ライフサイエンスコーパス: parahippocampal

1 ia and their healthy siblings showed reduced parahippocampal activation (bilaterally) and hippocampal

2 , carriers had greater right hippocampal and parahippocampal activation (p=0.001 and p<0.014, respect

3 hotic major depression group showed aberrant parahippocampal activation at a lower demand level than

4 to additional reductions in hippocampal and parahippocampal activation compared with NP.

5 s a significant positive correlation between parahippocampal activation during encoding and the visua

6 nduced withdrawal, cue-elicited craving, and parahippocampal activation to cannabis cues.

7 ble buyers that appeared, the more sensitive parahippocampal activation was to trial-by-trial uncerta

8 measures were task-dependent hippocampal or parahippocampal activations and precuneus or posterior c

9 he cortical nuclei, and amygdalo-hippocampal/parahippocampal-amygdala transition areas.

10 ory deficits shared an inability to suppress parahippocampal and anterior medial prefrontal cortex ac

11 effects within right posterior hippocampus, parahippocampal and fusiform gyri, and predominantly lef

12 Reduced cortical thickness in the right parahippocampal and fusiform gyrus across both time poin

13 Less gray matter loss in the left parahippocampal and fusiform gyrus and greater gray matt

14 Reduced right parahippocampal and fusiform gyrus thickness are familia

15 forebrain, in particular in the frontal and parahippocampal and hippocampal cortices.

16 hese disorders are accompanied by changes in parahippocampal and hippocampal structures.

17 ing into the precuneus/cuneus as well as the parahippocampal and inferior parietal area.

18 an object/item information pathway, whereas parahippocampal and medial entorhinal cortices are thoug

19 ppocampus, with a posterior stream including parahippocampal and medial lateral entorhinal cortex and

20 control) subjects had greater GM in the left parahippocampal and middle occipital, and bilateral supr

21 gyrus extending to the amygdala, insula, and parahippocampal and middle temporal gyri and in the left

22 ncreases in its functional connectivity with parahippocampal and orbitofrontal cortices.

23 n of the dorsolateral prefrontal, cingulate, parahippocampal and parietal cortex in patients.

24 Parahippocampal and perirhinal cortex showed different p

25 cortex, which are reciprocally connected to parahippocampal and perirhinal cortex, but evidence for

26 onal dissociation has been suggested between parahippocampal and perirhinal cortex.

27 ary roles of the hippocampus and surrounding parahippocampal and perirhinal cortices during the retri

28 Furthermore, parahippocampal and retrosplenial cortex involvement in

29 codes, (ii) posterior brain regions such as parahippocampal and retrosplenial cortices provide criti

30 Parahippocampal and retrosplenial cortices respond stron

31 Effects of inflammation on parahippocampal and rhinal glucose metabolism directly m

32 MTL)-hippocampus and surrounding perirhinal, parahippocampal, and entorhinal cortical areas-has long

33 ant activation of the amygdala, hippocampus, parahippocampal, and fusiform gyri in 30 of 31 subjects

34 ipital, anterior, and posterior hippocampal, parahippocampal, and fusiform regions, as well as a post

35 th neuropsychological scores and entorhinal, parahippocampal, and hippocampal volumes.

36 In discrete auditory, parahippocampal, and inferior parietal "hub" regions [12

37 interactions in regions (including frontal, parahippocampal, and lateral temporal cortex) in which V

38 ilateral occipital, right sensorimotor, left parahippocampal, and left inferior parietal cortices.

39 Cerebellar, parahippocampal, and temporal pole differences were obse

40 ex (i.e., orbitofrontal, cingulate, insular, parahippocampal, and temporopolar cortices) and limbic r

41 isual cortex, lateral occipital complex, the parahippocampal, and the fusiform gyri did not predict t

42 mance can arise by showing that both common (parahippocampal/anterior medial PFC) and differential (D

43 sal and pregenual anterior cingulate cortex, parahippocampal area and precuneus.

44 e and bilateral inferior temporal gyri, left parahippocampal area, left geniculum body, left precuneu

45 ons between this network and hippocampal and parahippocampal areas as well as primary visual cortex c

46 otentials generated by human hippocampal and parahippocampal areas have been related to both physiolo

47 We refer to these visual field maps as parahippocampal areas PHC-1 and PHC-2.

48 trhinal cortex, projections to the remaining parahippocampal areas were either absent or very sparse.

49 e memories via recruitment of left posterior parahippocampal, bilateral retrosplenial, and bilateral

50 the margins of resection, and contralateral parahippocampal changes may suggest a bitemporal disorde

51 ater dependence on other tracts, notably the parahippocampal cingulum (PHC).

52 ippocampal volumes in HS-TLE correlated with parahippocampal cingulum and anterior commissure atrophy

53 Similar associations were not found in the parahippocampal cingulum, a comparison temporal associat

54 mponents of memory networks: the fornix, the parahippocampal cingulum, and the uncinate fasciculus.

55 was also independently related to posterior parahippocampal connections.

56 striking topographic organization of OFC-to-parahippocampal connectivity.

57 plus one additional deposit in the posterior parahippocampal cortex (area TF, n = 1).

58 tudies have shown a relationship between the parahippocampal cortex (PHC) and the processing of spati

59 fferentially with perirhinal cortex (PRC) vs parahippocampal cortex (PHC) and with hippocampal subfie

60 ered during encoding are reinstated in human parahippocampal cortex (PhC) during retrieval.

61 The parahippocampal cortex (PHC) has been implicated in both

62 mportance of the perirhinal cortex (PRC) and parahippocampal cortex (PHC) in episodic memory.

63 gnals for all stimulus categories or whether parahippocampal cortex (PhC) may also play a role for st

64 ippocampal subfields CA2/CA3/DG, whereas the parahippocampal cortex (PHC) showed the opposite pattern

65 been proposed that perirhinal cortex (PRC), parahippocampal cortex (PHC), and hippocampus differenti

66 notably the perirhinal cortex (PrC) and the parahippocampal cortex (PhC).

67 oss the collateral sulcus into the posterior parahippocampal cortex (PHC).

68 nctional roles can be dissociated within the parahippocampal cortex anatomically.

69 ng an anticipatory response, and activity in parahippocampal cortex and hippocampus was greater durin

70 Functional connectivity patterns with parahippocampal cortex and premotor cortex again suggest

71 cited transient responses in the hippocampus/parahippocampal cortex and retrosplenial cortex, and to

72 cortex in humans, and between perirhinal and parahippocampal cortex as a function of information cont

73 arousal was correlated with activity in the parahippocampal cortex but not the amygdala, as is the c

74 These findings suggest that parahippocampal cortex embeds scenes in their temporal c

75 memory, we found that perirhinal cortex and parahippocampal cortex exhibited differential content se

76 The human parahippocampal cortex has been ascribed central roles i

77 VEGF was markedly increased in frontal and parahippocampal cortex in Alzheimer's disease but only s

78 dent postrhinal cortex (POR), homolog to the parahippocampal cortex in primates, is thought to proces

79 cruit hippocampus, retrosplenial cortex, and parahippocampal cortex in support of path integration, i

80 yses indicated that the posterior section of parahippocampal cortex is driven predominantly by judgme

81 oncholinergic projections from the BF to the parahippocampal cortex is more complex than previously d

82 Activity in the parahippocampal cortex predicted subsequent fine tempora

83 nal axis and suggesting that, in humans, the parahippocampal cortex serves as a functional interface

84 ore specifically, evidence suggests that the parahippocampal cortex subserves both the perceptual ana

85 oscillatory phase in visual regions and the parahippocampal cortex tracks the incidental reinstateme

86 rsa) BOLD signals in precuneus and posterior parahippocampal cortex were attenuated in patients relat

87 stem, hippocampus, retrosplenial cortex, and parahippocampal cortex were responsive to Euclidean dist

88 In contrast, posterior hippocampus, parahippocampal cortex, and fusiform gyrus activity line

89 fferent group of regions (perirhinal cortex, parahippocampal cortex, and inferior temporal gyrus) was

90 integrated system including the hippocampus, parahippocampal cortex, and orbitofrontal cortex is crit

91 episodic memory, including the hippocampus, parahippocampal cortex, and orbitofrontal cortex.

92 dorsal bank of the superior temporal sulcus, parahippocampal cortex, and posterior cingulate and retr

93 tion, hippocampus, retrosplenial cortex, and parahippocampal cortex, as well as medial prefrontal cor

94 ttern similarity in perirhinal cortex and in parahippocampal cortex, but greater pattern distinctiven

95 elated with local gray matter density in the parahippocampal cortex, but not in other brain areas.

96 s between latency and selectivity within the parahippocampal cortex, entorhinal cortex, and hippocamp

97 neurons recorded from microelectrodes in the parahippocampal cortex, entorhinal cortex, hippocampus,

98 rhinal cortex, rodent homolog of the primate parahippocampal cortex, processes spatial and contextual

99 Activity in the posterior MTL, including parahippocampal cortex, reflected how strongly one react

100 exposure, and found that perirhinal cortex, parahippocampal cortex, subiculum, CA1, and CA2/CA3/dent

101 activation in MTL, including hippocampus and parahippocampal cortex, uniquely predicted success on no

102 early (150-250 ms) only when it involved the parahippocampal cortex, whereas retrosplenial-medial pre

103 h non-depressed AD patients in precuneus and parahippocampal cortex.

104 pocampus, the perirhinal cortex, and rostral parahippocampal cortex.

105 e represented in a scene-selective region of parahippocampal cortex.

106 ssociated with increased activation of right parahippocampal cortex.

107 lesions may depend on damage in or near the parahippocampal cortex.

108 y the hippocampus, retrosplenial cortex, and parahippocampal cortex.

109 showing domain specificity in perirhinal and parahippocampal cortices (for object-processing vs scene

110 ingulate, lateral parietal, hippocampal, and parahippocampal cortices and amygdala, as well as lower

111 temporal lobe including both perirhinal and parahippocampal cortices and the posterior hippocampus.

112 ctivity in the left anterior hippocampus and parahippocampal cortices during goal-directed navigation

113 The hippocampus and parahippocampal cortices exhibit theta oscillations duri

114 Grid cells in parahippocampal cortices fire at vertices of a periodic

115 inking the medial prefrontal, cingulate, and parahippocampal cortices in processes of working memory,

116 ysfunction of right anterior hippocampus and parahippocampal cortices may underlie this deficit and s

117 s engagement of the anterior hippocampus and parahippocampal cortices relative to comparison subjects

118 n the lateral-occipital, inferotemporal, and parahippocampal cortices showed strong peaks of differen

119 n CA1, the subiculum, and the entorhinal and parahippocampal cortices, activity consistent with a str

120 in nucleus accumbens, lateral prefrontal and parahippocampal cortices, and other regions.

121 the hippocampus, entorhinal, perirhinal, and parahippocampal cortices, forms a functionally related s

122 n, located mainly in the vmPFC, temporal and parahippocampal cortices, thalamus, and brainstem.

123 ere preferentially connected to temporal and parahippocampal cortices.

124 anular insular, piriform, retrosplenial, and parahippocampal cortices.

125 erences across hippocampal subfields and the parahippocampal cortices.

126 cells in the hippocampus and the surrounding parahippocampal cortices.

127 uman subjects have demonstrated a perirhinal/parahippocampal division, such a division among subregio

128 be altered in schizophrenia, and hippocampal-parahippocampal dysfunction has been implicated in this

129 ese results suggest that altered hippocampal-parahippocampal function during encoding is an intermedi

130 Therefore, measuring hippocampal-parahippocampal function with neuroimaging represents a

131 traumatic brain injury results from altered parahippocampal functional connectivity, perhaps seconda

132 ivation of the cingulate, medial frontal and parahippocampal gryi, following weight loss, in response

133 FA in the parahippocampal gyri was significantly decreased in pati

134 ons, such as the posterior cingulate cortex, parahippocampal gyri, and frontal pole, that exhibited a

135 r 2 h induces changes in the hippocampus and parahippocampal gyri.

136 temporal region (areas TEO and TE1-TE3), and parahippocampal gyrus (areas TF, TH, and TL).

137 s; hyperactivation in thalamus (P < .03) and parahippocampal gyrus (P < .003) during affective proces

138 as vmPFC, lateral orbitofrontal cortex, and parahippocampal gyrus (PHG) during both rest and task.

139 Importantly, the right parahippocampal gyrus (PHG.R) was the only region with s

140 03, p=0.00780), Fusiform Gyrus (t=1.26), and Parahippocampal Gyrus (t=1.29).

141 nterior cingulate cortex [ACC] and the right parahippocampal gyrus [PHG]) compared to healthy control

142 t with a mechanism of phase resetting, while parahippocampal gyrus activity was indicative of evoked

143 ssociated with lower activation in the right parahippocampal gyrus and amygdala (R(2) = 0.45, P < 0.0

144 cal regions, and less frequently also in the parahippocampal gyrus and hippocampus.

145 ss positive) SCC connectivity with the right parahippocampal gyrus and left amygdala distinguished me

146 ased in the left middle temporal gyrus, left parahippocampal gyrus and left fusiform gyrus.

147 ted the amygdala bilaterally, right anterior parahippocampal gyrus and left insula.

148 ity in depression with memory systems in the parahippocampal gyrus and medial temporal lobe, especial

149 abnormal functional connectivity between the parahippocampal gyrus and posterior cingulate cortex.

150 fied confluent white matter abnormalities in parahippocampal gyrus and posterior cingulum, extending

151 -independent functional connectivity between parahippocampal gyrus and prefrontal cortex.

152 in the left entorhinal cortex, hippocampus, parahippocampal gyrus and temporal pole.

153 ed inversely with metabolic changes in right parahippocampal gyrus and temporoparietal cortex.

154 MTL, such that the hippocampus and posterior parahippocampal gyrus become increasingly specialized fo

155 hippocampus and decreased activation in the parahippocampal gyrus bilaterally compared with never us

156 onnectivity of the SCC with the amygdala and parahippocampal gyrus distinguished melancholic from non

157 on of Delta9-THC augmented activation in the parahippocampal gyrus during blocks 2 and 3 such that th

158 versus comparison subject activation in the parahippocampal gyrus during encoding and retrieval.

159 ignificantly greater activation in the right parahippocampal gyrus during the 2-back task, and the ps

160 correlated with the BOLD signal of the right parahippocampal gyrus during the processing of uncertain

161 gyrus and connectivity of the dACC with the parahippocampal gyrus predicted the magnitude of pretrea

162 dorsal prefrontal cortex (dPFC), and rostral parahippocampal gyrus regions.

163 ged regions of the hippocampus and posterior parahippocampal gyrus selectively for subsequent detail

164 ses revealed that posterior HC and posterior parahippocampal gyrus showed greater activity during sce

165 he cingulum bundle, the tract connecting the parahippocampal gyrus to the posterior cingulate cortex.

166 the mean response to the onset of objects in parahippocampal gyrus was predictive of trait difference

167 cortex, bilateral fusiform gyrus, and right parahippocampal gyrus were active during the processing

168 s variable) RSFC between MPFC and regions of parahippocampal gyrus within the default network, a patt

169 nsula), and learning and memory (caudate and parahippocampal gyrus).

170 ral to the seizure focus in the hippocampus, parahippocampal gyrus, amygdala, fusiform gyrus, and cho

171 ection regions (putamen, anterior cingulate, parahippocampal gyrus, and amygdala); and (3) hyperactiv

172 volume over 2 years in the left hippocampus, parahippocampal gyrus, and fusiform gyrus, and significa

173 gnificantly lower in temporal pole, anterior parahippocampal gyrus, and hippocampus of the schizophre

174 ivity in left supplementary motor area, left parahippocampal gyrus, and hippocampus; decreased brain

175 ed that there was reduced blood flood in the Parahippocampal Gyrus, and Left Fusiform Gyrus, of those

176 ior temporal cortex, inferior frontal gyrus, parahippocampal gyrus, and orbital frontal cortex.

177 in both hemispheres (frontotemporal cortex, parahippocampal gyrus, and precuneus) in highly educated

178 distributed network, including hippocampus, parahippocampal gyrus, and retrosplenial cortex.

179 y matter volume in the anterior hippocampus, parahippocampal gyrus, and superior temporal gyrus, and

180 ntorhinal cortex, beta = -0.005 [SE, 0.036]; parahippocampal gyrus, beta = -0.001 [SE, 0.027]; and in

181 ntorhinal cortex, beta = -0.125 [SE, 0.041]; parahippocampal gyrus, beta = -0.074 [SE, 0.030]; and in

182 rection at a resolution of 30 degrees in the parahippocampal gyrus, consistent with the head-directio

183 underpinned by over-activation of the right parahippocampal gyrus, in individuals with high trait an

184 o visual food cues in the brainstem, culmen, parahippocampal gyrus, inferior and middle frontal gyri,

185 l, removal of the amygdala, hippocampus, and parahippocampal gyrus, is based on the hypothesis that t

186 subsequent verbal memory effects within left parahippocampal gyrus, left orbitofrontal cortex and fus

187 strongly related to tau-tracer uptake in the parahippocampal gyrus, particularly the posterior entorh

188 bited increased loss signals in the midbrain/parahippocampal gyrus, possibly related to a disinhibiti

189 metry of the hippocampus, entorhinal cortex, parahippocampal gyrus, posterior cingulate gyrus, cortex

190 a scene-selective medial place patch in the parahippocampal gyrus, revealing a ventral network for v

191 gulate cortex, insula, medial temporal lobe, parahippocampal gyrus, striatum, and amygdala, this incr

192 ion between responses in the hippocampus and parahippocampal gyrus, suggesting that they play differi

193 een PTSD and smaller cortical volumes in the parahippocampal gyrus, superior temporal cortex, lateral

194 These regions include the parahippocampal gyrus, superior temporal gyrus, anterior

195 pocampus bilaterally, as well as in anterior parahippocampal gyrus, was associated with the actual ol

196 including right temporoparietal junction and parahippocampal gyrus, was more activated for inferentia

197 medial and lateral orbitofrontal cortex, and parahippocampal gyrus, while correlations with risk-aver

198 eral cerebellum, dorsal premotor cortex, and parahippocampal gyrus, with covarying reductions in the

199 e bilateral amygdala-hippocampal complex and parahippocampal gyrus, with the degree of disruption cor

200 medial temporal lobe cortices comprising the parahippocampal gyrus.

201 tidepressant-related angiogenesis in CA1 and parahippocampal gyrus.

202 r cingulate BA32), left precuneus, and right parahippocampal gyrus.

203 subgenual anterior cingulate cortex, and the parahippocampal gyrus.

204 , superior frontal gyrus, temporal lobe, and parahippocampal gyrus.

205 4Gy targeting the amygdala, hippocampus, and parahippocampal gyrus.

206 egion model, which included the hippocampus; parahippocampal gyrus; amygdala; superior, middle, and i

207 ; right temporal pole, anterior hippocampus, parahippocampal gyrus; and left middle temporal gyrus (a

208 (1) orbital frontal cortex with hippocampus/parahippocampal gyrus; and, (2) posterior cingulate cort

209 g., bilateral posterior cingulate; bilateral parahippocampal gyrus; left occipital cortex) demonstrat

210 omponent of episodic memory, mediated by the parahippocampal-hippocampal region.

211 ensory information, has direct access to the parahippocampal-hippocampal system.

212 or insula, subgenual anterior cingulate, and parahippocampal, inferior frontal, and parietal cortices

213 Finally, parahippocampal lesions that disrupted functional connec

214 Look OKN areas included the culmen, parahippocampal, lingual, middle temporal gyri, inferior

215 f functionally distinct subregions along the parahippocampal longitudinal axis and suggesting that, i

216 and contextual mnemonic processing along the parahippocampal longitudinal axis.

217 rieval of faces after distraction, whereas a parahippocampal-medial entorhinal pathway was more invol

218 correlated with pre- to postsleep changes in parahippocampal-medial prefrontal connectivity during re

219 n this study, we analyzed responses from 630 parahippocampal neurons in 24 neurosurgical patients dur

220 ssue; the behavior and selectivity of single parahippocampal neurons remains largely unknown.

221 Particularly, parahippocampal neurons were found to respond significan

222 FFA) (apparently selective for faces) to the parahippocampal place area (PPA) (apparently selective f

223 l cortex (LO) and scene-specific ROIs in the parahippocampal place area (PPA) and posterior collatera

224 distributed and complementary manner by the parahippocampal place area (PPA) and the lateral occipit

225 participants showed strong activation of the parahippocampal place area (PPA) and the retrosplenial c

226 e showed a stronger functional connection to parahippocampal place area (PPA) compared with adjacent

227 In humans, the ventral temporal parahippocampal place area (PPA) has been implicated in

228 For example, the parahippocampal place area (PPA) responds maximally to e

229 l vs. familiarity specific to words, and the parahippocampal place area (PPA) showed effects for reca

230 ions within the fusiform face area (FFA) and parahippocampal place area (PPA) was modulated such that

231 Here we show that the parahippocampal place area (PPA), a region in human occi

232 ex, including the primary visual cortex, the parahippocampal place area (PPA), and the retrosplenial

233 hip between scene and object patterns in the parahippocampal place area (PPA), even though this regio

234 esponses in the fusiform face area (FFA) and parahippocampal place area (PPA), respectively.

235 ng elicited similar activity patterns in the parahippocampal place area (PPA), retrosplenial complex

236 We found that area V1, the parahippocampal place area (PPA), retrosplenial cortex (

237 vely engaged in visual scene processing: the parahippocampal place area (PPA), the retrosplenial comp

238 elective regions in human visual cortex [the parahippocampal place area (PPA), transverse occipital s

239 has intact scene-selective responses in the parahippocampal place area (PPA), transverse occipital s

240 SC)/parietal-occipital sulcus region and the parahippocampal place area (PPA), which previous studies

241 cluding the fusiform face area (FFA) and the parahippocampal place area (PPA).

242 llateral sulcus (CoS) that overlaps with the parahippocampal place area (PPA).

243 leus on generating selective response within parahippocampal place area (PPA).

244 vely respond to visual scenes, including the parahippocampal place area (PPA).

245 This area (the parahippocampal place area [PPA]) was initially interpre

246 Moreover, one scene-selective region (the parahippocampal place area or PPA) was tolerant to mirro

247 Interestingly, the visual parahippocampal place area showed NF activation closer t

248 egions such as retrosplenial complex and the parahippocampal place area were sensitive to landmark re

249 superior temporal sulcus, STS)- and place ('parahippocampal place area', PPA)-selective cortices in

250 ]) and for the spatial layout of scenes (the parahippocampal place area).

251 rea, lateral occipital cortex, mid fusiform, parahippocampal place area, and extending superiorly to

252 onse observed with functional imaging in the parahippocampal place area.

253 ated with a face was only represented in the parahippocampal place area.

254 scenes and might be the homolog of the human parahippocampal place area.

255 eavily overlap with the functionally defined parahippocampal place area.

256 "scene-selective" visual cortical area (the parahippocampal place area; PPA) showed distinctively hi

257 vidual, the anterior, middle, posterior, and parahippocampal portions of the cingulum bundle were rec

258 atment response at 5-weeks, as was decreased parahippocampal-prefrontal cortex RSFC.

259 The subicular-parahippocampal projection has been proposed as the majo

260 hat an adult-like topography of subiculum-to-parahippocampal projections is present by postnatal day

261 the subiculum), but, in contrast, target the parahippocampal region (perirhinal, postrhinal, lateral

262 The rat parahippocampal region (PHR) and retrosplenial cortex (R

263 e dorsolateral prefrontal cortex (DLPFC) and parahippocampal region along with poor working memory ar

264 ins head direction cells and connects to the parahippocampal region and anterior thalamus.

265 The hippocampus and the parahippocampal region have been proposed to contribute

266 s from the orbitofrontal cortex (OFC) to the parahippocampal region in rats by injecting anterograde

267 r organization of insular projections to the parahippocampal region in the rat with the use of antero

268 Mean diffusivity in the parahippocampal region of the cingulum was negatively as

269 Mean diffusivity in the left parahippocampal region of the cingulum was negatively as

270 Moreover, a parahippocampal region that showed strong resting-state

271 Specifically, the left parahippocampal region was genetically correlated with a

272 ferences in the cingulum at the level of the parahippocampal region were only observed in the right h

273 The parahippocampal region, which comprises the perirhinal,

274 rs (layers I-III) than in deep layers in the parahippocampal region.

275 ubstantiating the PrS's critical role in the parahippocampal region.

276 ub-region of orbital frontal cortex, and the parahippocampal region.

277 to certain areas of the hippocampus and the parahippocampal region.

278 troop processing: ALC activated midbrain and parahippocampal regions more than CTL when processing al

279 bic (including the retrosplenial cortex) and parahippocampal regions similar to that previously obser

280 D showing greater connectivity to visual and parahippocampal regions than TD.

281 ls; alterations in the entorhinal cortex and parahippocampal regions were limited to schizophrenia an

282 l (BA25 extending into BA10) and hippocampal/parahippocampal regions.

283 We used fMRI to measure parahippocampal responses while participants engaged in

284 that the contextual network consists of the parahippocampal, retrosplenial, and medial prefrontal co

285 LD signal in the left posterior hippocampus, parahippocampal-retrosplenial gyrus and left superior fr

286 t in the dark, as in the light, interrelated parahippocampal sites are activated when rats explore no

287 interconnected components of the hippocampal-parahippocampal spatial-representation system.

288 context is represented in the brain and how parahippocampal structures are involved will enhance our

289 ial learning is dependent on hippocampal and parahippocampal theta oscillations, extending to humans

290 genu and splenium of the corpus callosum and parahippocampal tract bilaterally (P < .05).

291 eeking traits and abnormal orbitofrontal and parahippocampal volume were shared by individuals who we

292 l volumes: adjusted r = -0.46, P = .006; and parahippocampal volumes: adjusted r = -0.47, P = .005, n

293 om preoperative imaging, the fimbria-fornix, parahippocampal white matter bundle and uncinate fascicu

294 of the uncinate bilaterally, the ipsilateral parahippocampal white matter bundle, and the ipsilateral

295 teral dorsal fornix and in the contralateral parahippocampal white matter bundle.

296 nd radial (RD) diffusivity measured from the parahippocampal white matter in AD and NCI subjects diff

297 imaging (DTI) to assess the integrity of the parahippocampal white matter in mild cognitive impairmen

298 The use of DTI for in vivo assessment of the parahippocampal white matter may be useful for identifyi

299 Voxelwise analysis in the parahippocampal white matter revealed a progressive chan

300 long the left and right fimbria-fornix (FF), parahippocampal WM bundle (PWMB), arcuate fasciculus (AF