コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 nsula), and learning and memory (caudate and parahippocampal gyrus).
2 medial temporal lobe cortices comprising the parahippocampal gyrus.
3 tidepressant-related angiogenesis in CA1 and parahippocampal gyrus.
4 r cingulate BA32), left precuneus, and right parahippocampal gyrus.
5 subgenual anterior cingulate cortex, and the parahippocampal gyrus.
6 , superior frontal gyrus, temporal lobe, and parahippocampal gyrus.
7 4Gy targeting the amygdala, hippocampus, and parahippocampal gyrus.
8 t inferior parietal lobule, and left fusifom/parahippocampal gyrus.
9 bserved in DNA isolated from the hippocampus/parahippocampal gyrus.
10 mporal and frontal regions and none with the parahippocampal gyrus.
11 his association was not seen in the anterior parahippocampal gyrus.
12 t with a mechanism of phase resetting, while parahippocampal gyrus activity was indicative of evoked
13 mygdala, entorhinal cortex, hippocampus, and parahippocampal gyrus, allowing us to explore the neuron
14 gions of interest (ROIs) of the hippocampus, parahippocampal gyrus, amygdala, corpus callosum, and an
15 ral to the seizure focus in the hippocampus, parahippocampal gyrus, amygdala, fusiform gyrus, and cho
16 egion model, which included the hippocampus; parahippocampal gyrus; amygdala; superior, middle, and i
17 ssociated with lower activation in the right parahippocampal gyrus and amygdala (R(2) = 0.45, P < 0.0
18 tensive grey matter loss in the hippocampus, parahippocampal gyrus and frontal operculum/insular cort
20 y in the posterior hippocampal formation and parahippocampal gyrus and in the lingual and fusiform gy
21 ss positive) SCC connectivity with the right parahippocampal gyrus and left amygdala distinguished me
24 ity in depression with memory systems in the parahippocampal gyrus and medial temporal lobe, especial
26 abnormal functional connectivity between the parahippocampal gyrus and posterior cingulate cortex.
27 fied confluent white matter abnormalities in parahippocampal gyrus and posterior cingulum, extending
32 rom human medial temporal lobe (hippocampus, parahippocampal gyrus) and cerebellum using in-situ hybr
34 ection regions (putamen, anterior cingulate, parahippocampal gyrus, and amygdala); and (3) hyperactiv
35 volume over 2 years in the left hippocampus, parahippocampal gyrus, and fusiform gyrus, and significa
36 gnificantly lower in temporal pole, anterior parahippocampal gyrus, and hippocampus of the schizophre
37 ivity in left supplementary motor area, left parahippocampal gyrus, and hippocampus; decreased brain
38 temporal lobe, including the hippocampus and parahippocampal gyrus, and in the occipital lobe, the ri
39 ed that there was reduced blood flood in the Parahippocampal Gyrus, and Left Fusiform Gyrus, of those
41 in both hemispheres (frontotemporal cortex, parahippocampal gyrus, and precuneus) in highly educated
43 gs; such regions included the NAc/SCC, right parahippocampal gyrus, and some regions of lateral prefr
44 y matter volume in the anterior hippocampus, parahippocampal gyrus, and superior temporal gyrus, and
45 ippocampus, amygdala, anterior and posterior parahippocampal gyrus, and temporal pole CSF were measur
46 ate, and prefrontal cortex, basal forebrain, parahippocampal gyrus, and thalamus, and these declines
47 elicited greater responses in the amygdala, parahippocampal gyrus. and anterior fusiform gyrus when
48 ; right temporal pole, anterior hippocampus, parahippocampal gyrus; and left middle temporal gyrus (a
49 (1) orbital frontal cortex with hippocampus/parahippocampal gyrus; and, (2) posterior cingulate cort
51 MTL, such that the hippocampus and posterior parahippocampal gyrus become increasingly specialized fo
52 ntorhinal cortex, beta = -0.005 [SE, 0.036]; parahippocampal gyrus, beta = -0.001 [SE, 0.027]; and in
53 ntorhinal cortex, beta = -0.125 [SE, 0.041]; parahippocampal gyrus, beta = -0.074 [SE, 0.030]; and in
54 hippocampus and decreased activation in the parahippocampal gyrus bilaterally compared with never us
55 r they ate chocolate despite being satiated (parahippocampal gyrus, caudolateral OFC and prefrontal r
56 al forebrain, thalamus, insula, hippocampus, parahippocampal gyrus, cingulate, lateral prefrontal and
57 rection at a resolution of 30 degrees in the parahippocampal gyrus, consistent with the head-directio
58 onnectivity of the SCC with the amygdala and parahippocampal gyrus distinguished melancholic from non
59 on of Delta9-THC augmented activation in the parahippocampal gyrus during blocks 2 and 3 such that th
61 ignificantly greater activation in the right parahippocampal gyrus during the 2-back task, and the ps
63 correlated with the BOLD signal of the right parahippocampal gyrus during the processing of uncertain
64 rential activation was observed in the right parahippocampal gyrus during the retrieval of spatial-lo
65 (eg, insular cortex, nucleus accumbens, and parahippocampal gyrus) during the experience of unpleasa
66 matter neurons in the anterior region of the parahippocampal gyrus from 41 individuals with schizophr
67 he amygdala, hippocampus, entorhinal cortex, parahippocampal gyrus, fusiform gyrus, and superior, mid
68 of interstitial white matter neurons in the parahippocampal gyrus in schizophrenia may indicate an a
70 We found that caspase-3 is activated in the parahippocampal gyrus in subjects with mild AD and that
71 , in the vicinity of the hippocampus and the parahippocampal gyrus (in two subjects) and in posterior
72 underpinned by over-activation of the right parahippocampal gyrus, in individuals with high trait an
73 o visual food cues in the brainstem, culmen, parahippocampal gyrus, inferior and middle frontal gyri,
75 l, removal of the amygdala, hippocampus, and parahippocampal gyrus, is based on the hypothesis that t
76 , an injection into area TH of the posterior parahippocampal gyrus labeled neurons in a longitudinal
77 the right prefrontal cortex, posterior left parahippocampal gyrus, left medial parietal cortex and r
78 subsequent verbal memory effects within left parahippocampal gyrus, left orbitofrontal cortex and fus
79 g., bilateral posterior cingulate; bilateral parahippocampal gyrus; left occipital cortex) demonstrat
80 mine in humans how sustained activity in the parahippocampal gyrus may underlie long-term encoding as
81 ojections from area TF--to TH (in the medial parahippocampal gyrus; n = 5) and to posterior visual ar
82 ial recognition and naming), adjacent to the parahippocampal gyrus on the ventral occipitotemporal su
83 Anomalies of structure and asymmetry of the parahippocampal gyrus (origin of the perforant path inpu
84 s; hyperactivation in thalamus (P < .03) and parahippocampal gyrus (P < .003) during affective proces
85 strongly related to tau-tracer uptake in the parahippocampal gyrus, particularly the posterior entorh
86 group more than the other: the precuneus and parahippocampal gyrus (patients more than controls) and
87 as vmPFC, lateral orbitofrontal cortex, and parahippocampal gyrus (PHG) during both rest and task.
89 ivation within the hippocampal formation and parahippocampal gyrus (PHG) was correlated with better m
91 nterior cingulate cortex [ACC] and the right parahippocampal gyrus [PHG]) compared to healthy control
92 bited increased loss signals in the midbrain/parahippocampal gyrus, possibly related to a disinhibiti
93 metry of the hippocampus, entorhinal cortex, parahippocampal gyrus, posterior cingulate gyrus, cortex
94 gyrus and connectivity of the dACC with the parahippocampal gyrus predicted the magnitude of pretrea
95 , which, however, is also a component of the parahippocampal gyrus, receives dense inputs from severa
97 a scene-selective medial place patch in the parahippocampal gyrus, revealing a ventral network for v
98 ged regions of the hippocampus and posterior parahippocampal gyrus selectively for subsequent detail
99 ses revealed that posterior HC and posterior parahippocampal gyrus showed greater activity during sce
100 ct vision, and the hippocampal formation and parahippocampal gyrus, specialized for long-term memory.
101 gulate cortex, insula, medial temporal lobe, parahippocampal gyrus, striatum, and amygdala, this incr
102 locortex (including the amygdala, uncus, and parahippocampal gyrus), subjects with GSP produced a sig
103 ion between responses in the hippocampus and parahippocampal gyrus, suggesting that they play differi
104 een PTSD and smaller cortical volumes in the parahippocampal gyrus, superior temporal cortex, lateral
106 recollection, whereas adjacent cortex in the parahippocampal gyrus supports the process of familiarit
108 in white matter volume in the region of the parahippocampal gyrus that includes the perforant path.
109 hippocampus, amygdala, entorhinal cortex and parahippocampal gyrus that selectively altered their fir
110 he cingulum bundle, the tract connecting the parahippocampal gyrus to the posterior cingulate cortex.
111 lobe atrophy, including the hippocampus and parahippocampal gyrus was detected in Alzheimer's diseas
112 ntrast, activation in the right PFC and left parahippocampal gyrus was linked to successful memory fo
113 ng the recovery of semantic information, the parahippocampal gyrus was more activated for True than f
114 the mean response to the onset of objects in parahippocampal gyrus was predictive of trait difference
115 pocampus bilaterally, as well as in anterior parahippocampal gyrus, was associated with the actual ol
116 including right temporoparietal junction and parahippocampal gyrus, was more activated for inferentia
117 cortex, bilateral fusiform gyrus, and right parahippocampal gyrus were active during the processing
118 nd left amygdala, hippocampus, and posterior parahippocampal gyrus were significantly associated with
119 medial and lateral orbitofrontal cortex, and parahippocampal gyrus, while correlations with risk-aver
120 eral cerebellum, dorsal premotor cortex, and parahippocampal gyrus, with covarying reductions in the
121 e bilateral amygdala-hippocampal complex and parahippocampal gyrus, with the degree of disruption cor
122 s variable) RSFC between MPFC and regions of parahippocampal gyrus within the default network, a patt
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。