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1  in visual areas, particularly the bilateral fusiform gyri.
2  were identified in the inferior frontal and fusiform gyri.
3 ut was specific for areas in the lingual and fusiform gyri.
4 king on clear speech activated both anterior fusiform gyri.
5 egated area, including the right lingual and fusiform gyri.
6 parahippocampal gyrus and in the lingual and fusiform gyri.
7 l and frontal lobes, including cingulate and fusiform gyri and cerebellum.
8 ition elicited activation in the lingual and fusiform gyri and in the Brodmann areas 22 and 38 in sup
9 d enlarged GMV in the caudate, thalamus, and fusiform gyri and reduced GMV in the cerebellar vermis i
10 ial frontal gyri, bilateral middle occipital/fusiform gyri, and bilateral cerebella for both the rhym
11  the right posterior parahippocampal and mid-fusiform gyri, and in the hippocampal body in healthy yo
12 ding the hippocampus and parahippocampal and fusiform gyri, and increasing activation in the posterom
13 eas including right V1 and cuneus, bilateral fusiform gyri, and left parietal cortex.
14 ore by regions in the inferior occipital and fusiform gyri, and perception of eye gaze was mediated m
15 t posterior hippocampus, parahippocampal and fusiform gyri, and predominantly left hemisphere extra-t
16 Studies with functional MRI confirm that the fusiform gyri are involved in color and face perception,
17 xperiments have clearly established that the fusiform gyri are preferentially responsive to faces, wh
18 ons, including the primary visual cortex and fusiform gyri bilaterally were activated while the secon
19                                Activation of fusiform gyri by faces was strongly affected by attentio
20 ipital complex, the parahippocampal, and the fusiform gyri did not predict target presence, while hig
21  amygdala, hippocampus, parahippocampal, and fusiform gyri in 30 of 31 subjects compared with normal
22 posterior cingulate (cue-alpha) and the left fusiform gyri (item-gamma).
23 -wise differences in the cuneus, lingual and fusiform gyri, middle occipital lobe, inferior parietal
24 etry was reversed in the parahippocampal and fusiform gyri of the schizophrenic patients.
25 ower volumes of both the parahippocampal and fusiform gyri on the left side.
26 P < .05) and FA values in the cerebellum and fusiform gyri (P < .05).
27 ream of activation involving the lingual and fusiform gyri, perirolandic cortex, thalamus and anterio
28  stimuli resulted in greater deactivation in fusiform gyri, possibly reflecting greater suppression o
29 eam, particularly the inferior occipital and fusiform gyri, remained selective despite showing only 9
30  in other brain regions, including MT or V5, fusiform gyri, right premotor cortex, and the intraparie
31  within the inferior occipital gyri, lateral fusiform gyri, superior temporal sulci, amygdala, and th
32 the inferior frontal, inferior parietal, and fusiform gyri; the precuneus; and the dorsomedial prefro
33 icularly strong in the inferior temporal and fusiform gyri, two areas important for object recognitio
34 mary visual cortex, superior occipital gyri, fusiform gyri, ventral premotor area, superior parietal
35 er in the left and right parahippocampal and fusiform gyri were assessed with a stereological point-c
36 -famous) are the right lingual and bilateral fusiform gyri, while the areas specialized for famous st

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