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1 ral prefrontal and parietal cortex and right fusiform gyrus).
2 and FH effects were found bilaterally in the fusiform gyrus.
3 ct responses, especially in the amygdala and fusiform gyrus.
4 timuli, whereas the opposite was true in the fusiform gyrus.
5 pathway from the occipital visual cortex to fusiform gyrus.
6 ntal cortex and from orbitofrontal cortex to fusiform gyrus.
7 ortex, the inferior parietal lobule, and the fusiform gyrus.
8 ace-selective functional MRI response in the fusiform gyrus.
9 ositively with differential activity of left fusiform gyrus.
10 iation of activity in left amygdala and left fusiform gyrus.
11 reduced activation within the left anterior fusiform gyrus.
12 r temporal cortex, intraparietal sulcus, and fusiform gyrus.
13 eral temporal lobe (Brodmann area 20/21) and fusiform gyrus.
14 drites of neocortical pyramidal cells in the fusiform gyrus.
15 ween higher-level language areas and the mid fusiform gyrus.
16 evoked by words in the posterior part of the fusiform gyrus.
17 teral aspect of the collateral sulcus on the fusiform gyrus.
18 onse profiles such as the lateral and medial fusiform gyrus.
19 the downstream face-selective region in the fusiform gyrus.
20 9557 in the right occipital cortex and right fusiform gyrus.
21 t posterior hippocampus, parahippocampus and fusiform gyrus.
22 hesis in relation to face selectivity in the fusiform gyrus.
23 redict functional activation to faces in the fusiform gyrus.
24 tion following a lesion to the right lateral fusiform gyrus.
25 l gyrus, left parahippocampal gyrus and left fusiform gyrus.
26 parahippocampus (0.032 vs 0.037; p<0.0001), fusiform gyrus (0.036 vs 0.041; p<0.0001), inferior temp
27 emporal gyrus (13% difference) and bilateral fusiform gyrus (10% difference in both hemispheres).
28 0.001), anterior vermis (40%, P < 0.001) and fusiform gyrus (20%, P < 0.001) compared with controls o
29 as well as the insula, cingulate cortex, and fusiform gyrus, a regional distribution that was nearly
30 l thickness in the right parahippocampal and fusiform gyrus across both time points was found in both
31 was inversely correlated with the change in fusiform gyrus activation in the fasted state but not in
32 paired performance and reduced left anterior fusiform gyrus activation was observed when control subj
34 ior hippocampus, parahippocampal cortex, and fusiform gyrus activity linearly increased across the 30
40 matter loss in the left parahippocampal and fusiform gyrus and greater gray matter increases in the
41 s in the pars orbitalis, paracentral lobule, fusiform gyrus and inferior temporal gyrus was lowest in
43 ion and the ankle DF/PF tasks, the bilateral fusiform gyrus and middle temporal gyrus, right inferior
46 orm; (2) body-selective regions in posterior fusiform gyrus and posterior inferior temporal sulcus ov
47 in right lateral occipital cortex and right fusiform gyrus and sources in a control region (left V1)
48 in ReHo between the two bands were found in fusiform gyrus and superior frontal gyrus (slow-4> slow-
49 more left-sided in autism), whereas adjacent fusiform gyrus and temporooccipital inferior temporal gy
50 ted by visual semantic loops within the left fusiform gyrus and that these neural processes may be me
52 field being represented more medially on the fusiform gyrus and the inferior field more laterally, th
54 uced and increased fMRI responses in the mid-fusiform gyrus and the lateral occipital cortex, respect
55 in the left inferior prefrontal cortex, the fusiform gyrus and the medial temporal lobe including bo
56 ups predicted activity in the right anterior fusiform gyrus and the temporal poles, where accuracy li
57 amage to the inferior temporal gyrus, to the fusiform gyrus and to a white matter network including t
58 y-related patterns of activation in ventral (fusiform gyrus) and lateral (superior and middle tempora
59 dalar region) cingulate, parahippocampal and fusiform gyrus, and anterior insula were seen along with
61 emisphere in caudate, hippocampal formation, fusiform gyrus, and cerebellum, and in right temporal co
63 ippocampus, parahippocampal gyrus, amygdala, fusiform gyrus, and choroid plexus but not in other brai
64 rome group was found in the cingulate gyrus, fusiform gyrus, and frontal cortex in response to all fa
65 ed decreased activity in the right amygdala, fusiform gyrus, and inferior occipital gyrus compared wi
66 eral temporal lobe, including temporal pole, fusiform gyrus, and insula, and extending into occipital
69 as the lingual gyrus, middle temporal gyrus, fusiform gyrus, and precuneus all showed delayed hemodyn
70 lts showed that the visual cortex, bilateral fusiform gyrus, and right parahippocampal gyrus were act
71 ft lingual gyrus), anterior cingulate, right fusiform gyrus, and right sublobar insula were significa
72 including Brodmann's areas 18 and 19 and the fusiform gyrus, and several cortical regions associated
73 left hippocampus, parahippocampal gyrus, and fusiform gyrus, and significantly greater gray matter in
74 s, entorhinal cortex, parahippocampal gyrus, fusiform gyrus, and superior, middle, and inferior tempo
75 cur in the anterior medial temporal lobe and fusiform gyrus, and that these changes occur at least 3
76 ith word-related potentials in the posterior fusiform gyrus, and was independent of stimulus colour.
77 s in schizophrenia and draw attention to the fusiform gyrus as a structure of particular interest in
78 l resolution imaging techniques identify the fusiform gyrus as subserving processing of invariant fac
80 cortex), BA 37 (posterior, inferior temporal/fusiform gyrus), BA 38 (anterior temporal cortex) and BA
81 l gyrus) and 37 (posterior-inferior temporal/fusiform gyrus) best predicted impairment in reading wor
82 r areas are consistently activated: the left fusiform gyrus, bilateral middle and inferior frontal gy
83 was detected in the mesial temporal lobe and fusiform gyrus bilaterally among persons without a first
85 blood flow to left posterior middle temporal/fusiform gyrus, Broca's area, and/or Wernicke's area acc
86 ed face-responsive visual areas in the human fusiform gyrus, but their role in recognizing familiar i
89 ly increased in temporal regions, insula and fusiform gyrus, consistent with those areas known to be
90 iculum, and entorhinal cortex), and anterior fusiform gyrus (corrected P < .05; uncorrected P = .001)
91 that responded to viewing pictorial stimuli (fusiform gyrus) correlated with self-reported visualizer
92 s (Cohen's d=-0.293; P=1.71 x 10(-21)), left fusiform gyrus (d=-0.288; P=8.25 x 10(-21)) and left ros
93 cipants (both absolutely and relative to the fusiform gyrus), despite apparently normal levels of fac
94 temporal gyrus, superior temporal gyrus, and fusiform gyrus during memory encoding reduced odds of re
100 ns involved in face processing including the fusiform gyrus (FFG) and posterior cingulate cortex (PCC
101 ther than to identity changes, whereas right fusiform gyrus (FFG) shows sensitivity to identity rathe
103 ions for the size of activation in the right fusiform gyrus (FG) and right inferior temporal gyri (IT
104 own to respond to face and gaze stimuli, the fusiform gyrus (FG) and superior temporal sulcus (STS),
105 ction (IFJ), middle temporal gyrus (MTG) and fusiform gyrus (FG) are active during response inhibitio
106 hat spatially informative cues activated the fusiform gyrus (FG) as well as frontoparietal components
107 le of face-selective neural responses of the fusiform gyrus (FG) in face perception in a patient impl
113 ties in distinct but adjacent regions in the fusiform gyrus for only faces in one region (the FFA*) a
115 s (absolute volume/intracranial contents) of fusiform gyrus gray matter compared with controls (9%) a
116 is associated with a bilateral reduction in fusiform gyrus gray matter volume that is evident at the
117 For comparison, superior temporal gyrus and fusiform gyrus gray matter volumes were also measured.
118 had smaller bilateral anterior and posterior fusiform gyrus gray matter volumes, compared to the heal
120 nsisting of hippocampus, parahippocampus and fusiform gyrus (HPF) as defined by a published template.
121 ance imaging (fMRI), we found an area in the fusiform gyrus in 12 of the 15 subjects tested that was
122 sed to measure the gray matter volume of the fusiform gyrus in 22 patients with first-episode schizop
124 with ASD had lower FC than TC in cerebellum, fusiform gyrus, inferior occipital gyrus and posterior i
126 ed abnormal hyperactivation in the amygdala, fusiform gyrus, insula, anterior cingulate cortex, and d
127 ability was evident in the temporal pole and fusiform gyrus ipsilateral to the seizure focus followin
128 ese findings indicate that the right lateral fusiform gyrus is critically involved in object recognit
129 ative to healthy subjects, suggests that the fusiform gyrus is the site of a defective anatomical sub
131 ortical dysfunction in the temporal lobe and fusiform gyrus may be related to epileptic activity in I
134 d automatic semantic priming in the left mid-fusiform gyrus (mid-FFG) and strategic semantic priming
135 ces on post hoc analysis: posterior temporal fusiform gyrus (more left-sided in autism), whereas adja
136 ealthy participants showed activation in the fusiform gyrus, occipital lobe, and inferior frontal cor
137 ied a putative face-specific area within the fusiform gyrus of human visual cortex; the precise role
139 e area in specific cortical regions (cuneus, fusiform gyrus, pars triangularis) in both populations.
142 work and that a right anterior region of the fusiform gyrus plays a central role within the informati
143 creased rCBF to motor cortex, visual cortex, fusiform gyrus, posterolateral temporal lobe, and right
144 showed activations, not seen in normals, in fusiform gyrus, precentral gyrus, and intra-parietal sul
145 erior temporal gyrus reduction and bilateral fusiform gyrus reductions, these data suggest that schiz
147 gyrus and bilateral middle/inferior temporal/fusiform gyrus, respectively) that showed reversed effec
148 sults show that bilateral posterior areas in fusiform gyrus responded more strongly for faces with po
151 ons, the lateral section of the right middle fusiform gyrus showed the largest face-selective respons
153 s placed over high-order visual areas (e.g., fusiform gyrus) showed both effects of spatial and objec
154 ormality and anatomical abnormalities in the fusiform gyrus shown with magnetic resonance imaging (MR
155 ateral occipito-temporal sulcus and adjacent fusiform gyrus shows maximal selectivity for words and h
156 the visual word-form area (part of the left fusiform gyrus specialized for printed words); and persi
159 tentials recorded from nearby regions of the fusiform gyrus suggest that the attention effect is due
160 uperior Temporal Gyrus (t=1.403, p=0.00780), Fusiform Gyrus (t=1.26), and Parahippocampal Gyrus (t=1.
161 rebellum, including putamen, insula, cuneus, fusiform gyrus, thalamus and caudate nucleus, and increa
162 wer spectra in the primary visual cortex and fusiform gyrus that are maximally discriminative of data
163 ther fusiform face area (FFA)-the portion of fusiform gyrus that is functionally-defined by its prefe
164 eralized hyperactivation in the amygdala and fusiform gyrus that was subject to intersession habituat
165 ct patches of face-selective activity in the fusiform gyrus that were interspersed within a large exp
167 ies have described a localized region in the fusiform gyrus [the fusiform face area (FFA)] that respo
168 ted, in addition, more anterior parts of the fusiform gyrus, the hippocampus and the ventrolateral fr
169 Voxels in the right temporal pole, the right fusiform gyrus, the right caudate and right subcallosal
170 laims have been made, and within the lateral fusiform gyrus, they are restricted to a small area (200
172 ediated the association with inattention and fusiform gyrus thickness mediated the association with i
173 found positive correlations between the left fusiform gyrus to amygdala connectivity and different st
174 , and may serve in concert with amygdala and fusiform gyrus to modulate visual attention toward motiv
175 over time in activation of the amygdala and fusiform gyrus to neutral facial stimuli in adults with
177 ced modulation of connectivity from the left fusiform gyrus to the left amygdala and from the right a
179 e association of these deficits with smaller fusiform gyrus volume in patients with schizophrenia, re
181 that the intensity of the activation in the fusiform gyrus was associated with significantly stronge
184 s in orthographic processing circuits (i.e., fusiform gyrus) was predictive of smaller gains in fluen
185 wed that repetition suppression in bilateral fusiform gyrus, was selectively correlated with priming
187 ing, whereas PrC, anterior HC, and posterior fusiform gyrus were recruited during discrimination lear
188 mygdala, parahippocampal gyrus. and anterior fusiform gyrus when participants were in a hungry state
189 ocampal gyrus, left orbitofrontal cortex and fusiform gyrus whereas patients with left hippocampal sc
190 s activated a discrete region of the lateral fusiform gyrus, whereas letterstrings activated a nearby
191 , but previous studies have not included the fusiform gyrus (which may have a role in facial recognit
192 cal area in the collateral sulcus and medial fusiform gyrus, which was place-selective according to b
193 , ventral IPS, lateral occipital region, and fusiform gyrus], which was accompanied by activation tha
194 ed fMRI to measure neural responses from the fusiform gyrus while subjects observed a rapid stream of
195 ties in the right temporal pole and anterior fusiform gyrus; while in the Alzheimer's disease group,
196 us, left temporoparietal junction, and right fusiform gyrus, with patients showing relative hypoactiv
197 ivated inferior frontal gyrus, amygdala, and fusiform gyrus, with significantly stronger activation e
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