ライフサイエンスコーパス: parietal lobe

1 r white matter hyperintensities (frontal and parietal lobes).

2 at the juxtacortical region from frontal and parietal lobes).

3 the middle temporal gyrus with the inferior parietal lobe.

4 ound in areas of the left posterior-inferior parietal lobe.

5 more dorsomedial pattern, extending into the parietal lobe.

6 iated with grey matter in the right inferior parietal lobe.

7 tions in the white matter of the frontal and parietal lobe.

8 omedial frontal region but also in the right parietal lobe.

9 in the left thalamus and bilateral inferior parietal lobe.

10 and superior temporal lobes; and in the left parietal lobe.

11 of frontal and striatal regions, as well as parietal lobe.

12 ate may be related to hyperactivation in the parietal lobe.

13 right hemisphere, rather than the posterior parietal lobe.

14 l prefrontal cortex, anterior cingulate, and parietal lobe.

15 of the dorsal stream of visual areas in the parietal lobe.

16 ificant reduction of gray matter in the left parietal lobe.

17 d to recent single-unit data from the monkey parietal lobe.

18 ual 'neglect' after injury to regions in the parietal lobe.

19 l limbic area, anterior insula, and inferior parietal lobe.

20 , with the largest decreases observed in the parietal lobe.

21 appeared to be systematically linked to the parietal lobe.

22 ro-parieto-occipital junction and the medial parietal lobe.

23 etal lobe, was associated with tau in medial parietal lobe.

24 ontal, dorsolateral prefrontal, and inferior parietal lobe.

25 and lower surface area of the left inferior parietal lobe.

26 fic cortical networks converging in inferior parietal lobe.

27 g in the basal ganglia and the right temporo-parietal lobe.

28 lume, and cortical thickness in the inferior parietal lobe.

29 istinct time courses, overlapped in the left parietal lobe.

30 ring which we applied concurrent TDCS to the parietal lobes.

31 patterns, both of which are mediated by the parietal lobes.

32 sal ganglia and resulting dysfunction of the parietal lobes.

33 s are represented in an abstract way in both parietal lobes.

34 y the prefrontal cortex and the temporal and parietal lobes.

35 with higher MT in the bilateral frontal and parietal lobes.

36 ly between inferior prefrontal and occipital/parietal lobes.

37 considerable atrophy in some regions of the parietal lobes.

38 neonatal brain in the frontal, temporal, and parietal lobes.

39 ork of regions in the frontal, temporal, and parietal lobes.

40 a lesser degree in the frontal, temporal and parietal lobes.

41 greater in women than men in hippocampus and parietal lobes.

42 veral brain regions spanning the frontal and parietal lobes.

43 and evolved asymmetrically in the occipital-parietal lobes.

44 ociation zones in the frontal, temporal, and parietal lobes.

45 predominantly in the frontal, temporal, and parietal lobes.

46 ant WM abnormalities within the temporal and parietal lobes.

47 roximate number sense" (ANS) associated with parietal lobes.

48 In the non-dominant parietal lobe, 111 (27%) low-frequency and 176 (55%) hig

49 e: 2632 mm3, P = 0.002), right occipital and parietal lobes (12.7 14.3 mL . 100 g-1 . min-1, volume:

50 P < .001), with strongest reductions in the parietal lobes (22 mL/100 g/min +/- 6 vs 30 mL/100 g/min

51 track the accumulation of tau in the medial parietal lobe, a key region for memory processing that i

52 nd high-order visual areas and the posterior parietal lobe, a prominent node of the default mode netw

53 l association with surface area in the right parietal lobe, a region related to nonverbal cognitive f

54 Parietal lobe abnormalities might cause attentional dysf

55 At the same time, the parietal lobe activation associated with spatial process

56 eprived subjects was associated with greater parietal lobe activation.

57 Precuneus cortex, distributed parietal lobe activity, and microstructure of the sSTR s

58 only found in a small region of the inferior parietal lobe, adding evidence for its role in domain-ge

59 brain showed a 3-cm mass in the left mesial parietal lobe adjacent to the resection site.

60 ess, how tumours elsewhere in the frontal or parietal lobes affect functional connectivity in a weak

61 dual neurons, reversible inactivation of the parietal lobe affects only spatial orienting of attentio

62 ed activation in the right anterior inferior parietal lobe (aIPL), bilateral lingual gyrus and the cu

63 rical atrophy with the frontal, temporal and parietal lobes all affected.

64 The parietal lobe also started to become involved.

65 elated with iron accumulation in left SN and parietal lobe, although CR animals did not show this rel

66 sula/frontal operculum and the left superior parietal lobe, among other areas of the brain.

67 nnecting Broca's territory with the inferior parietal lobe and a posterior segment connecting the inf

68 icantly decreased DLPFC FC with the superior parietal lobe and attenuated negative connectivity in th

69 rony of neural processes within the superior parietal lobe and extrastriate visual cortex that in tur

70 th stroke involving regions within the right parietal lobe and insula.

71 tured by changes in connectivity between the parietal lobe and insula.

72 of the left inferior frontal gyrus, inferior parietal lobe and posterior middle temporal gyrus in act

73 Given the role of the inferior parietal lobe and posterior superior temporal sulcus in

74 DLPFC) during encoding, whereas the inferior parietal lobe and precuneus cortical sources were identi

75 vity (mediated by the beta band) to inferior parietal lobe and right middle temporal gyrus (MTG).

76 a spatial attention circuit in the superior parietal lobe and supplementary motor area was activated

77 rhemispheric metabolism bias in the inferior parietal lobe and temporoparietal junction.

78 asking effects (including bilateral inferior parietal lobe and thalamus), but groups did not differ i

79 o sites of the parietal cortex, the superior parietal lobe and the anterior intraparietal sulcus (aIP

80 tau abnormalities in frontal, temporal, and parietal lobes and basal ganglia of both hemispheres.

81 tricular (WMH principally in the frontal and parietal lobes and basal ganglia, especially in the peri

82 ated to differences in the left temporal and parietal lobes and cerebellum.

83 hip between abnormalities in the frontal and parietal lobes and clinical symptoms in people with AS.

84 eas in patients, only the bilateral superior parietal lobes and left insular cortex were less activat

85 ations of FC between left and right inferior parietal lobes and right insular cortex.

86 left precuneus, right temporal, frontal, and parietal lobes and right medial-frontal cortex) showed l

87 n, involving predominantly the occipital and parietal lobes and the putamen, and were dependent on th

88 odal association cortices in the frontal and parietal lobes and unimodal sensory areas of the occipit

89 he WML were predominantly in the frontal and parietal lobes and were mostly confluent, affecting the

90 insular cortex, prefrontal cortex, inferior parietal lobe, and cerebellum.

91 ncluding sensorimotor and premotor cortices, parietal lobe, and cerebellum.

92 e cortex, supplementary motor area, inferior parietal lobe, and dorsolateral prefrontal cortex despit

93 e insula, cingulate cortices, temporal lobe, parietal lobe, and medial frontal lobe.

94 teral dorsal premotor cortex, right superior parietal lobe, and midbrain.

95 w baseline in middle frontal gyrus, inferior parietal lobe, and middle temporal gyrus.

96 ual stream, superior parietal lobe, inferior parietal lobe, and postcentral gyrus abnormalities contr

97 frontal gyrus, orbitofrontal gyrus, superior parietal lobe, and precuneus compared to participants wi

98 ugar foods causes adaptions in the striatum, parietal lobe, and prefrontal and visual cortices in the

99 , insula, temporoparietal junction, inferior parietal lobe, and superior temporal gyrus during implic

100 rtex, the orbitofrontal cortex, the inferior parietal lobe, and the basal ganglia.

101 ng were performed to determine frontal lobe, parietal lobe, and total cerebral brain volume.

102 tex, then the precuneus, lateral frontal and parietal lobes, and finally the lateral temporal lobe.

103 , and radial diffusivity from frontal lobes, parietal lobes, and in the frontostriatal tract.

104 re principally in the frontal lobe, superior parietal lobes, and in the paramedian cerebral cortex.

105 s, temporal lobe, right superior frontal and parietal lobes, and paracentral lobule.

106 tability in the temporal poles, the inferior parietal lobes, and the superior and dorsolateral fronta

107 t not animals, were encoded in left inferior parietal lobe; and (3) LATL subregions exhibited distinc

108 insula and appearing as an extension of the parietal lobe; and (ii) a mosaic of orofacial motor prog

109 middle, and inferior temporal gyri; superior parietal lobe; and posterior cingulate gyrus, resulted i

110 cortical thinning in the medial and lateral parietal lobe appeared 10 and 5 y, respectively, before

111 In sum, the parietal lobe appears to have a critical role in recolle

112 Einstein's parietal lobes are also unusual and may have provided so

113 findings suggest that the human frontal and parietal lobes are not disproportionately enlarged when

114 Regions of the temporal and parietal lobes are particularly damaged in Alzheimer's d

115 The parietal lobes are prominent generators of alpha oscilla

116 usion, particularly in the posterior temporo-parietal lobes, are well recognized in Alzheimer's disea

117 inferior longitudinal fascicle (ILF) to the parietal lobe (areas POa and IPd), superior temporal sul

118 al lobe, the right frontal lobe and the left parietal lobe, as well as some subcortical regions.

119 increase of activation in the right superior parietal lobe at 3 and 12 months after surgery.

120 cycle were determined in the human occipital/parietal lobe at rest.

121 ations (at 3-4 months); to the occipital and parietal lobes (at 4-6 months); and then to the genu of

122 10.85, 95% CI -17.91, -3.79, p < 0.0125) and parietal lobes (B = -12.75, 95% CI -21.58, -3.91, p < 0.

123 l gyrus (BA 4), the left hemisphere superior parietal lobe (BA 7), and the bilateral superior tempora

124 dorsolateral frontal lobe (BA9), and dorsal parietal lobe (BA7) of each case.

125 Training transferred to proficiency in other parietal lobe-based quantity judgment, i.e., time and sp

126 an areas, occasionally with extension to the parietal lobes beyond the immediate perisylvian cortex.

127 tal gyri, bilateral inferior frontal gyrus), parietal lobe (bilateral inferior parietal lobule), insu

128 m of the corpus callosum, bilateral superior-parietal lobe, bilateral anterior forceps, and inferior-

129 the inferior frontal, posterior temporal and parietal lobes bilaterally and in posterior frontal lobe

130 asymmetry of metabolism, in the temporal and parietal lobes, Broca's area, thalamus, and hippocampus.

131 tivity detected by MEG in the right superior parietal lobe (Brodmann's Area 7).

132 ween impaired performance and lesions of the parietal lobe but there was no effect of laterality of l

133 a that was most prominent in the frontal and parietal lobes but involved other cortical areas as well

134 ilar findings were noted in the temporal and parietal lobes but not in the frontal and occipital lobe

135 establishes heavy interconnections with the parietal lobe, but the precise nature of these connectio

136 in bulk volume bilaterally in the occipital-parietal lobes, but a larger right caudate nucleus and l

137 ed with cortical activity in the frontal and parietal lobes, but also with increased activity in the

138 metry measures of the individual gyri of the parietal lobe by means of magnetic resonance imaging (MR

139 In the dominant parietal lobe, clinical responses were observed for 56 (

140 and higher MD in the frontal, temporal, and parietal lobes compared to the lower-stable group.

141 The human parietal lobe contains multiple maps of the external wor

142 Two patients with bilateral parietal lobe damage received detailed assessments of th

143 d memory-retrieval deficits in patients with parietal lobe damage.

144 h lesions involving the anterior temporal or parietal lobes displayed poor performance for stimuli pr

145 orbital prefrontal cortex, ventral striatum, parietal lobe, dorsal putamen, dorsal caudate, amygdala,

146 terior superior temporal sulcus and inferior parietal lobe during nonimitative action.

147 lity of using noninvasive stimulation to the parietal lobe during numerical learning to selectively i

148 th somatosensory cortex and lateral inferior parietal lobe during smoking cues compared with food cue

149 orsal anterior cingulate cortex and inferior parietal lobe during the methylphenidate condition for e

150 eral prefrontal and temporal lobes and right parietal lobe during the switch task.

151 Parietal lobe dysfunction and problems with sensory-moto

152 psychological examination also suggests that parietal lobe dysfunction is a characteristic feature of

153 anar, n = 58; PROPELLER, n = 1; P <.01), and parietal lobes (echo-planar, n = 5; PROPELLER, n = 0; P

154 d tenofovir), frontal lobe (lamivudine), and parietal lobe (efavirenz).

155 psy, five occipital lobe epilepsy (OLE), six parietal lobe epilepsy (PLE) and 19 neocortical epilepsy

156 l, 7 (35.0%) with frontal and 2 (10.0%) with parietal lobe epilepsy.

157 ions in the frontal lobe, temporal lobe, and parietal lobe exhibited the opposite pattern.

158 ian cerebral proportion toward a frontal and parietal lobe expansion in catarrhini (primate parvorder

159 l showed hypoperfusion in the right inferior parietal lobe extending into the bilateral posterior cin

160 metabolism was most commonly observed in the parietal lobe followed by the occipital lobe.

161 howed that the activation was located in the parietal lobe for the 70-100 ms timeframe, the frontal a

162 d FA: mean [SE] beta = 2.9 [1.0] x 10-4) and parietal lobes (for CBF and MD: mean [SE] beta = -1.5 [0

163 cortex, orbital frontal cortex and inferior parietal lobe) for 28 subjects with autism spectrum diso

164 The parietal lobe forms about 20% of the human cerebral cort

165 ing, parieto-occipital cortical anatomy, and parietal lobe function.

166 ent results reveal a left/right asymmetry in parietal lobe function.

167 .001), temporal lobe (g = -0.84; p < 0.001), parietal lobe (g = -0.73; p = 0.053), cerebellum (g = -1

168 he visual representation of the world in the parietal lobe generally find that it is based in a gaze-

169 Also noted was relative preservation of parietal lobe gray and temporal lobe white matter in sub

170 volumetric reductions in left occipital and parietal lobe grey matter.

171 Although the right posterior inferior parietal lobe has been implicated in temporal order judg

172 The parietal lobe has long been viewed as a collection of ar

173 Does the parietal lobe have a critical role in memory?

174 the cortical topography of the temporal and parietal lobes have revealed a common organisational pri

175 the posterior cingulate cortex and inferior parietal lobes, have also shown decreased metabolism ear

176 d measures of the prefrontal lobe in 11, the parietal lobe in 13, and both lobes in 10 subjects with

177 was involved in 14 patients (77.8%) and the parietal lobe in 4 patients (22.2%).

178 flect changes in cell density in the temporo-parietal lobe in developmental dyslexia and that the alt

179 Few studies have evaluated the parietal lobe in schizophrenia despite the fact that it

180 The exact role of the parietal lobe in spatial cognition is controversial.

181 here has been a debate about the role of the parietal lobe in the generation of behavior.

182 ronal integrity of the medial prefrontal and parietal lobes in 14 non-learning-disabled adults with A

183 ing the most relatively enlarged frontal and parietal lobes in an infraorder exhibiting a disproporti

184 we detected cortical thinning in frontal and parietal lobes in groups of Tourette syndrome children r

185 rger grey matter volumes in the temporal and parietal lobes in improvers compared with those who decl

186 sleep deprivation and implicate the PFC and parietal lobes in this compensation.

187 tum, as well as in the cuneus, cingulum, and parietal lobe, in all SCA17 patients and presymptomatic

188 ention share common neural mechanisms in the parietal lobes, in addition to task specific mechanisms

189 other regions within the medial and lateral parietal lobe including the medial place memory area (MP

190 gnificantly less activation in the bilateral parietal lobes (including the superior parietal gyrus an

191 n the Posterior Parietal Cortex and Inferior Parietal Lobe, indicating increases of cortical involvem

192 on system, a network comprising the inferior parietal lobe, inferior frontal gyrus, and posterior sup

193 magnocellular/dorsal visual stream, superior parietal lobe, inferior parietal lobe, and postcentral g

194 y matter volume of the frontal, temporal and parietal lobes, insula and whole brain.

195 ies have supported the notion of frontal and parietal lobe involvement in unawareness of illness in s

196 Turn-take and Compete, and greater Inferior Parietal Lobe (IPL) activation during Lead and Turn-take

197 nce to support the role of the left inferior parietal lobe (IPL) in processing syllable order.

198 e frontal gyrus (MFG) and bilateral inferior parietal lobe (IPL) of the DAN, as well as the left IPL

199 n fMRI research in adults, that (1) inferior parietal lobe (IPL) plays a central role in representing

200 Our understanding of the inferior parietal lobe (IPL) remains challenged by inconsistencie

201 purely perceptual function for the inferior parietal lobe (IPL), patients with lesions to this struc

202 tients was the angular gyrus of the inferior parietal lobe (IPL).

203 l prefrontal cortex (RLPFC) and the inferior parietal lobe (IPL).

204 g of hand gestures involve the left inferior parietal lobe (IPL).

205 Our findings suggest that the superior parietal lobe is critical for sensorimotor integration,

206 sentation of the external environment in the parietal lobe is highly selective for objects that are i

207 suggests that integrity of the left inferior parietal lobe is important for speech repetition and, as

208 e, the numerical representation in the right parietal lobe is notation dependent and thus includes no

209 udy was to examine whether the left inferior parietal lobe is recruited during temporal order judgmen

210 re-lateralized system including the inferior parietal lobe is specifically recruited for the computat

211 icant relationships within the left inferior parietal lobe, left middle temporal gyrus, and right ins

212 both these brain regions (Cho/NA in temporo-parietal lobe, left vs right, p< or =0.01; Cre/NA in cer

213 ects structures in the temporal, frontal and parietal lobes linking speech perception and production.

214 ons in regions such as the basal ganglia and parietal lobe may explain some CNS-related symptoms in C

215 They also suggest why areas in the inferior parietal lobe may play a prominent role in visual awaren

216 quantity of a number by the use of a similar parietal lobe mechanism.

217 ith occipital metabolism and positively with parietal lobe metabolism.

218 We found no significant differences in parietal lobe metabolite concentrations.

219 rs: B, 0.06; 95% CI, 0.01 to 0.11; P = .03), parietal lobe (mothers: B, 0.07; 95% CI, 0.03 to 0.11; P

220 t for the frontal lobe (for example, for the parietal lobe, mothers: B, -9.5; 95% CI, -13.8 to -5.3;

221 n = 117; temporal lobe, n = 244 vs n = 137; parietal lobe n = 240 vs n = 93; and occipital lobe, n =

222 additional loss in anterior temporal lobes, parietal lobes, occipital lobes and cerebellum.

223 ical measures of AD in brain tissue from the parietal lobe of AD cases and age-matched, cognitively n

224 ent mice were successfully inoculated in the parietal lobe of immunosuppressed, mixed-breed hound dog

225 Area 5 in the parietal lobe of the primate brain is thought to be invo

226 r accident involving anterior regions of the parietal lobe of the right hemisphere, which resulted in

227 th COS showing slower WM growth rates in the parietal lobes of the brain than age-matched healthy con

228 ctivation in frontal cortex and temporal and parietal lobes of the cerebrum in both groups.

229 n images were collected from the frontal and parietal lobes of the subject with a 4 tesla magnet.

230 , (4) eight electrodes in occipital combined parietal lobe (OPL8), (5) seven electrodes in occipital

231 op-down feedback originating from within the parietal lobe or from the frontal lobe.

232 striatal regions with structures within the parietal lobe (P < .05, corrected for multiple compariso

233 le frontal gyri (P <.001), and left inferior parietal lobe (P=.007).

234 lative to the CN group in the inferior right parietal lobe (P=.046), similar to the region of greates

235 erately intense stimulation was found in the parietal lobe (P2, P4, and P6 electrodes).

236 eglect, and suggest that in man the inferior parietal lobe plays a role not only in perception but al

237 hese findings suggest that the left inferior parietal lobe plays an important role in processing syll

238 ntal lobe (PRL3); (3) four electrodes in the parietal lobe (PLL4), (4) eight electrodes in occipital

239 duced changes of FCS and rCBF in the lateral-parietal lobe positively correlated with behavioral perf

240 increased in CD vs HC in the right inferior parietal lobe post-cocaine and in the left superior fron

241 e cortex, and increases in activation in the parietal lobe, posterior cingulate cortex, and inferior

242 symmetric uptake was evident in temporal and parietal lobes, precuneus, and posterior cingulate corte

243 amage or hypoperfusion, to the left inferior parietal lobe, rather than the underlying white matter,

244 yslexic men and controls in the left temporo-parietal lobe (ratio of choline-containing compounds [Ch

245 ep cortical layers of frontal, temporal, and parietal lobe regions.

246 ose metabolism in the occipital and inferior parietal lobes relative to controls.

247 may be divided between inferior and superior parietal lobes, respectively.

248 saic variants across 17 locations within one parietal lobe reveals that restriction of clonal spread

249 pramarginal and angular gyri of the inferior parietal lobe), right precuneus, and thalamus.

250 nd posterior cingulate gyrus, right superior parietal lobe, right intraparietal sulcus, right precune

251 e loss affected the hippocampi, temporal and parietal lobes, right caudate nucleus, and insulae in pa

252 t portion of the daily light-dark cycle, and parietal lobe seizures occurred nocturnally and out of p

253 The inferior parietal lobe showed greater activation for shorter lag

254 acies in intraparietal sulcus (IPS)/superior parietal lobe (SPL) for both sociality and transitivity

255 Activity in the superior parietal lobe (SPL) increased proportionally to viewpoin

256 higher brain activation in the left superior parietal lobe (SPL).

257 led that the structure of bilateral superior parietal lobes (SPL) could account for interindividual v

258 The functional complexity of the parietal lobe still represents a challenge for neurophys

259 of interest, covering frontal, temporal and parietal lobes, striatum, insula and supplemental motor

260 from areas S2/PV and aspects of the inferior parietal lobe such as PF, PFG, AIP, and the tip of the I

261 e, occipital lobe, cerebellum, temporal, and parietal lobe, suggesting its potential as a brain struc

262 us, precuneus, posterior cingulate, inferior parietal lobe, supramarginal gyrus, striatum, and thalam

263 us, precuneus, posterior cingulate, inferior parietal lobe, supramarginal gyrus, striatum, and thalam

264 x (EC) and RsC did not correlate with medial parietal lobe tau.

265 stronger correlation between MTL and medial parietal lobe tau.

266 in the temporal lobes as well as frontal and parietal lobes (temporofrontoparietal subtype).

267 egions, including left superior temporal and parietal lobes, temporoparietal junction and paracentral

268 acentral lobule, right superior temporal and parietal lobes, temporoparietal junction, and precuneus.

269 or cortex, prefrontal cortex, temporal lobe, parietal lobe, thalamus, basal ganglia, cingulate cortex

270 timodal associative areas in the frontal and parietal lobe than primary regions of sensorimotor and v

271 area (LIP) is a subdivision of the inferior parietal lobe that has been implicated in the guidance o

272 within the human medial temporal and medial parietal lobes that encode two fundamental spatial quant

273 st to an abstract representation in the left parietal lobe, the numerical representation in the right

274 ributes for the posteromedial portion of the parietal lobe, the precuneus.

275 in the isotope material: emanating from the parietal lobe, the superior longitudinal fasciculus subc

276 Normal symmetry of parietal lobe tissue observed in the comparison group wa

277 dorsolateral prefrontal cortex and inferior parietal lobe tissue were interrogated from 697 particip

278 lthough most studies show the right inferior parietal lobe to be crucial and new imaging modalities h

279 gates from the superficial cortex around the parietal lobe to the hippocampus.

280 a posterior segment connecting the inferior parietal lobe to Wernicke's territory.

281 y from associative areas in the temporal and parietal lobe toward functional connectivity with the fr

282 d superior temporal gyri and to the inferior parietal lobe was a predictor of deficits in processing

283 The right parietal lobe was compressed by the mass.

284 Damage to the frontal and parietal lobes was more common in apraxics, but neither

285 ial cortex (RsC), a key region of the medial parietal lobe, was associated with tau in medial parieta

286 dial part, at the junction with the inferior parietal lobe, was linked to speech production rather th

287 Core regions at the precuneus and inferior parietal lobe were activated for multiple orientation do

288 dorsolateral prefrontal cortex and inferior parietal lobe were activated to resolve the additional p

289 gions in left prefrontal cortex and superior parietal lobe were more active for calculation than for

290 ions in right prefrontal cortex and inferior parietal lobe were more active for reasoning than for ca

291 etween the intraparietal sulcus and inferior parietal lobe were significantly associated with this de

292 ontotemporal lobes, left thalamus, and right parietal lobe were strongly associated with PSCI (after

293 ot after sleep deprivation; in contrast, the parietal lobes were not activated after normal sleep but

294 ased neural recruitment in the left inferior parietal lobe when participants made judgments about syl

295 emonstrate that there is an area in the left parietal lobe where children without a deficit in calcul

296 gyrus in the occipital lobe and the inferior parietal lobe, which had normal morphology on structural

297 ignificantly smaller frontal, occipital, and parietal lobe white matter volumes; significantly lower

298 port a patient with a lesion of the superior parietal lobe who shows both sensory and motor deficits

299 l activity inside the precuneus and inferior parietal lobes, with space orientation activating poster

300 nificant main effects on total, frontal, and parietal lobe WM volumes (F = 3.98, P = .02; F = 4.95, P