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1 wer mean (SD) FA in white matter of the left postcentral (0.35 [0.05] vs 0.36 [0.04]; mean difference
2 , especially in the left insula and in right postcentral and middle frontal regions.
3                    Abnormalities in the left postcentral and middle occipital gyri were found only in
4  max, 3.76; P = .01; activation of the right postcentral and supramarginal gyrus: Z max, 3.73; P < .0
5 ral dorsolateral prefrontal, precuneus, left postcentral, and inferior parietal regions.
6 , pain contexts recruited the supramarginal, postcentral, and insular cortex, whereas disgust context
7  superior temporal, left supramarginal, left postcentral, and occipital regions (P values were betwee
8 n (areas 1 and 2) is connected with pre- and postcentral areas 3, 1, and 2 as well as SII.
9 synchronized neuronal assemblies in pre- and postcentral areas of two monkeys as they pressed a hand
10 ronized large-scale network linking pre- and postcentral areas.
11 lcarine (B [SE] = -0.077 [0.012]; P < .001), postcentral (B [SE] = -0.069 [0.012]; P < .001), precent
12  (BA 6), parietal (BA 7), precentral (BA 4), postcentral (BA 3), occipital (BA 18), and calcarine (BA
13  control ROIs (superior parietal, calcarine, postcentral, central, and precentral cortices), and to o
14 uted to writing words, while lesions to left postcentral contributed to writing numbers.
15 egion, which includes the caudal half of the postcentral convexity as well as the medial bank of the
16 ectivity in schizophrenia in insula, lateral postcentral cortex, striatum, and thalamus.
17  GMV reductions converged in insula, lateral postcentral cortex, striatum, and thalamus.
18 ble for migraine classification included the postcentral cortex, supramarginal gyrus, superior tempor
19   However, little is known about the role of postcentral cortical areas in motor maintenance and thei
20 associated with less left precuneus and left postcentral cortical thickness and smaller left superior
21 abnormalities occurring in the early folding postcentral cortices (three-path mediation).
22 ip of gyrification between the early folding postcentral cortices and associative temporal cortices,
23 late cortices and with lower GWC in pre- and postcentral cortices.
24 ses in activation in precentral (P<.001) and postcentral gyri (P = .03) and the cerebellum (P<.001),
25 y with the thickness of the precentral gyri, postcentral gyri and superior frontal gyrus in JME (left
26 re concentrated in premotor cortex, pre- and postcentral gyri and supramarginal gyrus with minimal ex
27   Regions of interest were drawn in pre- and postcentral gyri based on anatomic criteria.
28 ral, posterior middle temporal, and inferior postcentral gyri bilaterally, and enlarged superior fron
29 ral prefrontal cortex, as well as precentral/postcentral gyri during processing of threatening faces
30 n number of activated voxels in the pre- and postcentral gyri induced by active and passive movements
31                In the insula, precentral and postcentral gyri NTDE signals were greater, and PTDE-rel
32 ncreases in blood flow in the precentral and postcentral gyri of the right hemisphere.
33 owed altered nodal centralities in left pre-/postcentral gyri relative to controls.
34 n the other pathologies, although precentral/postcentral gyri volume was reduced in comparison with o
35 cluding the sylvian fissure and temporal and postcentral gyri, by using magnetic resonance data and a
36 tic posterior shift of the inferior pre- and postcentral gyri, indicative of reorganization of the fr
37     The modulated happiness network included postcentral gyri, left caudate, right cingulate cortex,
38 cluded insulae, cingulate cortices, pre- and postcentral gyri, precunei, cunei, bilateral putamena, r
39 rates in the formation of the precentral and postcentral gyri, right superior temporal gyrus, and ope
40 eas, including bilateral STG, precentral and postcentral gyri, supplementary motor area, supramargina
41 lcus: small gyri bridging the precentral and postcentral gyri.
42 e relapsed group with the bilateral pre- and postcentral gyri.
43 losum, superior temporal gyrus, and pre- and postcentral gyri.
44 al gyri and in the left inferior frontal and postcentral gyri.
45  skill who activated both the precentral and postcentral gyri.
46 i, precuneus, cingulate cortex, caudate, and postcentral gyrus (all regions: p < .001, etap(2) > .06)
47 ion (left IFG BA 46), and dual-tasking [left postcentral gyrus (BA 40)].
48 ificantly associated with stimulation of the postcentral gyrus (odds ratio: 5.83, P < 0.001; odds rat
49                                          The postcentral gyrus (PCG) was included to control for any
50  lateral/posterolateral nucleus (VL/VPL) and postcentral gyrus (PoCG) and between the dorsal/ventral
51 and were not predicted to be adjacent in the postcentral gyrus (PoCG), suggesting that representation
52  activation response in areas of the ventral postcentral gyrus (POG) in the patients relative to cont
53 ficant modulation of neural activity in left postcentral gyrus (PostCG), right culmen and, co-varying
54 he parietal operculum (related to speed) and postcentral gyrus (related to dot periodicity).
55 stigate whether neural activity in the right postcentral gyrus (rPoG) and right lateral premotor cort
56 r parietal lobe, inferior parietal lobe, and postcentral gyrus abnormalities contributing to deficits
57 uding the bilateral insula, thalamus and pre/postcentral gyrus across both groups.
58 torhinal cortex, superior-frontal gyrus, and postcentral gyrus across the lifespan of 55 cognitively
59 a positive component, were recorded over the postcentral gyrus and a later one, consisting of only a
60 f focal activity located in the ipsilesional postcentral gyrus and cingulate cortex (p < 0.05, correc
61 he first few days after stroke, of which the postcentral gyrus and cingulate cortex are a part, that
62 ntral prefrontal cortices (vPFC), as well as postcentral gyrus and global cerebrum control regions.
63 tive reasoning (superior temporal and medial postcentral gyrus and parahippocampus) were the main pos
64 bilateral amygdala connectivity to the right postcentral gyrus and right precuneus.
65                              Activity in the postcentral gyrus and superior parietal lobule was sensi
66 metry was altered in left-handedness: on the postcentral gyrus and the inferior occipital cortex, fun
67 the left or right hemisphere, but not in the postcentral gyrus as the entry site of cortical somatose
68 dings suggest anatomical displacement of the postcentral gyrus in psychotic disorders and support the
69 a robust somatosensory MMN was recorded from postcentral gyrus in the absence of an auditory MMN.
70 monization process across the precentral and postcentral gyrus might not be possible because of diver
71  representations (FRs) in the precentral and postcentral gyrus of 25 5-fingered participants (8 femal
72 th overrepresented L-shape triads, where the postcentral gyrus shared different edges with the latera
73           But which brain regions beyond the postcentral gyrus specifically contribute to the percept
74 are patient with a focal lesion of the right postcentral gyrus that interferes with the processing of
75 W.) with a circumscribed lesion of the right postcentral gyrus that overlapped the human eye proprioc
76 alateral primary somatosensory cortex on the postcentral gyrus together with the bilateral parietal o
77 For processing of happy faces, activation in postcentral gyrus was a significant predictor of treatme
78 nity similarity between lateral thalamus and postcentral gyrus was enhanced in migraine.
79 P = .002) or healthy controls (P = .04), the postcentral gyrus was thinner in patients with MDD than
80 , whereas the increases in blood flow in the postcentral gyrus were not.
81 ulate gyrus, inferior parietal lobule (IPL), postcentral gyrus) areas.
82 cingulate and medial superior gyrus and left postcentral gyrus).
83 nging along to the trained song in the right postcentral gyrus, and in the right posterior superior t
84 ocity in the contralateral precentral gyrus, postcentral gyrus, and inferior parietal lobule.
85  supramarginal gyrus, ventral precentral and postcentral gyrus, and insula), and concrete words (pars
86 with greater CT in the left lateral fissure, postcentral gyrus, and middle/lateral occipital cortex,
87 ral gyri, left inferior parietal region with postcentral gyrus, and right superior frontal and inferi
88  premotor cortex, anterior cingulate cortex, postcentral gyrus, and the inferior parietal lobule.
89 e that localized to the anterior bank of the postcentral gyrus, area 3b of SI.
90 in bilateral parietal and occipital regions (postcentral gyrus, cuneus, lingual gyrus, pericalcarine
91 greater activation in the bilateral caudate, postcentral gyrus, hippocampus, and inferior frontal gyr
92 tical thickness in cuff tear patients in the postcentral gyrus, inferior parietal lobule, temporal-pa
93 d tactile FRs within both the precentral and postcentral gyrus, integrating finger-specific motor and
94                                       In the postcentral gyrus, only the shoulder revealed a signific
95 stable showed decreases in activation in the postcentral gyrus, prefrontal cortex, insula, and anteri
96 esentations exist in both the precentral and postcentral gyrus, supported by a finger-specific patter
97 enomic risk loci, we found that in the right postcentral gyrus, the left paracentral lobule and the p
98 h ALS in brain regions of the precentral and postcentral gyrus, the paracentral lobule, the superior
99 lar gyrus and the posterior bank of the left postcentral gyrus, the right posterior superior temporal
100 gion, which lies outside the confines of the postcentral gyrus, whereas the ventrorostral premotor co
101 actile representations in the precentral and postcentral gyrus, while finger kinematics better descri
102       The M20 is generated in area 3b of the postcentral gyrus.
103 function and structure in the precentral and postcentral gyrus.
104 the fingers are mapped in the precentral and postcentral gyrus.
105 ly (4) behavioral response representation in postcentral gyrus.
106 tive input, such as the posterior insula and postcentral gyrus.
107 ence trials was only found in the precentral/postcentral gyrus.
108 anterior cingulate cortex and central sulcus/postcentral gyrus.
109 plementary motor area, precentral gyrus, and postcentral gyrus.
110 was generally confined to the cerebellum and postcentral gyrus.
111 nteraction in the left amygdala and left pre/postcentral gyrus.
112 eus, left inferior parietal lobule, and left postcentral gyrus.
113  and near the parietal operculum and ventral postcentral gyrus.
114 it CCEPs in language areas but rather in the postcentral gyrus.
115 ures, anterior superior parietal cortex, and postcentral gyrus.
116 the left supplementary motor cortex and left postcentral gyrus/precuneus after ECT.
117 s, right inferior temporal gyrus (ITG), left postcentral gyrus/precuneus, left supplementary motor ar
118 lus extent of injury to precentral gyrus and postcentral gyrus; lesion volume; and lesion topography)
119 t is, in the granular insular cortex and the postcentral insular gyrus.
120 tal (gyrus rectus and orbital gyri) and then postcentral neocortex and striatum.
121 ietal opercular region is connected with the postcentral portions of areas 3, 1, and 2; areas 5, 7, a
122  an occipito-parietal network comprising the postcentral (PostCG) and the superior occipital (SOG) gy
123 olved the posterior superior-frontal and pre/postcentral regions, bilaterally.
124 ns; surface area decline in the fusiform and postcentral regions; and in older adults, greater subcor
125 wise rCBF differences in the OA group in the postcentral, rostral/subgenual cingulate, mid/anterior i
126 anger causal influences from motor cortex to postcentral sites, however, were weak in one monkey and
127 r time of -0.5 or less included the pre- and postcentral subcortical white matter in the hand knob ar
128  activated regions along the central and the postcentral sulci and in lobules V, VI, and VIII of the
129 sulcus, and ventral portions of the pre- and postcentral sulci in both hemispheres.
130 a and has non-confluent Sylvian and inferior postcentral sulci.
131 hs predicting acuity converged from the left postcentral sulcus and right frontal eye field onto the
132 with the parietal face and body areas in the postcentral sulcus at the most anterior border of the do
133 he dorsal and ventral precentral sulcus, the postcentral sulcus, and the anterior intraparietal sulcu
134 n cortex-namely, in the superior part of the postcentral sulcus.
135 at the intersection of the intraparietal and postcentral sulcus; SPL1 branches off the IPS and extend
136 superior temporal sulcus, inferior temporal, postcentral/superior parietal and supramarginal gyri).
137 ty in fronto-temporo-limbic, precentral, and postcentral/supramarginal regions (critical for emotiona
138 -pronounced layer appearance was as follows: postcentral (variance, 0.04), posterior frontal (varianc

 
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