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1 llosum voxels, including the genu, body, and splenium.
2 ith controls, without changes in the genu or splenium.
3 ntrols, while no difference was found in the splenium.
4 ing indicated T2-hyperintense lesions of her splenium.
5 through the inferior-anterior corner of the splenium.
6 egular organization of the fibers within the splenium.
7 converged onto the same positions within the splenium.
8 ocampal border is at the ventral edge of the splenium.
9 us callosum except the posterior midbody and splenium.
10 sue of sex differences in axon number in the splenium.
12 disruption) in the genu (-0.02; p = .04) and splenium (-0.01; p = .02) of the corpus callosum and ant
13 holism, with the genu more affected than the splenium, a pattern even more pronounced in the fibre tr
14 ee regions of the corpus callosum: the genu, splenium and callosal fibres connecting the motor cortic
17 The trajectories of two inter-hemispheric (splenium and genu), two projection (cortico-pontine and
18 ubjects had smaller volumes in the thalamus, splenium and pons, but not in the caudate or putamen.
19 ior midbody, posterior midbody, isthmus, and splenium) and for overall CC size, with left-handed chim
20 a rostrocaudal organization of axons in the splenium based on rostral to caudal cortical location th
21 f visuomotor integration and FA in bilateral splenium, but not temporal regions were observed within
22 fibre bundles coursing through the genu and splenium, but these effects were only significant in the
24 matter tracts, such as the callosal genu and splenium, cingulum, optic radiations, and the superior l
27 Among the psychosis groups, the anterior splenium in probands with PBD showed a stronger correlat
29 tching BPA, FA in posterior corpus callosum (splenium-occipital) correlated with face-matching BPA.
30 integrity, in a priori regions of interest: splenium of corpus callosum (SPCC) and posterior limb of
32 es, although not in FA values, including the splenium of corpus callosum, left posterior corona radia
33 pied by myelin were examined in the genu and splenium of male and female rats in adulthood, middle ag
35 tooccipital fasciculi (IFOF), genu (GCC) and splenium of the corpus callosum (SCC), posterior limbs o
36 correlated with diffusion anisotropy of the splenium of the corpus callosum and adjacent parietal wh
37 l interhemispheric connectivity (through the splenium of the corpus callosum and anterior commissure)
38 eonatal diffusion properties of the genu and splenium of the corpus callosum and corticospinal tracts
39 transversely sectioned nerve fibers from the splenium of the corpus callosum and from the vertical bu
40 te matter tract degeneration spread into the splenium of the corpus callosum and motor cortex white m
41 capsule; proceeding caudocranially from the splenium of the corpus callosum and optic radiations (at
42 OAD also had specific damage to the genu and splenium of the corpus callosum and parahippocampal trac
43 ft inferior fronto-occipital fasciculus, and splenium of the corpus callosum compared with controls.
44 with the microstructural organization of the splenium of the corpus callosum in low-risk infants, but
45 ibers in area 46 of prefrontal cortex and in splenium of the corpus callosum show age-related alterat
47 he left uncinate fasciculus and the genu and splenium of the corpus callosum were also obtained for c
49 D, respectively]) of frontal lobe, genu, and splenium of the corpus callosum WM (FWM, GWM, and SWM, r
50 signal in white matter areas, especially the splenium of the corpus callosum, and no gray matter abno
51 ral fornix (cres)/stria terminalis, genu and splenium of the corpus callosum, bilateral anterior and
52 owth in diabetes, as did white matter areas (splenium of the corpus callosum, bilateral superior-pari
53 ule, forceps minor and major, genu, body and splenium of the corpus callosum, inferior fronto-occipit
55 controls in the left dorsal cingulum bundle, splenium of the corpus callosum, right corticospinal tra
58 nal anisotropy values along the body and the splenium of the corpus callosum, the left cingulum, and
59 ed radial diffusivity in the genu, body, and splenium of the corpus callosum, the right posterior lim
60 of the internal capsule (RLIC), the body and splenium of the corpus callosum, the superior and poster
68 groups of interhemispheric fibres within the splenium, only those connecting the temporal lobes were
69 mum in the body, and 10.6 vs 8.2 mum in the splenium; P < .05) and decreased axon density ([0.48 vs
73 adiations, posterior corona radiata, and the splenium region of the corpus callosum) were found to ha
74 the right posterior cingulum, left callosal splenium, right inferior fronto-occipital fasciculus, an
76 duced fractional anisotropy in a portion the splenium, the forceps major, which provides interhemisph
78 corpus callosum, the gyrus curves around the splenium, turns laterally and forms a region called the
79 impact the number of myelinated axons in the splenium was confirmed in a subset of animals using quan
82 etween the visuomotor task and FA within the splenium were not significant within the control group,
83 differences in axon density in the adult rat splenium were regional and did not result in overall sex
84 ns through a large band in the middle of the splenium, whereas ventral visual maps (ventral V3, V4) s
85 s detected in the posterior corpus callosum (splenium), which contains interhemispheric connections b
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