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Compared with the values transformed by square-root (not shown), the skewness for the log data is comparable for week 32 or above, while slightly larger for week 31 or below.
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(66% vs. 34%, P < 0.05), but the data was comparable for Troponin I. Compared to group-1, APACHE II score in group-2 significantlyicantly higher values (31.9 ± 9.3 vs.16.2 ± 7.1, P < 0.001).
(32.3 ± 8.7 vs. 20.1 ± 11 of pts., P < 0.001), but the data was comparable for Troponin I. Despite the positive H-FABP pts.
Compared to group-1, H-FABP of group-2 showed a significant higher values (76.3% vs. 33.3% of pts., P < 0.05), but the data was comparable for Troponin I.
This means that the revenue data are comparable for the whole period.
Data were comparable for scans from patients in the observational cohort (Table 1).
Each study measured "identification" in such a way that data were comparable (for instance, based on clinical encounter).
This survival data is comparable to the survival rates published for patients with colorectal peritoneal metastasis.
However, the disability measure based on impairment-based examination conducted in 2006 was similar to that in 1987, and thus the two surveys' data are comparable except for the data on hearing disability and speech disability.
Predictive performance for pre-1999 data was comparable with that for post-1999 data (cross-validation R = 0.33).
In addition, in a separate analysis of these surveillance data, we have demonstrated that the cumulative susceptibility reports generated from these data are comparable with those for organisms reported to be associated with definitive hospital-acquired infection (25).
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