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We demonstrate this effect using an event-related fMRI study of single word reading during blocked and randomized trial presentations.
The cortical areas localized in the blocked design experiment comparing anti- and pro-saccades were then used to examine activation during widely spaced event-related trial presentations.
Each trial type was presented once within a block of six trials and the order of 48 trial presentations was fixed for all mice.
Risk assessments were performed using data from a number of sources (as available) including trial primary publications, trial design manuscript, trial protocol, and trial presentations.
Target detectability was measured using the method of constant stimuli, with 120 trial presentations for each of seven equally log-spaced Michelson contrast levels (840 trials contributing to each threshold estimate).
Similar(55)
Subjects were presented with the same trial presentation as in the calibration procedure and in the main part of the experiment, but this time they needed to report first the direction of motion in the cued diagonal and then the direction of motion in the uncued diagonal.
Trial presentation order was randomised within each condition and the two conditions were presented as separate counterbalanced blocks.
To control for effects of activation history, the order of trial presentation was 'one back' counterbalanced so that trials from each condition listed above were preceded equally often by all trial types for one trial back [43].
This finding indicates that PD patients benefited from the blocked trial presentation of CM location as their anticipatory digit force control improved with repeated lifts (see also 'trial-to-trial learning' below).
In the motor conditions (mEXT and mEXP) synchronized horizontal and vertical displacements are evident with a characteristic frequency that matches the trial presentation rate (one outbound and one return saccade approximately every 3.2 seconds).
The rate of trial presentation was controlled by the experimenter.
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