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T2-w hyperintense areas were first defined by visual analysis during which the window settings could be freely adjusted to the personal preference of the observer and were manually contoured.
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These are determined by visual analysis of the particle trajectories.
These results were confirmed by visual analysis and optical microscopy.
Fig. 1 Intestinal 18F-FDG uptakes classified by visual analysis.
We assessed intestinal 18F-FDG uptake by visual analysis and quantitative analysis.
Second, we grouped subjects by visual analysis in the assessment of bowel FDG uptake.
However, in these two studies microplastics were only identified by visual analysis.
Comparison of PFGE patterns was done by visual analysis.
IZ locations were identified by visual analysis of sEMG signals.
No perfusion defect at rest was detected by visual analysis.
Maximum luminal narrowing was estimated by visual analysis as described.
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