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1 occurred in the left inferior frontal gyrus (Broca's area).
2 nsula and lateral premotor cortex and not of Broca's area.
3 subjects with PTSD showed decreased rCBF in Broca's area.
4 The pars triangular is a portion of Broca's area.
5 activation of the ventral temporal lobes and Broca's area.
6 o ventral premotor cortex, not the classical Broca's area.
7 racy in the left ventral premotor cortex and Broca's area.
8 correlation between left striate cortex and Broca's area.
9 dle temporal gyrus and the dorsal portion of Broca's area.
10 cortical networks, neither of which involves Broca's area.
11 lood oxygen level-dependent (BOLD) signal in Broca's area.
12 reas with premotor/motor areas, and not with Broca's area.
13 , in close topographical relationship to the Broca's area.
14 power in both Sylvian-parietal-temporal and Broca's areas.
15 logic cell counting in postmortem samples of Broca's area 44 in 9 schizophrenic patients and 14 norma
17 y identified by Broca and what is now called Broca's area, a finding with significant ramifications f
18 is discovery of language-specific regions in Broca's area advances our understanding of the cortical
19 ded during awake neurosurgical operations in Broca's area and in the dominant temporal lobe with the
20 tex in relation to bulbar disability, and in Broca's area and its homologue in relation to verbal flu
21 vation relative to the unaffected members in Broca's area and its right homolog, as well as in other
22 chronous delays led to increased activity in Broca's area and its right homologue, whereas disruptive
23 tion: storage for verbal materials activates Broca's area and left-hemisphere supplementary and premo
25 Heschl's gyrus, the parietal operculum, left Broca's area and the left arcuate fasciculus (similar to
26 s between FFG and phonology-related regions (Broca's area and the left inferior parietal lobule), and
28 ral prefrontal cortex (areas 45, 46 and 47), Broca's area and the right temporal (area 21) and right
29 ract that lies deep to posterior portions of Broca's area and the sensory-motor cortex, is a robust p
30 the input language resulted in activation of Broca's area and the supramarginal gyri, areas associate
32 ing was restricted to left inferior frontal (Broca's area) and bilateral posterior perisylvian (Werni
33 ic activations in the left inferior frontal (Broca's area) and posterior superior temporal (Wernicke'
34 or prefrontal regions bilaterally (including Broca's area) and superior temporal regions bilaterally
35 rea, and the left inferior frontal gyrus, or Broca's area) and their homologous right-hemisphere area
37 ask-relevant anatomic regions (sensorimotor, Broca's area, and superior temporal gyrus), these behavi
38 ft posterior middle temporal/fusiform gyrus, Broca's area, and/or Wernicke's area accounted for most
39 ions including frontopolar cortex (area 10), Broca's area (area 45), frontoinsular cortex (area FI),
40 inal patients and the increasing reliance on Broca's area as a major speech centre, we thought it imp
42 assical theories of brain organization (e.g. Broca's area as speech output region) and provide a dist
43 imaging studies often rely on activation in Broca's area as verification that tasks have successfull
44 d by left-hemisphere speech areas, including Broca's area as well as the premotor and supplementary m
45 ur findings strongly indicate that a part of Broca's area (BA 44, pars opercularis) is critically imp
47 BA 44 (part of Broca's area), BA 45 (part of Broca's area), BA 21 (inferior temporal cortex), BA 37 (
48 (including Wernicke's area), BA 44 (part of Broca's area), BA 45 (part of Broca's area), BA 21 (infe
49 Repetition of single words did not activate Broca's area but activity in three left-lateralised regi
51 rior temporal) as well as motor brain areas (Broca's area, cerebellum) in response to speech, and equ
53 reviously obtained cytoarchitectonic maps of Broca's area confirmed lack of homology between activati
54 ect fMRI, we find that both ideas are right: Broca's area contains two sets of subregions lying side
57 whether the electrophysiological activity of Broca's area correlates with the sound of the utterances
58 vity in the left ventral premotor cortex and Broca's area exhibited effective phoneme categorization
59 ith resting fMRI signals in the thalamus and Broca's area extending to Wernicke's area, supporting th
60 utational systems, and a common substrate in Broca's area for hierarchical processing has recently be
63 llustrate the interindividual variability of Broca's area homologue in the chimpanzee and support the
64 ly prior study documenting the morphology of Broca's area homologue in the chimpanzee, we report grea
66 that the region of cortex commonly known as Broca's area (i.e., the posterior LIFG) serves to bias c
68 Contrary to classic notions of the role of Broca's area in speech, while motor cortex is activated
70 ominant distribution of activation involving Broca's area in the generation tasks and a more bilatera
71 ions dorsal to the traditional boundaries of Broca's area in the inferior frontal sulcus and the post
73 issociation of language lateralization (e.g. Broca's area in the left, and Wernicke's area in the rig
74 r fMRI examinations showed activation of the Broca's area in the right hemisphere in 3/4 cases of low
75 gnificant cytoarchitectonic abnormalities in Broca's area in the same brains in which the dlPFC exhib
78 showed significantly increased activation in Broca's area, in addition to the well known visuospatial
84 t ventrolateral prefrontal cortex (including Broca's area), left premotor cortex, and left and right
85 mal naming network and as such indicate that Broca's area may be a suitable candidate site for tDCS i
87 as the recurrence of the tumor near the left Broca's area might be the factors leading to reorganizat
88 e primary auditory cortex (p </= .001), left Broca's area (p </= .001), and cingulate gyrus (p </= .0
89 dings to reflect preferential recruitment of Broca's area, part of the neural substrate supporting si
90 independent datasets strongly indicate that Broca's area participates in categorical speech percepti
91 e whether the posterior, superior portion of Broca's area performs operations on phoneme segments spe
94 ize (RR, 2.0; 95% CI, 1.2-3.2) and injury to Broca's area (RR, 2.5; 95% CI, 1.3-5.0), internal capsul
95 the frontal-lobe language-sensitive regions (Broca's area), second languages acquired in adulthood ('
96 PF), left superior temporal region (ST), and Broca's area showed sustained activation during the memo
97 audate, as well as primary motor cortex, the Broca's area, superior temporal gyrus, insula, and claus
99 area; the inferior lateral premotor cortex (Broca's area); the anterior insula; and the cerebellum.
101 implicate anterior cortical regions such as Broca's area, the left anterior insula, and deep white m
102 d by left-hemisphere speech areas, including Broca's area, the premotor area, and the supplementary m
103 ntoparietal motor-related network (including Broca's area, the premotor region, the intraparietal sul
104 g the Sylvian fissure bilaterally including "Broca's area," the primary language area, by disrupting
105 uage network on epicentres in Wernicke's and Broca's areas; the explicit memory/emotion network on ep
106 patients are due entirely to dysfunction in Broca's area, thereby attributing all aspects of the dis
108 lization index was calculated separately for Broca's area versus its right-hemisphere homolog and Wer
109 t the AF connects posterior brain areas with Broca's area via a relay station in the premotor/motor a
117 ectly involved in language generation, or in Broca's area when the participants were executing a repe
118 iculus, a long associative bundle connecting Broca's area with Wernicke's area, and other language re
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