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1 ft inferior temporal gyri, and left superior parietal lobule.
2 ciated with activation in the right inferior parietal lobule.
3 ntral gyrus, postcentral gyrus, and inferior parietal lobule.
4 predicted by per cent damage to the inferior parietal lobule.
5 uperior temporal gyrus and the left inferior parietal lobule.
6 to-occipital cortex and the rostral superior parietal lobule.
7 olved the pre-central gyrus and the anterior parietal lobule.
8 es off the IPS and extends into the superior parietal lobule.
9 the middle frontal gyrus, ACC, and superior parietal lobule.
10 yrus, posterior cingulate, and left inferior parietal lobule.
11 sula, supramarginal gyrus, and left inferior parietal lobule.
12 otor cortex, as well as the rostral inferior parietal lobule.
13 across the cortical surface of the inferior parietal lobule.
14 HF and the contralateral DLPFC and inferior parietal lobule.
15 y in the striatum and the posterior superior parietal lobule.
16 left posterior temporal cortex and inferior parietal lobule.
17 ortex, superior temporal gyrus, and superior parietal lobule.
18 s gyrus [planum temporale (PT)] and inferior parietal lobule.
19 marginal gyrus (SMG), a part of the inferior parietal lobule.
20 he rostral-most region of the right superior parietal lobule.
21 as of the IPS, superior temporal sulcus, and parietal lobule.
22 dorsolateral prefrontal cortex, and inferior parietal lobule.
23 in the medial prefrontal cortex and inferior parietal lobule.
24 premotor cortex originates from the superior parietal lobule.
25 cortical sites: bilateral DLPFC and inferior parietal lobule.
26 with a weak contribution from right superior parietal lobule.
27 and low-ED vs. non-food cues in the inferior parietal lobule.
28 orized sound in auditory cortex and superior parietal lobule.
29 cortex, postcentral gyrus, and the inferior parietal lobule.
30 left anterior hippocampus and right inferior parietal lobule.
31 y decoded from activity in the left inferior parietal lobule.
32 a significant decrease in the right inferior parietal lobule.
33 , the inferior parietal sulcus, and superior parietal lobule.
34 c stimulation (rTMS) applied to the inferior parietal lobule.
35 precuneus and intraparietal sulcus/inferior parietal lobule.
36 argest correlations observed in the inferior parietal lobule.
37 dorsolateral prefrontal cortex and inferior parietal lobule.
38 ex face area and bilaterally in the inferior parietal lobule.
39 ingulate gyrus, the putamen and the superior parietal lobules.
40 extent of the lateral superior and inferior parietal lobules.
41 ns of the occipital lobe and of the superior parietal lobules.
42 d grossly asymmetrical inferior and superior parietal lobules.
44 l (PMv)-motor cortex (M1), anterior inferior parietal lobule (aIPL)-M1, and dorsal inferior parietal
45 al field representation in the left inferior parietal lobule and a significant decrease in the right
46 ateral prefrontal cortex, and right inferior parietal lobule and caudate nucleus, perhaps reflecting
48 ork involving primary motor cortex, superior parietal lobule and cerebellum that were specifically re
49 reased neural activity in bilateral inferior parietal lobule and dorsolateral prefrontal cortex in bo
50 in the cuneus and cingulate for NS; inferior parietal lobule and frontal regions for SI; and parahipp
51 py and increased diffusivity in the superior parietal lobule and increased diffusivity in the hippoca
53 iments, signal in the left anterior inferior parietal lobule and posterior inferior temporal gyrus an
54 sociated cortical network including inferior parietal lobule and posterior inferolateral temporal gyr
55 ggest that parts of gestalt cortex (inferior parietal lobule and posterior temporal cortex) and poste
57 versely, activity patterns in right superior parietal lobule and premotor cortex, and also left front
58 lower fractional anisotropy in the superior parietal lobule and reduced mean diffusivity in the thal
60 We identified decreased MTR in left inferior parietal lobule and right superior parietal lobule in su
61 pected sex differences in the right inferior parietal lobule and superior marginal gyrus, and display
62 and suggests a crucial role of the superior parietal lobule and supramarginal gyrus in mediating com
64 , and a region on the border of the superior parietal lobule and the inferior parietal lobule (SPL/IP
65 ed to the coupling between the left inferior parietal lobule and the left anterior insula, which, in
66 refrontal cortex and both the right superior parietal lobule and the left lateral occipital cortex) i
70 r functional connectivity with left inferior parietal lobule and ventral premotor cortex, indicating
71 middle temporal gyri, inferior and superior parietal lobules and precuneus, all of which were unilat
72 regions (Broca's area and the left inferior parietal lobule), and with stronger negative relationshi
73 siform gyri, middle occipital lobe, inferior parietal lobule, and also cingulate, paracentral, and pr
74 n in the lateral prefrontal cortex, inferior parietal lobule, and cerebellum, relative to the compari
76 ed functional connectivity with the inferior parietal lobule, and children with ASD showed atypical f
77 ay (i.e., superior occipital gyrus, superior parietal lobule, and dorsal premotor area) was relevant
78 l gyrus, orbital prefrontal cortex, superior parietal lobule, and hippocampus; right claustrum/putame
79 on during motor imagery in the left inferior parietal lobule, and in the anterior cingulate gyrus and
80 vity in left middle temporal gyrus, inferior parietal lobule, and inferior frontal gyrus as videos we
81 ft posterior cingulate cortex, left inferior parietal lobule, and left fusifom/parahippocampal gyrus.
83 eral supplementary motor area, left inferior parietal lobule, and left superior temporal gyrus) when
84 nd right transverse temporal gyrus, superior parietal lobule, and paracentral, lateral orbitofrontal,
86 gyrus, motion sensitive area MT/V5, superior parietal lobule, and primary visual cortex, while showin
87 supplementary motor area, anterior superior parietal lobule, and striatum) already known for their c
88 impaired group (left temporal pole, inferior parietal lobule, and superior temporal gyrus) correspond
89 rontal gyrus, middle frontal gyrus, superior parietal lobule, and supramarginal gyrus, comparison sub
90 portions of the prefrontal cortex, inferior parietal lobule, and temporoparietal junction, as well a
92 st three (anterior cingulate, right inferior parietal lobule, and the caudate/lateral dorsal nucleus)
94 ons, particularly the right and left lateral parietal lobule, and the Language Network, including the
95 rticularly the angular gyrus of the inferior parietal lobule, and the planum temporale are brain regi
96 rior intraparietal sulcus, anterior superior parietal lobule, and the ventral object-specific lateral
97 hway (i.e., middle occipital gyrus, inferior parietal lobule, and ventral premotor area) was specific
98 ontal eye fields, both superior and inferior parietal lobules, and regions within the prefrontal cort
99 ingulate cortex, right superior and inferior parietal lobules, and right superior frontal, middle tem
100 of the right frontal pole, the right lateral parietal lobules, and the left posterior cingulate corte
101 efault mode network, precuneus, and inferior parietal lobule; and, within the dorsal attention networ
102 with higher metabolic values in the inferior parietal lobule, anterior cingulate, inferior temporal l
103 The premotor cortex face area and inferior parietal lobule are both implicated in the cortical mirr
105 ivation in the left hippocampus and inferior parietal lobule (area 40), left middle (area 10) and sup
107 MIND values between the insula and superior parietal lobule, as well as between the superior frontal
108 y corresponded to activation in the inferior parietal lobule, as well as to activation around the inf
109 premotor cortex (PMd) and anterior superior parietal lobule (aSPL) showed substantial activation dur
110 s, left dorsolateral PFC, and right inferior parietal lobule at rest in the treatment group compared
112 rietal areas [e.g., SFG (BA8) right inferior parietal lobule (BA 40), left precuneus (BA 7)], and sub
115 ntary motor area, premotor area and superior parietal lobule, based on the anatomic location of the h
116 ion contrast map included bilateral superior parietal lobule, bilateral dorsolateral prefrontal corte
119 ation in occipital regions and left inferior parietal lobule but increased activation in parietal-occ
120 siform gyri, ventral premotor area, superior parietal lobule, cerebellum and primary sensorimotor are
122 uospatial representation within the inferior parietal lobule changes, with a decrease of the ipsilate
123 ateral to the intraparietal sulcus [inferior parietal lobule complex (IPLC)] and two regions in the m
124 ) and anterior intraparietal sulcus/superior parietal lobule (consistent with sensorimotor output).
125 we show that activity in the human inferior parietal lobule correlates with the divergence of such o
126 dorsolateral prefrontal cortex and superior parietal lobule, corresponded to the decision variables
128 plementary motor area and the right inferior parietal lobule demonstrated a positive linear relations
129 rietal lobule (aIPL)-M1, and dorsal inferior parietal lobule (dIPL)-M1 before and after inducing a lo
130 ial and decreased activation in the inferior parietal lobule during storage of nonverbal material.
131 strogen increased activation in the inferior parietal lobule during storage of verbal material and de
133 task-related BOLD responses in the superior parietal lobule during WM encoding, and the bilateral hi
134 on, and the left superior and right inferior parietal lobules during cognitive experiments, while hyp
135 illustrated in a patient with left inferior parietal lobule embolic infarction in whom a significant
136 ontal gyrus, cuneus, precuneus, and superior parietal lobule [F=19.04-28.51, df=1, 189, partial eta s
137 (p < 0.0003), and a decrease in NAc-inferior parietal lobule FC relative to controls (p < 0.001).
138 nal evoked by switch cues in medial superior parietal lobule for both domains of control, revealing a
139 tic processing occurred in the left inferior parietal lobule for words, and the right middle occipita
141 egions of the default mode network, superior parietal lobule, fusiform gyrus and anterior insula.
143 ymmetry in this region and had left inferior parietal lobule gray matter volumes that were significan
145 th and suggest vulnerability of the superior parietal lobule, hippocampus, and thalamus to glycemic e
146 ng attention has been linked to the superior parietal lobule; however, the neural substrates associat
147 ereas stimulation over right medial superior parietal lobule impaired target discrimination after a s
148 d with higher activity of the right inferior parietal lobule in all participants and also engagement
149 hinner angular gyrus, precuneus and superior parietal lobule in carriers compared to non-carriers, wi
150 ight middle frontal gyrus and right inferior parietal lobule in ECN, as well as increased RSFC betwee
151 inferior parietal lobule and right superior parietal lobule in suicide attempters relative to both n
152 rom the middle frontal gyrus to the superior parietal lobule in the right hemisphere in healthy contr
155 ve to HC in both the left and right inferior parietal lobule, including the supramarginal and angular
156 he primary somatosensory cortex and superior parietal lobule influences brain networks associated wit
157 al gyrus), parietal lobe (bilateral inferior parietal lobule), insula, and limbic lobe (anterior and
158 the posterior intraparietal sulcus/inferior parietal lobule interfered with perceptual conflict proc
159 aptation paradigm, we show that the inferior parietal lobule (IPL) (corresponding to the supramargina
160 trongly lateralized network, where the infra-parietal lobule (IPL) activation was lateralized to the
161 parieto-temporal network; bilateral inferior parietal lobule (IPL) activity was larger in HC versus S
162 the levels of HSPs in hippocampus, inferior parietal lobule (IPL) and cerebellum of subjects with aM
163 labeled by tracer injections in the inferior parietal lobule (IPL) and dorsolateral prefrontal cortex
164 protein nitration is higher in the inferior parietal lobule (IPL) and hippocampus in MCI compared to
165 associated with damage to the right inferior parietal lobule (IPL) and the right temporo-parietal jun
167 vely covalently bound by HNE in EAD inferior parietal lobule (IPL) compared to age-related control br
168 n primary motor cortex (M1) and the inferior parietal lobule (IPL) have been identified with supporti
169 superior temporal gyrus (STG), and inferior parietal lobule (IPL) in Non-prehensile Use trials as co
172 rther, dorsolateral PFC (dlPFC) and inferior parietal lobule (IPL) reactivity to threat varied positi
173 retrieval success pattern, a larger inferior parietal lobule (IPL) region tracked the validity of the
174 reveal the contribution of rostral inferior parietal lobule (IPL) regions, in particular PFt, and th
176 x (AIC), premotor cortex (PMd), and inferior parietal lobule (IPL) were modulated by prior belief on
177 he supramarginal gyrus (SMG) of the inferior parietal lobule (IPL) where we observed a double dissoci
178 orsomedial prefrontal cortex (PFC), inferior parietal lobule (IPL), and hippocampal activity varied w
179 in posterior temporal gyrus (pSTG), inferior parietal lobule (IPL), and ventral central sulcus (vCS)
180 nvolved stronger signal in the left inferior parietal lobule (IPL), bilateral precuneus (PCN), bilate
181 relative to the pop-out task in the inferior parietal lobule (IPL), frontal eye field (FEF), middle f
182 al prearcuate cortex and the caudal inferior parietal lobule (IPL), interconnected regions that are p
184 , ventral premotor cortex (PMv) and inferior parietal lobule (IPL), presumably consisting of motor-re
185 uperior temporal sulcus (pSTS), the inferior parietal lobule (IPL), the premotor cortex (PM), and the
190 on was found for the left and right inferior parietal lobules (IPL), the left superior parietal lobul
191 , posterior cingulate cortex [PCC], inferior parietal lobule [IPL], and superior temporal gyrus (STG]
192 ed with social and moral cognition (inferior parietal lobule [IPL], prefrontal cortex [PFC], and cing
194 ence that a specific sector of left inferior parietal lobule is devoted to tool use in humans, but no
195 n patients to determine whether the superior parietal lobule is indeed necessary for working memory.
196 g semantic information and the left inferior parietal lobule is involved in mapping between orthograp
197 ate cortex/retrosplenial (PCC/Rsp), inferior parietal lobule, lateral temporal cortex, and hippocampu
198 eased GMV in the right insula, left inferior parietal lobule, left dorsolateral prefrontal cortex/sup
199 lt network node (the left posterior inferior parietal lobule, lpIPL) induced two topographically dist
200 e network (DMN), the left and right superior parietal lobules (LSPL/RSPL) and DMN, and the LSPL/RSPL
201 the posterior intraparietal sulcus/inferior parietal lobule may resolve perceptual conflicts selecti
202 intraparietal sulcus and bilateral superior parietal lobule, met our criteria for transsaccadic orie
203 uditory stream, specifically in the inferior parietal lobule, middle frontal gyrus, and dorsal parts
204 ecific areas were identified in the superior parietal lobule, middle temporal and lateral prefrontal
205 ition, and cortical atrophy, in the inferior parietal lobule, middle temporal gyrus, precuneus, and i
206 mplicated a common region of medial superior parietal lobule (mSPL) as a domain-independent source of
207 hemodynamic activity in the medial superior parietal lobule (mSPL), previously implicated in volunta
209 Neurons have been described in the inferior parietal lobule of monkeys, which besides encoding a spe
210 targeting the dorsal pathway's left inferior parietal lobule or the ventral reading pathway's left mi
213 lateral, and ventral temporal lobe; inferior parietal lobule; posterior cingulate gyrus and precuneus
214 cts showed greater activation in the cuneus, parietal lobule, precentral gyrus, and superior temporal
215 sely correlated with FC in the LOC, superior parietal lobule, precuneus, and default mode networks (r
216 hand, and included the inferior and superior parietal lobule, precuneus, and posterior superior tempo
217 reading by the blind activated the inferior parietal lobule, primary visual cortex, superior occipit
219 ts interactions between the central inferior parietal lobule region and the anterior prefrontal corte
220 second key system in the precuneus/superior parietal lobule region with reduced functional connectiv
221 d significantly reduced MTR in left inferior parietal lobule relative to controls, as well as an MTR
223 ft supplementary motor area (SMA), bilateral parietal lobule, right hippocampus, bilateral middle fro
224 he left anterior hippocampus, right inferior parietal lobule, right posterior cingulate cortex, and r
226 ychological evidence supporting the superior parietal lobule's purported role in working memory has b
227 ivity analyses with hippocampal and inferior parietal lobule seed regions and the rest of the brain a
230 (dlPFC), frontal eye fields (FEF), superior parietal lobule (SPL) and intraparietal sulcus (IPS).
231 or parietal lobules (IPL), the left superior parietal lobule (SPL) and the right precuneus-SPL, which
232 ce periods each highlight the right superior parietal lobule (SPL) as a source for training-related c
233 al (LFP) activity obtained from the superior parietal lobule (SPL) as non-human primates performed a
234 intraparietal sulcus (IPS) and left superior parietal lobule (SPL) differing in time and sign for rec
235 rior intraparietal sulcus (aIPS) or superior parietal lobule (SPL) disrupts on-line adaptive adjustme
236 s revealed the critical role of the superior parietal lobule (SPL) in shifting spatial attention, a f
237 ithin the frontal eye fields (FEF), superior parietal lobule (SPL), and right supramarginal gyri (SMG
238 F, the frontal eye field (FEF), the superior parietal lobule (SPL), and the right ventrolateral prefr
239 rior insula with regions within the superior parietal lobule (SPL), including the left precuneus.
241 reas (IPS1-IPS5) and an area in the superior parietal lobule (SPL1)] to examine their spatial attenti
243 ases in cortical activity in medial superior parietal lobule, suggesting that this may be the source
245 patients in the postcentral gyrus, inferior parietal lobule, temporal-parietal junction and the pulv
246 x (the "retrosplenial complex") and superior parietal lobule that exhibited reliable tuning as a func
248 We identified a region in the right superior parietal lobule that responded to both types of visuomot
249 rus (SMG) is a structure within the inferior parietal lobule that specifically processes object-direc
250 showed a reversed asymmetry in the inferior parietal lobule that was localized to the angular gyrus,
251 ng the inferior parietal sulcus and superior parietal lobule, the frontal eye-movement field, and the
252 hemispheric areas, namely the right superior parietal lobule, the insula, and the temporal pole.
253 striate and prestriate cortex, the superior parietal lobules, the frontal eye fields, the supplement
255 gnetic resonance imaging to measure inferior parietal lobule volumes of 15 pairs of male and female s
257 eft IFG and the right IFG and right inferior parietal lobule was also significantly correlated with a
260 operculum, middle frontal gyri, and inferior parietal lobule were specifically associated with trace
261 the left prefrontal cortex and left superior parietal lobule, were selectively activated for verb tri
262 anges were found bilaterally in the inferior parietal lobule when prisms, but not plain glasses, were
263 al gyrus, mediodorsal thalamus, and inferior parietal lobule, whereas perceptual beliefs were encoded
264 stimated generators within the left superior parietal lobule, which may reflect post-lexical activati
265 ation and movement direction in the superior parietal lobule, which may underlie a transformation fro
266 n, especially its connection to the inferior parietal lobule, which was particularly prominent in ear
267 or superior temporal gyrus, and the inferior parietal lobule, while those of patients with atypical l
268 cortex (IMC) and in the ipsilateral inferior parietal lobule with increasing global disability (as as
269 er; conversely, connectivity of the superior parietal lobules within the lateral motor network was ab