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1 nferior frontal gyrus, and the right parieto-occipital region.
2 and a larger effect in a neighboring lateral occipital region.
3 ion, showed a similar pattern as the ventral occipital region.
4 cluding V5, V3A, and a new area, the kinetic occipital region.
5 medial-frontal, orbito-frontal, parietal and occipital regions.
6 alternative pathway directly to extrastriate occipital regions.
7 ion in a number of prefrontal, parietal, and occipital regions.
8 acentral, lateral orbitofrontal, and lateral occipital regions.
9 oglial activation in temporal, parietal, and occipital regions.
10 ronto-central, right parietal, temporal, and occipital regions.
11 uperior temporal, posterior white matter, or occipital regions.
12 al thickness in frontal, medial parietal and occipital regions.
13 , and PMG most severe in the temporo-parieto-occipital regions.
14 icant in right frontal and bilateral parieto-occipital regions.
15 mm per year, most prominently in frontal and occipital regions.
16 s in orbitofrontal, midtemporal, and parieto-occipital regions.
17 more widespread and primarily located in the occipital regions.
18 metabolism in the posterior temporo-parieto-occipital regions.
21 ive patients known to have MCD affecting the occipital region and seven normal subjects using H2 (15)
24 decreased GMV in medial frontal and temporal-occipital regions and increased GMV in lateral prefronta
25 tractors, patients showed less activation in occipital regions and left inferior parietal lobule but
26 nce quotient to GMV were found in cerebellar-occipital regions and medial prefrontal cortex for contr
27 score and grey matter volume of the temporo-occipital regions and the corpus striatum; (ii) emotiona
28 osterior hippocampus, medial cingulo-parieto-occipital regions and the dorsal raphe nucleus, but inte
29 ory regions [LIP, IPSa, ventral IPS, lateral occipital region, and fusiform gyrus], which was accompa
30 refrontal regions, larger volumes in parieto-occipital regions, and smaller inferior occipital volume
31 al white matter (beta = -0.13, P = .02), and occipital regions (beta = -0.15, P = .03) in the whole s
32 -0.15, P = .03) in the whole sample and the occipital regions (beta = -0.21, P = .01) in the CN subs
33 l thinning, predominantly in the frontal and occipital regions (both p < 0.01) in multiple linear reg
34 directional connectivity from PFC to parieto-occipital regions commensurate with executive processing
36 fluctuant mass was present in the midline in occipital region covered with alopecic skin with dimplin
37 tter anisotropy with age, and prefrontal and occipital regions evidenced the greatest age-related dif
38 n the deep white matter of the left parietal-occipital region extending anteriorly along the superior
40 owth compared with white matter growth, with occipital regions growing much faster than prefrontal re
42 regional decreases involving paracentral and occipital regions in both PD + VH and PD - VH patients (
43 blished that multiple frontal, parietal, and occipital regions in humans are involved in anticipatory
44 aled subtle activity deficits in frontal and occipital regions in the patients with schizophrenia.
45 nation tasks, in blind subjects, the ventral occipital regions, including the primary visual cortex a
46 arousal is associated with MS lesions in the occipital region, integrating visual information and mod
47 ugmented by progesterone in the parietal and occipital regions, it was suppressed in the frontal regi
49 ied reductions of grey matter of the parieto-occipital regions, left putamen/globus pallidus and thal
50 termined with proton decoupling in a parieto-occipital region (n = 9) and without proton decoupling i
55 etabolism in precuneus, lateral parietal and occipital regions of interest (controlling for age, educ
57 as significantly blunted in the parietal and occipital regions of the cerebrum and the suprapyramidal
59 l, left supramarginal, left postcentral, and occipital regions (P values were between <.001 and .03 a
60 ajectories emerged in bilateral parietal and occipital regions (postcentral gyrus, cuneus, lingual gy
62 ended deactivations of superior parietal and occipital regions representing parts of the dorsal atten
65 ht superior frontal gyrus and left and right occipital regions, such that psychosis patients showed a
66 L further showed increased connectivity with occipital regions suggesting an active top-down mechanis
67 c activity from HCs in medial prefrontal and occipital regions, suggesting that these groups may use
68 shed in anatomically segregated temporal and occipital regions, sustained delay related memory for th
71 cortices in the left and right parietal and occipital regions, the mesial frontal lobe of the right
72 ted cortical thickness ranged from 1.5 mm in occipital regions to 5.5 mm in dorsomedial frontal corte
73 , with directional connectivity from parieto-occipital regions to PFC, regardless of processing deman
74 the significant contribution of parietal and occipital regions to such estimation challenges the trad
75 he simulations predict that the temporal and occipital regions undergo the most axonal strain and str
76 nd that stimulus-bound responses in superior occipital regions were linearly predictive of trial-by-t
78 sciculus, which projects between frontal and occipital regions where activity predicted word recognit
79 positively correlated with that in the right occipital region, whereas in sighted subjects correlatio
80 inately associated with motor, parietal, and occipital regions, while interhemispheric expression pro
81 beta oscillations were observed over parieto-occipital regions, with directional connectivity from pa
82 ations was more severe over the parietal and occipital regions, XLIS mutations produced the reverse g
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