ライフサイエンスコーパス: fasciculus

1 n and the processing of reward (the uncinate fasciculus).

2 teral anterior forceps, and inferior-frontal fasciculus).

3 he dorsal pathway underpinned by the arcuate fasciculus).

4 and approximately 1.5 (superior longitudinal fasciculus).

5 of g and working memory include the arcuate fasciculus.

6 rticospinal tracts and superior longitudinal fasciculus.

7 capsule and the right superior longitudinal fasciculus.

8 ine the fractional anisotropy of the arcuate fasciculus.

9 ffusivity in the right superior longitudinal fasciculus.

10 ate cortex and the amygdala via the uncinate fasciculus.

11 or corona radiata, and superior longitudinal fasciculus.

12 uperior longitudinal fasciculus and uncinate fasciculus.

13 s the anterior cingulum, fornix and uncinate fasciculus.

14 he fiber bundle of the superior longitudinal fasciculus.

15 tegrity) in the cingulum bundle and uncinate fasciculus.

16 rpus callosum and inferior frontal-occipital fasciculus.

17 and the right temporal inferior longitudinal fasciculus.

18 longitudinal fasciculus, but not the arcuate fasciculus.

19 sociation tracts, most commonly the uncinate fasciculus.

20 eak in the right-sided superior longitudinal fasciculus.

21 s and superior and inferior fronto-occipital fasciculus.

22 to the anterior segment of the left arcuate fasciculus.

23 ipital fasciculus, and inferior longitudinal fasciculus.

24 ht arcuate fasciculus, and the left uncinate fasciculus.

25 b of the internal capsule and right uncinate fasciculus.

26 reduced structural integrity of the uncinate fasciculus.

27 pocampal commissure, and medial longitudinal fasciculus.

28 al tract, and left inferior fronto-occipital fasciculus.

29 rtico-spinal tract and superior longitudinal fasciculus.

30 w, within, and above the medial longitudinal fasciculus.

31 lateral areas were connected via the arcuate fasciculus.

32 ic radiations, and the superior longitudinal fasciculus.

33 culus, superior corona radiata, and uncinate fasciculus.

34 e parahippocampal cingulum, and the uncinate fasciculus.

35 beta = .142, q = .026) in the right uncinate fasciculus.

36 the limbic system, particularly the uncinate fasciculus.

37 cted by the white matter of the left arcuate fasciculus.

38 e fasciculus and right inferior longitudinal fasciculus.

39 m were primarily associated with the arcuate fasciculus.

40 the arcuate or the inferior-fronto-occipital fasciculus.

41 l fasciculus, and left inferior longitudinal fasciculus.

42 tropy of the right inferior fronto-occipital fasciculus.

43 rontal cortex via forceps minor and uncinate fasciculus; 2) rostral and dorsal cingulate cortex via t

44 ate fasciculus and the inferior longitudinal fasciculus, a control tract that we hypothesized was not

45 well as on the integrity of the left arcuate fasciculus, a fiber bundle linking the posterior suprate

46 Our study focused on the arcuate fasciculus, a language pathway composed of three segment

47 ity lies along the inferior fronto-occipital fasciculus, a large intrahemispheric association pathway

48 yed development of the inferior longitudinal fasciculus, a prominent occipitotemporal fiber.

49 ition, tractography analysis of the uncinate fasciculus, a tract associated with semantic processing

50 iction model also included the left uncinate fasciculus, a white matter tract connecting the middle a

51 greater structural integrity of the uncinate fasciculus, a white matter tract that connects the amygd

52 hat the anterior segment of the left arcuate fasciculus, a white matter tract that lies deep to poste

53 eg, corona radiata and inferior longitudinal fasciculus) across all individuals, regardless of diagno

54 is revealed that involvement of the uncinate fasciculus adjudicated between Broca's and global aphasi

55 We focused on the arcuate fasciculus (AF) and inferior longitudinal fasciculus (IL

56 Most researchers agree that the arcuate fasciculus (AF) is the neuroanatomical correlate of the

57 demonstrated in the strength of the arcuate fasciculus (AF), a fiber pathway interlinking the left-h

58 ), parahippocampal WM bundle (PWMB), arcuate fasciculus (AF), inferior longitudinal fasciculus (ILF),

59 l and temporal cortex) by way of the arcuate fasciculus (AF).

60 The uncinate fasciculus also is a conduit for vPFC fibers to reach ot

61 ven fibre pathways-the superior longitudinal fasciculus and arcuate fasciculus, the uncinate fascicul

62 at were observed throughout the left arcuate fasciculus and associated with age-related differences i

63 e relatively increased superior longitudinal fasciculus and cerebellar FA in men may reflect their in

64 hese findings suggest that abnormal uncinate fasciculus and cingulum WM structure may underlie emotio

65 e x FA in left corpus callosum, longitudinal fasciculus and corona radiata were independent contribut

66 ffusivity of the right superior longitudinal fasciculus and heritable aspects of the default mode net

67 ulate, anterior thalamic radiation, uncinate fasciculus and hippocampal portion of the cingulum bundl

68 fronto-occipital fasciculus and the uncinate fasciculus and in the left parietal regions that include

69 ngitudinal fasciculus, inferior longitudinal fasciculus and inferior fronto-occipital fasciculus-that

70 MWF in the left inferior fronto-occipital fasciculus and inferior longitudinal fasciculus was posi

71 white-matter index for the fornix, uncinate fasciculus and inferior longitudinal fasciculus, show di

72 circuitry that is connected by the uncinate fasciculus and is critical in the regulation of mood and

73 beled fibers were distributed in the cuneate fasciculus and lateral funiculus.

74 ificant increase in FA in bilateral uncinate fasciculus and right inferior longitudinal fasciculus.

75 from the JHU ICBM atlas, including uncinate fasciculus and sagittal stratum as a control tract, were

76 r white matter tracts: superior longitudinal fasciculus and superior and inferior fronto-occipital fa

77 eases of MD in the superior fronto-occipital fasciculus and superior longitudinal fasciculus between

78 ificantly lower in the inferior longitudinal fasciculus and superior longitudinal fasciculus in all p

79 rostructure were calculated for the uncinate fasciculus and the inferior longitudinal fasciculus, a c

80 ocated between the inferior fronto-occipital fasciculus and the uncinate fasciculus and in the left p

81 le temporal gyrus, inferior fronto-occipital fasciculus and uncinate fasciculus, while exhibiting les

82 us callosum, posterior superior longitudinal fasciculus and uncinate fasciculus.

83 orona radiata, and superior fronto-occipital fasciculus) and cortical gray matter (in medial frontal

84 attention control (inferior fronto-occipital fasciculus) and emotion regulation and the processing of

85 cortex (via forceps minor and left uncinate fasciculus) and to the cingulate cortex (via left cingul

86 ndicated that both dorsally located (arcuate fasciculus) and ventrally located (inferior frontal-occi

87 nnectivity of the amygdala, fornix, uncinate fasciculus, and cingulum was assessed using fractional a

88 losum, corona radiata, superior longitudinal fasciculus, and corticospinal tracts.

89 regulation circuitry (ie, cingulum, uncinate fasciculus, and forceps minor) and (1) broader diagnosti

90 (beta = .149, q = .012) in the left uncinate fasciculus, and higher axial diffusivity (beta = .142, q

91 corona radiata, right superior longitudinal fasciculus, and in a left cluster including the posterio

92 rcuate fasciculus, inferior fronto-occipital fasciculus, and inferior longitudinal fasciculus.

93 alamic radiations, inferior fronto-occipital fasciculus, and inferior temporal and superior orbital g

94 al splenium, right inferior fronto-occipital fasciculus, and left fornix crus (six studies; 323 voxel

95 halamic radiate, right superior longitudinal fasciculus, and left inferior longitudinal fasciculus.

96 hippocampus, left inferior fronto-occipital fasciculus, and splenium of the corpus callosum compared

97 tal fasciculus (IFOF), inferior longitudinal fasciculus, and superior longitudinal fasciculus (SLF).

98 r longitudinal fasciculus, the right arcuate fasciculus, and the left uncinate fasciculus.

99 ft arcuate fasciculus, inferior longitudinal fasciculus, and the parietal portion of the superior lon

100 um, temporal cingulum, superior longitudinal fasciculus, arcuate fasciculus, inferior fronto-occipita

101 anterior segment) connections of the arcuate fasciculus are left and right lateralized, respectively,

102 rior part of right inferior fronto-occipital fasciculus are putative neurocognitive endophenotypes in

103 emisphere tracts (e.g. superior longitudinal fasciculus) are also present in younger children who stu

104 dered language pathways, such as the arcuate fasciculus, are now argued to be domain-general rather t

105 Using the arcuate fasciculus as an example of discontinuity in the evoluti

106 , ventral amygdalofugal pathway and uncinate fasciculus) as well as the internal and external capsule

107 otropy values in the left and right uncinate fasciculus, as measured by tract-based analysis for diff

108 branches of the right superior longitudinal fasciculus, as well as in the splenium of the corpus cal

109 xtensive lesion of the contralateral cuneate fasciculus at C5-C6.

110 , a complete but lower lesion of the cuneate fasciculus at C8 produced some abnormalities in the reac

111 In the uncinate fasciculus, autistic individuals who decreased in autism

112 also found in the left superior longitudinal fasciculus (beta = -0.194, pcorrected = 0.025), superior

113 nd volume of the long segment of the arcuate fasciculus [beta = 0.730, t(2.732), P = 0.020] were pred

114 cipital fasciculus and superior longitudinal fasciculus between scans correlating with greater improv

115 ona radiata, bilateral superior longitudinal fasciculus, bilateral fornix (cres)/stria terminalis, ge

116 omplete lesions of the contralateral cuneate fasciculus, but afferents from the digits may not contri

117 cluding the middle and superior longitudinal fasciculus, but not the arcuate fasciculus.

118 ly correlated with the volume of the arcuate fasciculus, but not with other tracts.

119 left arcuate and left inferior longitudinal fasciculus, children with above-average reading skills i

120 hite matter bundles (forceps minor, uncinate fasciculus, cingulum and fronto-striatal fibers).

121 he anterior and long segments of the arcuate fasciculus, cingulum and uncinate--predominantly in the

122 the GNW network (inferior frontal-occipital fasciculus, cingulum, and corpus callosum).

123 ngitudinal fasciculus, superior longitudinal fasciculus, cingulum, and uncinate underlie these associ

124 culi, and in the right inferior longitudinal fasciculus compared with control subjects (P < .05).

125 mised white-matter integrity of the uncinate fasciculus connecting the insula with the amygdala and o

126 sures from the three segments of the arcuate fasciculus connecting Wernicke's to Broca's region (i.e.

127 The arcuate fasciculus, connecting both of them, was most severely a

128 C efferent axons travel through the uncinate fasciculus, connecting different vPFC regions and linkin

129 inly located in the corona radiata, uncinate fasciculus, corpus callosum, optic radiation, internal a

130 eased risk taking and reduced FA in uncinate fasciculus correlated significantly with increased risk

131 Conversely, damage to the uncinate fasciculus correlated with deficits in semantic processi

132 of the ventral stream and the corticospinal fasciculus, depicting a gradual reorganisation of these

133 that developmental sculpting of the arcuate fasciculus determines acquisition, storage, and access o

134 ciculus or a small percentage of the cuneate fasciculus did not produce changes in the gross hand rep

135 trahemispheric pathways included the arcuate fasciculus (dorsal language pathway) and uncinate fascic

136 ected white matter reductions in the arcuate fasciculus (dorsal language stream) bilaterally, but not

137 ciculus and arcuate fasciculus, the uncinate fasciculus, extreme capsule, middle longitudinal fascicu

138 culus (dorsal language pathway) and uncinate fasciculus/extreme capsule (ventral language pathway).

139 understand whether the reduction in uncinate fasciculus FA exists in children with anxiety disorders

140 ders have significant reductions in uncinate fasciculus FA.

141 had the greatest change within left uncinate fasciculus (FA: -7.9%/yr, p < 0.001; MD: 10.9%/yr, p < 0

142 gray matter structures, namely, the uncinate fasciculus, fornix, and ventral prefrontal tract, showed

143 atter structural alterations in the uncinate fasciculus, fornix, and ventral prefrontal tract: tracts

144 ivity of the right inferior fronto-occipital fasciculus (genetic correlation, rhog = -0.45, P = .02).

145 ity during infancy presaged greater uncinate fasciculus GFA in children 9-11 years of age (n = 69, 29

146 c radiations, and left superior longitudinal fasciculus (>2,000 voxels) were observed.

147 The left arcuate fasciculus had decreased fractional anisotropy, particul

148 Although abnormalities in the uncinate fasciculus have been associated with several psychiatric

149 the cerebellum and the superior longitudinal fasciculus have not previously been noted.

150 cingulum bundle and inferior frontooccipital fasciculus (IFOF) was associated with higher executive f

151 fic WM tracts: the inferior fronto-occipital fasciculus (IFOF), inferior longitudinal fasciculus, and

152 cture integrity of inferior fronto-occipital fasciculus (IFOF).

153 SLF I-III) and the inferior fronto-occipital fasciculus (IFOF).

154 l anisotropy values in superior longitudinal fasciculus II/III for subacute patients and in its cauda

155 increased in the right inferior longitudinal fasciculus (ILF) (P = .0008).

156 te fasciculus (AF) and inferior longitudinal fasciculus (ILF) as fiber tracts that connect regions al

157 cuate fasciculus (AF), inferior longitudinal fasciculus (ILF), uncinate fasciculus (UF) and cingulum

158 n one tract, the right inferior longitudinal fasciculus (ILF).

159 orm, and reduced FA in inferior longitudinal fasciculus (ILF).

160 along a segment of the inferior longitudinal fasciculus (ILF).

161 Microstructure of inferior longitudinal fasciculus (ILF, connecting occipital and ventro-anterio

162 erstanding how lateralization of the arcuate fasciculus impacts on severity of symptoms and their rec

163 tudinal fasciculus and superior longitudinal fasciculus in all patients compared with all healthy vol

164 rols, structural terminations of the arcuate fasciculus in inferior frontal gyrus were indistinguisha

165 or corona radiata, and superior longitudinal fasciculus in remitted vs persistent PTSD patients.

166 am accounts that deny a role for the arcuate fasciculus in semantic processing, and for ventral-strea

167 and further confirm the role of the uncinate fasciculus in semantic processing.

168 al degeneration of the superior longitudinal fasciculus in the executive control network better expla

169 ues, the authors assessed FA in the uncinate fasciculus in unmedicated boys and girls with anxiety di

170 reased axial diffusivity within the uncinate fasciculus in youth with emotional DDs vs those with beh

171 is represented directly beneath the cuneate fasciculus, in a region devoid of barrelettes.

172 ere dorsal tracts--the superior longitudinal fasciculus including its arcuate component--was strongly

173 al awareness and right superior longitudinal fasciculus (including arcuate fasciculus) white-matter o

174 t WM differences bilaterally in the uncinate fasciculus (increased fractional anisotropy in the right

175 anisotropy values in the bilateral uncinate fasciculus indicated reduced frontolimbic structural con

176 m, superior longitudinal fasciculus, arcuate fasciculus, inferior fronto-occipital fasciculus, and in

177 iculus, extreme capsule, middle longitudinal fasciculus, inferior longitudinal fasciculus and inferio

178 nd white matter organization in left arcuate fasciculus, inferior longitudinal fasciculus, and the pa

179 The bidirectionality of the uncinate fasciculus information flow allows orbital frontal corte

180 fied a negative correlation between uncinate fasciculus integrity and subgenual ACC functional connec

181 This reduction in uncinate fasciculus integrity was most pronounced for patients wi

182 n the cingulum bundle, superior longitudinal fasciculus, internal capsule, and splenium of the corpus

183 The uncinate fasciculus is a bidirectional, long-range white matter t

184 The arcuate fasciculus is a central connection in this architecture,

185 suggested that lateralization of the arcuate fasciculus is a heterogeneous process that depends on th

186 ose that an overarching role of the uncinate fasciculus is to allow temporal lobe-based mnemonic asso

187 e fasciculus, left inferior fronto-occipital fasciculus, left cerebral peduncle, posterior thalamic r

188 left and right corona radiata, left uncinate fasciculus, left inferior fronto-occipital fasciculus, l

189 hemisphere stroke patients without uncinate fasciculus lesions in the emotional empathy task.

190 Participants with right uncinate fasciculus lesions were significantly more impaired than

191 corpus callosum (CC), superior longitudinal fasciculus (LF), corona radiata (CR), internal capsule (

192 cabulary knowledge are influenced by arcuate fasciculus macrostructure (i.e., shape and volume) prope

193 icrostructure in the fornix and the uncinate fasciculus make critical but differential contributions

194 al PNSE was associated with altered uncinate fasciculus microstructure in offspring.

195 In contrast, a decline in uncinate fasciculus microstructure was linked to impaired error m

196 ally that lesions of the medial longitudinal fasciculus (MLF) and the medial vestibular nucleus are a

197 oneer neurons but on the medial longitudinal fasciculus (MLF), a bundle of axons lying ventral to the

198 axons course through the medial longitudinal fasciculus (MLF), and neurons in the lateral vestibular

199 -17, -78, 6), left inferior fronto-occipital fasciculus ( MNI Montreal Neurological Institute coordin

200 However, atypical patterns of arcuate fasciculus morphology or macrostructure were associated

201 We tested the hypothesis that arcuate fasciculus morphology, which supports the development of

202 ed in the nucleus of the medial longitudinal fasciculus (NMLF) and entopeduncular nucleus (EN), respe

203 ctum, the nucleus of the medial longitudinal fasciculus (nMLF) and the hindbrain.

204 ns of the nucleus of the medial longitudinal fasciculus (nMLF) to dissect their contribution to contr

205 le of the nucleus of the medial longitudinal fasciculus (nMLF), a small group of reticulospinal neuro

206 that deterioration of tissue in the arcuate fasciculus occurs with normal aging, while having limite

207 luent/agrammatic variant and in the uncinate fasciculus of patients with the semantic variant.

208 The superior fasciculus of the accessory optic tract, which innervate

209 Lesions that damaged only the gracile fasciculus or a small percentage of the cuneate fascicul

210 were found for the inferior-fronto-occipital fasciculus or the arcuate.

211 not related to abnormalities of the arcuate fasciculus (or its subsegments), but was associated with

212 ation, FA was increased in the right arcuate fasciculus (P = .0015), and in right-handers, FA was als

213 onal anisotropy in the superior longitudinal fasciculus (P = .006), white matter around the nucleus a

214 ze [d] = 0.34) and the inferior longitudinal fasciculus (P = .03; d = 0.17).

215 by genotype interaction within the uncinate fasciculus (P0.05), with BD subjects carrying the T (ris

216 ean diffusivity of the superior longitudinal fasciculus, particularly the premotor components.

217 The human arcuate fasciculus pathway is crucial for language, interconnect

218 The right uncinate fasciculus plays an important role in the emotional empa

219 right corpus callosum, superior longitudinal fasciculus, posterior thalamic radiation, and corona rad

220 iata, corpus callosum, superior longitudinal fasciculus, posterior thalamic radiations, and sagittal

221 t aphasia, such as the superior longitudinal fasciculus, precentral, inferior frontal, supramarginal

222 properties of the left inferior-longitudinal fasciculus predict contextual learning, whereas the left

223 rom fMRI(LI) and optic radiation and arcuate fasciculus probabilistic tractography was performed for

224 = -0.66, P = .01) and superior longitudinal fasciculus (r = -0.65, P = .05).

225 tions of the right inferior fronto-occipital fasciculus (reduced radial diffusivity in approximately

226 ract, although the integrity of the uncinate fasciculus remained unchanged.

227 l diffusivity in the left [P = .01] uncinate fasciculus, respectively).

228 entral, and parateanial thalamic nuclei, the fasciculus retroflexus of Meynert, basolateral and basom

229 medial habenula (MHb), its output tract, the fasciculus retroflexus, and its principal target, the in

230 t this effect is prevented by lesions of the fasciculus retroflexus, the principal output pathway of

231 lencephalon, relayed by the habenula via the fasciculus retroflexus.

232 a primate auditory prototype for the arcuate fasciculus, reveals an earlier phylogenetic origin and i

233 ropy (FA) was lower within the left uncinate fasciculus, right caudate and occipital regions (p < 0.0

234 tral pathway); and the superior longitudinal fasciculus segmented into its frontosupramarginal, front

235 onally introduced the left and right arcuate fasciculus (separate analysis for each segment).

236 ncinate fasciculus and inferior longitudinal fasciculus, show differential contributions to the three

237 ntials elicited from the medial longitudinal fasciculus significantly increased in average size after

238 three branches of the superior longitudinal fasciculus (SLF I-III) and the inferior fronto-occipital

239 lusters located in the superior longitudinal fasciculus (SLF) when compared with the psychiatric and

240 related changes in the superior longitudinal fasciculus (SLF), are responsible for the deterioration

241 alamic radiation (TR), superior longitudinal fasciculus (SLF), corpus callosum (CC), and corticospina

242 udinal fasciculus, and superior longitudinal fasciculus (SLF).

243 nix, left fimbria, and superior longitudinal fasciculus (SLF).

244 weeks after complete lesions of the cuneate fasciculus subserving the forelimb at cervical levels 5-

245 e measured in the following tracts: uncinate fasciculus, superior cingulum, temporal cingulum, superi

246 tudinal fasciculi, inferior fronto-occipital fasciculus, superior corona radiata, and uncinate fascic

247 microstructure in the inferior longitudinal fasciculus, superior longitudinal fasciculus, cingulum,

248 strongly for the right superior longitudinal fasciculus (t = -3.05; P = .003).

249 xtreme capsule and the inferior longitudinal fasciculus, that mediated auditory comprehension.

250 nal fasciculus and inferior fronto-occipital fasciculus-that have been proposed to support language i

251 perior longitudinal fasciculus, the uncinate fasciculus, the forceps minor, and in the genu and splen

252 integrity, has been observed in the uncinate fasciculus, the major tract that connects limbic and pre

253 We focused on the uncinate fasciculus, the primary fiber bundle connecting the amyg

254 d structural integrity in the right uncinate fasciculus, the primary white matter connection between

255 controls at the right inferior longitudinal fasciculus, the right arcuate fasciculus, and the left u

256 superior longitudinal fasciculus and arcuate fasciculus, the uncinate fasciculus, extreme capsule, mi

257 spinal tract, the left superior longitudinal fasciculus, the uncinate fasciculus, the forceps minor,

258 gical word forms is supported by the arcuate fasciculus, these findings demonstrate that learning new

259 ogical word forms is mediated by the arcuate fasciculus, these findings show that the temporal pathwa

260 We found the left inferior-longitudinal fasciculus to be predictive of word-learning success in

261 ffusivity of the right superior longitudinal fasciculus to h2 = 0.46 (SE, 0.15; P = .0009) for fracti

262 ctography of the right inferior longitudinal fasciculus together with a data-driven multivoxel patter

263 resent in association fibers of the uncinate fasciculus (UF) and cingulum bundle (CB) among MDD subje

264 rior longitudinal fasciculus (ILF), uncinate fasciculus (UF) and cingulum bundle (CB).

265 ficantly decreased FA values in the uncinate fasciculus (UF) bilaterally (mean FA, 0.425; 95% confide

266 n structural characteristics of the uncinate fasciculus (UF) measured by Diffusion Tensor Imaging (DT

267 d fractional anisotropy (FA) of the uncinate fasciculus (UF) were considered.

268 hildren suggests alterations in the uncinate fasciculus (UF), the white matter tract that connects pr

269 This demonstrates that the arcuate fasciculus underwent additional evolutionary modificatio

270 we quantified the integrity of the uncinate fasciculus using generalized fractional anisotropy (GFA)

271 arietal portion of the superior longitudinal fasciculus using probabilistic tractography.

272 ly, but not in the inferior fronto-occipital fasciculus (ventral language stream) nor in primary moto

273 llum; white matter integrity in the uncinate fasciculus, ventral frontal, and right cerebellum region

274 The vertical occipital fasciculus (VOF) is the only major fiber bundle connecti

275 between language lateralisation and arcuate fasciculus volume.

276 uded, of which the integrity of the uncinate fasciculus was assessed that connects the subgenual ante

277 in left corpus callosum, or in longitudinal fasciculus was associated with MCCB mazes and Trail Maki

278 gh fractional anisotropy of the left arcuate fasciculus was decreased in autistic children relative t

279 tum, uncinate, and inferior fronto-occipital fasciculus was found in both HS-TLE and MRI-neg TLE, sug

280 , but only percentage damage to the uncinate fasciculus was independently associated with error rate.

281 cipital fasciculus and inferior longitudinal fasciculus was positively associated with intelligence q

282 onal anisotropy of the inferior longitudinal fasciculus was positively associated with psychomotor sp

283 that white matter integrity of the uncinate fasciculus was reduced and that functional connectivity

284 Fractional anisotropy in the left arcuate fasciculus was significantly related to individual varia

285 extreme capsule fiber system or the uncinate fasciculus--was not associated with syntactic deficits.

286 from damage along the superior longitudinal fasciculus were associated with both types of neglect an

287 ract and the anterior segment of the arcuate fasciculus were particularly engaged with the quantity a

288 hippocampal white matter bundle and uncinate fasciculus were reconstructed, and scalar diffusion metr

289 pyramidal tract and the medial longitudinal fasciculus were recorded and compared with control respo

290 rtion of the right inferior fronto-occipital fasciculus were shared between ADHD probands and their u

291 ting neocortical areas, such as the uncinate fasciculus, were observed only in schizophrenia.

292 (IQ) in the right inferior fronto-occipital fasciculus when both sexes were looked at together.

293 m, and the anterior part of the left arcuate fasciculus when controlling for age, sex, and acquisitio

294 hese findings indicate that the left arcuate fasciculus, which connects anterior and posterior langua

295 rtion of the left inferior frontal-occipital fasciculus, which projects between frontal and occipital

296 ior fronto-occipital fasciculus and uncinate fasciculus, while exhibiting lesions in areas typically

297 These findings provide evidence of uncinate fasciculus white matter alterations in boys with anxiety

298 r longitudinal fasciculus (including arcuate fasciculus) white-matter organization significantly pred

299 ciated with higher integrity of the uncinate fasciculus with no effect on a second corticolimbic path

300 matter and in the left superior longitudinal fasciculus; women had higher FA in the corpus callosum,