dorso-temporal region of the retina.
198                             In both taxa the temporal region of the skull is enclosed by bone and the
199 we demonstrated that in affected frontal and temporal regions of AD brains the amount of 12/15-LOX wa
200 eased in pathologically affected frontal and temporal regions of Alzheimer's disease (AD) brains comp
201 ated with activation in inferior frontal and temporal regions of both cerebral hemispheres in the tit
202  SERT binding in the basal ganglia or medial temporal regions of interest did not significantly diffe
203 to measure cortical thickness of frontal and temporal regions of interest.
204 lassify language patterns within frontal and temporal regions of interest.
205 their natural target population, fibers from temporal regions of retinae failed to invade areas of gr
206  loss and Lewy-body pathology in the ventral-temporal regions of the brain.
207  selectively prevent extension of axons from temporal regions of the retinae.
208 ificantly lower in the inner nasal and inner temporal regions of the study group compared to the cont
209  from the choroid fissure into the nasal and temporal regions of the ventral retina by 70 hpf.
210  neural dysfunction within auditory sensory (temporal) regions, or of increased distractibility, whic
211  were correctly classified using frontal and temporal region oxy-haemoglobin, respectively.
212 ); (b) weighted local efficiency in the left temporal region (P < .05); and (c) weighted clustering c
213 oefficient in the bilateral frontal and left temporal regions (P < .05).
214 teral frontal, right parietal, and bilateral temporal regions (P < .05); (b) weighted local efficienc
215 were localized to medial and inferio-lateral temporal regions (p < 0.007); Abeta + women exhibited gr
216 on of naming sites in anterior and posterior temporal regions (P = 0.03).
217 nces were found in the outer nasal and outer temporal regions (p = 0.659, p < 0.825, respectively).
218                 Connections originating from temporal regions peaked at alpha frequency, whereas conn
219  are consistent indications that frontal and temporal regions play a crucial role in these disorders.
220 he posterior parietal cortex and the central temporal region (PMLS) provide network points required f
221 t fractional anisotropy in the left parietal-temporal region positively correlated with the performan
222 d categorical representations in frontal and temporal regions predicted forgetting.
223 d with blood flow increases in a left medial temporal region previously implicated in episodic memory
224 (r = 0.56; P < 0.01) regions, but not in the temporal region (r = 0.20; P = 0.10).
225 f the heartbeat-evoked potential in the left temporal region reflected the proarrhythmic status of th
226 gions were also observed: a lateral parietal/temporal region related to recollection and a more super
227 l thickness across prefrontal, parietal, and temporal regions relative to community control subjects.
228 linical seizure onset localizing to the left temporal region revealed a significant increase in diffu
229                           Bilateral anterior temporal regions show sensitivity to identity change tha
230         In contrast, prefrontal and anterior temporal regions showed activity reductions to repeated
231                        Prefrontal and medial temporal regions showed greater functional MRI activatio
232                                        Other temporal regions showed similar but attenuated associati
233 is: F, 3.68; P = .004), with the frontal and temporal regions showing the greatest between-group diff
234        The pattern of findings suggests that temporal regions specialize in processing voices very ea
235 he spreading of atrophy to posterior ventral temporal regions specialized for representing this infor
236 eral prefrontal cortex (DLPF), left superior temporal region (ST), and Broca's area showed sustained
237 chitecture of auditory areas of the superior temporal region (STR) in the human was analyzed in Nissl
238 P = .03) and lateral (beta = -0.08, P = .03) temporal regions, subcortical white matter (beta = -0.13
239 (ACC)) and neocortical (superior frontal and temporal) regions subserving affective and cognitive emp
240 t frontotemporal network (including superior temporal regions surrounding auditory cortex) during lex
241 n increased compensative connectivity of the temporal regions (temporal pole and posterior temporal c
242 ontal cortex, orbitofrontal cortex, superior temporal region, temporal pole, amygdala, insula, and do
243 eft superior frontal region and right middle temporal region than did NW and obese controls-a pattern
244  activity was less desynchronized within the temporal regions than at 21% FI,O2 .
245 lower nodal efficiency in bilateral superior temporal regions than controls, probands with SAD only e
246 oss in the medial temporal lobe and inferior temporal regions than the DLB group.
247 pain usually in the orbital, supraorbital or temporal region that typically last minutes.
248 cted activations in a left hemisphere middle temporal region that was part of the normal sentence rea
249 unfamiliar information in a posterior medial-temporal region that were focused in the parahippocampal
250 remembered information in an anterior medial-temporal region that were focused in the subiculum.
251 e-developing ventrolateral prefrontal-limbic-temporal regions that are known to mediate late-developi
252 ing inferior frontal, parietal, and superior temporal regions that may participate in both the percep
253 nt with this, left mid-fusiform and superior temporal regions that showed reading-related activations
254 ivity with memory load, and mediofrontal and temporal regions that were decreasing.
255                Critically, in prefrontal and temporal regions that were modulated by novelty, the mag
256 e and arcuate fasciculus; from the occipital-temporal region, the inferior longitudinal fasciculus; a
257  including ventral prefrontal cortex, medial temporal regions, the ventral striatal complex, and ante
258  tract tracing methods to examine the ferret temporal region: the lateral rostral suprasylvian sulcal
259 with ADHD, mainly in frontal, cingulate, and temporal regions; the largest significant effect was for
260 y be functionally related to nearby superior temporal regions thought to be involved in lip-reading a
261 ntified inferior frontal cortex and anterior temporal regions to receive widespread input and middle
262 gions to receive widespread input and middle temporal regions to send widespread output.
263       Connections originating from the right-temporal regions to these areas emerged when newborns li
264 nhanced activation in the posterior occipito-temporal regions (V5), reflecting the greater movement c
265 pect to major sulci and gyri in the superior temporal region varied most in the chimpanzee and human
266 vation profiles, hypertrophy in the anterior temporal region was associated with improving behaviour,
267  to that observed previously when the entire temporal region was deleted.
268 osterior cortical regions; atrophy in medial temporal regions was also observed.
269                                   GMV in the temporal regions was associated with contemporaneous per
270 rden in the left precuneus/cuneus and medial-temporal regions was associated with increased brain atr
271 pants, elevated baseline cortical tau-PET in temporal regions was associated with lower baseline WM v
272 Increased uptake at low tau stages in medial temporal regions was only observed in cases with a high
273 etwork integration in the medial and lateral temporal regions was related to surgical outcomes.
274 eriod activity in the frontal, parietal, and temporal regions was strongly contralateral.
275 nguals, activations in the bilateral frontal/temporal regions were maintained at a higher level than
276 subthreshold and suprathreshold AB groups in temporal regions were nonsignificantly elevated compared
277          In controls, MTR/FA in the occipito-temporal regions were not associated with PS.
278                                        These temporal regions were not atrophic, displayed normal evo
279 ration and FA in bilateral splenium, but not temporal regions were observed within the FASD group.
280 hanges in oxy-haemoglobin in the frontal and temporal regions were quantified.
281 ary VD in the superior temporal and inferior temporal regions were significantly associated with incr
282  that retinotopic activations in frontal and temporal regions were synchronous, indicating that these
283 ments reliably revealed a posterior superior temporal region (Wernicke's area, traditionally consider
284 t bilateral insular, left frontal, and right temporal regions when compared with responders (all clus
285 e and exhibited similar activation of medial temporal regions when judging nonoverlapping pairs.
286  effects were inverted in the left posterior temporal region, where GMD gain continued up to age 30 a
287 obability were sex specific (eg, in inferior temporal regions, where ASD has different neurobiologica
288 to concepts is situated in posterior lateral temporal regions, whereas additional and deeper levels o
289 ral fronto-striato-thalamic and left lateral temporal regions, whereas genetic risk for bipolar disor
290 rior parietal, and to a lesser extent mesial temporal regions, whereas white matter changes were wide
291 ts, showing that the left posterior inferior temporal region, which has previously been termed the La
292 s early signs of tauopathy, and the inferior temporal region, which is more closely associated with A
293 w a region of hyperperfusion in the anterior temporal region, which often also involves the basal gan
294 ea and the prefrontal, inferior parietal and temporal regions, which were connected through the aslan
295 cits are associated with lesions in anterior temporal regions while verb deficits arise from left inf
296 ced FDG metabolism in posterior parietal and temporal regions, while attentional performance was asso
297 tion in left anterior and posterior superior temporal regions, while environmental sounds enhanced ac
298 d syntactic processes, anterior and inferior temporal regions with lexical retrieval, and posterior t
299 egions with lexical retrieval, and posterior temporal regions with phonological errors and several ot
300  by quadrant (superior, inferior, nasal, and temporal), regions within each quadrant, and distance fr

 
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