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1 ferior parietal, middle frontal, and lateral occipital regions).
2 left sided and occasionally radiated to the occipital region.
3 left sided and occasionally radiated to the occipital region.
4 ssing oscillations in the alpha range in the occipital region.
5 nferior frontal gyrus, and the right parieto-occipital region.
6 and a larger effect in a neighboring lateral occipital region.
7 ion, showed a similar pattern as the ventral occipital region.
8 cluding V5, V3A, and a new area, the kinetic occipital region.
9 ndence of hippocampal connectivity to medial occipital regions.
10 al networks located in the orbitofrontal and occipital regions.
11 a in the superior temporal gyrus and parieto-occipital regions.
12 acy of ErrPs, especially in the parietal and occipital regions.
13 cortex and impoverished item specificity in occipital regions.
14 iated with hypergyrification in temporal and occipital regions.
15 edominantly in the left temporal and parieto-occipital regions.
16 s, the left fusiform, and right parietal and occipital regions.
17 encoding across many frontal, parietal, and occipital regions.
18 ons, and with modest correlations in parieto-occipital regions.
19 ificantly higher FA values than parietal and occipital regions.
20 itively with alpha-band power in frontal and occipital regions.
21 density, particularly strong in frontal and occipital regions.
22 ontoparietal, cingulo-opercular, and temporo-occipital regions.
23 ut the larger effect were localised in visuo-occipital regions.
24 cessing mechanisms, was localized to lateral occipital regions.
25 arietal, rostral middle frontal, and lateral occipital regions.
26 al thickness in frontal, medial parietal and occipital regions.
27 medial-frontal, orbito-frontal, parietal and occipital regions.
28 alternative pathway directly to extrastriate occipital regions.
29 ion in a number of prefrontal, parietal, and occipital regions.
30 acentral, lateral orbitofrontal, and lateral occipital regions.
31 oglial activation in temporal, parietal, and occipital regions.
32 t observed in scalp electrodes over parietal-occipital regions.
33 ronto-central, right parietal, temporal, and occipital regions.
34 uperior temporal, posterior white matter, or occipital regions.
35 , and PMG most severe in the temporo-parieto-occipital regions.
36 icant in right frontal and bilateral parieto-occipital regions.
37 mm per year, most prominently in frontal and occipital regions.
38 lower lGI in left frontal and right parieto-occipital regions.
39 s in orbitofrontal, midtemporal, and parieto-occipital regions.
40 more widespread and primarily located in the occipital regions.
41 metabolism in the posterior temporo-parieto-occipital regions.
42 usters involving left temporal, parietal and occipital regions (32, and 18 voxels, CCLAV = 0.02 and 0
44 activity in the frontal, motor, parietal and occipital regions, aiming to better understand the brain
46 ive patients known to have MCD affecting the occipital region and seven normal subjects using H2 (15)
49 nd decreased functional connectivity between occipital regions and frontal, parietal, and cerebellar
50 decreased GMV in medial frontal and temporal-occipital regions and increased GMV in lateral prefronta
51 tractors, patients showed less activation in occipital regions and left inferior parietal lobule but
52 nce quotient to GMV were found in cerebellar-occipital regions and medial prefrontal cortex for contr
53 egional sensitivity in bilateral frontal and occipital regions and strengthening of feedforward conne
54 roup also had larger cortical thicknesses in occipital regions and surface areas in frontal regions.
55 score and grey matter volume of the temporo-occipital regions and the corpus striatum; (ii) emotiona
56 osterior hippocampus, medial cingulo-parieto-occipital regions and the dorsal raphe nucleus, but inte
57 ory regions [LIP, IPSa, ventral IPS, lateral occipital region, and fusiform gyrus], which was accompa
58 ivity strength in the frontal, temporal, and occipital regions, and increased phase synchrony value (
60 refrontal regions, larger volumes in parieto-occipital regions, and smaller inferior occipital volume
61 egional sensitivity in bilateral frontal and occipital regions, and strengthened feedforward connecti
62 ations of global shape properties in lateral occipital regions, and these representations were predic
63 nal gradients between early and higher-order occipital regions are retained, at least for reading.
64 rength with CA between frontal, central, and occipital regions at low-delta and alpha frequencies tog
65 SR in four brain regions: (a) right temporal-occipital region, (b) right dorsomedial prefrontal corte
66 al white matter (beta = -0.13, P = .02), and occipital regions (beta = -0.15, P = .03) in the whole s
67 5% CI, -0.23 to -0.04; P = .02), and lateral occipital regions (beta = -0.15; 95% CI, -0.24 to -0.06;
68 -0.15, P = .03) in the whole sample and the occipital regions (beta = -0.21, P = .01) in the CN subs
69 l thinning, predominantly in the frontal and occipital regions (both p < 0.01) in multiple linear reg
70 ently appeared in middle frontal and parieto-occipital regions but were not moderated by Abeta burden
71 rontal (|Cohen's D|< 0.6, P(FWER) < .01) and occipital regions (|Cohen's D|< 0.5, P(FWER) < .01).
72 directional connectivity from PFC to parieto-occipital regions commensurate with executive processing
73 These results suggest frontal and parieto-occipital regions communicate through theta-alpha/beta P
76 fluctuant mass was present in the midline in occipital region covered with alopecic skin with dimplin
77 t of hippocampi, temporo-parietal and medial occipital regions during judgements of semantic relatedn
78 tter anisotropy with age, and prefrontal and occipital regions evidenced the greatest age-related dif
79 n the deep white matter of the left parietal-occipital region extending anteriorly along the superior
81 owth compared with white matter growth, with occipital regions growing much faster than prefrontal re
83 miniaturized hair follicles from vertex and occipital region in males with and without androgenetic
84 ssociated with less atrophy within the right occipital region in presymptomatic carriers at baseline,
86 all sighted and blind groups is enhanced in occipital regions in blind groups , suggesting that the
87 regional decreases involving paracentral and occipital regions in both PD + VH and PD - VH patients (
88 blished that multiple frontal, parietal, and occipital regions in humans are involved in anticipatory
89 r atrophy rate within the right temporal and occipital regions in presymptomatic carriers, and within
90 aled subtle activity deficits in frontal and occipital regions in the patients with schizophrenia.
91 nation tasks, in blind subjects, the ventral occipital regions, including the primary visual cortex a
93 arousal is associated with MS lesions in the occipital region, integrating visual information and mod
94 learly differentiated from posterior parieto-occipital regions involved in visuospatial cognition and
95 alpha-band waves propagating from frontal to occipital regions ipsilateral to the attended location,
96 ugmented by progesterone in the parietal and occipital regions, it was suppressed in the frontal regi
98 ied reductions of grey matter of the parieto-occipital regions, left putamen/globus pallidus and thal
99 termined with proton decoupling in a parieto-occipital region (n = 9) and without proton decoupling i
104 etabolism in precuneus, lateral parietal and occipital regions of interest (controlling for age, educ
106 as significantly blunted in the parietal and occipital regions of the cerebrum and the suprapyramidal
107 carriers consisting of focal slowing in the occipital regions often preceding irregular generalized
110 l, left supramarginal, left postcentral, and occipital regions (P values were between <.001 and .03 a
111 ajectories emerged in bilateral parietal and occipital regions (postcentral gyrus, cuneus, lingual gy
113 l trajectory of motion area respect to other occipital regions, probably reflecting also a different
114 d automatic contour integration over lateral occipital regions relative to neurotypical controls.
115 ended deactivations of superior parietal and occipital regions representing parts of the dorsal atten
116 lerated and attenuated in the prefrontal and occipital regions, respectively, in the asymmetric condi
119 ht superior frontal gyrus and left and right occipital regions, such that psychosis patients showed a
120 L further showed increased connectivity with occipital regions suggesting an active top-down mechanis
121 c activity from HCs in medial prefrontal and occipital regions, suggesting that these groups may use
122 shed in anatomically segregated temporal and occipital regions, sustained delay related memory for th
124 role in surface perception for this lateral occipital region that includes V3A, V4v, V7, and V8.
125 cortices in the left and right parietal and occipital regions, the mesial frontal lobe of the right
126 ted cortical thickness ranged from 1.5 mm in occipital regions to 5.5 mm in dorsomedial frontal corte
127 , with directional connectivity from parieto-occipital regions to PFC, regardless of processing deman
128 the significant contribution of parietal and occipital regions to such estimation challenges the trad
129 ion emerged in distinct parietal and temporo-occipital regions, unassociated with familial depression
130 he simulations predict that the temporal and occipital regions undergo the most axonal strain and str
131 ysis revealed that the volume of this dorsal occipital region was strongly correlated in VAC-FTD, but
132 nd that stimulus-bound responses in superior occipital regions were linearly predictive of trial-by-t
133 mulation in all cortical regions, the medial occipital regions were spared in people with Down syndro
135 the prefrontal region and attenuated in the occipital region when exposed to asymmetric, as compared
136 sciculus, which projects between frontal and occipital regions where activity predicted word recognit
137 positively correlated with that in the right occipital region, whereas in sighted subjects correlatio
138 shoulders, and neck muscles inserted in the occipital region, whereas the second suggests that these
139 covariance from lateral frontal to posterior occipital regions, which differentiated the dominance of
140 as V4, but is found more strongly in lateral occipital regions, which exhibit responses and represent
141 inately associated with motor, parietal, and occipital regions, while interhemispheric expression pro
142 ing sensory inference and memory in parietal-occipital regions, while the cumulative exposure to cons
143 phy network mapping identified a dorsomedial occipital region whose activity inversely correlated, in
144 grity of late-visual pathways connecting the occipital regions with ipsilateral fronto-parieto-tempor
145 beta oscillations were observed over parieto-occipital regions, with directional connectivity from pa
146 u pathology in this case was confined to the occipital region without evidence of spread, potentially
147 ations was more severe over the parietal and occipital regions, XLIS mutations produced the reverse g