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4 superior temporal, left supramarginal, left postcentral, and occipital regions (P values were betwee
6 synchronized neuronal assemblies in pre- and postcentral areas of two monkeys as they pressed a hand
8 (BA 6), parietal (BA 7), precentral (BA 4), postcentral (BA 3), occipital (BA 18), and calcarine (BA
9 control ROIs (superior parietal, calcarine, postcentral, central, and precentral cortices), and to o
10 egion, which includes the caudal half of the postcentral convexity as well as the medial bank of the
11 However, little is known about the role of postcentral cortical areas in motor maintenance and thei
12 ses in activation in precentral (P<.001) and postcentral gyri (P = .03) and the cerebellum (P<.001),
13 re concentrated in premotor cortex, pre- and postcentral gyri and supramarginal gyrus with minimal ex
15 ral, posterior middle temporal, and inferior postcentral gyri bilaterally, and enlarged superior fron
16 ral prefrontal cortex, as well as precentral/postcentral gyri during processing of threatening faces
17 n number of activated voxels in the pre- and postcentral gyri induced by active and passive movements
20 n the other pathologies, although precentral/postcentral gyri volume was reduced in comparison with o
21 cluding the sylvian fissure and temporal and postcentral gyri, by using magnetic resonance data and a
23 cluded insulae, cingulate cortices, pre- and postcentral gyri, precunei, cunei, bilateral putamena, r
24 rates in the formation of the precentral and postcentral gyri, right superior temporal gyrus, and ope
25 eas, including bilateral STG, precentral and postcentral gyri, supplementary motor area, supramargina
30 i, precuneus, cingulate cortex, caudate, and postcentral gyrus (all regions: p < .001, etap(2) > .06)
31 ificantly associated with stimulation of the postcentral gyrus (odds ratio: 5.83, P < 0.001; odds rat
33 and were not predicted to be adjacent in the postcentral gyrus (PoCG), suggesting that representation
34 activation response in areas of the ventral postcentral gyrus (POG) in the patients relative to cont
35 ficant modulation of neural activity in left postcentral gyrus (PostCG), right culmen and, co-varying
37 stigate whether neural activity in the right postcentral gyrus (rPoG) and right lateral premotor cort
38 r parietal lobe, inferior parietal lobe, and postcentral gyrus abnormalities contributing to deficits
39 torhinal cortex, superior-frontal gyrus, and postcentral gyrus across the lifespan of 55 cognitively
40 a positive component, were recorded over the postcentral gyrus and a later one, consisting of only a
41 f focal activity located in the ipsilesional postcentral gyrus and cingulate cortex (p < 0.05, correc
42 he first few days after stroke, of which the postcentral gyrus and cingulate cortex are a part, that
43 ntral prefrontal cortices (vPFC), as well as postcentral gyrus and global cerebrum control regions.
45 the left or right hemisphere, but not in the postcentral gyrus as the entry site of cortical somatose
46 dings suggest anatomical displacement of the postcentral gyrus in psychotic disorders and support the
47 a robust somatosensory MMN was recorded from postcentral gyrus in the absence of an auditory MMN.
49 are patient with a focal lesion of the right postcentral gyrus that interferes with the processing of
50 W.) with a circumscribed lesion of the right postcentral gyrus that overlapped the human eye proprioc
51 alateral primary somatosensory cortex on the postcentral gyrus together with the bilateral parietal o
52 For processing of happy faces, activation in postcentral gyrus was a significant predictor of treatme
53 P = .002) or healthy controls (P = .04), the postcentral gyrus was thinner in patients with MDD than
57 ral gyri, left inferior parietal region with postcentral gyrus, and right superior frontal and inferi
59 in bilateral parietal and occipital regions (postcentral gyrus, cuneus, lingual gyrus, pericalcarine
60 greater activation in the bilateral caudate, postcentral gyrus, hippocampus, and inferior frontal gyr
62 h ALS in brain regions of the precentral and postcentral gyrus, the paracentral lobule, the superior
63 lar gyrus and the posterior bank of the left postcentral gyrus, the right posterior superior temporal
64 gion, which lies outside the confines of the postcentral gyrus, whereas the ventrorostral premotor co
76 s, right inferior temporal gyrus (ITG), left postcentral gyrus/precuneus, left supplementary motor ar
79 ietal opercular region is connected with the postcentral portions of areas 3, 1, and 2; areas 5, 7, a
80 an occipito-parietal network comprising the postcentral (PostCG) and the superior occipital (SOG) gy
82 wise rCBF differences in the OA group in the postcentral, rostral/subgenual cingulate, mid/anterior i
83 anger causal influences from motor cortex to postcentral sites, however, were weak in one monkey and
84 r time of -0.5 or less included the pre- and postcentral subcortical white matter in the hand knob ar
85 activated regions along the central and the postcentral sulci and in lobules V, VI, and VIII of the
88 hs predicting acuity converged from the left postcentral sulcus and right frontal eye field onto the
89 with the parietal face and body areas in the postcentral sulcus at the most anterior border of the do
91 at the intersection of the intraparietal and postcentral sulcus; SPL1 branches off the IPS and extend
92 superior temporal sulcus, inferior temporal, postcentral/superior parietal and supramarginal gyri).
93 -pronounced layer appearance was as follows: postcentral (variance, 0.04), posterior frontal (varianc
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