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1 the left posterior superior temporal cortex (Wernicke's area).
2 rior temporal regions bilaterally (including Wernicke's area).
3 demonstrated SSC's superiority at localizing Wernicke's area.
4  risk allele, p=7.64x10(-5)), which contains Wernicke's area.
5 ic error production to lesions in and around Wernicke's area.
6 erior and middle temporal gyri, in classical Wernicke's area.
7 e temporal and angular gyri corresponding to Wernicke's area.
8 essive right-sided activation of Broca's and Wernicke's areas.
9 other motor regions, and between Broca's and Wernicke's areas.
10 emporal/fusiform gyrus, Broca's area, and/or Wernicke's area accounted for most acute improvement aft
11 he temporal-lobe language-sensitive regions (Wernicke's area) also show effectively little or no sepa
12                                         Both Wernicke's area and its right homolog displayed a negati
13 ds); (2) the VWFA has preferential RSFC with Wernicke's area and other core regions of the language s
14  and verbal fluency (FAS), in localizing the Wernicke's area and studied the association between geno
15  the left posterior superior temporal gyrus (Wernicke's area) and motor production processes occurred
16 -correlated activity with auditory (only for Wernicke's area) and visual cortices that suggests integ
17 ociative bundle connecting Broca's area with Wernicke's area, and other language regions of the tempo
18 (the left laterosuperior temporal cortex, or Wernicke's area, and the left inferior frontal gyrus, or
19 four regions of interest (ROIs): Broca's and Wernicke's areas, and their anatomic homologues in the r
20 n various Brodmann's areas--BA 22 (including Wernicke's area), BA 44 (part of Broca's area), BA 45 (p
21 l links with posterior language areas (e.g., Wernicke's area), because it is presumed to be involved
22 y encompassing temporoparietal components of Wernicke's area, Broca's area, and dorsal premotor corte
23 add further evidence for the crucial role of Wernicke's area (Brodmann's area 22) in word comprehensi
24  demonstrated foci not only within classical Wernicke's area but also within the middle and inferior
25 nd not only in language regions (Broca's and Wernicke's areas), but also specific regions in bilatera
26 sical arcuate pathway connecting Broca's and Wernicke's areas directly, we show a previously undescri
27 r, a memory-specific left-sided dominance in Wernicke's area for speech perception has been demonstra
28 guage processing regions such as Broca's and Wernicke's areas for the word problems and the horizonta
29 the functional and anatomical boundaries of 'Wernicke's area' have become so broad as to be meaningle
30 ined activation only in the right hemisphere Wernicke's area in 4/5 of the cases.
31                                Activation in Wernicke's area in both hemispheres was obtained irrespe
32  Our results highlight the important role of Wernicke's area in forming vivid musical imagery through
33 lization (e.g. Broca's area in the left, and Wernicke's area in the right hemisphere) have been repor
34 humans, Broca's area in the frontal lobe and Wernicke's area in the temporal lobe are crucially invol
35 while they were remote from both Broca's and Wernicke's areas in the remainder.
36                                      Whereas Wernicke's area interacted within the intrinsic auditory
37                    HGG tumors localized near Wernicke's area lead to transfer its function to the hea
38 arietal areas, traditionally included within Wernicke's area, leave single word comprehension intact
39      SSC is a robust paradigm for localizing Wernicke's area, making it an important clinical tool fo
40  with tumors located close to the Broca's or Wernicke's areas of the left hemisphere.
41  with the magnitude of delay in perfusion of Wernicke's area on magnetic resonance perfusion-weighted
42 s area) and bilateral posterior perisylvian (Wernicke's area on the left) regions.
43 he strength of the RSFC between the VWFA and Wernicke's area predicts performance on a semantic class
44            These regions include Broca's and Wernicke's areas, primary auditory and visual cortex, an
45 bidirectional connection between Broca's and Wernicke's areas probably through the arcuate fasciculus
46 cal network, but independently of awareness, Wernicke's area processes predictive events in time and
47 oca's area) and posterior superior temporal (Wernicke's area) regions, in addition to other language
48 in time-to-peak concentration of contrast in Wernicke's area, relative to the homologous region on th
49 tion of the underlying lesion site, known as Wernicke's area, remains controversial.
50 ith a different functional specificity; e.g. Wernicke's area responded specifically to speech sounds
51     Language areas of the brain (Broca's and Wernicke's area) responded as the premises and the concl
52 internal capsule (RR, 2.2; 95% CI, 1.1-4.4), Wernicke's area (RR, 2.0; 95% CI, 1.1-3.8), or basal gan
53  because of its functional connectivity with Wernicke's area.SIGNIFICANCE STATEMENT The visual word f
54 n the thalamus and Broca's area extending to Wernicke's area, supporting the hypothesized (negative)
55 ge functional connectivity (except posterior Wernicke's area that exhibited predominant long-range co
56 tivity was left lateralized (except anterior Wernicke's area that exhibited rightward lateralization)
57 lative underactivation in posterior regions (Wernicke's area, the angular gyrus, and striate cortex)
58  Transmodal areas in the midtemporal cortex, Wernicke's area, the hippocampal-entorhinal complex and
59 vealed a posterior superior temporal region (Wernicke's area, traditionally considered a language-spe
60 area versus its right-hemisphere homolog and Wernicke's area versus its right-hemisphere homolog.
61           For 50 patients without infarct in Wernicke's area, we found a strong Pearson correlation b
62  the presence of hypoperfusion or infarct in Wernicke's area, we tested the hypothesis that the sever
63 ng activations at the anterolateral belt and Wernicke's area, where the responses were correlated wit

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