I. Architectures and methodsNeural correlates of partial transmission of sensorimotor information in the cerebral cortex
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Cited by (23)
Cognitive and motor event-related potentials in Tourette syndrome and tic disorders: A systematic review
2019, Clinical NeurophysiologyElectrophysiological predictors of cognitive-behavioral therapy outcome in tic disorders
2018, Journal of Psychiatric ResearchCognitive-behavioral therapy induces sensorimotor and specific electrocortical changes in chronic tic and Tourette's disorder
2015, NeuropsychologiaCitation Excerpt :Lateralized readiness potentials (LRP), which are a subtype of motor ERP derived from the readiness potential, can yield significant information on preparation and executions of movements (Coles, 1989). Several experiments showed that LRPs have generators located in the primary motor cortex (Coles, 1989; Miller and Hackley, 1992; Praamstra et al., 1999; Requin and Riehle, 1995) and the SMA (Rektor, 2002). This component is a good candidate as a psychophysiological marker of TD, since patients often face motor impairments thought to be related, at least partially, to SMA and the CSTC motor loop (Eddy et al., 2009).
Neural Mechanisms of Speed-Accuracy Tradeoff
2012, NeuronCitation Excerpt :With unprecedented resolution of the neural mechanisms mediating SAT, we found adjustments in preperceptual, perceptual, categorical, and response processes. The distinction between perceptual and response stages is beyond dispute (e.g., Miller, 1983; Osman et al., 1995; Requin and Riehle, 1995; Sato et al., 2001; Murthy et al., 2009; reviewed by Sternberg, 2001). Our results indicate that adjustments mediating SAT occur in both perceptual and response stages.
Visual stimuli evoke rapid activation (120 ms) of sensorimotor cortex for overt but not for covert movements
2011, Brain ResearchCitation Excerpt :In the following, different interpretations will be discussed regarding the absence of significant latN120 in covert movements, which might in general contribute to the absence of later muscle contraction. As reviewed above, the very early activity (< 150 ms) in the primary motor (single cell data) and sensorimotor cortices (EEG data) strongly suggest that neuronal processing at this time most likely reflects stimulus identification and stimulus–response mappings, e.g., hand selection (Georgopoulos et al., 1982; Requin and Riehle, 1995; Carrillo-de-la-Peña et al., 2008). Interestingly, experimental evidence supported the assumption of “sensory” neurons in the monkey primary motor cortex being reactive not to visual stimuli per se, but only when the stimulus indicated a forthcoming motor response (Kwan et al., 1985; Riehle, 1991; Requin and Riehle, 1995), i.e., such neurons are stronger reactive in stimulus- than in response-locked data which might reflect processes of stimulus identification.