Interventions: In the acute study, subjects were given a placebo and fluoxetine (40mg) 6 hours before testing, in the chronic study, they were given fluoxetine (40mg/d) and an identical placebo for 2 weeks before testing.
Fig. 1 Polarity contour maps of MEG data recorded from a representative chronic migraine subject, acute migraine subject, and control subject during left finger movements.
Fig. 6 Magnetic source imaging (MSI) showing the locations of neuromagnetic activation in response to left-finger movement in a representative chronic migraine subject, acute migraine subject, and control subject.
The low abundance of interferon and interferon-induced transcripts was also observed in a study of gene expression profiles in acute KD subjects compared to subjects with adenovirus infection [ 16].
All diabetic patients, both acute Charcot case subjects and control subjects, were on insulin therapy.
"L" indicates left; "R" indicates right; "F" indicates frontal; "O" indicates occipital Fig. 2 Polarity contour maps of MEG data recorded from a representative chronic migraine subject, an acute migraine subject and a control during right finger movements.
"**" indicates p < 0.001; "*" indicates p < 0.01 Fig. 4 Global spectrograms of MEG data recorded from a representative chronic migraine subject, an acute migraine subject and a control during left finger movements.
"L" indicates left; "R" indicates right; "F" indicates frontal; "O" indicates occipital Fig. 3 Global spectrograms of MEG data recorded from a representative chronic migraine subject, an acute migraine subject, and a control during left finger movements.
The mean duration of diabetes in acute Charcot case subjects and diabetic control subjects with or without oseomyelitis was 31 ± 5.1, 27 ± 4.6, and 36 ± 2.9 years, respectively.
As shown in Table 3, the serum ACE2 level was significantly higher in the acute MI subjects than that in the control subjects (p<0.05).
