ライフサイエンスコーパス: fasciculus

1 he dorsal pathway underpinned by the arcuate fasciculus).

2 and approximately 1.5 (superior longitudinal fasciculus).

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

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

5 e fasciculus and right inferior longitudinal fasciculus.

6 he fiber bundle of the superior longitudinal fasciculus.

7 tegrity) in the cingulum bundle and uncinate fasciculus.

8 rpus callosum and inferior frontal-occipital fasciculus.

9 and the right temporal inferior longitudinal fasciculus.

10 sociation tracts, most commonly the uncinate fasciculus.

11 eak in the right-sided superior longitudinal fasciculus.

12 s and superior and inferior fronto-occipital fasciculus.

13 to the anterior segment of the left arcuate fasciculus.

14 ipital fasciculus, and inferior longitudinal fasciculus.

15 ht arcuate fasciculus, and the left uncinate fasciculus.

16 b of the internal capsule and right uncinate fasciculus.

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

18 reduced structural integrity of the uncinate fasciculus.

19 pocampal commissure, and medial longitudinal fasciculus.

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

21 rtico-spinal tract and superior longitudinal fasciculus.

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

23 lateral areas were connected via the arcuate fasciculus.

24 ic radiations, and the superior longitudinal fasciculus.

25 l fasciculus, and left inferior longitudinal fasciculus.

26 culus, superior corona radiata, and uncinate fasciculus.

27 e parahippocampal cingulum, and the uncinate fasciculus.

28 in the posterior portion of the left arcuate fasciculus.

29 of the fronto-parietal superior longitudinal fasciculus.

30 and transverse in the inferior longitudinal fasciculus.

31 onal anisotropy in the inferior longitudinal fasciculus.

32 nificantly decreased FA in the left uncinate fasciculus.

33 mmissure, corpus callosum and right uncinate fasciculus.

34 , extreme capsule, and inferior longitudinal fasciculus.

35 en memory performance and FA in the uncinate fasciculus.

36 mance and FA in a ROI placed in the uncinate fasciculus.

37 erstitial nucleus of the medial longitudinal fasciculus.

38 tropy of the right inferior fronto-occipital fasciculus.

39 rticospinal tracts and superior longitudinal fasciculus.

40 capsule and the right superior longitudinal fasciculus.

41 ffusivity in the right superior longitudinal fasciculus.

42 ate cortex and the amygdala via the uncinate fasciculus.

43 or corona radiata, and superior longitudinal fasciculus.

44 uperior longitudinal fasciculus and uncinate fasciculus.

45 s the anterior cingulum, fornix and uncinate fasciculus.

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

47 k and integrity of the superior longitudinal fasciculus (a primary fronto-parietal connection) shared

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

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

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

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

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

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

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

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

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

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

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

59 age impairment due to lesions of the arcuate fasciculus (AF) that disconnect receptive language areas

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

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

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

63 and production are connected by the arcuate fasciculus (AF).

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

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

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

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

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

69 m the temporal lobe, the middle longitudinal fasciculus and from rostral to caudal, the uncinate fasc

70 ft inferior longitudinal fasciculus, arcuate fasciculus and fronto-parietal superior longitudinal fas

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

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

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

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

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

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

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

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

79 -occipital fasciculus, superior longitudinal fasciculus and sagittal stratum.

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

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

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

83 The left uncinate fasciculus and the genu and splenium of the corpus callo

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

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

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

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

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

89 r fronto-occipital tract, superior occipital fasciculus, and anterior thalamic radiation for the hear

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

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

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

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

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

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

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

99 tter, corpus callosum, superior longitudinal fasciculus, and white matter core of the temporal lobe.

100 l-temporal region, the inferior longitudinal fasciculus; and from the cingulate gyrus, the cingulum b

101 The left inferior longitudinal fasciculus, arcuate fasciculus and fronto-parietal super

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

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

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

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

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

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

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

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

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

111 nterior portion of the superior longitudinal fasciculus (aSLF), a pathway connecting parietal and fro

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

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

114 nted for two years by section of the cuneate fasciculus at the C1 level, there was extensive withdraw

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

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

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

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

119 s major (bilaterally), inferior longitudinal fasciculus (bilaterally), and the genu and splenium of t

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

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

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

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

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

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

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

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

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

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

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

135 lus and from rostral to caudal, the uncinate fasciculus, extreme capsule and arcuate fasciculus; from

136 culus, fronto-occipital fasciculus, uncinate fasciculus, extreme capsule, and inferior longitudinal f

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 f correlation between attention and uncinate fasciculus FA and the lack of correlation between memory

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

141 , sagittal stratum and superior longitudinal fasciculus for the mild TBI group.

142 nate fasciculus, extreme capsule and arcuate fasciculus; from the occipital-temporal region, the infe

143 ipital-parietal region, the fronto-occipital fasciculus; from the temporal lobe, the middle longitudi

144 ite matter tracts: the superior longitudinal fasciculus, fronto-occipital fasciculus, uncinate fascic

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

146 i in the anterior columns, and the bilateral fasciculus gracilis and cuneatus in the posterior column

147 alities and massive axon degeneration in the fasciculus gracilis of mutant animals, as indicated by u

148 P <or= .05 corrected) in the right uncinate fasciculus (greater radial diffusivity).

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

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

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

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

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

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

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

156 culus (ILF) and/or inferior fronto-occipital fasciculus (IFOF)] connecting the visual cortex with emo

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

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

159 lower MD in the right inferior longitudinal fasciculus (ILF) and left forceps major (>/=164mul, p<.0

160 ociation fiber tracts [inferior longitudinal fasciculus (ILF) and/or inferior fronto-occipital fascic

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

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

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

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

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

166 higher AD in the right superior longitudinal fasciculus, ILF, and forceps minor (>/= 164mul, p<.01).

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

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

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

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

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

172 t SLF or the bilateral inferior longitudinal fasciculus in WS subjects.

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

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

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

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

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

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

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

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

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

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

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

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

185 optic radiations, superior fronto-occipital fasciculus, internal capsule, callosal isthmus, and the

186 g anteriorly along the superior longitudinal fasciculus into the deep white matter of the frontal lob

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

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

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

190 The arcuate fasciculus is a white-matter fiber tract that is involve

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

192 ociated with involvement of the left arcuate fasciculus, its specific lesion correlate remains elusiv

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

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

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

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

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

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

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

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

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

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

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

204 -17, -78, 6), left inferior fronto-occipital fasciculus ( MNI Montreal Neurological Institute coordin

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

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

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

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

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

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

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

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

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

214 ed in the nucleus of the medial longitudinal fasciculus of the tegmentum.

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

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

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

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

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

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

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

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

223 ystem, in particular the medial longitudinal fasciculus pathway, may be a way to measure body tempera

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

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

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

227 = -0.66, P = .01) and superior longitudinal fasciculus (r = -0.65, P = .05).

228 , P <or= .05 corrected) in the left uncinate fasciculus (reduced radial diffusivity distally and incr

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

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

231 Electrolytic lesions of the fasciculus retroflexus blocked the effects of LHb stimul

232 In Brn3a mutant embryos, the fasciculus retroflexus is directed appropriately, but ha

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

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

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

236 subnuclei and a principal output tract, the fasciculus retroflexus, which together form a link betwe

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

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

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

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

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

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

243 ulum, left Broca's area and the left arcuate fasciculus (similar to previous findings in adult-onset

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

245 as higher in the right superior longitudinal fasciculus (SLF) in WS compared with both control groups

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

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

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

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

250 the parietal lobe, the superior longitudinal fasciculus subcomponents I, II and III; from the occipit

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

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

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

254 e corpus callosum, inferior fronto-occipital fasciculus, superior longitudinal fasciculus and sagitta

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

256 emporal lobe projection of the human arcuate fasciculus that is much smaller or absent in nonhuman pr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

272 The human brain uncinate fasciculus (UF) is an important cortico-cortical white m

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

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

275 babilistically defined tract of the uncinate fasciculus (UF), a WM pathway connecting the amygdala to

276 or longitudinal fasciculus, fronto-occipital fasciculus, uncinate fasciculus, extreme capsule, and in

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

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

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

280 between language lateralisation and arcuate fasciculus volume.

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

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

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

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

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

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

287 The fronto-parietal superior longitudinal fasciculus was relatively spared, with a significant dif

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

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

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

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

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

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

294 us and fronto-parietal superior longitudinal fasciculus were tracked in five semantic dementia patien

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

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

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

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

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

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