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If visual discrimination benefits from intentional processing of A's communicative gesture – as we hypothesize here – contrasting visual discrimination in the communicative and the individual conditions should reveal differential activation in regions associated the processing of communicative intentions [29], [30].
Moreover, the processing of communicative intentions has been shown to engage a common neural network independently of the modality: that is, for both speech and gestures (Enrici et al. 2011).
Several recent brain imaging studies have attempted to investigate some aspects of the neural processing of communicative actions (Van Ackeren et al. 2012; Basnáková et al. 2013; Egorova et al. 2013).
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One hypothesis that our observations lead to is that language delay might be a residual effect of a less well-developed neural system underpinning processing of social-communicative cues.
The neurobiological basis and temporal dynamics of communicative language processing pose important yet unresolved questions.
The data so far obtained suggest that neuropragmatic processes draw upon brain regions for action, mentalising, and social interactive knowledge processing to compute different aspects of communicative meaning (Frith 2007; Spunt et al. 2011; Spunt and Lieberman 2013).
Habermas calls such speech that is not dependent on these conditions of communicative rationality "distorted communication".
Our present data thus confirm a stronger involvement of the right hemisphere in the processing of pragmatic and social-communicative information.
A major open question in natural language research is the role of communicative efficiency in the origin and on-line processing of language structures.
Children with an APD diagnosis (N=25) were compared with children with dyslexia (N=19) on a battery of standardised auditory processing, language, literacy and non-verbal intelligence quotient measures as well as parental report measures of communicative skill and listening behaviour.
A recent optical brain imaging study [28] using a similar paradigm in 5-month-old infants showed that young infants also recruit prefrontal regions when processing communicative signals of different modalities, although not directly overlapping.
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