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This difference may due to different study patient populations (racial and environmental differences), different tumor stage, or different criteria used for identification of micropapillary component.
No pronounced difference was found according to different study base.
This difference may be due to different study populations and settings.
This difference may be due to different study designs and populations.
This difference is possibly due to different study design and different study population recruited.
7, 19 These differences may be attributable to different study populations, as patients in Medicare generally tend to be older and of poorer health.
The difference seen may be due to different study population or sample size.
11 The differences in PD-MCI and PD-D frequencies between studies are probably due to different study methods, varying criteria, and differences in disease severity.
This fact can be related, on one hand, to differences among populations and, on the other hand, to different study designs.
We anticipated heterogeneity between studies due to different study methodologies and geographical and population differences.
These differences in prevalence may be attributed to different study designs as well as the presence and number of MRSA and C. difficile patients during the study period.
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