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1 nsula), and learning and memory (caudate and parahippocampal gyrus).
2 his association was not seen in the anterior parahippocampal gyrus.
3 s are disynaptic through the hippocampus and parahippocampal gyrus.
4 it decreases in the HC and increases in the parahippocampal gyrus.
5 medial temporal lobe cortices comprising the parahippocampal gyrus.
6 tidepressant-related angiogenesis in CA1 and parahippocampal gyrus.
7 r cingulate BA32), left precuneus, and right parahippocampal gyrus.
8 subgenual anterior cingulate cortex, and the parahippocampal gyrus.
9 , superior frontal gyrus, temporal lobe, and parahippocampal gyrus.
10 4Gy targeting the amygdala, hippocampus, and parahippocampal gyrus.
11 t inferior parietal lobule, and left fusifom/parahippocampal gyrus.
12 bserved in DNA isolated from the hippocampus/parahippocampal gyrus.
13 mporal and frontal regions and none with the parahippocampal gyrus.
14 sue contrast in the orbitofrontal cortex and parahippocampal gyrus; (2) greater changes in markers of
15 t with a mechanism of phase resetting, while parahippocampal gyrus activity was indicative of evoked
16 mygdala, entorhinal cortex, hippocampus, and parahippocampal gyrus, allowing us to explore the neuron
17 efrontal cortex, posterior cingulate cortex, parahippocampal gyrus, amygdala, and nucleus accumbens.
18 gions of interest (ROIs) of the hippocampus, parahippocampal gyrus, amygdala, corpus callosum, and an
19 ral to the seizure focus in the hippocampus, parahippocampal gyrus, amygdala, fusiform gyrus, and cho
20 egion model, which included the hippocampus; parahippocampal gyrus; amygdala; superior, middle, and i
21 ssociated with lower activation in the right parahippocampal gyrus and amygdala (R(2) = 0.45, P < 0.0
22 tensive grey matter loss in the hippocampus, parahippocampal gyrus and frontal operculum/insular cort
23 d lateral orbitofrontal cortex and amygdala, parahippocampal gyrus and hippocampus, and temporal lobe
25 y in the posterior hippocampal formation and parahippocampal gyrus and in the lingual and fusiform gy
26 ss positive) SCC connectivity with the right parahippocampal gyrus and left amygdala distinguished me
29 ity in depression with memory systems in the parahippocampal gyrus and medial temporal lobe, especial
30 hippocampus, grey matter in the hippocampus, parahippocampal gyrus and middle temporal gyrus, were de
32 abnormal functional connectivity between the parahippocampal gyrus and posterior cingulate cortex.
33 fied confluent white matter abnormalities in parahippocampal gyrus and posterior cingulum, extending
38 re, magnitudes of the activation of the left parahippocampal gyrus and the left fusiform gyrus, recru
39 attack before the scan and activation of the parahippocampal gyrus and the right hippocampus yielded
40 rom human medial temporal lobe (hippocampus, parahippocampal gyrus) and cerebellum using in-situ hybr
42 ection regions (putamen, anterior cingulate, parahippocampal gyrus, and amygdala); and (3) hyperactiv
43 l gyrus, right angular gyrus, right amygdala/parahippocampal gyrus, and bilaterally in the middle tem
44 volume over 2 years in the left hippocampus, parahippocampal gyrus, and fusiform gyrus, and significa
45 gnificantly lower in temporal pole, anterior parahippocampal gyrus, and hippocampus of the schizophre
46 ivity in left supplementary motor area, left parahippocampal gyrus, and hippocampus; decreased brain
47 temporal lobe, including the hippocampus and parahippocampal gyrus, and in the occipital lobe, the ri
48 homogeneity (ReHo) in the left hippocampus, parahippocampal gyrus, and inferior temporal gyrus, alon
49 reover showed that the mesial frontal lobes, parahippocampal gyrus, and lateral temporal neocortex we
50 anterior lobes of the cerebellum, bilateral parahippocampal gyrus, and left anterior cingulate corte
51 ed that there was reduced blood flood in the Parahippocampal Gyrus, and Left Fusiform Gyrus, of those
53 ght amygdala with the hippocampus, posterior parahippocampal gyrus, and posterior cingulate cortex an
54 in both hemispheres (frontotemporal cortex, parahippocampal gyrus, and precuneus) in highly educated
57 gs; such regions included the NAc/SCC, right parahippocampal gyrus, and some regions of lateral prefr
59 y matter volume in the anterior hippocampus, parahippocampal gyrus, and superior temporal gyrus, and
60 ippocampus, amygdala, anterior and posterior parahippocampal gyrus, and temporal pole CSF were measur
61 , frontal orbital cortex, putamen, posterior parahippocampal gyrus, and temporal pole, along the infe
62 ate, and prefrontal cortex, basal forebrain, parahippocampal gyrus, and thalamus, and these declines
63 elicited greater responses in the amygdala, parahippocampal gyrus. and anterior fusiform gyrus when
64 al temporal lobe structures encompassing the parahippocampal gyrus; and (iii) a delta/theta band netw
65 ; right temporal pole, anterior hippocampus, parahippocampal gyrus; and left middle temporal gyrus (a
66 (1) orbital frontal cortex with hippocampus/parahippocampal gyrus; and, (2) posterior cingulate cort
68 ater in controls compared to patients in the parahippocampal gyrus (BA27) and perirhinal cortex (BA36
69 MTL, such that the hippocampus and posterior parahippocampal gyrus become increasingly specialized fo
70 ntorhinal cortex, beta = -0.005 [SE, 0.036]; parahippocampal gyrus, beta = -0.001 [SE, 0.027]; and in
71 ntorhinal cortex, beta = -0.125 [SE, 0.041]; parahippocampal gyrus, beta = -0.074 [SE, 0.030]; and in
72 hippocampus and decreased activation in the parahippocampal gyrus bilaterally compared with never us
73 r they ate chocolate despite being satiated (parahippocampal gyrus, caudolateral OFC and prefrontal r
74 al forebrain, thalamus, insula, hippocampus, parahippocampal gyrus, cingulate, lateral prefrontal and
75 rection at a resolution of 30 degrees in the parahippocampal gyrus, consistent with the head-directio
76 onnectivity of the SCC with the amygdala and parahippocampal gyrus distinguished melancholic from non
77 on of Delta9-THC augmented activation in the parahippocampal gyrus during blocks 2 and 3 such that th
79 ignificantly greater activation in the right parahippocampal gyrus during the 2-back task, and the ps
81 correlated with the BOLD signal of the right parahippocampal gyrus during the processing of uncertain
82 rential activation was observed in the right parahippocampal gyrus during the retrieval of spatial-lo
83 (eg, insular cortex, nucleus accumbens, and parahippocampal gyrus) during the experience of unpleasa
85 matter neurons in the anterior region of the parahippocampal gyrus from 41 individuals with schizophr
87 he amygdala, hippocampus, entorhinal cortex, parahippocampal gyrus, fusiform gyrus, and superior, mid
88 ckening or attenuated thinning) of temporal (parahippocampal gyrus, hazard ratio=3.73; fusiform gyrus
90 of interstitial white matter neurons in the parahippocampal gyrus in schizophrenia may indicate an a
92 We found that caspase-3 is activated in the parahippocampal gyrus in subjects with mild AD and that
93 , in the vicinity of the hippocampus and the parahippocampal gyrus (in two subjects) and in posterior
94 underpinned by over-activation of the right parahippocampal gyrus, in individuals with high trait an
95 o visual food cues in the brainstem, culmen, parahippocampal gyrus, inferior and middle frontal gyri,
96 he hippocampus, amygdala, entorhinal cortex, parahippocampal gyrus, insula and superior frontal gyrus
97 he hippocampus, amygdala, entorhinal cortex, parahippocampal gyrus, insula, temporal pole and superio
99 l, removal of the amygdala, hippocampus, and parahippocampal gyrus, is based on the hypothesis that t
100 , an injection into area TH of the posterior parahippocampal gyrus labeled neurons in a longitudinal
101 ildren showed less upregulation in posterior parahippocampal gyrus, lateral occipital cortex, and cer
102 the right prefrontal cortex, posterior left parahippocampal gyrus, left medial parietal cortex and r
103 subsequent verbal memory effects within left parahippocampal gyrus, left orbitofrontal cortex and fus
104 g., bilateral posterior cingulate; bilateral parahippocampal gyrus; left occipital cortex) demonstrat
105 mine in humans how sustained activity in the parahippocampal gyrus may underlie long-term encoding as
106 -associated increased uptake in hippocampus, parahippocampal gyrus, middle temporal pole, inferior te
107 ojections from area TF--to TH (in the medial parahippocampal gyrus; n = 5) and to posterior visual ar
108 ial recognition and naming), adjacent to the parahippocampal gyrus on the ventral occipitotemporal su
110 Anomalies of structure and asymmetry of the parahippocampal gyrus (origin of the perforant path inpu
111 s; hyperactivation in thalamus (P < .03) and parahippocampal gyrus (P < .003) during affective proces
113 ssociated with lower Lewy body counts in the parahippocampal gyrus (P = 3.30 x 10(-5)), with weaker a
114 strongly related to tau-tracer uptake in the parahippocampal gyrus, particularly the posterior entorh
115 group more than the other: the precuneus and parahippocampal gyrus (patients more than controls) and
116 as vmPFC, lateral orbitofrontal cortex, and parahippocampal gyrus (PHG) during both rest and task.
118 ivation within the hippocampal formation and parahippocampal gyrus (PHG) was correlated with better m
119 in task-related brain regions, including the parahippocampal gyrus (PHG), hippocampus, inferior tempo
120 ain regions from two large-scale ad cohorts [parahippocampal gyrus (PHG), sample size n = 190; dorsol
122 nterior cingulate cortex [ACC] and the right parahippocampal gyrus [PHG]) compared to healthy control
123 bited increased loss signals in the midbrain/parahippocampal gyrus, possibly related to a disinhibiti
124 r frontal areas, medial occipital areas, the parahippocampal gyrus, post- and precentral gyri, and th
125 metry of the hippocampus, entorhinal cortex, parahippocampal gyrus, posterior cingulate gyrus, cortex
126 gyrus and connectivity of the dACC with the parahippocampal gyrus predicted the magnitude of pretrea
127 ally, women and men differed in amygdala and parahippocampal gyrus reactivity to cued versus non-cued
128 , which, however, is also a component of the parahippocampal gyrus, receives dense inputs from severa
129 erior temporal, entorhinal cortex, amygdala, parahippocampal gyrus regions after adjusting for age an
130 al temporal, entorhinal cortex, amygdala and parahippocampal gyrus regions retained a significant APO
132 l recruitment of classically place-selective parahippocampal gyrus, retrosplenial complex, and transv
133 a scene-selective medial place patch in the parahippocampal gyrus, revealing a ventral network for v
134 ged regions of the hippocampus and posterior parahippocampal gyrus selectively for subsequent detail
135 ses revealed that posterior HC and posterior parahippocampal gyrus showed greater activity during sce
136 ct vision, and the hippocampal formation and parahippocampal gyrus, specialized for long-term memory.
137 gulate cortex, insula, medial temporal lobe, parahippocampal gyrus, striatum, and amygdala, this incr
138 locortex (including the amygdala, uncus, and parahippocampal gyrus), subjects with GSP produced a sig
139 ion between responses in the hippocampus and parahippocampal gyrus, suggesting that they play differi
140 een PTSD and smaller cortical volumes in the parahippocampal gyrus, superior temporal cortex, lateral
142 cross-brain concordance, with PCNs striatum, parahippocampal gyrus, superior temporal sulcus, ACC, an
143 recollection, whereas adjacent cortex in the parahippocampal gyrus supports the process of familiarit
145 in white matter volume in the region of the parahippocampal gyrus that includes the perforant path.
146 hippocampus, amygdala, entorhinal cortex and parahippocampal gyrus that selectively altered their fir
147 h T1D had higher T1w/T2w ratios in the right parahippocampal gyrus, the executive part of both putami
148 he cingulum bundle, the tract connecting the parahippocampal gyrus to the posterior cingulate cortex.
149 The exception was place-selective regions (parahippocampal gyrus, transverse occipital sulcus, retr
150 ex volume (0.94 [0.91-0.97], P < .001), left parahippocampal gyrus volume (0.93 [0.91-0.96], P < .001
151 lobe atrophy, including the hippocampus and parahippocampal gyrus was detected in Alzheimer's diseas
152 ntrast, activation in the right PFC and left parahippocampal gyrus was linked to successful memory fo
153 ng the recovery of semantic information, the parahippocampal gyrus was more activated for True than f
155 the mean response to the onset of objects in parahippocampal gyrus was predictive of trait difference
156 pocampus bilaterally, as well as in anterior parahippocampal gyrus, was associated with the actual ol
157 including right temporoparietal junction and parahippocampal gyrus, was more activated for inferentia
158 cortex, bilateral fusiform gyrus, and right parahippocampal gyrus were active during the processing
159 erior lobes of the cerebellum, and bilateral parahippocampal gyrus were negatively correlated with th
160 nd left amygdala, hippocampus, and posterior parahippocampal gyrus were significantly associated with
161 medial and lateral orbitofrontal cortex, and parahippocampal gyrus, while correlations with risk-aver
162 eral cerebellum, dorsal premotor cortex, and parahippocampal gyrus, with covarying reductions in the
163 e bilateral amygdala-hippocampal complex and parahippocampal gyrus, with the degree of disruption cor
164 s variable) RSFC between MPFC and regions of parahippocampal gyrus within the default network, a patt