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Still, large and highly significant differences on most tests were detected between patients with LLS and those without a psychiatric diagnosis who were referred by their primary care physicians due to memory or cognitive complaints and found to have normal cognition.
No positive HNPP gene tests were detected in any of the studied patients.
An estimated overall seroprevalence of 49.623% by DAT and 40.49% by ELISA tests were detected.
49,840 (62.1%) tests were detected for one pathogen or TRG.
While improvements for the jump tests were detected following a PT on unstable surfaces, significant increases in the testing results were amiss for the STAB group.
These significant tests were detected across several subspecies (C. a. actites, C. a. pacifica, and C. a. sakhalina) and could have been observed by chance alone given the large number of individual tests that were performed.
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The temperature evolution during the tests was detected by means of IR cameras to study the temperature effect on the material response.
Few ASPV isolates escaped detection by IC-RT-PCR, while all isolates tested were detected using the SC-RT-PCR with the new primers.
Consistent with our design, in which the Life/Nb antibody pair detects total α-syn, AlphaLISA signals from all the fractions tested were detected using this antibody pair (Fig. 1G for AlphaLISA and Fig. S2F for TR-FRET).
Interestingly, in reconstituted ZAP-70-/ mice, all the TCRV transcripts tested were detected in thymus or spleen (Figure 5A).
None of the 88 Hi isolates (Table 2) or the 100 Hi culture-positive Brazilian and CHOA carriage specimens tested were detected by this Nm sodC assay.
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