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1 to-occipital cortex and the rostral superior parietal lobule.
2 olved the pre-central gyrus and the anterior parietal lobule.
3 es off the IPS and extends into the superior parietal lobule.
4 the middle frontal gyrus, ACC, and superior parietal lobule.
5 yrus, posterior cingulate, and left inferior parietal lobule.
6 sula, supramarginal gyrus, and left inferior parietal lobule.
7 otor cortex, as well as the rostral inferior parietal lobule.
8 across the cortical surface of the inferior parietal lobule.
9 HF and the contralateral DLPFC and inferior parietal lobule.
10 y in the striatum and the posterior superior parietal lobule.
11 left posterior temporal cortex and inferior parietal lobule.
12 ortex, superior temporal gyrus, and superior parietal lobule.
13 s gyrus [planum temporale (PT)] and inferior parietal lobule.
14 marginal gyrus (SMG), a part of the inferior parietal lobule.
15 left anterior hippocampus and right inferior parietal lobule.
16 he rostral-most region of the right superior parietal lobule.
17 as of the IPS, superior temporal sulcus, and parietal lobule.
18 dorsolateral prefrontal cortex, and inferior parietal lobule.
19 y decoded from activity in the left inferior parietal lobule.
20 in the medial prefrontal cortex and inferior parietal lobule.
21 premotor cortex originates from the superior parietal lobule.
22 a significant decrease in the right inferior parietal lobule.
23 c stimulation (rTMS) applied to the inferior parietal lobule.
24 precuneus and intraparietal sulcus/inferior parietal lobule.
25 argest correlations observed in the inferior parietal lobule.
26 dorsolateral prefrontal cortex and inferior parietal lobule.
27 ex face area and bilaterally in the inferior parietal lobule.
28 ft inferior temporal gyri, and left superior parietal lobule.
29 ciated with activation in the right inferior parietal lobule.
30 ntral gyrus, postcentral gyrus, and inferior parietal lobule.
31 predicted by per cent damage to the inferior parietal lobule.
32 ingulate gyrus, the putamen and the superior parietal lobules.
33 extent of the lateral superior and inferior parietal lobules.
34 ns of the occipital lobe and of the superior parietal lobules.
35 d grossly asymmetrical inferior and superior parietal lobules.
37 al field representation in the left inferior parietal lobule and a significant decrease in the right
38 ateral prefrontal cortex, and right inferior parietal lobule and caudate nucleus, perhaps reflecting
40 py and increased diffusivity in the superior parietal lobule and increased diffusivity in the hippoca
42 iments, signal in the left anterior inferior parietal lobule and posterior inferior temporal gyrus an
43 sociated cortical network including inferior parietal lobule and posterior inferolateral temporal gyr
44 versely, activity patterns in right superior parietal lobule and premotor cortex, and also left front
45 lower fractional anisotropy in the superior parietal lobule and reduced mean diffusivity in the thal
47 We identified decreased MTR in left inferior parietal lobule and right superior parietal lobule in su
48 pected sex differences in the right inferior parietal lobule and superior marginal gyrus, and display
49 and suggests a crucial role of the superior parietal lobule and supramarginal gyrus in mediating com
51 refrontal cortex and both the right superior parietal lobule and the left lateral occipital cortex) i
55 r functional connectivity with left inferior parietal lobule and ventral premotor cortex, indicating
56 middle temporal gyri, inferior and superior parietal lobules and precuneus, all of which were unilat
57 regions (Broca's area and the left inferior parietal lobule), and with stronger negative relationshi
58 siform gyri, middle occipital lobe, inferior parietal lobule, and also cingulate, paracentral, and pr
59 n in the lateral prefrontal cortex, inferior parietal lobule, and cerebellum, relative to the compari
61 ed functional connectivity with the inferior parietal lobule, and children with ASD showed atypical f
62 ay (i.e., superior occipital gyrus, superior parietal lobule, and dorsal premotor area) was relevant
63 l gyrus, orbital prefrontal cortex, superior parietal lobule, and hippocampus; right claustrum/putame
64 on during motor imagery in the left inferior parietal lobule, and in the anterior cingulate gyrus and
65 vity in left middle temporal gyrus, inferior parietal lobule, and inferior frontal gyrus as videos we
66 ft posterior cingulate cortex, left inferior parietal lobule, and left fusifom/parahippocampal gyrus.
68 nd right transverse temporal gyrus, superior parietal lobule, and paracentral, lateral orbitofrontal,
70 gyrus, motion sensitive area MT/V5, superior parietal lobule, and primary visual cortex, while showin
71 impaired group (left temporal pole, inferior parietal lobule, and superior temporal gyrus) correspond
72 rontal gyrus, middle frontal gyrus, superior parietal lobule, and supramarginal gyrus, comparison sub
73 portions of the prefrontal cortex, inferior parietal lobule, and temporoparietal junction, as well a
75 st three (anterior cingulate, right inferior parietal lobule, and the caudate/lateral dorsal nucleus)
77 rticularly the angular gyrus of the inferior parietal lobule, and the planum temporale are brain regi
78 rior intraparietal sulcus, anterior superior parietal lobule, and the ventral object-specific lateral
79 hway (i.e., middle occipital gyrus, inferior parietal lobule, and ventral premotor area) was specific
80 ontal eye fields, both superior and inferior parietal lobules, and regions within the prefrontal cort
81 ingulate cortex, right superior and inferior parietal lobules, and right superior frontal, middle tem
82 of the right frontal pole, the right lateral parietal lobules, and the left posterior cingulate corte
83 efault mode network, precuneus, and inferior parietal lobule; and, within the dorsal attention networ
84 with higher metabolic values in the inferior parietal lobule, anterior cingulate, inferior temporal l
85 The premotor cortex face area and inferior parietal lobule are both implicated in the cortical mirr
87 ivation in the left hippocampus and inferior parietal lobule (area 40), left middle (area 10) and sup
89 y corresponded to activation in the inferior parietal lobule, as well as to activation around the inf
90 s, left dorsolateral PFC, and right inferior parietal lobule at rest in the treatment group compared
93 ntary motor area, premotor area and superior parietal lobule, based on the anatomic location of the h
94 ion contrast map included bilateral superior parietal lobule, bilateral dorsolateral prefrontal corte
97 ation in occipital regions and left inferior parietal lobule but increased activation in parietal-occ
98 siform gyri, ventral premotor area, superior parietal lobule, cerebellum and primary sensorimotor are
100 uospatial representation within the inferior parietal lobule changes, with a decrease of the ipsilate
101 ateral to the intraparietal sulcus [inferior parietal lobule complex (IPLC)] and two regions in the m
102 we show that activity in the human inferior parietal lobule correlates with the divergence of such o
103 dorsolateral prefrontal cortex and superior parietal lobule, corresponded to the decision variables
105 plementary motor area and the right inferior parietal lobule demonstrated a positive linear relations
106 ial and decreased activation in the inferior parietal lobule during storage of nonverbal material.
107 strogen increased activation in the inferior parietal lobule during storage of verbal material and de
109 illustrated in a patient with left inferior parietal lobule embolic infarction in whom a significant
110 nal evoked by switch cues in medial superior parietal lobule for both domains of control, revealing a
111 tic processing occurred in the left inferior parietal lobule for words, and the right middle occipita
113 egions of the default mode network, superior parietal lobule, fusiform gyrus and anterior insula.
115 ymmetry in this region and had left inferior parietal lobule gray matter volumes that were significan
117 th and suggest vulnerability of the superior parietal lobule, hippocampus, and thalamus to glycemic e
118 ng attention has been linked to the superior parietal lobule; however, the neural substrates associat
119 ereas stimulation over right medial superior parietal lobule impaired target discrimination after a s
120 hinner angular gyrus, precuneus and superior parietal lobule in carriers compared to non-carriers, wi
121 inferior parietal lobule and right superior parietal lobule in suicide attempters relative to both n
122 rom the middle frontal gyrus to the superior parietal lobule in the right hemisphere in healthy contr
125 he primary somatosensory cortex and superior parietal lobule influences brain networks associated wit
126 al gyrus), parietal lobe (bilateral inferior parietal lobule), insula, and limbic lobe (anterior and
127 the posterior intraparietal sulcus/inferior parietal lobule interfered with perceptual conflict proc
128 aptation paradigm, we show that the inferior parietal lobule (IPL) (corresponding to the supramargina
129 trongly lateralized network, where the infra-parietal lobule (IPL) activation was lateralized to the
130 parieto-temporal network; bilateral inferior parietal lobule (IPL) activity was larger in HC versus S
131 the levels of HSPs in hippocampus, inferior parietal lobule (IPL) and cerebellum of subjects with aM
132 labeled by tracer injections in the inferior parietal lobule (IPL) and dorsolateral prefrontal cortex
133 protein nitration is higher in the inferior parietal lobule (IPL) and hippocampus in MCI compared to
134 associated with damage to the right inferior parietal lobule (IPL) and the right temporo-parietal jun
135 vely covalently bound by HNE in EAD inferior parietal lobule (IPL) compared to age-related control br
136 n primary motor cortex (M1) and the inferior parietal lobule (IPL) have been identified with supporti
137 superior temporal gyrus (STG), and inferior parietal lobule (IPL) in Non-prehensile Use trials as co
140 retrieval success pattern, a larger inferior parietal lobule (IPL) region tracked the validity of the
142 he supramarginal gyrus (SMG) of the inferior parietal lobule (IPL) where we observed a double dissoci
143 in posterior temporal gyrus (pSTG), inferior parietal lobule (IPL), and ventral central sulcus (vCS)
144 nvolved stronger signal in the left inferior parietal lobule (IPL), bilateral precuneus (PCN), bilate
145 relative to the pop-out task in the inferior parietal lobule (IPL), frontal eye field (FEF), middle f
146 al prearcuate cortex and the caudal inferior parietal lobule (IPL), interconnected regions that are p
151 on was found for the left and right inferior parietal lobules (IPL), the left superior parietal lobul
152 , posterior cingulate cortex [PCC], inferior parietal lobule [IPL], and superior temporal gyrus (STG]
154 ence that a specific sector of left inferior parietal lobule is devoted to tool use in humans, but no
155 n patients to determine whether the superior parietal lobule is indeed necessary for working memory.
156 g semantic information and the left inferior parietal lobule is involved in mapping between orthograp
157 ate cortex/retrosplenial (PCC/Rsp), inferior parietal lobule, lateral temporal cortex, and hippocampu
158 lt network node (the left posterior inferior parietal lobule, lpIPL) induced two topographically dist
159 the posterior intraparietal sulcus/inferior parietal lobule may resolve perceptual conflicts selecti
160 uditory stream, specifically in the inferior parietal lobule, middle frontal gyrus, and dorsal parts
161 ecific areas were identified in the superior parietal lobule, middle temporal and lateral prefrontal
162 mplicated a common region of medial superior parietal lobule (mSPL) as a domain-independent source of
163 hemodynamic activity in the medial superior parietal lobule (mSPL), previously implicated in volunta
166 cts showed greater activation in the cuneus, parietal lobule, precentral gyrus, and superior temporal
167 hand, and included the inferior and superior parietal lobule, precuneus, and posterior superior tempo
168 reading by the blind activated the inferior parietal lobule, primary visual cortex, superior occipit
170 ts interactions between the central inferior parietal lobule region and the anterior prefrontal corte
171 second key system in the precuneus/superior parietal lobule region with reduced functional connectiv
172 d significantly reduced MTR in left inferior parietal lobule relative to controls, as well as an MTR
174 ft supplementary motor area (SMA), bilateral parietal lobule, right hippocampus, bilateral middle fro
175 he left anterior hippocampus, right inferior parietal lobule, right posterior cingulate cortex, and r
176 ychological evidence supporting the superior parietal lobule's purported role in working memory has b
177 ivity analyses with hippocampal and inferior parietal lobule seed regions and the rest of the brain a
180 (dlPFC), frontal eye fields (FEF), superior parietal lobule (SPL) and intraparietal sulcus (IPS).
181 or parietal lobules (IPL), the left superior parietal lobule (SPL) and the right precuneus-SPL, which
182 intraparietal sulcus (IPS) and left superior parietal lobule (SPL) differing in time and sign for rec
183 rior intraparietal sulcus (aIPS) or superior parietal lobule (SPL) disrupts on-line adaptive adjustme
184 s revealed the critical role of the superior parietal lobule (SPL) in shifting spatial attention, a f
185 ithin the frontal eye fields (FEF), superior parietal lobule (SPL), and right supramarginal gyri (SMG
186 F, the frontal eye field (FEF), the superior parietal lobule (SPL), and the right ventrolateral prefr
187 reas (IPS1-IPS5) and an area in the superior parietal lobule (SPL1)] to examine their spatial attenti
189 ases in cortical activity in medial superior parietal lobule, suggesting that this may be the source
190 We identified a region in the right superior parietal lobule that responded to both types of visuomot
191 showed a reversed asymmetry in the inferior parietal lobule that was localized to the angular gyrus,
192 ng the inferior parietal sulcus and superior parietal lobule, the frontal eye-movement field, and the
193 striate and prestriate cortex, the superior parietal lobules, the frontal eye fields, the supplement
195 gnetic resonance imaging to measure inferior parietal lobule volumes of 15 pairs of male and female s
197 eft IFG and the right IFG and right inferior parietal lobule was also significantly correlated with a
200 operculum, middle frontal gyri, and inferior parietal lobule were specifically associated with trace
201 the left prefrontal cortex and left superior parietal lobule, were selectively activated for verb tri
202 anges were found bilaterally in the inferior parietal lobule when prisms, but not plain glasses, were
203 ation and movement direction in the superior parietal lobule, which may underlie a transformation fro
204 or superior temporal gyrus, and the inferior parietal lobule, while those of patients with atypical l
205 cortex (IMC) and in the ipsilateral inferior parietal lobule with increasing global disability (as as
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