ライフサイエンスコーパス: subfield

1 absence of significant edema in the central subfield.

2 ied Spectralis software for the central 3 mm subfield.

3 mum (standard deviation, 4.8 mum) at central subfield.

4 t Diabetic Retinopathy Study (ETDRS) macular subfields.

5 nated central region flanked by ON-dominated subfields.

6 that extended beyond CA1 to all of the other subfields.

7 hat auditory cortex is populated by multiple subfields.

8 ippocampus consists of anatomically distinct subfields.

9 nd pyramidal cell layer of CA3, CA2, and CA1 subfields.

10 ht hippocampus and also selected hippocampal subfields.

11 in different layers of the CA1, CA3, and DG subfields.

12 arly Treatment of Diabetic Retinopathy Study subfields.

13 effect was not apparent in other hippocampal subfields.

14 has shown adult neurogenesis in hippocampal subfields.

15 s had spatially overlapping ON/OFF receptive subfields.

16 lor-made for a better involvement in several subfields.

17 ats in the dentate gyrus and CA3 hippocampal subfields.

18 ubfield and then by 200 mum within the inner subfields.

19 eneity in the spatial matrix of facilitatory subfields.

20 , requiring spatially separate ON and/or OFF subfields.

21 IBRA in the hippocampus, particularly in the subfields.

22 e in area of retinal nonperfusion in central subfields.

23 fovea, parafovea, and temporal and superior subfields.

24 l tissue was used to label seven hippocampal subfields.

25 issue) was used to delineate the hippocampal subfields.

26 ers may be localized to specific hippocampal subfields.

27 on distribution across all major hippocampal subfields.

28 that extended beyond CA1 to all of the other subfields.

29 tibodies bind to specific rodent hippocampal subfields.

30 (mean 334.5 mum) and thinnest in the center subfield (285.4 mum).

31 ippocampal cortex (PHC) and with hippocampal subfields along the proximo-distal axis.

32 ficantly reduced in patients and hippocampal subfield analysis revealed bilateral atrophy of the inpu

33 A hippocampal subfield analysis shows that a locus within the MSRB3 ge

34 thickness measurement of the central macular subfield and 35 mum in subfoveal choroidal thickness is

35 (EZ) were determined within the 1-mm central subfield and correlated with VA at baseline and follow-u

36 Hippocampal subfield and metabolic abnormalities detected at 7T appe

37 two hippocampal-related subregions: the CA2 subfield and the entorhinal cortex (EC).

38 in steps of 100 mum within the central 1-mm subfield and then by 200 mum within the inner subfields.

39 was used to objectively measure hippocampal subfield and whole brain volumes.

40 phrenia, with extension to other hippocampal subfields and accompanying clinical sequelae over time.

41 differential development of intrahippocampal subfields and associated networks.

42 odic memory for which individual hippocampal subfields and entorhinal cortex layers contribute by car

43 reflecting loss of volume in all hippocampal subfields and in both dorsal and ventral hippocampus.

44 standard error, 2.42; P = .009) hippocampal subfields and left amygdalar (simple slope, -34.62; stan

45 with left dentate gyrus and CA3 hippocampal subfields and left amygdalar volumes.

46 de in vivo measurement of entire hippocampal subfields and separation between unmedicated and medicat

47 showed evidence of localization to specific subfields and subregions, findings that appear, on the s

48 these volume changes in specific anatomical subfields and their functional significance is unclear.

49 in CFT, presence of hard exudates in center subfield, and absence of renal disease.

50 of segmentation error in the central macular subfield, and after exclusion of these eyes the revised

51 olateral amygdaloid nucleus, hippocampal CA3 subfield, and dentate gyrus; in contrast, the level is g

52 ompanied by phosphorylated TDP-43 in the CA1 subfield, and ubiquitin and mitochondria accumulations i

53 41; P = .04) and CA4/DG (r = -0.43; P = .03) subfields, and impaired left hippocampal microstructural

54 mework, and focusing on the hippocampus, its subfields, and specialization along its longitudinal axi

55 cessing can be organized amongst hippocampal subfields, and that CA1 pyramidal cells are less critica

56 ly Treatment Diabetic Retinopathy Study grid subfields, and total grid area of 6 mm on both scans and

57 n the human hippocampus and whether specific subfields are differentially affected by KIBRA genotype.

58 By contrast, the centres of the ON subfields are distributed over a wider region of visual

59 CT was measured in nine subfields as defined by the ETDRS-style grid using a DRI

60 nd microstructure of the hippocampus and its subfields as indicated by the mean diffusivity on diffus

61 pocampal, dentate gyrus, and CA3 hippocampal subfields as well as amygdalar volumes were assessed usi

62 ssociated with significantly thicker central subfield at baseline (347.6 vs 258.1 mum; P = .02) and r

63 applied multimodal 7T MRI to assess if focal subfield atrophy and deviations in brain metabolites cha

64 Volume analyses identified hippocampal subfield atrophy in 9/12 patients (75%), commonly affect

65 g lower field strengths, such as hippocampal subfield atrophy in mild cognitive impairment.

66 Fourth, CA3 subfield atrophy was associated with severe episodic but

67 egulation is observed in the CA1 hippocampal subfield but not in CA3 and is thus subfield/celltype-sp

68 and retrospective modes exist in hippocampal subfield CA1 and that slow and fast gamma rhythms differ

69 al subfields, such as the cornu ammonis (CA) subfields CA1-4, the dentate gyrus (DG) including a gran

70 mous body of literature on other hippocampal subfields (CA1 and CA3), relatively little is known abou

71 Recent studies have implicated hippocampal subfield CA2 in social and contextual memory but how it

72 atient groups had smaller cornu ammonis (CA) subfields CA2/3 (left, p = 7.2 x 10(-6); right, p = 2.3

73 al contextual representations in hippocampal subfields CA2/CA3/DG, whereas the parahippocampal cortex

74 t variation in the size of human hippocampal subfield CA3 predicted the amount of neural interference

75 pocampal subfield but not in CA3 and is thus subfield/celltype-specific.

76 (the majority of which examined hippocampal subfield changes), and 4 investigated HD.

77 Volumes of hippocampal subfields cornu ammonis (CA) 2+3, CA4+dentate gyrus, and

78 by pronounced hippocampal atrophy, including subfields cornu ammonis 2/3 (CA2/3) and CA4/dentate gyru

79 isons and that MRI landmarks approximate the subfields defined by cellular microstructure.

80 The measurements of the 9 subfields defined by the Early Treatment Diabetic Retino

81 t-synaptic potentials in the hippocampal CA1 subfield demonstrate that TBI inhibits the expression of

82 ually segment hippocampal cornu ammonis (CA) subfields, dentate gyrus (DG), and the subiculum as well

83 reliable and accurate segmentation of the HF subfields DG, CA3, CA2, CA1, prosubiculum, subiculum, pr

84 rmine whether in vivo volumes of hippocampal subfields differ between clinical groups and healthy con

85 hronic stress and MDD may affect hippocampal subfields differently, but MRI spatial resolution has pr

86 ional contribution of individual hippocampal subfields during a perceptual discrimination task for sc

87 offset light-preferring and dark-preferring subfields, each obliquely oriented in spacetime.

88 available on detailed parcellation of the HF subfields, especially in the complex, curved hippocampal

89 ontains several small, functionally distinct subfields, examining the role of these in scene processi

90 vancing age, synapses in various hippocampal subfields exhibit impaired long-term potentiation, an el

91 large-scale reorganization in forepaw barrel subfield (FBS) cortex.

92 ortical reorganization in the forepaw barrel subfield (FBS) of primary somatosensory cortex (SI) that

93 eview preliminary findings from this nascent subfield, focusing on observational learning and strateg

94 The centres of OFF subfields for neurons in a given region of cortex are co

95 PR103 particularly in the cornu ammonis (CA) subfield from AD patients suffering from early onset fam

96 ells, identified by their overlapping on/off subfields, had significantly weaker OS than simple cells

97 ells, identified by their overlapping on/off subfields, has significantly weaker orientation selectiv

98 mple, memory improvement was associated with subfield hippocampal volume increase independent of mood

99 Even in this rare successful subfield, however, more data are still unshared than sha

100 ale firing correlations across those ACC/PFC subfields implicated to control and monitor attention.

101 ignal profiles in the dentate gyrus (DG)/CA3 subfield in human subjects.

102 athology and its distribution in hippocampal subfields in 95 clinically and neuropathologically chara

103 Treatment Diabetes Retinopathy Study (ETDRS) subfields in Egypt using deep-range imaging swept source

104 e whether the spatial map of receptive-field subfields in individual V2 neurons is sufficiently matur

105 stigate coding of vocal stimuli in different subfields in macaque auditory cortex.

106 y in statistical power is common across most subfields in neuroscience.

107 of HF to allow segmentation into individual subfields in order to identify specific functions in bot

108 novel insight into the roles of hippocampal subfields in support of recognition memory and further p

109 accurate segmentation and measurement of HF subfields in the human brain on MRI scans.

110 eceptor levels were increased in hippocampal subfields in the mice and in resected hippocampus from p

111 ked ipsilateral load of anomalies across all subfields in TLE-HS, whereas anomalies in TLE-G were res

112 ently decreased network embedding across all subfields in TLE-HS, while changes in TLE-G were limited

113 agement of therapies in specific hippocampus subfields in vivo that underlie abnormal behavior.

114 decline of CA1, but not of other hippocampal subfields, in the non-remitters was associated with incr

115 rch terms were "infusion, intraosseous" (all subfields included), and intraosseous access" as key wor

116 with neuronal loss affecting all hippocampal subfields including CA1, CA4 and dentate gyrus (HS ILAE

117 s, interaction between human CA3 and dentate subfields is difficult to investigate due to small size

118 in pain processing, the role of hippocampal subfields is uncertain.

119 sence of macular fluid and automated central subfield macular thickness (CSMT) at year 1 and 2, were

120 ving DME and VA </=79 ETDRS letters, central subfield macular thickness (CST) >/=350 mum on Topcon 3D

121 ss was 107.6 +/- 1.2 mum and average central subfield macular thickness was 271.2 +/- 2.0 mum.

122 e superior and inferior sectors, and central subfield macular thickness was significantly correlated

123 increase from preoperative baseline central subfield macular thickness) within 90 days after catarac

124 Both drugs reduced the central subfield macular thickness, with a mean decrease of 95 m

125 ver, approximately 25% of V2 neurons had the subfield map where the neighboring facilitatory subfield

126 ts had "tuned" suppressive profiles in their subfield maps that could alter the tuning properties of

127 l organization, the ontogenetic timing of HC subfield maturation remains controversial.

128 entral macular fields as well as the central subfield may be useful in the early detection and treatm

129 n optical coherence tomography (OCT) central subfield mean thickness (CSMT) was -89 mum for bevacizum

130 times on ERG, mean deviation on VF, central subfield mean thickness, and total macular volume did no

131 How these alterations and hippocampal subfields might differ across the psychosis spectrum rem

132 quantified cell loss pattern in hippocampal subfields obtained from the same patients using the new

133 S letters (20/41 Snellen) and a mean central subfield of 422 mum at baseline.

134 It is a subfield of biomedical natural language processing that

135 The subfield of evanescent wave fluorescence biosensors has

136 d as a result is perhaps the fastest growing subfield of mass spectrometry.

137 Recently, this subfield of microfluidics has started to attract greater

138 As the subfield of MOF-based sensing has developed, many divers

139 In the artificial intelligence subfield of neural networks, a barrier to that goal is t

140 subset of superficial mPFC projections to a subfield of nucleus accumbens (NAc) neurons naturally en

141 outlook toward the future of this promising subfield of organic synthesis.

142 fluids, in particular in the rapidly growing subfield of quantum turbulence which elucidates the evol

143 ied a preferential response in the subiculum subfield of the hippocampus during scene, but not face o

144 ior work has shown that the volume of CA1, a subfield of the hippocampus, is selectively reduced in t

145 e highly expressed in the dentate gyrus (DG) subfield of the hippocampus, where they generate a tonic

146 diated by reversal of brain matter loss in a subfield of the left hippocampus.

147 Because not all subfields of biology use mathematics for this purpose, m

148 inputs arise not from the major hippocampal subfields of CA1 and CA3, but from area CA2, a region th

149 at aims to bring together leading experts in subfields of cardiovascular biomedicine to focus on topi

150 at aims to bring together leading experts in subfields of cardiovascular biomedicine to focus on topi

151 difference between line scans/corresponding subfields of cube scans (outer nasal 0.92-1.11, inner na

152 ial genomics, functional evolution and other subfields of microbiology.

153 sult and that it varies substantially across subfields of neuroscience, with particularly low power i

154 Collaborative efforts across these subfields of regenerative medicine seek to ultimately pr

155 show that the spatially separate ON and OFF subfields of simple cells in layer 2/3 exhibit topologic

156 tensive in the temporal and nasal parafoveal subfields of the deep plexus with sickle SC or prolifera

157 nalysis of granule-cell neurons spanning the subfields of the dentate gyrus revealed significant redu

158 etailed organization and parcellation of all subfields of the hippocampal head and body regions on th

159 ts in schizophrenia are confined to specific subfields of the hippocampus and to measure the subfield

160 However, the roles of the various subfields of the hippocampus are poorly understood.

161 ell neurons within the dentate gyrus and CA1 subfields of the hippocampus exhibited significant reduc

162 munoblotting and immunohistochemistry in all subfields of the hippocampus in young and adult mice.

163 romising in vivo paradigm for bridging brain subfield oxidative stress and behavior in animal models

164 In vivo imaging of prodromal hippocampus CA1 subfield oxidative stress in models of Alzheimer disease

165 ker retinas than eyes in women in the center subfield (P < .001) and inner circle (P < .001).

166 3.20 x 10(-9), respectively) and the center subfield (P = 1.24 x 10(-9) and P = 6.68 x 10(-8), respe

167 First, hippocampal subfield quantitative morphometry indicated significant

168 The CR for the other macular subfields ranged from 7.0 mum to 38.2 mum.

169 In turn, decreased volume of the left CA2/3 subfield (RAVLT delayed recall, r = 0.40; P = .047) and

170 e structural morphology of human hippocampal subfields represents one factor determining vulnerabilit

171 e mild; the overall strength of facilitatory subfield responses was lower than that in adults, and th

172 Significant decreases in central subfield retinal thickness on optic coherence tomography

173 n improvement in vision, a decreased central subfield retinal thickness, and an increase in fluid-fre

174 her outcomes included visual acuity, central subfield retinal thickness, and number of anti-VEGF inje

175 A consecutive analysis of hippocampal subfields revealed a spatially distinct profile for each

176 us were performed using a recently validated subfield segmentation approach, and cortical thickness e

177 r, our results demonstrate that kindling has subfield-selective effects on the different functional c

178 ein, we tested the hypothesis of hippocampal subfield specialization in a series of 100 consecutive p

179 s with BD had reduced volumes of hippocampal subfields, specifically in the left CA4, GCL, ML and bot

180 endent but converging influences of both MTL subfield structure and function contribute to age-relate

181 Here, human hippocampal subfield (subiculum, cornu ammonis 1-3, and dentate gyru

182 field map where the neighboring facilitatory subfields substantially differed in their preferred orie

183 a uniform structure and consists of several subfields, such as the cornu ammonis (CA) subfields CA1-

184 we carried out a novel MRI-based hippocampal subfield surface analysis that integrated volume, T2 sig

185 mplate activity patterns in each hippocampal subfield that corresponded to the attentional state indu

186 its most recent role in cancer signaling, a subfield that is expected to grow exponentially.

187 Hippocampal subfields that participate in memory-related processes s

188 d the lateral part of entorhinal cortex, the subfields that receive the predominant olfactory input t

189 Fields spawn subfields that then become entities in themselves that p

190 In addition to the central subfield, the average mean change in thickness of the mo

191 ormed fewer contacts in specific hippocampal subfields, their stereotyped connectivity was largely pr

192 iabetic retinopathy without definite central subfield thickening on optical coherence tomography (OCT

193 ive ranibizumab with persistent DME (central subfield thickness >/=250 mum on time domain optical coh

194 t of ERM patients who had severe ME (central subfield thickness >/=450 mum on spectral domain optical

195 persistent DME (failure to achieve a central subfield thickness <250 mum and at least a 10% reduction

196 rval [CI], 2.3-5.8) and of 57 mum in central subfield thickness (95% CI, -84 to -30) in the study eye

197 Central subfield thickness (CFT), horizontal and vertical extent

198 Center subfield thickness (CSF) between the internal limiting m

199 t-corrected visual acuity (BCVA) and central subfield thickness (CSFT) from baseline to month 24, and

200 bjectives included change in retinal central subfield thickness (CSFT) from baseline to the end of st

201 e change from baseline to month 1 in central subfield thickness (CSFT) measured by spectral-domain op

202 BCVA, central subfield thickness (CSFT), and morphologic features were

203 s were best-corrected visual acuity, central subfield thickness (CSFT), and rates of macular edema im

204 Central subfield thickness (CST) and cube volume decreased in st

205 y Study protocol, and measurement of central subfield thickness (CST) by spectral-domain optical cohe

206 s optical coherence tomography (OCT) central subfield thickness (CST) can yield different prevalence

207 greater reduction from baseline mean central subfield thickness (CST) in the 2.0-mg versus 0.5-mg gro

208 acula was completely dry or when the central subfield thickness (CST) measured by optical coherence t

209 ic macular edema, defined as Stratus central subfield thickness (CST) of 250 mum or greater, particip

210 stics associated with 6-month VA and central subfield thickness (CST) outcomes in participants in the

211 ) area under the curve and change in central subfield thickness (CST) within subgroups based on wheth

212 best-corrected visual acuity (BCVA), central subfield thickness (CST), and DRSS score.

213 Mean change from baseline central subfield thickness (CST, mum) at week 12 in Group 1 vs 2

214 T functional MRI (hr-fMRI), we evaluated MTL subfield thickness and function in older adults represen

215 pical dorzolamide-timolol may reduce central subfield thickness and subretinal fluid in eyes with per

216 Central subfield thickness changes beyond 10% when using the sam

217 Mean central subfield thickness decreased by 67.0 mum, 55.4 mum, and

218 Optical coherence tomography central subfield thickness decreased by 85.90 mum, 70.39 mum, an

219 The mean central subfield thickness decreased from 419.7 mum at enrollmen

220 There was a minimal mean change in central subfield thickness from baseline in these eyes at the ti

221 ange in optical coherence tomography central subfield thickness from baseline to month 12 was -107 an

222 a mean optical coherence tomography central subfield thickness improvement from baseline of -48.4 mu

223 e associated with similar effects on central subfield thickness in patients with DME through 1 year o

224 figure of 14 mum for central macular retinal subfield thickness in the absence of segmentation error.

225 ME defined as the following: (1) OCT central subfield thickness of 250 mum or greater (time-domain OC

226 5% CI, -1.0 to 4.4) and a decrease in center subfield thickness of 34 mum (95% CI, -75 to 6.8) for th

227 crease in center point thickness and central subfield thickness of 38.9% and 33.7%, respectively.

228 y level, area of retinal thickening, central subfield thickness on optical coherence tomography, and

229 less of baseline VA, lesion size, or central subfield thickness on optical coherence tomography.

230 at least a 1-step increase in logOCT central subfield thickness preoperatively to the 16-week visit;

231 at least a 2-step increase in logOCT central subfield thickness preoperatively to the 16-week visit;

232 edema was 5.2 (1.3) days; the final central subfield thickness ranged from 193 to 293 microm.

233 Mean [SD] central subfield thickness reduced by -50 [97] mum, with 8 parti

234 nt differences in mean BCVA gains or central subfield thickness reductions at month 15 between the PR

235 acuity letter score and OCT-measured central subfield thickness similar to those without prior anti-V

236 ckness) and resolution (reduction of central subfield thickness to <315 mum) at 3 and 6 months follow

237 nce tomography has focused mainly on central subfield thickness to quantify macular edema in central

238 dard deviation) change from baseline central subfield thickness was -247.8 +/- 207.5 mum in the PRN g

239 n postoperative day 4, the mean (SD) central subfield thickness was 309 (78) microm in the 6 eyes wit

240 Mean central subfield thickness was 325 mum.

241 coherence tomography (OCT)-measured central subfield thickness was 678 mum (range, 300-1203 mum), an

242 nibizumab at baseline and monthly if central subfield thickness was greater than 275 mum.

243 A significant reduction in mean central subfield thickness was observed in both groups at all st

244 The mean central retinal subfield thickness was significantly higher in IMU (368.

245 Change in central subfield thickness was the primary outcome measure.

246 st-corrected visual acuity (BCVA) and center subfield thickness were measured every 4 weeks.

247 edema improvement (>20% reduction in central subfield thickness) and resolution (reduction of central

248 ab, 0.5 mg, if foveal thickness (FTH, center subfield thickness) was 250 mum or greater.

249 baseline center-involved DME (SD-OCT central subfield thickness, >/= 320 microm for men and >/= 305 m

250 Evaluation of central retinal subfield thickness, 3 mm and 6 mm perifoveal rings was p

251 ary outcomes included visual acuity, central subfield thickness, and adverse events.

252 ere visual acuity, optical coherence central subfield thickness, and number of injections through 5 y

253 cluded best-corrected visual acuity, central subfield thickness, and rates of macular edema improveme

254 Central subfield thickness, maximum subretinal fluid height, and

255 int thickness of central fovea, central 1-mm subfield thickness, the occurrence of intraretinal cysts

256 ratory flow rate were associated with center subfield thickness.

257 erence tomography of 2 eyes revealed central subfield thicknesses of 909 and 873 microm.

258 At 6 months of follow-up the mean central subfield thicknesses were: eyes without an epiretinal me

259 Postmortem hippocampal subfield tissue (CA3, CA1) from subjects with schizophre

260 amined macular fields other than the central subfield to determine if they are possibly independent i

261 ctural magnetic resonance imaging data of HC subfields to behavioral memory performance in children a

262 the differential contribution of hippocampal subfields to compromised learning and memory in humans.

263 We also correlated these subfields to macro-anatomical landmarks, which are visib

264 ging to characterize human auditory cortical subfields using a variety of low-level acoustic features

265 prior episodes, current stress, hippocampal subfield volume and cortical thickness.

266 We also demonstrated that hippocampal subfield volume reduction was associated with the progre

267 Hippocampal subfield volume reductions are found in patients with sc

268 fields of the hippocampus and to measure the subfield volume trajectories over the course of the illn

269 ion between chronic pain and hippocampal and subfield volume using linear regression.

270 decreased dentate gyrus volume, and no other subfield volume, mediates adverse effects of aging on me

271 examine the relationship between hippocampal subfield volumes and chronic pain in nondemented older a

272 ate the link between the in vivo hippocampal subfield volumes and specific mood disorders, such as bi

273 ho sequences at 4.7 T to compare hippocampal subfield volumes at .09 muL voxel volume.

274 ver time, a greater decline in bilateral CA1 subfield volumes was found in the subgroup of UHR subjec

275 Hippocampal subfield volumes were estimated using FreeSurfer softwar

276 Hippocampal subfield volumes were estimated with FreeSurfer.

277 xplore diagnostic differences in hippocampal subfield volumes, covarying for age, intracranial volume

278 ed with the volume of any of the hippocampal subfield volumes.

279 has previously been insufficient to measure subfield volumes.

280 Using 3 T MR hippocampal subfield volumetry combined with a behavioural pattern s

281 lusion of these eyes the revised CR for this subfield was 13.7 mum (95% CI 13.3-14.1 mum).

282 ar thickness (CMT) in the central 1-mm ETDRS subfield was 264.5 (22.9) mum, with 95% confidence limit

283 of repeatability (CR) of the central macular subfield was 30.6 mum (95% confidence interval [CI] 29.8

284 The hippocampal CA2 subfield was initially identified by Lorente de No as an

285 Of note, macular thickness in other subfields was negatively correlated with older age and g

286 ent synaptic plasticity in other hippocampal subfields, we speculated that the metabotropic glutamate

287 in volumes of the overall hippocampus or its subfields were found among the groups.

288 e cross-sectional volume deficits across all subfields were found in the more chronic and ill schizop

289 Hippocampal subfields were manually segmented from 600mum isotropic

290 hat among the mood disorders the hippocampal subfields were more affected in BD-I compared with BD-II

291 Medial temporal lobe and hippocampal subfields were quantified with an automated parcellation

292 Smaller volumes across the hippocampal subfields were seen in all 3 psychotic disorders, with t

293 inal thickness measurements in all 9 macular subfields were significantly lower (<40 mum) in the affe

294 ior outer, inferior outer and temporal outer subfields were statistically significant (p = 0.038, p =

295 me deficits in the CA1, but not of the other subfields, were found in the schizophrenia patients of D

296 y, and mean diffusivity increases across all subfields, whereas TLE-G presented with dentate gyrus hy

297 d MS hippocampi, mainly in the CA3/2 and CA1 subfields, which also showed a marked decrease in synapt

298 One subfield whose function is poorly known is the subiculum

299 aging that combined volumetry of hippocampal subfields with analysis of hippocampal microstructural i

300 ferential phase relationships of hippocampal subfields within the overall theta rhythm enable a power