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1 ular gyrus, mid-frontal cortex, and anterior cingulate gyrus).
2 ula, and limbic lobe (anterior and posterior cingulate gyrus).
3 own the medial prefrontal cortex, toward the cingulate gyrus).
4 teral prefrontal cortices, and the posterior cingulate gyrus.
5 or occipital cortex, fusiform areas, and the cingulate gyrus.
6 binding in orbitofrontal cortex and anterior cingulate gyrus.
7 ects found in the thalamus, hippocampus, and cingulate gyrus.
8 primary role for dysfunction of the anterior cingulate gyrus.
9 e left fronto-temporal junction and anterior cingulate gyrus.
10 ntly lower metabolism in the dorsal anterior cingulate gyrus.
11 th glucose metabolism in the dorsal anterior cingulate gyrus.
12 ad greater activation in the right posterior cingulate gyrus.
13 ventromedial nucleus of the hypothalamus and cingulate gyrus.
14 tal and temporal regions and in the anterior cingulate gyrus.
15 phenotypic changes in a control area of the cingulate gyrus.
16 us, posterior parietal cortex, and posterior cingulate gyrus.
17 o examine regional glucose metabolism in the cingulate gyrus.
18 s discussed with particular reference to the cingulate gyrus.
19 e ventral prefrontal cortex and the anterior cingulate gyrus.
20 ed additional areas of hypometabolism in the cingulate gyrus.
21 ison group had greater increases in anterior cingulate gyrus.
22 the piriform cortex, Purkinje cells and the cingulate gyrus.
23 eft middle temporal gyrus, and the posterior cingulate gyrus.
24 l and functional alterations in the anterior cingulate gyrus.
25 n the right parietal cortex and the anterior cingulate gyrus.
26 11, 5-HTR1b and 5-HTR4 in the hippocampus or cingulate gyrus.
27 people by opposite activity in the anterior cingulate gyrus.
28 pus callosum, i.e., the anterior part of the cingulate gyrus.
29 campus, anterior cingulate gyrus, and medial cingulate gyrus.
30 , and inferior/middle temporal gyri) and the cingulate gyrus.
31 o impending sudden task disengagement in mid-cingulate gyrus.
32 lving the motor/premotor cortex and anterior cingulate gyrus.
33 tter volume in the frontal pole and anterior cingulate gyrus.
34 s, cingulate gyrus, and striatum/subcallosal cingulate gyrus.
35 umulation of cNFT pathology in the posterior cingulate gyrus.
36 and both NAA/Cr and NAA/mI in the posterior cingulate gyrus.
37 sponses in the hippocampus and the posterior cingulate gyrus.
38 esonance spectroscopy in the dorsal anterior cingulate gyrus.
39 ter of the basal ganglia and right posterior cingulate gyrus.
40 ative decrease in activation in the anterior cingulate gyrus.
41 sorder-specific dysfunction in the posterior cingulate gyrus.
42 s), primarily in the precuneus and posterior cingulate gyrus.
43 ingulate sulcus, connecting the SMA with the cingulate gyrus; (3) frontal 'aslant' fascicle, directly
44 activation foci bilaterally in the posterior cingulate gyrus (+/-8, -48, 26; left P < 0.001; right P
45 planum temporale, angular gyrus and anterior cingulate gyrus: a cortical network that has previously
46 5), and in the contralateral dorsal anterior cingulate gyrus (ACC; r = 0.43, P < 0.05), dorsolateral
48 e neural signature of effort in the anterior cingulate gyrus (ACCg) for prosocial acts, both when cho
51 campus, orbitofrontal cortex (OFC), anterior cingulate gyrus (aCING), and peripeduncular nucleus of t
52 zophrenia showed significantly less anterior cingulate gyrus activation while naming the color of col
54 s associated with activation of the anterior cingulate gyrus, amygdala, orbitofrontal cortex, and dor
55 m in limbic regions (eg, perigenual anterior cingulate gyrus and amygdala) and ratings of state and t
56 gender-related structural differences in the cingulate gyrus and corresponding differences in cingula
57 ly lower glucose metabolism in the posterior cingulate gyrus and cuneus, whereas the nonhoarding OCD
58 portant revisions to the organization of the cingulate gyrus and demonstrate four structure/function
59 corpus callosum, and anterior and posterior cingulate gyrus and from automatically defined frontal,
60 n deficits were noted in the dorsal anterior cingulate gyrus and hippocampus of the depressed geriatr
61 Broca's and prefrontal areas combined, left cingulate gyrus and left superior temporal gyrus and a f
62 icated in reward processing (e.g., subgenual cingulate gyrus and medial orbitofrontal cortex) and con
64 al lobe; inferior parietal lobule; posterior cingulate gyrus and precuneus; and medial, dorsal, ventr
66 PTSD had increased rCBF in ventral anterior cingulate gyrus and right amygdala when generating menta
67 e occipital/ middle temporal gyri, bilateral cingulate gyrus and right sensorimotor and pre-motor reg
68 ray and white matter volumes of the anterior cingulate gyrus and superior frontal gyrus were computed
69 a K(i)(o) were observed in the left anterior cingulate gyrus and the dorsal midbrain region (P < 0.05
70 l behavior of primates and that the anterior cingulate gyrus and the mSTS support these computations.
72 rs investigated the function of the anterior cingulate gyrus and the related neural systems that are
73 revealed that the network from the posterior cingulate gyrus and the semiology of PCE (motor manifest
74 most of the medial surface of the posterior cingulate gyrus and the ventral bank of the posterior ci
77 al cortex, supplementary motor area, anteior cingulate gyrus) and parietal (precuneus, posterior cing
79 er connectivity with the precuneus, anterior cingulate gyrus, and areas of the occipital cortex, part
80 mpus, insula, orbitofrontal cortex, anterior cingulate gyrus, and caudate in subjects with high CTQ s
81 e content in the prefrontal cortex, anterior cingulate gyrus, and hippocampus between healthy control
82 fferent cortical regions (prefrontal cortex, cingulate gyrus, and hippocampus) that are routinely inv
84 al, inferior frontal, middle frontal cortex, cingulate gyrus, and left middle frontal), with no signi
85 region (supramarginal gyri), right posterior cingulate gyrus, and left occipital lobe (lingual gyrus)
89 udate and putamen, globus pallidum, anterior cingulate gyrus, and medial temporal regions, including
90 frontal and temporal lobes, caudate nucleus, cingulate gyrus, and mediodorsal nucleus of the thalamus
92 dent functional connectivity with precuneus, cingulate gyrus, and striatum/subcallosal cingulate gyru
93 anterior and posterior cerebellum, posterior cingulate gyrus, and superior and inferior frontal gyrus
95 brain regions, including the precuneus, the cingulate gyrus, and the hippocampus, regions commonly a
96 tal gyri, the left anterior cingulate cortex/cingulate gyrus, and the left middle frontal/precentral
97 bilateral prefrontal cortices, the anterior cingulate gyrus, and the precuneus; and induced a more "
98 f the amygdala, the left insula and anterior cingulate gyrus, and the right subcallosal gyrus and nuc
99 tal gyrus, left superior temporal gyrus, and cingulate gyrus/anterior cingulate cortex (Brodmann area
100 Volumetric abnormalities in the anterior cingulate gyrus appear specific to the gray matter in OC
101 as 6, 7, 8, 9, 10, 11, 44, 45, 47), anterior cingulate gyrus (areas 24, 32), temporal cortex (area 21
103 ala, anterior insula, striatum, and anterior cingulate gyrus as well as in regions associated with sy
104 activity in the orbitofrontal cortex and the cingulate gyrus associated with emotional responses when
105 level, except for the final tone, where the cingulate gyrus assumes the top position within the hier
106 derwent antemortem (1)H-MRS of the posterior cingulate gyrus at 3 tesla were included in this study.
107 ith elevated metabolic rates in the anterior cingulate gyrus at baseline are more likely to respond t
108 veral cortical areas, including the anterior cingulate gyrus (BA 24 and 25), the lateral basal fronta
109 gyrus (BA9), spreading to the right anterior cingulate gyrus (BA32); and in the left middle temporal
110 ties of areas, including the frontal cortex, cingulate gyrus, basal ganglia, and temporal cortex.
111 , reduced area of the right posterior middle cingulate gyrus (beta = -0.09, p = 8.01 x 10(-4)) and re
112 ith a smaller volume in the rostral anterior cingulate gyrus (beta [SE], -166.3 [65.1] mm3; P = .006)
113 edly greater activation of the left anterior cingulate gyrus, bilateral frontopolar regions, bilatera
114 ivations were observed in the right anterior cingulate gyrus (Brodmann area 24), in the intraparietal
115 tate was detected most frequently within the cingulate gyrus but it was also present in the subcortic
116 s had more total gray matter in the anterior cingulate gyrus but not the superior frontal gyrus.
117 e inferior frontal gyrus and dorsal anterior cingulate gyrus, but act on distinct affect-generating r
118 estimated for 7 structures: rostral anterior cingulate gyrus, caudal anterior cingulate gyrus, poster
119 ain regions such as the precuneus, posterior cingulate gyrus, cerebellum, as well as basal ganglia an
120 gyrus (SFG), supramarginal gyrus (SMG), and cingulate gyrus (CG) from 4 parcellation protocols as im
122 30 identify them on the ventral bank of the cingulate gyrus (CGv), whereas standardized atlases show
123 reduced gray matter volumes in the anterior cingulate gyrus compared with individuals with BD (Montr
125 0.89 +/- 0.04, ADs 0.72 +/- 0.04; posterior cingulate gyrus: controls 1.05 +/- 0.09, ADs 0.79 +/- 0.
126 nal cortex, parahippocampal gyrus, posterior cingulate gyrus, cortex of the temporal lobes and corpus
127 frontal cortex and supplementary motor area, cingulate gyrus, cuneus and occipital gyrus, and insula
128 tivity in the orbito-frontal cortex, ventral cingulate gyrus, dorsal cingulate cortex, hypothalamus,
129 ) binding in several brain regions (anterior cingulate gyrus, dorsolateral prefrontal cortex, and par
130 o-parietal association cortex, precuneus and cingulate gyrus during and following seizures, similar t
131 schizophrenia fail to activate the anterior cingulate gyrus during selective attention performance.
132 insula and middle cingulate/dorsal anterior cingulate gyrus during the processing of fearful faces.
133 so-medial prefrontal cortex and the anterior cingulate gyrus, encode social prediction errors and con
134 tivated microglia distributed throughout the cingulate gyrus, entorhinal cortex, hippocampus and dent
135 articipants included 14 consecutive cases of cingulate gyrus epilepsies confirmed by restricted magne
136 NG, AND PARTICIPANTS: We studied consecutive cingulate gyrus epilepsy cases identified retrospectivel
139 es between SLF-I models with and without the cingulate gyrus excluded, suggesting that the SLF-I may
141 n group and age, were found in retrosplenial cingulate gyrus, found to be metabolically affected in p
142 he fragile X syndrome group was found in the cingulate gyrus, fusiform gyrus, and frontal cortex in r
143 ve (P = .04), and right posterior (P = .003) cingulate gyrus gray matter subregions compared with HCs
145 rains, the monkey frontal lobe and posterior cingulate gyrus had significantly less metabolic activit
147 ere and, to a lesser extent, in the anterior cingulate gyrus, head of the caudate nucleus and the pos
148 nt multivariate classifications included the cingulate gyrus, hippocampal subfields and amygdalar nuc
150 , caudal anterior cingulate gyrus, posterior cingulate gyrus, hippocampus, basal forebrain, amygdala,
151 opulations from four brain regions (anterior cingulate gyrus, hippocampus, prefrontal cortex, and nuc
153 brain have suggested the involvement of the cingulate gyrus in a wide variety of affective, cognitiv
155 metabolism of the amygdala, hippocampus, and cingulate gyrus in an expanded group of 17 patients with
157 e of the prefrontal cortex, hippocampus, and cingulate gyrus in major depressive disorders (MDD), but
159 oups shared underactivation in the posterior cingulate gyrus in relation to comparison subjects.
160 and superior frontal gyri, frontal pole, and cingulate gyrus in S-allele carriers compared with parti
161 ice variants in the hippocampus and anterior cingulate gyrus in suicide completers with and without a
162 ulty in localizing seizures arising from the cingulate gyrus in the absence of a magnetic resonance i
164 tion with tissue loss in the right subgenual cingulate gyrus in the VMPC, and aberrant motor behaviou
165 iddle and inferior frontal gyri and anterior cingulate gyrus, in addition to regions of the parietal
166 he right caudate nucleus and bilateral (para)cingulate gyrus increased in patients after real-rTMS wh
167 CBF increases in insular cortex and anterior cingulate gyrus; increases in anterior cingulate gyrus w
168 te gyrus) and parietal (precuneus, posterior cingulate gyrus, inferior parietal lobule (IPL), postcen
169 a bilateral lower activity in the posterior cingulate gyrus, insula and precuneus in the bed rest gr
170 multiple foci in dorsal anterior and middle cingulate gyrus, insula/claustrum, amygdala/periamygdala
171 halamus, amygdala, caudate nucleus, anterior cingulate gyrus, insular cortex and orbitofrontal cortex
172 nferior frontal gyri, anterior and posterior cingulate gyrus, insular cortex, and medial temporal lob
176 At 1-year follow-up, WM volume in the left cingulate gyrus isthmus correlated with clinical scores
177 terior cingulate WM bilaterally and the left cingulate gyrus isthmus WM, as well as the right precune
178 r, the anterior part of the cingulum and the cingulate gyrus isthmus, as well as the precuneal GM, ma
179 grey matter loss over time in the posterior cingulate gyrus, lateral and medial temporal lobe, and o
180 thalamus) and extrathalamic regions such as cingulate gyrus, lateral geniculate, temporal cortex, an
181 osteroinferior temporal lobe, left posterior cingulate gyrus, left frontal lobe expressive language r
182 re identified in the frontal lobes, anterior cingulate gyrus, left temporal lobe, and of white matter
183 hroughout the sequences, the hippocampus and cingulate gyrus maintain the same hierarchical level, ex
184 results suggest that damage to the anterior cingulate gyrus may be the cause of changes in social in
186 rapy-treated on the right) and left anterior cingulate gyrus metabolism, and increases in normalized
187 ctivation was observed across studies in the cingulate gyrus, middle frontal gyrus, caudate, and insu
188 ry: entorhinal cortex, retrosplenial cortex, cingulate gyrus, midline thalamic nuclei and prefrontal
190 individuals, differences in C(p), lambda and cingulate gyrus nodal centrality were significantly redu
191 ain tissues from cerebellum, midfrontal, and cingulate gyrus obtained at autopsy from 11 patients wit
192 asolateral amygdala and the rostral anterior cingulate gyrus of the medial prefrontal cortex while mo
193 umes of the superior frontal gyrus, anterior cingulate gyrus, orbital frontal region, hippocampus, an
194 accumbens, right and left insula, and right cingulate gyrus (P < 0.005, corrected for multiple compa
196 patients had decreased rCBF in the posterior cingulate gyrus (P = .01) with extension to the medial p
197 nts had increased rCBF in the right anterior cingulate gyrus (P = .02) compared with that in control
198 th reduced fractional anisotropy in the left cingulate gyrus part of the cingulum, left posterior tha
199 entral precuneus (BA7), along with posterior cingulate gyrus (PCC, BA23, sad condition) and anteromed
200 vity for gains was reduced in CD in the left cingulate gyrus post-cocaine and in the left putamen in
201 al prefrontal cortex (DLPFC), medial frontal/cingulate gyrus, posterior cingulate cortex (PCC), and v
202 al anterior cingulate gyrus, caudal anterior cingulate gyrus, posterior cingulate gyrus, hippocampus,
203 d temporal cortices as well as the posterior cingulate gyrus, precuneus, and mesial temporal cortex.
205 in seven prefrontal subregions: the anterior cingulate, gyrus rectus, orbitofrontal cortex, precentra
206 sion in the right superior frontal gyrus and cingulate gyrus, regions associated with pain processing
207 gyri; superior parietal lobe; and posterior cingulate gyrus, resulted in a fitted accuracy of 94% an
208 ol (mI), and mI/Cr measured in the posterior cingulate gyrus reveal evidence of disease progression i
209 patients presented decreased activity in the cingulate gyrus, right PrCS and right PPC and increased
210 mentary motor cortex, anterior and posterior cingulate gyrus, right superior parietal lobe, right int
211 ddle frontal gyrus (MFG) and the subcallosal cingulate gyrus (SCG) showed enrichment for the common a
212 nificantly raised regional CBF (rCBF) in the cingulate gyrus, sensorimotor cortex, superior temporal
214 showed reduced volume of the right anterior cingulate gyrus, specifically in Brodmann's area 24'.
215 k map, which comprised the insular cortices, cingulate gyrus, striatum, globus pallidus internus, tha
216 lated smaller gray matter volumes in various cingulate gyrus subregions in schizophrenia and bipolar
217 e bilateral cerebellum, middle and posterior cingulate gyrus, supplementary motor cortex, precentral
219 edial prefrontal cortex and rostral anterior cingulate gyrus (Talairach coordinates: x=0, y=62, z=10)
220 g network-medial prefrontal cortex, anterior cingulate gyrus, temporoparietal junction, and precuneus
222 ed greater activation in the dorsal anterior cingulate gyrus than did low-risk participants, who show
224 ule, the superior temporal gyrus, the middle cingulate gyrus, the putamen and the superior parietal l
226 including superior frontal gyrus and rostral cingulate gyrus; the ACD group had significant reduction
227 physiological connections from the posterior cingulate gyrus to parietal, temporal, mesial occipital
228 al evaluation was performed on the posterior cingulate gyrus using antibodies to synaptic vesicles, h
229 ity (CNBD), CNBD:CNFD ratio (P < 0.0001) and cingulate gyrus volume (P < 0.05) but comparable volume
231 fied a reduction in corneal nerve fibers and cingulate gyrus volume in schizophrenia, but no associat
234 ated in patients; in contrast, the posterior cingulate gyrus was activated in patients and deactivate
235 al areas combined and fewer NODs in the left cingulate gyrus was associated with better phonological
236 m-level analysis, the right posterior middle cingulate gyrus was negatively associated with "tense, s
238 ) voxel matrix) acquired axially through the cingulate gyrus was used to quantify regional brain chem
239 this follow-up study of postmortem anterior cingulate gyrus, we have found evidence of increased TDO
240 ain activations in the midbrain and anterior cingulate gyrus were further associated with higher leve
241 erior cingulate gyrus; increases in anterior cingulate gyrus were greater in the comparison group tha
243 ll as between the superior frontal gyrus and cingulate gyrus, were positively correlated with the tot
244 ight inferior parietal cortex, and posterior cingulate gyrus when compared with control subjects.
245 in the right cerebellar cortex and the left cingulate gyrus when executing the prelearned sequence,
246 The orbitofrontal cortex and the anterior cingulate gyrus, which are regions neuroanatomically con
248 tal cortex) and inhibitory control (anterior cingulate gyrus), whose disruption results in compulsivi
249 patterns were also observed in the anterior cingulate gyrus with the proximal esophagus being repres
251 metabolic products were observed in anterior cingulate gyrus without proton decoupling in one subject