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The images shown in Fig. 4a f depict the 3D topographical comparison between the uncoated and coated formulations.
Topographical comparison of significant EEG power differences (p <.05) between migraine patients in different migraine phases and HCs during eyes-closed recording.
Fig. 2 Topographical comparison of significant EEG power differences (p <.05) between migraine patients in different migraine phases and HCs during eyes-open recording.
The purpose here is to describe two approaches for improving the detection of glaucomatous damage; one approach combines a topographical comparison of OCT and VFs and a second involves a qualitative analysis of OCT scans.
We argued above that the effectiveness of the OCT could be improved by a qualitative analysis of enlarged, high-quality images and by a topographical comparison of the abnormal regions seen on OCT to those seen on VFs.
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Topographical comparisons of significant EEG coherence differences (p <.05) between patients in different migraine phases and HCs during eyes-closed recording.
Topographical comparisons of significant EEG power differences (p <.05) between patients in each of the four migraine phases during eyes-closed recording.
Topographical comparisons of significant EEG coherence differences (p <.05) between migraine patients in each of the four phases of the migraine cycle during eyes-closed recording.
The directions of arrows represent the direct paths of inter-channel coupling Fig. 5 Topographical comparisons of significant EEG coherence differences (p <.05) between migraine patients in each of the four phases of the migraine cycle during eyes-open recording.
Color intensity indicates the magnitude of the power difference (red for increased power, blue for decreased power) in each channel Fig. 4 Topographical comparisons of significant EEG coherence differences (p <.05) between patients in different migraine phases and HCs during eyes-open recording.
Color intensity indicates the magnitude of the power difference (red for increased power, blue for decreased power) in each channel Fig. 3 Topographical comparisons of significant EEG power differences (p <.05) between patients in each of the four migraine phases during eyes-open recording.
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