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1 a 5 could be considered a highly specialized sensorimotor area.
2 associated with reversal of asymmetry in the sensorimotor area.
3 ource of beta band (13-30 Hz) coherence over sensorimotor areas.
4 significantly attenuated over the bilateral sensorimotor areas.
5 ontal pyramidal neurons developed later than sensorimotor areas.
6 ation in the prefrontal cortex compared with sensorimotor areas.
7 sequence being encoded as in other cortical sensorimotor areas.
8 es (affordances) are visually represented in sensorimotor areas.
9 of connectivity between dorsal striatum and sensorimotor areas.
10 yllables were least likely to engage the lip sensorimotor area and they were least impaired by TMS.
11 on between two major brain systems: unimodal sensorimotor areas and the higher-order association cort
13 n is disentangled from perceptual decisions, sensorimotor areas are not involved in accumulating sens
14 rior parietal lobule, cerebellum and primary sensorimotor area bilaterally, also the right dorsal pre
16 s demonstrated for the ipsilateral secondary sensorimotor area (compared with the ipsilateral primary
17 AG was functionally correlated with cortical sensorimotor areas, conducive to facilitating fight/flig
18 PMV and PMDc, and a more posterior cingulate sensorimotor area (CSMA) with motor connections that may
19 ase together with increased connectedness of sensorimotor areas facilitates successful facial affect
21 area (compared with the ipsilateral primary sensorimotor area) for movement of the hemiplegic hand t
22 tivity in pons, thalamus, medial frontal and sensorimotor areas, hippocampus, supramarginal and infer
23 used throughout life, those in higher-order sensorimotor areas (i.e., inferior parietal cortex and r
24 between reward-related prefrontal areas and sensorimotor areas in the basal ganglia and frontal cort
25 ly -400 ms before response, originating from sensorimotor areas including dmFC, precuneus, and poster
26 n, significant fMRI activities were found in sensorimotor areas including superior parietal lobule bi
27 synchronized beta oscillations bind multiple sensorimotor areas into a large-scale network during mot
29 differing complexity, the bilateral primary sensorimotor area, left ventral premotor cortex, posteri
31 flow between lateral and mesial premotor and sensorimotor areas of both hemispheres, even if the move
32 functional impairments suggests that lateral sensorimotor areas of caudate putamen are important for
35 to reinforcement, with connectivity between sensorimotor areas of putamen and the reward-related ven
38 his distinction is particularly relevant for sensorimotor areas such as parietal cortex, where both v
39 the right premotor area (PMA), superolateral sensorimotor areas, thalamus, and bilaterally in the cer
40 transfer of visual motion information to the sensorimotor areas that transform visual information int
41 gnalled by these cells could be used by this sensorimotor area to detect novel objects and motion in
42 anial direct current stimulation (tDCS) over sensorimotor areas to modulate neural lateralization pat
43 -15 Hz power increase localized in bilateral sensorimotor areas, together with occipital power decrea
44 ols are visually represented within the same sensorimotor areas underlying their dexterous use accord
45 nd that hemodynamic signals in contralateral sensorimotor areas vary with the direction of movements,
46 gnificant functional connectivity within the sensorimotor area was identified using independent compo
47 we recorded neural activity in a prefrontal sensorimotor area while monkeys naturally switched betwe
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