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1 ns of the link between speech perception and speech production.
2 ct provide a rich source of sensory input in speech production.
3 in deformation that would normally accompany speech production.
4 modulation of activity in SII during normal speech production.
5 d to minimize artifact associated with overt speech production.
6 tion of motor sequences necessary for fluent speech production.
7 motor areas associated with articulation and speech production.
8 ntary spasms in the laryngeal muscles during speech production.
9 h perception for the motor system underlying speech production.
10 al procedures typically lead to worsening of speech production.
11 tal role in the construction of syllables in speech production.
12 ated a frontal-temporal system implicated in speech production.
13 eedback, and modulation of learned voice for speech production.
14 Human frontal cortex plays a crucial role in speech production.
15 ced neural activation in the left IFG during speech production.
16 aoperative cortical cooling in humans during speech production.
17 t of finer vocal motor control necessary for speech production.
18 ch is commonly seen as a neural correlate of speech production.
19 LMC functionality for finer motor control of speech production.
20 highly learned and uniquely human behavior: speech production.
21 and is activated by auditory feedback during speech production.
22 s of speech perception and motor programs of speech production.
23 al roles, only one of which was activated in speech production.
24 ar-striatal network previously implicated in speech production.
25 mpensate for loss of the left putamen during speech production.
26 r sensory target and state maps during overt speech production.
27 ly overlapping networks that are involved in speech production.
28 e during complex voluntary behavior, such as speech production.
29 ntary spasms in the laryngeal muscles during speech production.
30 r different underlying impairments affecting speech production.
31 nt phase using speech entrainment to improve speech production.
32 orrelated with somatosensory feedback during speech production.
33 ing periods of auditory perception and overt speech production.
34 ferior frontal gyrus, a region implicated in speech production.
35 pecific components of the neural network for speech production.
36 the increased motor demands associated with speech production?
37 The mechanisms underlying the acquisition of speech-production ability in human infancy are not well
38 positively with the longitudinal recovery of speech production across the two time points (as measure
39 uggested that variability in the recovery of speech production after aphasic stroke may relate in par
41 communication is a joint activity; however, speech production and comprehension have primarily been
42 February 2005, we discuss imaging studies of speech production and comprehension in patients with aph
44 n this important brain area involved in both speech production and domain-general cognitive processin
45 tudy examined the spontaneous rhythmicity in speech production and its relationship to cortex-muscle
48 rlap between altered dopamine release during speech production and reduced 11C-raclopride binding to
49 he auditory system is critically involved in speech production and that the motor system is criticall
51 es of speech, the motor commands involved in speech production, and a Direct Realist approach that em
52 empirical data between the resting state and speech production, and dopaminergic neurotransmission ev
53 occurring among brain areas associated with speech production, and white matter tracts that intercon
55 lose relationship between (left-lateralized) speech production areas and the implementation of top-do
59 al right hemispheric (RH) lateralization for speech production, based on a previous large-scale scree
61 the human brain and is a critical region for speech production, being larger in the left hemisphere t
63 support a modular view of word retrieval in speech production but rather support substantial overlap
64 he left putamen is known to be important for speech production, but some patients with left putamen d
65 findings demonstrate that the development of speech production capacity relies on changes in selectiv
66 evel of activation within this region during speech production correlated positively with the longitu
68 ility to articulate our thoughts by means of speech production depends critically on the integrity of
69 liminary evidence suggests that treatment of speech production difficulties, even years after stroke,
70 n have greater difficulty with variations in speech production encountered in everyday listening.
71 the relation between hearing loss and human speech production especially where there is consideratio
74 ic lateralization of neural processes during speech production has been known since the times of Broc
76 heard speech sounds with motor programs for speech production; imitation and self-imitation mechanis
78 at training with speech entrainment improves speech production in Broca's aphasia providing a potenti
80 neural activation during natural, connected speech production in children who stutter demonstrates t
82 to improve the characterization of connected speech production in each variant of primary progressive
83 promise for the use of fNIRS during natural speech production in future research with typical and at
86 o explore auditory-motor interactions during speech production in other human populations, particular
87 al magnetic stimulation (TMS) to investigate speech production in pre-surgical epilepsy patients and
88 ed semantic matching, perceptual matching or speech production in response to familiar or unfamiliar
89 nguage changes may be reflected in connected speech production in the earliest stages of typical Alzh
90 sensorimotor interaction primarily supports speech production, in the form of a state feedback contr
91 onses over neural regions integral to fluent speech production including inferior frontal gyrus, prem
92 dioxide levels is among the prerequisites to speech production insofar as speech often induces hypoca
94 e ability to express thoughts through fluent speech production is a most human faculty, one that is o
95 multidimensional quantification of connected speech production is necessary to characterize the diffe
97 This response of cortical regions related to speech production is not predicted by the classical mode
98 tering, atypical functional organization for speech production is present and suggests promise for th
99 ed the crucial role of the frontal cortex in speech production, it has remained uncertain whether the
100 dopaminergic transmission during symptomatic speech production may represent a disorder-specific path
101 al premotor cortex that largely overlapped a speech production motor area centered just posteriorly o
102 ected regions comprised nodes of the Bohland speech-production (motor activity regulation), default-m
103 y shows that left WM pathways connecting the speech production network are selectively damaged in nfv
104 ossing white matter (WM) tracts within this "speech production network" is complex and has rarely bee
108 and quantitative differences in the impaired speech production observed in aphasic stroke patients.
112 isphere activations predict chronic aphasia; speech production recovery appears to depend on left fro
113 of auditory speech comprehension, but unlike speech production, recovery of speech comprehension appe
114 how this premotor activity influenced other speech production regions and whether the same neural pa
118 ested that other regions also play a role in speech production, some of which are medial to the area
119 ted to language production (sentential overt speech production-Speech task) and activation related to
121 stem to accurately predict less prototypical speech productions suggests that the efferent-driven sup
125 ubject to subject and performance on certain speech production tasks can be relatively preserved in s
126 release during sequential finger tapping and speech production tasks in 15 patients with writer's cra
127 es in SII/OP1 activity during three familiar speech production tasks: object naming, reading and repe
128 aptation to altered auditory feedback led to speech production that fell into the phonetic range of t
129 -filter model describes the mechanics behind speech production: the identity of the speaker is carrie
130 hat were correlated positively were those of speech production: the mouth representation in the prima
132 rforming sensory-motor tasks involving overt speech production to show that sensory-motor transformat
133 has been suggested that, analogous to human speech production, tongue movements observed in parrot v
134 te selective cognitive impairments affecting speech production, visual recall memory and executive fu
135 networks controlling two tasks necessary for speech production: voluntary voice as repetition of two
137 o account for temporal irregularities during speech production, we introduced a non-linear time align
138 substrates for left-hemisphere dominance in speech production were evident at least five million yea
139 tory cortical responses to less prototypical speech productions were less suppressed, resembling resp
140 g impairs the normally effortless process of speech production, which requires precise coordination o
141 ogical retrieval) is an essential process in speech production whose neural localization is not clear
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