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Same effects have been reported in visual cortex using phosphene thresholds (Antal et al., 2003), whereas contrast detection thresholds were only changed by cathodal tDCS (Antal et al., 2001).
Consistent with our current findings, these effects have been reported in visual processing [ 20] and in flexibility of switching attention [ 21].
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Responses to human stimuli are reported in visual areas V3, V4 [44] and V5 [50], and in temporal areas responding to the perception of faces (fusiform face area FFA [48], lateral face area LFA [46]) and actions (superior temporal gyrus, [49]).
Visual analogues of such activity have been reported in extrastriate visual areas during discrimination and reproduction of visual durations [21], [22], and in association with visually guided timed motor responses [20], [23].
Furthermore, a similar increase of response has been reported in the visual word form area of the ventral occipital cortex when the visual appearance of a written word is degraded, Altogether, increased response to robot compared to human gestures in visual areas implicated in the perception of faces and actions is likely to reflect additional processing of the unfamiliar stimulus [64].
In contrast to the evidence favoring a gain-based model of selective attention, increase in neuronal selectivity [17] and shifts in receptive fields towards attended location have been reported in the visual cortex [18].
Current-orientation-specific effects have not only been shown in the primary motor area [20], [29] but have also been reported in prefrontal and visual cortices [24], [25].
Extreme differences between upper right and lower left visual quadrants have been reported in the rather different context of visual search (visual search asymmetries in three-dimensional space) [101].
Increased, decreased or normal excitability to transcranial magnetic stimulation (TMS) has been reported in the motor (M1) and visual cortices of patients with migraine.
This has been reported in a number of attentional demanding visual tasks, such as object tacking [12], short-term memory for spatial locations [13], item identification [14] and orientation discrimination and detection [15] among other visual tasks.
In addition, activation in DLPFC and middle frontal gyrus (MFG) and ACC has frequently been reported in fMRI studies using auditory and visual oddball tasks (McCarthy et al. 1997; Menon et al. 1997; Linden et al. 1999; Yoshiura et al. 1999; Clark et al. 2000; Stevens et al. 2000; Kiehl and Liddle 2001; Ardekani et al. 2002).
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