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

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

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

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

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

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

9 The change in parahippocampal/amygdala and insula responses during the

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

11 nts' production accuracy and originates from parahippocampal and cerebellar sources.

12 ve information processing carried out in the parahippocampal and cingulate regions.SIGNIFICANCE STATE

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

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

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

16 Reduced right parahippocampal and fusiform gyrus thickness are familia

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

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

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

20 ecreased response in right prefrontal, right parahippocampal and left striatal regions; also, a gradi

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

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

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

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

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

26 Parahippocampal and perirhinal cortex showed different p

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

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

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

30 Furthermore, parahippocampal and retrosplenial cortex involvement in

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

32 Parahippocampal and retrosplenial cortices respond stron

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

34 ce that WM performance critically depends on parahippocampal and striatal integrity, while theta-alph

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

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

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

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

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

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

41 Cerebellar, parahippocampal, and temporal pole differences were obse

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

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

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

45 ipsilateral mesial temporal lobe (p = 0.02), parahippocampal area (p = 0.03) and thalamus (p = 0.006)

46 nd a significant increase in the ipsilateral parahippocampal area (p = 0.03).

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

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

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

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

51 lar and rostral temporal association cortex, parahippocampal areas TH / TF, the ventral posterior mid

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

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

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

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

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

57 ith hippocampal sclerosis in the ipsilateral parahippocampal cingulum and external capsule, with smal

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

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

60 ch arise from dysfunction in hippocampal and parahippocampal circuits.

61 was also independently related to posterior parahippocampal connections.

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

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

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

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

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

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

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

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

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

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

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

73 sults provide novel support for the roles of parahippocampal cortex and frontal areas in conscious pr

74 mpus and vector-based retrieval supported by parahippocampal cortex and lateral parietal cortex.

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

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

77 urthermore, we found that representations in parahippocampal cortex are hierarchical, reflecting both

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

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

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

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

82 The human parahippocampal cortex has been ascribed central roles i

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

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

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

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

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

88 s: an auditory cortex related tinnitus and a parahippocampal cortex related tinnitus.

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

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

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

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

93 regions showing peripheral preference (e.g. parahippocampal cortex).

94 (2) source memory signals in posterior CA1, parahippocampal cortex, and angular gyrus.

95 restricted to the hippocampus, amygdala, and parahippocampal cortex, and applied separately for respo

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

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

98 occipital complex, inferior temporal cortex, parahippocampal cortex, and prefrontal cortex.

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

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

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

102 topographic spatial learning relies upon the parahippocampal cortex, damage to which renders patients

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

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

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

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

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

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

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

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

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

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

113 ssociated with increased activation of right parahippocampal cortex.

114 p tinnitus instead relates to changes in the parahippocampal cortex.

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

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

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

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

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

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

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

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

123 cells in the hippocampus and the surrounding parahippocampal cortices.

124 ere preferentially connected to temporal and parahippocampal cortices.

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

126 but not in the posteromedial entorhinal and 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 trate that hippocampal theta phase modulates parahippocampal gamma amplitude during retrieval of spat

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

134 ) and with smaller grey matter volume of the parahippocampal gyri (r(s) =-0.31, p=0.004).

135 FA in the parahippocampal gyri was significantly decreased in pati

136 the predictive models involved the bilateral parahippocampal gyri, as well as the superior temporal g

137 activation in the amygdala, the hippocampal/parahippocampal gyri, the dorsomedial/pulvinar nuclei of

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

139 tivation in the amygdala and the hippocampal/parahippocampal gyri.

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

141 ater in controls compared to patients in the parahippocampal gyrus (BA27) and perirhinal cortex (BA36

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

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

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

145 03, p=0.00780), Fusiform Gyrus (t=1.26), and Parahippocampal Gyrus (t=1.29).

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

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

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

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

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

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

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

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

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

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

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

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

158 re, magnitudes of the activation of the left parahippocampal gyrus and the left fusiform gyrus, recru

159 attack before the scan and activation of the parahippocampal gyrus and the right hippocampus yielded

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

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

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

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

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

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

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

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

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

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

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

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

172 l gyrus, right angular gyrus, right amygdala/parahippocampal gyrus, and bilaterally in the middle tem

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 reover showed that the mesial frontal lobes, parahippocampal gyrus, and lateral temporal neocortex we

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

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

178 e cortex, superior temporal gyrus, amygdala, parahippocampal gyrus, and prefrontal areas.

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

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

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

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

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

189 l recruitment of classically place-selective parahippocampal gyrus, retrosplenial complex, and transv

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 h T1D had higher T1w/T2w ratios in the right parahippocampal gyrus, the executive part of both putami

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

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

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

196 medial temporal lobe cortices comprising the parahippocampal gyrus.

197 tidepressant-related angiogenesis in CA1 and parahippocampal gyrus.

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

199 subgenual anterior cingulate cortex, and the parahippocampal gyrus.

200 it decreases in the HC and increases in the parahippocampal gyrus.

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

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

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

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

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

206 ytoarchitectural transition from six-layered parahippocampal isocortex to three-layered hippocampal a

207 Finally, parahippocampal lesions that disrupted functional connec

208 insular-limbic, occipito-temporal, temporal, parahippocampal-limbic, and inferior fronto-temporal), c

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

210 and contextual mnemonic processing along the parahippocampal longitudinal axis.

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

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

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

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

215 ion index in two regions of interest (ROIs): parahippocampal place area (PPA) and lateral occipital c

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

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

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

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

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

221 al neuroimaging studies have argued that the parahippocampal place area (PPA) represents such navigat

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

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

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

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

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

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

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

229 hree gradients extending anteriorly from the parahippocampal place area (PPA), retrosplenial complex

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

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

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

233 level image features of the stimuli, and the parahippocampal place area (PPA), which showed better te

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

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

236 ate parametric effects in the MTL, mPFC, and Parahippocampal Place Area (PPA).

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

238 area (FBA), retrosplenial complex (RSC) and parahippocampal place area (PPA).

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

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

241 and scene selectivity (including the "proto" parahippocampal place area and retrosplenial complex) by

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

243 found in other scene-selective regions (the parahippocampal place area or retrosplenial complex) or

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

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

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

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

248 regions that respond selectively to scenes: parahippocampal place area, retrosplenial complex/medial

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

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

251 strong functional connectivity with anterior parahippocampal place area.

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

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

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

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

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

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

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

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

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

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

262 with age, from 14 to 19 years, in the right parahippocampal region and left insular cortical area.

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

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

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

266 The parahippocampal region is thought to be critical for mem

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

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

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

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

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

272 The parahippocampal region, which comprises the perirhinal,

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

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

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

276 ortex showing face selectivity and posterior parahippocampal regions showing scene selectivity.

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

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

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

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

281 cortex (mPFC) and also receives inputs from parahippocampal regions.

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

283 The parahippocampal, retrosplenial and parietal cortices, as

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

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

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

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

288 ronal activation was observed in hippocampus parahippocampal structures: subiculum, entorhinal cortex

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

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

291 ry 2 years) and total brain, hippocampal and parahippocampal volumes (by magnetic resonance) in a sub

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