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Micronuclei formation was assessed by phase contrast microscopy in Table 2 after 20 hours.
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The status of laboratory equipments regarding blood smear microscopy is presented in Table 2.
The semiquantitative analysis of lung and diaphragm electron microscopy is shown in Table 2.
Primary antibodies used for flow cytometry, paraffin immunohistochemistry and confocal microscopy are recapitulated in Table 1.
The semiquantitative analysis of lung and diaphragm electron microscopy is shown in Table 6 and Figures 6 and 7.
not analysed The age-stratified prevalence of D. fragilis detected with microscopy is shown in Table 1.
Secondly, to evaluate relevant inflammatory reaction patterns in HD-OCT images, Ackerman's algorithmic method of pattern recognition in the perivascular dermatitis group was applied (Table 3).>> A set of morphological features generated by HD-OCT imaging very similar to those described for reflectance confocal microscopy are summarized in Table 3.
When considering the incremental cost per additional case correctly diagnosed and treated, which was considered as the baseline ICER results, values reduced from USD 3 to USD 2.6 for RDT and from USD 10.2 to USD 9.6 for microscopy as shown in table 6.
The overall sensitivities, specificities, NPV and PPV for the three RDTs, evaluated against microscopy and microscopy and PCR are detailed in Table 2.
The fluorescence markers that are linked to the 3'-end and enable the detection of the molecules with fluorescence microscopy are also listed in Table 1.
The root mean square of roughness (RRMS) of Au NPs film and the sizes of Au NPs were determined from the surface morphological images of the atomic force microscopy (AFM), as shown in Table 1.
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