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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 tical regions that overlap with the forelimb sensorimotor area.
4  of connectivity between dorsal striatum and sensorimotor areas.
5 ource of beta band (13-30 Hz) coherence over sensorimotor areas.
6  significantly attenuated over the bilateral sensorimotor areas.
7 ontal pyramidal neurons developed later than sensorimotor areas.
8 ation in the prefrontal cortex compared with sensorimotor areas.
9  sequence being encoded as in other cortical sensorimotor areas.
10 es (affordances) are visually represented in sensorimotor areas.
11 ralleled by an increase or lack of change in sensorimotor areas.
12 cs correlates mostly with neural activity in sensorimotor areas.
13 e outputs with those from posterior parietal sensorimotor areas.
14 chronization of beta-band neural activity in sensorimotor areas.
15 yllables were least likely to engage the lip sensorimotor area and they were least impaired by TMS.
16 m(2)) were applied for 20 min over bilateral sensorimotor areas and EEG was recorded at rest before a
17 tests, the elderly showed the recruitment of sensorimotor areas and increased muscle activity level,
18 on between two major brain systems: unimodal sensorimotor areas and the higher-order association cort
19         Elevated coherence was found between sensorimotor areas and the prefrontal and mesial frontal
20 nd local correlations is stronger in primary sensorimotor areas and weaker in association areas such
21     We also highlight how neural dynamics in sensorimotor areas are involved in beat-based timing.
22 n is disentangled from perceptual decisions, sensorimotor areas are not involved in accumulating sens
23  revealed by the activation of participants' sensorimotor areas before the agent's movement.
24 rior parietal lobule, cerebellum and primary sensorimotor area bilaterally, also the right dorsal pre
25 y index the downstream modulation of primary sensorimotor areas by engaging mirror neuron activity.
26 ) right-hemispheric prefrontal, premotor and sensorimotor areas compared to 'stimulation off'.
27 at athletes had enhanced rsFC within CAN and sensorimotor areas compared to non-athletes.
28 s demonstrated for the ipsilateral secondary sensorimotor area (compared with the ipsilateral primary
29 AG was functionally correlated with cortical sensorimotor areas, conducive to facilitating fight/flig
30 PMV and PMDc, and a more posterior cingulate sensorimotor area (CSMA) with motor connections that may
31 ase together with increased connectedness of sensorimotor areas facilitates successful facial affect
32 Less consistent labeling was seen in somatic sensorimotor areas FL, HL and Par 1.
33  area (compared with the ipsilateral primary sensorimotor area) for movement of the hemiplegic hand t
34 tivity in pons, thalamus, medial frontal and sensorimotor areas, hippocampus, supramarginal and infer
35  used throughout life, those in higher-order sensorimotor areas (i.e., inferior parietal cortex and r
36                                              Sensorimotor areas in anterior and posterior cerebellar
37                        In 2p recordings from sensorimotor areas in mice performing a forelimb reach t
38  between reward-related prefrontal areas and sensorimotor areas in the basal ganglia and frontal cort
39         Structural brain imaging showed that sensorimotor areas in the cerebellum, including lobules
40 During early learning, we found that several sensorimotor areas in the dorsal attention network exhib
41 wed a significant MPH-induced FC increase in sensorimotor areas in the functional circuit associated
42 ly -400 ms before response, originating from sensorimotor areas including dmFC, precuneus, and poster
43 n, significant fMRI activities were found in sensorimotor areas including superior parietal lobule bi
44 rganized corticocortical inputs from distant sensorimotor areas, including the secondary somatosensor
45 typical subsequent upregulation of beta over sensorimotor areas, indicating that their ability to imp
46 synchronized beta oscillations bind multiple sensorimotor areas into a large-scale network during mot
47            Instead, the neural plasticity in sensorimotor areas is sensitive to the temporal structur
48  differing complexity, the bilateral primary sensorimotor area, left ventral premotor cortex, posteri
49  late learning, these effects reversed, with sensorimotor areas now exhibiting increased covariance w
50 ic than interhemispheric connectivity in the sensorimotor area of naturally sleeping infants.
51 ain nucleus HVC (proper name), a cortex-like sensorimotor area of songbirds, otherwise known for bein
52 flow between lateral and mesial premotor and sensorimotor areas of both hemispheres, even if the move
53 functional impairments suggests that lateral sensorimotor areas of caudate putamen are important for
54 ensory signals are represented in multimodal sensorimotor areas of cortex in macaque monkeys.
55 itive, spatially selective activity found in sensorimotor areas of nonhuman primates.
56  to reinforcement, with connectivity between sensorimotor areas of putamen and the reward-related ven
57 h modulation of the signal-to-noise ratio in sensorimotor areas of the brain, while the decoupling of
58 alamus, but was also observed in sensory and sensorimotor areas of the midbrain and hindbrain.
59 th kinematics measures of successful RtGs in sensorimotor areas only.
60 , supplementary motor area (SMA) and primary sensorimotor area (S1M1).
61 ms; and (4) higher alpha and beta power over sensorimotor areas seem to be a maladaptive compensatory
62 road-band neural signals from three cortical sensorimotor areas simultaneously.
63 ight patients with intractable supplementary sensorimotor area (SSMA) seizures.
64 his distinction is particularly relevant for sensorimotor areas such as parietal cortex, where both v
65                                           In sensorimotor areas, T1w/T2w ratio measures start at high
66 the right premotor area (PMA), superolateral sensorimotor areas, thalamus, and bilaterally in the cer
67 in semantic processing in general as well as sensorimotor areas that process specific aspects/categor
68 transfer of visual motion information to the sensorimotor areas that transform visual information int
69 gnalled by these cells could be used by this sensorimotor area to detect novel objects and motion in
70 anial direct current stimulation (tDCS) over sensorimotor areas to modulate neural lateralization pat
71 -15 Hz power increase localized in bilateral sensorimotor areas, together with occipital power decrea
72 ols are visually represented within the same sensorimotor areas underlying their dexterous use accord
73 nd that hemodynamic signals in contralateral sensorimotor areas vary with the direction of movements,
74 gnificant functional connectivity within the sensorimotor area was identified using independent compo
75  gyrus and the visual occipital and superior sensorimotor areas when compared to healthy controls.
76 ompanied by beta-band desynchronization over sensorimotor areas, whereas movement cancellation is acc
77  we recorded neural activity in a prefrontal sensorimotor area while monkeys naturally switched betwe
78 ributed, and broadly similar across multiple sensorimotor areas while also exhibiting area- and submo
79         These results suggest that aPCu is a sensorimotor area whose sensory input is primarily propr
80                     A small set of conserved sensorimotor areas with well-defined thalamic input anch