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1 ostnatally in the granule cell layer and the dentate nucleus.
2 ia and had abnormal signals in brainstem and dentate nucleus.
3 volvement of white matter and the cerebellar dentate nucleus.
4 ated amino acid precursors injected into the dentate nucleus.
5 tDNA-encoded proteins only in neurons of the dentate nucleus.
6 images relative to reference tissues in the dentate nucleus (0.53% signal intensity increase per inj
7 lesions in the substantia nigra, caudate and dentate nucleus, a reliable and repeatable 12-tiered gra
8 tract changes correlated with reductions in dentate nucleus activation recorded during task performa
9 coustic transmissions to click change in the dentate nucleus after conditioning, that changes in resp
10 present in a small number of neurones in the dentate nucleus and diffusely in cerebellar astrocytes.
12 these neurons were found in portions of the dentate nucleus and the internal segment of the globus p
13 mapping, we identified distinct areas in the dentate nucleus and the lateral cerebellum of both hemis
14 rimotor cortex, the right cerebellum (dorsal dentate nucleus), and the right superior temporal gyrus
16 of these proteins in the cerebellar cortex, dentate nucleus, and inferior olivary nucleus from 2 aut
17 ites, neurons in internal granular layer and dentate nucleus, and neuronal elements in gut and kidney
18 The SI in the globus pallidus, thalamus, dentate nucleus, and pons was measured at unenhanced T1-
19 ior cingulate, inferior temporal lobule, the dentate nucleus, and the cerebellar lobules IV/V, VI, an
20 ections from caudal and ventral parts of the dentate nucleus appear to overlap oculomotor inputs to r
21 The findings support the hypothesis that the dentate nucleus can play a significant role in short as
22 ls in the basal ganglia, midbrain, thalamus, dentate nucleus, cerebellar peduncles, cerebellar vermis
23 ry indices for frontal cortex, thalamus, and dentate nucleus combined as well as individually for fro
24 e results indicated that inactivation of the dentate nucleus disrupted effort-based decision making.
25 ighted signal intensity (SI) increase in the dentate nucleus (DN) and globus pallidus (GP) in relatio
26 eglumine on the signal intensity (SI) of the dentate nucleus (DN) of the pediatric brain on nonenhanc
27 (GBCAs) on the signal intensity (SI) of the dentate nucleus (DN) on unenhanced T1-weighted magnetic
28 est for measurable visual enhancement of the dentate nucleus (DN) on unenhanced T1-weighted magnetic
29 ) in the globus pallidus (GP), thalamus (T), dentate nucleus (DN), and pons (P) were measured on unen
30 llowing five regions of interest (ROIs): the dentate nucleus (DN), pons, substantia nigra (SN), pulvi
32 is, and deep cerebellar nuclei including the dentate nucleus during absolute, duration-based timing a
33 ce imaging of the lateral cerebellar output (dentate) nucleus during passive and active sensory tasks
34 gest that mitochondrial abnormalities in the dentate nucleus in conjunction with loss of Purkinje cel
36 minations had increased SI ratios within the dentate nucleus (mean SI ratio +/- standard error of the
37 wed visually detectable T1 shortening in the dentate nucleus (n = 13), globus pallidus (n = 13), subs
39 Recordings were made from 95 units of the dentate nucleus of naive cats to determine if patterns o
40 nts and controls, although R2* values in the dentate nucleus of patients were significantly higher, w
41 en, pallidum, thalamus, midbrain, and in the dentate nucleus of the cerebellum (t's > 2.7, P's < 0.02
42 e targets of disynaptic projections from the dentate nucleus of the cerebellum and from the internal
44 were found in frontal cortex, thalamus, and dentate nucleus of the cerebellum in all 7 boys, but not
45 ined organization of the projection from the dentate nucleus of the cerebellum to the ventral lateral
48 euronal transport of virus were found in the dentate nucleus only after injections into areas 46d, 9m
49 .026) and T2 of the whole brain (P = .004), dentate nucleus (P = .023), and thalamus (P = .002) show
50 rain (P < .001), globus pallidus (P = .002), dentate nucleus (P = .046), and thalamus (P = .026) and
52 and spinal cord, including the hippocampus, dentate nucleus, pontine nuclei, locus coeruleus, and pa
53 neurons, the locus ceruleus, the cerebellar dentate nucleus, Purkinje cells, the basis pontis, numer
55 putamen, subthalamic nucleus, midbrain, and dentate nucleus relative to controls and PD patients (vo
57 [CI]: 0.03, 0.67; P = .03), but not between dentate nucleus SI and patient age (r = 0.23; 95% CI: -0
58 There was a significant correlation between dentate nucleus SI and total cumulative gadolinium dose
59 levated free-water in all regions except the dentate nucleus, subthalamic nucleus, and corpus callosu
61 olliculus, the Edinger-Westphal nucleus, the dentate nucleus, the raphes linearis and pontis, the dor
62 s pallidus, substantia nigra, and cerebellar dentate nucleus); this suggests a much more extensive ro
66 n output stage of cerebellar processing, the dentate nucleus, with an input stage of basal ganglia pr
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