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The neural correlates of motor execution in Amyotrophic Lateral Sclerosis (ALS) are challenging to investigate due to muscle weakness.
A functional magnetic resonance imaging experiment at 3 tesla was performed to investigate the collaborative mechanism between visuospatial processing and motor execution in performing visual language generation tasks.
This indicates that TMS did not modify substantially motor execution, in agreement with previous study [37].
The preparation map, however, also includes activity in motor structures (vPM, dPM, SMA, and PPC [posterior parietal cortex]) involved in motor preparation, leading to a conservative estimate of brain areas involved in motor execution in the remaining Hexe.
Interestingly, MPX, in addition, showed a drug-specific upregulation effect during the executive go process of the task in key regions for response selection and motor execution in ACC/SMA, left premotor cortex, and basal ganglia (Haber 2003).
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Such findings demonstrate that short-timescale processes, such as motor execution, may relate in systematic ways to longer-timescale cognitive processes, such as learning.
The increased activation for response anticipation/preparation in more apathetic individuals occurred in the absence of any difference in motor execution itself (no correlation between apathy scores and force production).
The supplementary motor area (SMA) is strongly involved in motor planning but is also involved in motor execution and seems to represent mainly the dynamics of the movement [45].
The contrast between the cortical activities generated by 1SYL and 1SYLx3 indexes an increase in motor execution but not motor planning.
Convincing evidence of mGluR participation in motor execution comes from an mGluR-autoantibody study by Coesmans et al. [26].
Existing studies show that aging is accompanied by general declines in motor execution such as reaction time speed and accuracy [3].
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