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3 ands produced increases in blood flow in the precentral and postcentral gyri of the right hemisphere.
4 elative growth rates in the formation of the precentral and postcentral gyri, right superior temporal
5 uage-related areas, including bilateral STG, precentral and postcentral gyri, supplementary motor are
7 associated with ALS in brain regions of the precentral and postcentral gyrus, the paracentral lobule
8 ncreased connectivity in a network including precentral and sensory-motor areas, whereas after 30 min
10 amaged left hemisphere language areas, right precentral and superior temporal gyrus, as well as left
11 ortical motor (ProM) areas is connected with precentral areas 3, 1, and 2 as well as with the rostral
12 , posterior frontal (BA 6), parietal (BA 7), precentral (BA 4), postcentral (BA 3), occipital (BA 18)
13 and rostral subdivisions of gigantocellular precentral cortex (areas 4c, 4i, and 4r) in macaque monk
14 luding medial agranular cortex (AGm), medial precentral cortex (PrCm), and frontal orienting field (F
16 ve data showing that microstimulation of the precentral cortex evokes complex movements, and conclude
19 he brainstem, centrum semiovale, frontal and precentral cortex, and significantly reduced NA/Cho in t
21 cortex [frontal eye field (FEF), PreCC/IFS (precentral cortex/inferior frontal sulcus)] and parietal
22 tomical and functional lesions spread beyond precentral cortices and corticospinal tracts, to include
23 e infralimbic, dorsal peduncular, and medial precentral cortices have dense intrinsic projections, bu
24 rietal, calcarine, postcentral, central, and precentral cortices), and to obtain an unbiased estimate
27 involved the bilateral superior-temporal and precentral gyri immediately following question onset; at
30 ric functional connectivity of the bilateral precentral gyri positively correlated with fractional an
31 he healthy comparison group in the bilateral precentral gyri, anterior cingulate cortex, and middle a
32 lobule, and also cingulate, paracentral, and precentral gyri, compared with the non-hallucinators.
33 nterior cingulate cortex, the left and right precentral gyri, the left and right anterior temporal co
37 ent conditions namely in the left hemisphere precentral gyrus (BA 4), the left hemisphere superior pa
39 tex (Brodmann area [BA] 22) bilaterally, the precentral gyrus (BA 9) on the left, and the precentral
41 c masks of the superior frontal gyrus (SFG), precentral gyrus (PcG), middle frontal gyrus (MFG), orbi
43 posterior inferior frontal gyrus (PIFG) and precentral gyrus (PrG); the impairment was immediately r
44 oca's region) and the ventral portion of the precentral gyrus (speech motor cortex) resulted in the m
45 herapy in the right prefrontal cortex (right precentral gyrus [Brodmann's area 9], inferior frontal g
48 d increases in ECN connectivity in the right precentral gyrus and decreases in DMN connectivity in th
49 elated positively with RSFC between the left precentral gyrus and other motor regions, and between Br
50 , and dorsal cortical areas (checking); left precentral gyrus and right orbitofrontal cortex (hoardin
51 n cortical areas were identified between the precentral gyrus and the anterior bank of the intraparie
52 anxiety with cortical thickness in bilateral precentral gyrus and the dorsolateral prefrontal cortex.
53 ing in the precentral sulcus, connecting the precentral gyrus and the SMA; (2) U-fibres running in th
55 11)C-CNS 5161 uptake in caudate, putamen and precentral gyrus compared to the patients without dyskin
56 RI), that a region of the medial wall of the precentral gyrus consistently activates during both volu
57 ate, right superior temporal gyrus and right precentral gyrus during psychography compared to their n
58 al gyrus with high correlation with the left precentral gyrus for the finger-tapping state versus the
60 ignificantly compared to the activity in the precentral gyrus from control samples (22.7 +/- 0.5 nmol
61 atched on reading abilities, with only right precentral gyrus GMV surviving this second analysis.
62 primary motor cortical region in the caudal precentral gyrus is not connected with the posterior par
66 ap study identified the superior part of the precentral gyrus of the insula (in the anterior insula)
67 that included a discrete region of the left precentral gyrus of the insula, a cortical area beneath
69 talase were not significantly altered in the precentral gyrus or cerebellar cortex in the patient sam
70 This sound-related somatotopic activation in precentral gyrus shows that, during speech perception, s
71 ally, however, distinct motor regions in the precentral gyrus sparked by articulatory movements of th
72 ildren had a stronger activation in the left precentral gyrus than did adults in response to unhealth
73 kening relative to HR-well subjects and left precentral gyrus thickening relative to HR-well and HC i
74 mproving behaviour, while hypertrophy in the precentral gyrus was associated with declining behaviour
80 with low-ED cues in the insula, declive, and precentral gyrus were negatively related to appetitive t
83 egions (e.g., in the caudate, cingulate, and precentral gyrus) and decreased activation in the insula
84 et regions (cLBP study, thalamus; ALS study, precentral gyrus) was normalized with the SUV from candi
85 previously, such as parafascicular thalamus, precentral gyrus, and dentate nucleus of the cerebellum.
90 ior temporal and middle occipital gyri, left precentral gyrus, bilateral opercular part of the inferi
91 ead rotation was observed bilaterally in the precentral gyrus, both medial and lateral to the hand ar
92 ared with passive movements, although in the precentral gyrus, hand, elbow, and shoulder movements sh
93 l area 6VR, in the most anterior part of the precentral gyrus, has strong connections with the rostra
94 electrically excitable cortex located on the precentral gyrus, including cortex sometimes considered
95 significantly less gray matter volume in the precentral gyrus, middle and superior frontal gyri, fron
96 nia patients exhibited decreased ReHo in the precentral gyrus, middle occipital gyrus, and posterior
97 elated to hand velocity in the contralateral precentral gyrus, postcentral gyrus, and inferior pariet
98 s, frontal inferior operculum, Heschl gyrus, precentral gyrus, rolandic operculum, and superior and i
99 rality in the medial superior frontal gyrus, precentral gyrus, Rolandic operculum, superior parietal
100 ngulate, gyrus rectus, orbitofrontal cortex, precentral gyrus, superior frontal cortex, middle fronta
101 he left pars opercularis, extending into the precentral gyrus, was activated to a greater extent by d
102 hout special foot skill mainly activated the precentral gyrus, which differed from those with more ad
103 tations of rules from both levels except for precentral gyrus, which represented only low-level rule
104 reductions in the left inferior frontal and precentral gyrus, which were greater in HR-well subjects
105 f an association between hand preference and precentral gyrus-morphology in chimpanzees (Pan troglody
113 e and expressive aphasia; and (iv) bilateral precentral/left posterior superior-frontal regions and s
114 ingulate cortex has extensive projections to precentral medial cortex and caudally directed projectio
115 ing in rhesus monkey to define subregions in precentral motor cortex (M1), injected isotope tracers i
116 with significant increases in activation in precentral (P<.001) and postcentral gyri (P = .03) and t
117 ventrolateral prefrontal cortex, as well as precentral/postcentral gyri during processing of threate
118 me loss than the other pathologies, although precentral/postcentral gyri volume was reduced in compar
120 s showed higher BOLD activation to SS in the precentral, prefrontal, fusiform, and posterior cingulat
121 neural stimulation studies (suppressing the precentral region and/or enhancing the anterior temporal
123 ntrast to the LOTC, the early recruitment of precentral regions does not contain the detailed informa
127 lpha-band oscillations (9-13 Hz) recorded at precentral sites strongly predicted scaling exponents of
128 Here, we recorded neurons from the medial precentral subregion of mouse prefrontal cortex to exami
129 lcal pattern, namely, the interposition of a precentral sulcal segment between the central sulcus and
130 perior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), anatomically interdigitated wi
131 perior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), interleaved with two bilateral
132 01) and was more frequently connected to the precentral sulcus (P < .001) in patients with FCD2 than
134 arietal sulcus (IPS0-IPS3) and two along the precentral sulcus (PCS) that contained reliable retinoto
135 decreased right-lateralized activity in the precentral sulcus (PrCS) and posterior parietal cortex (
136 at are biased for visual attention, superior precentral sulcus (sPCS) and inferior precentral sulcus
137 regions in lateral frontal cortex, superior precentral sulcus (sPCS) and inferior precentral sulcus
138 ently shown that the superior element of the precentral sulcus (sPCS), near the caudal end of the sup
139 ory attention, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal su
140 ntion regions, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal su
141 he lateral parietal cortex, and the superior precentral sulcus (thought to contain the human homolog
143 ided bias in the bifurcation of the inferior precentral sulcus, an anatomical feature that occurs muc
144 reconstructions: (1) U-fibres running in the precentral sulcus, connecting the precentral gyrus and t
145 uction in the cerebral cortex, including the precentral, superior and middle temporal, and lingual gy
146 d points, the middle temporal (T = 4.25) and precentral (T = 6.47) gyri, and one right ILF end point,
149 variance, 0.05), calcarine (variance, 0.05), precentral (variance, 0.06), parietal (variance, 0.08),
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