ライフサイエンスコーパス: parietal lobe

1 in the left thalamus and bilateral inferior parietal lobe.

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

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

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

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

6 fic cortical networks converging in inferior parietal lobe.

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

8 right hemisphere, rather than the posterior parietal lobe.

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

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

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

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

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

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

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

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

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

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

19 the middle temporal gyrus with the inferior parietal lobe.

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

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

22 more dorsomedial pattern, extending into the parietal lobe.

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

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

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

26 sal ganglia and resulting dysfunction of the parietal lobes.

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

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

29 considerable atrophy in some regions of the parietal lobes.

30 ly between inferior prefrontal and occipital/parietal lobes.

31 and evolved asymmetrically in the occipital-parietal lobes.

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

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

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

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

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

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

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

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

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

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

42 Parietal lobe abnormalities might cause attentional dysf

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

44 eprived subjects was associated with greater parietal lobe activation.

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

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

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

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

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

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

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

52 The parietal lobe also started to become involved.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 The parietal lobes are prominent generators of alpha oscilla

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 Parietal lobe dysfunction and problems with sensory-moto

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 The inferior parietal lobe showed greater activation for shorter lag

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

232 The right parietal lobe was compressed by the mass.

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

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

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

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

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

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

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

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

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

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

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

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

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

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