ライフサイエンスコーパス: fractional anisotropy

1 rostructural integrity (mean diffusivity and fractional anisotropy).

2 ffects (deletion > control > duplication) on fractional anisotropy.

3 rebrospinal fluid were associated with lower fractional anisotropy.

4 gray matter volume, hippocampal volume, and fractional anisotropy.

5 ec vs [0.9 +/- 0.09] x 10(-3) mm(2)/sec), or fractional anisotropy (0.43 +/- 0.05 vs 0.42 +/- 0.06).

6 95% confidence interval, -25.1 to -2.2) and fractional anisotropy (-0.0073; 95% confidence interval,

7 r in patients with Fabry disease had reduced fractional anisotropy [0.422 (SD 0.022) versus 0.443 (SD

8 Lower fractional anisotropy-a common sign of impaired WM-and s

9 genual structures, with frontal white matter fractional anisotropy abnormalities partially encircling

10 ion, female patients had significantly lower fractional anisotropy across all tracts compared with fe

11 r agreement between diffusion tensor imaging fractional anisotropy across the brain in an individual

12 A positive relation between fractional anisotropy (across much of the brain) and gen

13 ruption in interhemispheric circuitry (i.e., fractional anisotropy alterations in the corpus callosum

14 However, fractional anisotropy alterations may be more widespread

15 g a significant negative association between fractional anisotropy and age in the entire cohort.

16 entify: (i) the relationships between median fractional anisotropy and apathy, depression and cogniti

17 onvolution-based tractography indicated that fractional anisotropy and apparent fiber density in trac

18 age immersion program were best predicted by fractional anisotropy and COMT genotype.

19 increasing age was associated with increased fractional anisotropy and decreased apparent diffusion c

20 tiple regression analyses revealed decreased fractional anisotropy and decreased axial diffusivity wi

21 network by way of increased network density, fractional anisotropy and decreased diffusivities.

22 Increased fractional anisotropy and decreased mean diffusivity in

23 Results showed reduced fractional anisotropy and fewer streamlines in chronic s

24 group demonstrated lower CC integrity (lower fractional anisotropy and higher mean diffusivity) and p

25 3 months post-optic neuritis predicted lower fractional anisotropy and higher radial diffusivity at 1

26 Wolfram patients had lower fractional anisotropy and higher radial diffusivity in m

27 schizophrenia patients tended to have lower fractional anisotropy and lower IQ than healthy particip

28 ne (Val) and Val/Val genotypes showed higher fractional anisotropy and lower radial diffusivity durin

29 ish immersion program correlated with higher fractional anisotropy and lower radial diffusivity in th

30 ve symptoms and white matter microstructure (fractional anisotropy and mean diffusivity [MD]) in the

31 fasciculus, and cingulum was assessed using fractional anisotropy and mean diffusivity and analyzed

32 Syndrome-specific fractional anisotropy and mean diffusivity differences w

33 tics was used to derive skeletonized maps of fractional anisotropy and mean diffusivity for each part

34 also observed limited change in white matter fractional anisotropy and mean diffusivity in 13 players

35 ed that the diffusion abnormalities for both fractional anisotropy and mean diffusivity were anatomic

36 Fractional anisotropy and mean diffusivity were measured

37 Global fractional anisotropy and mean diffusivity were not asso

38 Fractional anisotropy and mean diffusivity were the same

39 We obtained average values of fractional anisotropy and mean diffusivity within the wh

40 s of white matter microstructural integrity (fractional anisotropy and mean diffusivity) and cerebrov

41 umetric and Diffusion Tensor Imaging derived fractional anisotropy and mean diffusivity.

42 by classical diffusion MRI metrics, such as fractional anisotropy and mean diffusivity.

43 ied using tractography to derive measures of fractional anisotropy and mean, axial, and radial diffus

44 Fractional anisotropy and normalized streamlines, an est

45 f diffusion tensor metrics showed widespread fractional anisotropy and radial diffusivity differences

46 pattern of ischemic brain injury (increased fractional anisotropy and reduced radial diffusivity).

47 t with diffusion tensor imaging by measuring fractional anisotropy and the apparent diffusion coeffic

48 ce in an age-independent association between fractional anisotropy and vocabulary.

49 ed abnormal age-related changes with greater fractional anisotropy and volume than normal at younger

50 Within patients, average white matter fractional anisotropy and white matter lesion volume sho

51 wed the most significant correlation between fractional anisotropy and white matter longitudinal atro

52 age-independent negative association between fractional anisotropy and years since most severe blast

53 , we examined the microstructure (indexed by fractional anisotropy) and volume of axon pathways using

54 l measures (free-water (FW) and FW-corrected fractional anisotropy), and functional connectivity of t

55 mong AT, UF microstructure (as measured with fractional anisotropy), and sex.

56 Myofiber helix angle, mean diffusivity, fractional anisotropy, and 3D tractograms were analyzed

57 FPN (i.e., gray matter volume, white matter fractional anisotropy, and intra/internetwork functional

58 using regional grey and white matter volume, fractional anisotropy, and mean diffusivity (MD) analyse

59 tween regional WM structures (WM volume, and fractional anisotropy, and mean diffusivity [MD]), and f

60 Mean diffusivity, fractional anisotropy, and myocyte aggregate orientation

61 bjects with calculation of mean diffusivity, fractional anisotropy, and sheetlet orientation (seconda

62 rity of damage within these connections, (i) fractional anisotropy as a measure for integrity; (ii) t

63 Fractional anisotropy as well as axial and radial diffus

64 global structural connectivity, with higher fractional anisotropy associated with higher IQ.

65 e influence of age on gray matter volume and fractional anisotropy at a whole-brain and voxel level.

66 of diffuse axonal injury, with reductions of fractional anisotropy at baseline and follow-up in large

67 sess white matter integrity, with indices of fractional anisotropy, axial diffusivity, and radial dif

68 ers of brain microstructural integrity (i.e. fractional anisotropy, axial, mean and radial diffusivit

69 -0.17 to -0.03 cm3; P = .006), lower global fractional anisotropy (b = -0.12; 95% CI, -0.24 to -0.01

70 remor relief in ET was associated with lower fractional anisotropy before treatment (R = -0.5; P = .0

71 HCC was associated with higher left amygdala fractional anisotropy (beta = 0.677, p=0.010), lower lef

72 While mean diffusivity and fractional anisotropy brain images were generated from d

73 fect; P = .041) and by PEs being mediated by fractional anisotropy changes in these regions.

74 ime had a slower developmental trajectory of fractional anisotropy compared with individuals whose au

75 rrying the T (risk) allele showing decreased fractional anisotropy compared with other subgroups, ind

76 analysis was used to calculate both a global fractional anisotropy component (gFA) and a fractional a

77 fractional anisotropy component (gFA) and a fractional anisotropy component for six long association

78 Average white matter fractional anisotropy correlated with the overall Mainz

79 ain a voxel-wise statistical analysis of the fractional anisotropy data.

80 We show that fractional anisotropy declined once the subjects finishe

81 er, in participants with multiple sclerosis, fractional anisotropy decreased and mean diffusivity of

82 10-14) as well as a significant whole-brain fractional anisotropy deficit (Cohen d = 0.63; P = 2.20

83 ith the severity of schizophrenia-associated fractional anisotropy deficits in the corresponding whit

84 zophrenia only after age 35, and the rate of fractional anisotropy deterioration with age was constan

85 he diffusion biomarkers mean diffusivity and fractional anisotropy effectively discriminate CA from h

86 In contrast, significant reductions in fractional anisotropy emerged in schizophrenia only afte

87 al diffusivities (RD/AD = 0.40 +/- 0.02) and fractional anisotropy (FA = 0.53 +/- 0.01) differentiate

88 lobal white matter integrity, as measured by fractional anisotropy (FA) (beta = -0.182, p = 0.005).

89 Compared to HCs, patients had increased fractional anisotropy (FA) along with decreased mean dif

90 The primary measure was voxelwise fractional anisotropy (FA) analyzed via tract-based spat

91 , whole brain voxel-wise regressions between fractional anisotropy (FA) and ADHD composite score were

92 Fractional anisotropy (FA) and blood oxygen level-depend

93 gions, normative percentiles of variation in fractional anisotropy (FA) and cortical thickness (CT) w

94 M) volume, white matter (WM) microstructure (fractional anisotropy (FA) and diffusivity), white matte

95 hosis risk symptoms had lower whole-brain WM fractional anisotropy (FA) and higher radial diffusivity

96 ract-specific microstructure was assessed by fractional anisotropy (FA) and mean diffusivity (MD) by

97 Accurate quantification of fractional anisotropy (FA) and mean diffusivity (MD) in

98 e obtained at child's 9-12 years of age, and fractional anisotropy (FA) and mean diffusivity (MD) wer

99 assessed white matter integrity measured by fractional anisotropy (FA) and mean diffusivity (MD) wit

100 Fractional anisotropy (FA) and mean diffusivity images w

101 Fractional anisotropy (FA) and mean diffusivity were der

102 ysis by determination of helical angle (HA), fractional anisotropy (FA) and myocardial disarray index

103 hrough diffusion-weighted imaging, measuring fractional anisotropy (FA) and streamlines.

104 Fractional anisotropy (FA) and the apparent diffusion co

105 brain white matter microstructure indexed by fractional anisotropy (FA) and three broad cognitive dom

106 imes through age 4 months; diffusivities and fractional anisotropy (FA) assessed in 7 white matter tr

107 ith DKI, ADC obtained with DTI (ADCDTI), and fractional anisotropy (FA) at DTI.

108 s as demonstrated by widespread reduction in fractional anisotropy (FA) based on diffusion-weighted i

109 ted up to 2014 to identify studies comparing fractional anisotropy (FA) between patients and control

110 ale participants were evaluated for seasonal fractional anisotropy (FA) changes in specific WM tracts

111 perform voxel-wise statistical comparison of fractional anisotropy (FA) data and computational morpho

112 Over the 2.0-year follow-up interval, global fractional anisotropy (FA) decreased by 0.0042 (P < .001

113 Mean fractional anisotropy (FA) from 43 regions of interest (

114 Amygdala-vPFC pathway fractional anisotropy (FA) from 669 diffusion magnetic r

115 White matter integrity was measured with fractional anisotropy (FA) from diffusion tensor magneti

116 We observed subtle, but widespread, lower fractional anisotropy (FA) in adult MDD patients compare

117 22q11DS patients showed higher mean fractional anisotropy (FA) in callosal and projection fi

118 Purpose To analyze if fractional anisotropy (FA) in nonenhancing peritumoral r

119 und increased cortical volumes and decreased fractional anisotropy (FA) in SAD compared with healthy

120 Significant reductions in fractional anisotropy (FA) in schizophrenia patients wer

121 ia and frontoparietal network with decreased fractional anisotropy (FA) in the right hemisphere and a

122 white matter organization measured by lower fractional anisotropy (FA) in the tapetum region of the

123 t SLF structural connectivity as measured by fractional anisotropy (FA) in the Tenacity group only.

124 the temporal lobes and corpus callosum, and fractional anisotropy (FA) index measurement of the corp

125 Fractional anisotropy (FA) maps of the control participa

126 ose without PTMs on the basis of analysis of fractional anisotropy (FA) maps.

127 In particular, the fractional anisotropy (FA) of auditory and visual system

128 using functional magnetic resonance imaging, fractional anisotropy (FA) of diffusion tensor imaging,

129 EC function was attributed to the fractional anisotropy (FA) of left (correlation was driv

130 ze groups that show a critical difference in fractional anisotropy (FA) of the left and right cingulu

131 Fractional anisotropy (FA) quantifies directionality of

132 ied by significant corticospinal tract (CST) fractional anisotropy (FA) reductions.

133 diffusion tensor imaging (DTI) studies used fractional anisotropy (FA) to investigate disrupted whit

134 s, and cognition with cortical thickness and fractional anisotropy (FA) using general linear models.

135 conduct genome-wide association analysis of fractional anisotropy (FA) value measured using diffusin

136 efore gene therapy revealed lower total mean fractional anisotropy (FA) values in patients than in th

137 nitive Battery (MCCB) and the voxel-wised WM fractional anisotropy (FA) values were examined using DT

138 Fractional anisotropy (FA) was a predictor of neuronal d

139 e values lower than controls (p < 0.05), and fractional anisotropy (FA) was lower within the left unc

140 Fractional anisotropy (FA) was reduced in the PC (-11.98

141 ellar peduncle and frontal white matter) and fractional anisotropy (FA) was used to compute an FA sco

142 Within-subject measures of STN volume and fractional anisotropy (FA) were derived from high-resolu

143 Significant reductions in fractional anisotropy (FA) were detected in the BN compa

144 sor was calculated in each voxel and maps of fractional anisotropy (FA) were generated.

145 al changes of cortical mean kurtosis (MK) or fractional anisotropy (FA) were heterogeneous across the

146 DTI axial diffusivity and fractional anisotropy (FA) were sensitive to axonal inte

147 The sciatic nerve's fractional anisotropy (FA), a marker of structural nerve

148 in adults with anxiety disorders, decreased fractional anisotropy (FA), a measure of white matter in

149 Our main outcome measure was fractional anisotropy (FA), a measure of WM tract integr

150 ed white matter trajectories, as measured by fractional anisotropy (FA), across the course of schizop

151 thickness, subcortical volume, white matter fractional anisotropy (FA), and behavioral measures in 1

152 cross-sectional area (CSA), lateral funiculi fractional anisotropy (FA), and brain GM volume as indep

153 (FFs), T2 relaxation of muscle (T2(water)), fractional anisotropy (FA), and diffusivity (mean, axial

154 regional volumes, global and tract-specific fractional anisotropy (FA), and global mean diffusivity

155 atistics were used to investigate changes in fractional anisotropy (FA), axial diffusivity (AD) and r

156 ing diffusion tensor imaging (DTI) measures: fractional anisotropy (FA), axial diffusivity (AD), and

157 myelin water fraction (MWF), T1w/T2w ratio, fractional anisotropy (FA), axial diffusivity (AD), radi

158 I with apparent diffusion coefficient (ADC), fractional anisotropy (FA), fiber number (FN) and cerebr

159 ow cell, collagen and elastin content effect fractional anisotropy (FA), mean diffusivity (MD) and tr

160 ffusivity (AD) without significant change in fractional anisotropy (FA), mean diffusivity (MD) or rad

161 imaging (n = 300), we compared white matter fractional anisotropy (FA), mean diffusivity (MD), and f

162 Various DTI indices such as Fractional Anisotropy (FA), Mean Diffusivity (MD), Radia

163 data were acquired and analyzed in terms of fractional anisotropy (FA), mean diffusivity (MD), radia

164 The mean and standard deviation of fractional anisotropy (FA), mean diffusivity (MD), radia

165 Baseline fractional anisotropy (FA), mean diffusivity (MD), T2, a

166 We compared whole-brain fractional anisotropy (FA), mean diffusivity, axial diff

167 Voxel-wise correlation analyses of fractional anisotropy (FA), measured with diffusion tens

168 tatistics analytic pipeline to first analyze fractional anisotropy (FA), the most commonly employed m

169 er total gray matter volume and lower global fractional anisotropy (FA), whereas maternal depressive

170 The outcome measure was change in fractional anisotropy (FA), which was assessed in three

171 metastasis and assessed mean diffusivity and fractional anisotropy (FA).

172 OCD < CONT; F([1,87]) = 5.3; P = 0.024) upon fractional anisotropy (FA, a measure of fiber collineari

173 m damage was found in the ablated core (mean fractional anisotropy [FA] at baseline, 0.41 +/- 0.10, a

174 atter tracts, and microstructural integrity (fractional anisotropy, FA) was assessed using tract-base

175 er volume, and white matter tract integrity (fractional anisotropy, FA) within brain regions implicat

176 lume and thickness, and mean diffusivity and fractional anisotropy from co-registered diffusion maps

177 cerebral white matter damage as evaluated by fractional anisotropy from diffusion tensor MRI schedule

178 hem with cortical thickness and white matter fractional anisotropy further improved accuracy.

179 of the uncinate fasciculus using generalized fractional anisotropy (GFA).

180 Overall, fractional anisotropy had the best reliability, with mea

181 -frontal pathway; weaker connectivity (lower fractional anisotropy, higher mean diffusivity) was asso

182 Lower fractional anisotropy in additional white matter tracts

183 arger visual cortex effects also had reduced fractional anisotropy in an anterior portion of the left

184 he tract segment [P </= .0001] and increased fractional anisotropy in approximately 16% of the tract

185 n index (beta = -0.597, p=0.034), and higher fractional anisotropy in connections between the right a

186 nternal capsule and a tendency for decreased fractional anisotropy in duplication.

187 Fractional anisotropy in left frontomedial WM was signif

188 Treatment responders demonstrated greater fractional anisotropy in left thalamocortical, limbic, a

189 found a negative relation between AT and UF fractional anisotropy in male but not female monkeys (AT

190 D) in the ventral thalamus and a decrease in fractional anisotropy in optic nerve and optic tract in

191 The fractional anisotropy in patients' optic radiations decr

192 er was associated with significantly reduced fractional anisotropy in regions that included frontal l

193 arpal tunnel syndrome demonstrated increased fractional anisotropy in several regions and, for these

194 in frontolimbic regions at rest and reduced fractional anisotropy in several white matter tracts.

195 ren were found to have slower development of fractional anisotropy in the cingulum bundle, superior l

196 = 34,194), 2) basal ganglia volumes, and 3) fractional anisotropy in the corpus callosum and corona

197 oral epilepsies had pronounced reductions in fractional anisotropy in the corpus callosum, corona rad

198 and nonimpaired groups in the association of fractional anisotropy in the forceps major with number o

199 Higher widespread white matter FW and lower fractional anisotropy in the fornix showed a stronger as

200 This identified reduced fractional anisotropy in the hippocampal CA3 area in abs

201 Fractional anisotropy in the left arcuate fasciculus was

202 cts, ever smoked was associated with reduced fractional anisotropy in the left cingulate gyrus part o

203 Post hoc t tests showed reduced fractional anisotropy in the left ventrolateral prefront

204 tract, and a correlation between preablation fractional anisotropy in the motor thalamus and clinical

205 ulcal regions with a significant decrease in fractional anisotropy in the patient group compared to c

206 rtate ratio in the thalamus and in preserved fractional anisotropy in the posterior limb of the inter

207 h structural connectivity as measured by the fractional anisotropy in the white matter underlying the

208 -65 and glutamine synthetase in PFC; reduced fractional anisotropy in various brain regions revealed

209 sue volumes and white matter microstructure (fractional anisotropy) in 134 PLWH receiving suppressive

210 res reflecting neuroanatomical connectivity (fractional anisotropy) in 77 children [40 controls (20 f

211 The regions showing the effect on fractional anisotropy included voxels both within and be

212 tial statistics showed a marked reduction of fractional anisotropy, increase of radial diffusivity (P

213 We show that fractional anisotropy increases (from 0.1 to 0.5), diffu

214 icant regional gray matter volume decreases, fractional anisotropy increases, and mean diffusivity de

215 resonance imaging in awake mice showed that fractional anisotropy is reduced in Plp-Nf1 (fl/+) corpu

216 Corpus callosal fractional anisotropy led to the lowest sample size esti

217 Free-water and free-water-corrected fractional anisotropy maps were compared across 72 indiv

218 ric mean ratio 1.09, 95% CI 0.90 to 1.32) or fractional anisotropy (mean difference -0.01, 95% CI -0.

219 95% CI: 0.051, 0.129; P < .001), with lower fractional anisotropy (mean difference in z score per st

220 The fractional anisotropy, mean diffusion, and radial diffus

221 DTI-derived fractional anisotropy, mean diffusivity (MD), axial diff

222 , and diffusion tensor imaging metrics, i.e. fractional anisotropy, mean, axial and radial diffusivit

223 Conventional mean diffusivity and fractional anisotropy metrics were also assessed for com

224 white matter hyperintensities (N = 42,310), fractional anisotropy (N = 17,663) and mean diffusivity

225 rve latency was associated with reduction of fractional anisotropy near (i) contralesional hand area

226 ing finger tapping rate (p = 0.027), whereas fractional anisotropy of aMF originating in the contrale

227 IOP loading also increased fractional anisotropy of CSS in diffusion tensor MRI wit

228 d in less white matter damage as measured by fractional anisotropy of diffusion tensor MRI.

229 tal-motor cortex FC, accompanied by a higher fractional anisotropy of left corona radiata, predicted

230 Fractional anisotropy of PLIC (n=65) had an AUC of 0.82

231 volume of the visual association cortex and fractional anisotropy of pontine white matter pathways w

232 n in the brain and with MRI to determine the fractional anisotropy of the arcuate fasciculus.

233 (P = 8.8 x 10(-7)) negative association with fractional anisotropy of the forceps major (effect size

234 Fractional anisotropy of the inferior longitudinal fasci

235 The fractional anisotropy of the optic radiations was lower

236 Regression analyses revealed that fractional anisotropy of the PT explained (p = 0.050) di

237 fusion tensor imaging analysis revealed that fractional anisotropy of the right cingulum was inversel

238 culus to h2 = 0.46 (SE, 0.15; P = .0009) for fractional anisotropy of the right inferior fronto-occip

239 Fractional anisotropy of this tract correlated positivel

240 call test) improved significantly; increased fractional anisotropy of white matter (a measure of cere

241 = 0.015)] and white matter changes including fractional anisotropy of white matter (DeltaR2 = 0.417,

242 correlated negatively with the mean general fractional anisotropy of white matter tracts exclusively

243 d N-acetylaspartate (NAA)/choline (Cho), and fractional anisotropy of white-matter pathways was asses

244 than previously used diffusion MRI metrics (fractional anisotropy or fiber-tracking recovered stream

245 No significant changes in fractional anisotropy over time were observed.

246 th subcortical gray matter volume and global fractional anisotropy over time.

247 rsion (P < 0.001 by paired t-test) and lower fractional anisotropy (P < 0.001 by related-samples Wilc

248 an 16% reduction of spinal cord white matter fractional anisotropy (P </= 0.0003) with a concomitant

249 the frontostriatal tract at follow-up: lower fractional anisotropy (p=0.069), higher axial diffusivit

250 The left arcuate fasciculus had decreased fractional anisotropy, particularly near the anterior no

251 njury predicted the degree of brain atrophy: fractional anisotropy predicted progressive atrophy in b

252 responded to lower structural integrity (DTI fractional anisotropy) (r=0.347, p=0.038).

253 ted with a more abnormal functional network (fractional anisotropy: r = 0.226).

254 structural network efficiency and cognition (fractional anisotropy: r = 0.329 and r = 0.447 number of

255 -weighted imaging (to derive optic radiation fractional anisotropy, radial diffusivity, and axial dif

256 on tensor imaging metrics (mean diffusivity, fractional anisotropy, radial diffusivity, axial diffusi

257 ted faster brain development in white matter fractional anisotropy (rate of increase, 2.2%; 95% CI, 0

258 Results Mean diffusivity was elevated and fractional anisotropy reduced in CA compared with both c

259 who stutter exhibited significantly reduced fractional anisotropy relative to controls in white matt

260 s, the more anxious twin exhibited decreased fractional anisotropy (t = -2.22, p = 0.032) and axial d

261 CD had lower fractional anisotropy than controls in white matter bund

262 free-water and altered free-water corrected fractional anisotropy that included the basal ganglia, t

263 white matter (white matter hyperintensities, fractional anisotropy [theoretical range, 0 {diffusion i

264 Using a fractional anisotropy threshold of 0.15 and an angle thr

265 Higher fractional anisotropy throughout the brain appears to be

266 howed a significant association pathway from fractional anisotropy to processing speed to working mem

267 etween head impact exposure and change of FA fractional anisotropy value of whole, core, and terminal

268 he age-, sex-, and site-adjusted mean global fractional anisotropy value was 3.8% higher (95% CI, 1.1

269 Spatial Statistics analysis revealed higher fractional anisotropy values for bilinguals vs. monoling

270 The severity of neglect correlated with fractional anisotropy values in superior longitudinal fa

271 l precentral gyri positively correlated with fractional anisotropy values of the CC subregion III, wh

272 The mean global fractional anisotropy values were 0.433 (SD, 0.028) in t

273 Compared with controls, free-water-corrected fractional anisotropy values were increased for multiple

274 f white matter pathways, as indexed by lower fractional anisotropy values, uniquely within the pons.

275 ces in brain function and also in volume and fractional anisotropy values.

276 of injury severity and microbleeds (>50% for fractional anisotropy versus <5% for other measures).

277 whereas in the short-range connections only fractional anisotropy was affected (z = -0.34, P = 0.03)

278 Fractional anisotropy was calculated from diffusion tens

279 Fractional anisotropy was increased in the hypothalamus

280 extracellular volume (r=0.68, P=0.004), and fractional anisotropy was inversely correlated with circ

281 ility analyses revealed that variation in UF fractional anisotropy was largely due to nonheritable fa

282 althy controls the mean average white matter fractional anisotropy was lower in [0.423 (standard devi

283 Fractional anisotropy was lower in the ASD and ADHD grou

284 Global fractional anisotropy was negatively associated with del

285 Across 'all epilepsies' lower fractional anisotropy was observed in most fibre tracts

286 Global fractional anisotropy was positively associated with sel

287 Fractional anisotropy was significantly lower in the inf

288 METHOD: Gray matter volume and fractional anisotropy were mapped in 326 individuals dia

289 Gray matter volume and fractional anisotropy were mapped in 326 individuals dia

290 -group differences in gray matter volume and fractional anisotropy were regionally localized across t

291 rates of reduction of gray matter volume and fractional anisotropy were significantly faster in males

292 sonance imaging and diffusion tensor imaging fractional anisotropy were used to measure functional co

293 -brain and regional diffusion tensor imaging fractional anisotropy were used to measure white matter

294 e deletion group showed widespread increased fractional anisotropy when compared with duplication.

295 mptom severity also had greater increases in fractional anisotropy with age.

296 Relationships of fractional anisotropy with dimensional measures of inatt

297 ostructure were also seen, including reduced fractional anisotropy with increased mean and radial dif

298 Lower fractional anisotropy within the splenium of the corpus

299 Moreover, age-associated differences in fractional anisotropy within these tracts were comparabl

300 connections showed the largest reduction in fractional anisotropy (z = -1.03, P < 0.001) and total n