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1 ppocampus; decreased brain activity in right lateral orbitofrontal cortex).
2 ower GM in bilateral temporal poles and left lateral orbitofrontal cortex.
3 correlates directly with BOLD signal in the lateral orbitofrontal cortex.
4 tional, particularly sad, distractors in the lateral orbitofrontal cortex.
5 reas, the BPM group exhibited decreased left lateral orbitofrontal cortex activation compared with bo
6 ons of the OFC, the agranular insula and the lateral orbitofrontal cortex (AI-OPNs and LO-OPNs, respe
7 ts), the lower was their D2-type BPND in the lateral orbitofrontal cortex, an important region in val
8 irrored by opposite aversion-like signals in lateral orbitofrontal cortex and anterior cingulate cort
9 long-range white matter tract that connects lateral orbitofrontal cortex and Brodmann area 10 with t
12 f attention from dorsolateral prefrontal and lateral orbitofrontal cortex and may represent an organi
13 uctural and functional abnormalities in left lateral orbitofrontal cortex and right supplementary mot
14 , basolateral and other), amygdala nuclei to lateral orbitofrontal cortex and stronger connections of
15 the ventromedial prefrontal cortex (VMPFC), lateral orbitofrontal cortex, and amygdala] while it sim
16 al connectivity among regions such as vmPFC, lateral orbitofrontal cortex, and parahippocampal gyrus
17 perior and inferior frontal gyri, medial and lateral orbitofrontal cortex, and parahippocampal gyrus,
18 ation in the ventromedial prefrontal cortex, lateral orbitofrontal cortex, and periaqueductal gray re
19 m, especially the left hippocampus, the left lateral orbitofrontal cortex, and the bilateral isthmus
20 ecreased grey matter in the anterior insula, lateral orbitofrontal cortex, anterior cingulate and dor
21 nd evaluation of wrong choices activated the lateral orbitofrontal cortex, anterior insula, superior
23 the increased functional connectivity of the lateral orbitofrontal cortex Brodmann area 47/12 is rela
24 owed that the functional connectivity of the lateral orbitofrontal cortex Brodmann area 47/12 with th
26 ns (in particular angry expressions); namely lateral orbitofrontal cortex (Brodmann area 47) and medi
27 -dorsolateral prefrontal cortex and amygdala-lateral orbitofrontal cortex coupling were shown in male
28 n of several cortical regions, including the lateral orbitofrontal cortex, during reversal learning i
29 brain stem regions and less deactivation in lateral orbitofrontal cortex in hypoglycemia unawareness
30 d receipt of food but less activation in the lateral orbitofrontal cortex in response to receipt of f
32 cit was dependent on a circuit involving the lateral orbitofrontal cortex, insula, amygdala and tempo
35 computationally distinct learning signals in lateral orbitofrontal cortex (lOFC) and the dopaminergic
37 Recent work in macaques has suggested the lateral orbitofrontal cortex (lOFC) is relatively more c
38 en assessed if pharmacologic inactivation of lateral orbitofrontal cortex (lOFC) or DBS of the ventra
39 ctivity in three frontal cortical areas, the lateral orbitofrontal cortex (lOFC), medial orbitofronta
41 ed MRI-based segmentations of the medial and lateral orbitofrontal cortex (OFC) and hippocampal volum
42 studies have demonstrated activations in the lateral orbitofrontal cortex (OFC) and the inferior fron
44 le/parietal operculum (PT/PO), and posterior lateral orbitofrontal cortex (plOFC) had local gray matt
46 children had greater activation in the left lateral orbitofrontal cortex than did low-risk children
47 lphenidate induced greater increases in left lateral orbitofrontal cortex than when it was expected.
48 roach restricting analysis to the medial and lateral orbitofrontal cortex, the amygdala, the anterior
49 ard-guided learning and decision-making: the lateral orbitofrontal cortex, the ventromedial prefronta
50 ofrontal cortex and in the reward-evaluating lateral orbitofrontal cortex underlie a diminished smoki
52 dify behaviour through interactions with the lateral orbitofrontal cortex, which provides valence-bas
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