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1 frontal and the paracentral motor cortex and cerebellar vermis.
2 the prefrontal cortex, corpus callosum, and cerebellar vermis.
3 Two of these are ongoing within the cerebellar vermis.
4 Controls had greater activation in the cerebellar vermis.
5 rietal sulcus, insula, frontal operculum and cerebellar vermis.
6 leus, and lobules I, IV, V, IX, and X of the cerebellar vermis.
7 ly, frontal operculum bilaterally and in the cerebellar vermis.
8 ecrease of vascular resistance in the dorsal cerebellar vermis.
9 oys in the posterior-inferior lobules of the cerebellar vermis.
10 te nucleus, globus pallidus, cerebellum, and cerebellar vermis.
11 kinases (ERKs) and p38 MAPK in the anterior cerebellar vermis.
12 total and frontal brain, basal ganglia, and cerebellar vermis.
13 recursor pool of cells that develop into the cerebellar vermis.
14 sels particularly in the cerebral cortex and cerebellar vermis.
15 ateral thalamus and premotor cortex, and the cerebellar vermis.
16 after transection of the posterior inferior cerebellar vermis.
17 the dorsal striatum, olfactory tubercle, and cerebellar vermis.
18 l cortex, the left prefrontal cortex and the cerebellar vermis.
19 of the frontal lobes but not in the superior cerebellar vermis.
20 taining GABA-A/BDZ receptors in the superior cerebellar vermis.
21 ns of K1, and DV bilaterally in the superior cerebellar vermis.
22 f-generated head movements in the rat caudal cerebellar vermis, an area essential for graviceptive fu
23 me is a congenital brain malformation of the cerebellar vermis and brainstem with abnormalities of ax
24 characterized by hypoplasia/dysplasia of the cerebellar vermis and by ataxia, hypotonia, oculomotor a
25 tter reduction in anterior subregions of the cerebellar vermis and hemisphere in the asymptomatic pre
26 fect in GCP proliferation was similar in the cerebellar vermis and hemispheres in all patients with c
27 uronal loss/dysfunction was indicated in the cerebellar vermis and hemispheres in both diseases by lo
29 amus, dentate nucleus, cerebellar peduncles, cerebellar vermis and lobules V and VI, and corpus callo
30 e ataxic, attributed to the reduction of the cerebellar vermis and some regions of the hemispheres.
34 input and motor output (anterior and dorsal cerebellar vermis) and the maintenance of equilibrium (v
35 l cortices as well as the caudate, thalamus, cerebellar vermis, and cerebrum in 20 first-episode psyc
37 infancy, atrophy of the cerebral cortex and cerebellar vermis, and mild atrophy of the cerebellar he
38 the thalamus, globus pallidus, hippocampus, cerebellar vermis, and very low expression was detected
39 same distribution, and also in the superior cerebellar vermis; and the non-ACD group had significant
41 (Senior-Loken syndrome), liver fibrosis, and cerebellar vermis aplasia (Joubert syndrome) in approxim
43 ts association with retinal degeneration and cerebellar vermis aplasia in Joubert syndrome are poorly
45 men/globus pallidus, sensorimotor cortex and cerebellar vermis, as well as increases in the precuneus
46 recessive disorder marked by agenesis of the cerebellar vermis, ataxia, hypotonia, oculomotor apraxia
47 trophy, progressive gait ataxia with tremor, cerebellar vermis atrophy, and optic-nerve thinning.
48 failure in early infancy and are affected by cerebellar vermis atrophy, ataxia, and peripheral neurop
49 ctivations (increased rCBF) were observed in cerebellar vermis, brainstem and right anterior cingulat
50 Using whole-cell recording from slices of cerebellar vermis derived from juvenile (P18-25) or adul
51 ion, activation patterns were present in the cerebellar vermis during bimanual coordination tasks, wi
54 and posterior fossa malformations including cerebellar vermis hypoplasia (CVH), mega-cisterna magna
58 The children presented congenital ataxia and cerebellar vermis hypoplasia with elongated superior cer
59 cessive multisystem disease characterized by cerebellar vermis hypoplasia with prominent superior cer
60 The ciliopathy Joubert syndrome is marked by cerebellar vermis hypoplasia, a phenotype for which the
61 evelopmental brain disorder characterized by cerebellar vermis hypoplasia, abnormal eye movement, ata
62 atrophy, dysgenesis of the corpus callosum, cerebellar vermis hypoplasia, and facial dysmorphism.
63 ooth sign" on axial brain MRI, together with cerebellar vermis hypoplasia, ataxia, and psychomotor de
64 and abnormal signal), thin corpus callosum, cerebellar vermis hypoplasia, optic nerve hypoplasia and
66 ic resonance image analysis, we measured the cerebellar vermis in 125 normal individuals with a broad
67 us, and fusiform gyri and reduced GMV in the cerebellar vermis in FXS at both timepoints, suggesting
70 daloid, and hippocampal volumes, and smaller cerebellar vermis lobules VI and VII, in comparison with
71 ly smaller volumes in the posterior-inferior cerebellar vermis (lobules VIII-X; effect size, 0.54; P
72 ized developmental links between frontal and cerebellar vermis neural abnormalities were supported, i
73 nsors but similar to lobules 9 and 10 of the cerebellar vermis (nodulus and uvula), MSTd neurons resp
74 nuclear fractions of postmortem samples from cerebellar vermis of 10 patients with schizophrenia and
76 jection of low doses of kainic acid into the cerebellar vermis of mice elicited reliable and reproduc
78 and linear density of Purkinje cells in the cerebellar vermis of subjects with and without schizophr
81 metabolism in right amygdala/hippocampus and cerebellar vermis (P < 0.001), relative to global brain.
82 his tumor, which arises predominantly in the cerebellar vermis, preferentially affects children betwe
84 thies characterized by severe defects of the cerebellar vermis, ranging from hypoplasia to aplasia.
85 cts, including mediolateral expansion of the cerebellar vermis, reduced thickness of the granule cell
86 e and mental stress tasks, increased rCBF in cerebellar vermis, right anterior cingulate and right in
87 loss of volume was observed in the superior cerebellar vermis; the volume loss persisted regardless
89 al cortex, hippocampus, corpus callosum, and cerebellar vermis were compared between mother-reared (n
91 of abnormal levels of the MAP kinases in the cerebellar vermis were linked to additional downstream t
92 brain malformation characterized by missing cerebellar vermis with apparent fusion of the cerebellar
93 tify a group of Purkinje cells in the caudal cerebellar vermis with responses that reflect an estimat
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