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In the present health-care environment, it is critical to develop a cost-effective, efficient testing strategy that maximizes the diagnostic potential of even limited specimens.
In addition, due to the limited specimens obtained by the needle biopsies, we could not determine the intrarenal localization of the specimens.
However most of these studies were performed through limited specimens due to the high cost of UHPC.
Due to the limited specimens available at this time, only preliminary findings were reported in this study.
The preparation of vitreous samples for cytopathological analysis has also changed over time to improve yields from these limited specimens.
It should be noted that no sample tested positive for Vibrio parahaemolyticus, Campylobacter jejuni, Yersinia, and Vibrio cholera with limited specimens.
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CD4+ T-cell testing of blood specimens collected in standard EDTA Vacutainer tubes and transported at ambient temperature, must be completed within 48 hours with the BD FACSCount™ flow cytometer, restricting specimen collection in remote clinics with no on-site testing and limited specimen transport services.
Of the three remaining species, heteroplasmy was limited to specimens from the Moloka'i population in H. angustulus, specimens from the East Maui population in H. haleakalae, and 11 out of 13 individuals in H. unicus.
The crack was more and more difficult to be repaired with the increase of average crack width and the repair ability of microbial repair agent was limited for specimens with crack width up to 0.8 mm.
Inclusion in the study was limited to specimens growing Mycobacterium tuberculosis which were tested for first and second line DST by request of the physician, and which were available for our evaluation (ordered from the department of Medicine or from TB clinic).
We were also limited by specimens that were submitted to PHOL for screening.
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