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Both TBI groups were similarly impaired in the Morris water-maze at 2 wk post-TBI.
The admission mobility status accounted for 61% and 60% of variability of the discharge mobility status for the stroke and TBI groups, respectively.
The admission mobility status accounted for 40% and 50% of the variability in rehabilitation LOS for the stroke and TBI groups, respectively.
Fifty-one were allocated to the Mild (n = 26) or Severe (n = 25) TBI groups, according to preset determinants of severity; 30 admissions with non-TBI trauma constituted the control group.
The 2 TBI groups did not differ on measures of severity of injury, but the TBI-NOT MET group performed significantly below the TBI-MET group on executive functioning.
Figure 1 illustrates the distribution of index scores for the two TBI groups.
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The rats were randomly allocated to 3 groups (n = 8 per group): (1) the TBI + VPA (VPA-treated TBI) group, (2) the TBI (vehicle-treated TBI) group, and (3) the sham (sham-operated control) group.
Full donor chimerism at day 100 was observed in 82% vs. 64% in the TBI and no-TBI groups, respectively (p=0.006).
For UCH-L1, strong staining tended to decrease for TBI + HH group compared to TBI group in the neocortex (NS).
For GFAP, immunostaining revealed a decrease of strong staining (p < 0.001) in the neocortex for TBI + HH group compared to TBI group (Fig. 101).
After the ANOVA analysis, it was determined that patients with mild to moderate TBI group scored significantly higher than severe TBI group on auditory immediate (P = 0.001) and auditory delayed (P < 0.001) indices.
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