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1 y for the diagnosis of PTB, in comparison to culture test.
2 e sol-gel TiO2 devices through in-vitro cell culture tests.
3 sensitivity remains suboptimum compared with culture tests.
4                    Of 370 isolates and stock cultures tested, 327 (88%) were given species names by t
5  show data that indicate that, while PCR and culture testing agree in the majority of cases, there ar
6                      While using semi-annual culture test and culling of low and high shedders with a
7 certainty analysis showed that, using annual culture test and culling of only high shedders or cullin
8 ion, empirical therapy for UTI without urine culture testing and overdiagnosis of UTI were common and
9 n the same sputum specimen was compared with culture tests and drug susceptibility testing as referen
10 98 significantly reduced Sox9 transcripts in cultured testes and increased Sox9 levels in ovaries.
11 perfect test performance, incomplete PCR and culture testing, and time-varying changes in cholera inc
12 ology and transmission of tinea imbricata by culturing, testing antifungal sensitivities, and sequenc
13 he Gen-Probe AccuProbe Group B Streptococcus Culture Test (APGB) and the BD GeneOhm StrepB assay (GOS
14 age of time to result and in scenarios where culture tests are not feasible.
15 on of the rapid Verigene Gram-negative blood culture test (BC-GN), a microarray that detects 9 genus/
16 ificity) of the Verigene Gram-Positive Blood Culture Test (BC-GP) test to identify 12 Gram-positive b
17 inistic cell cycle IBM model fails the batch culture test, because it has an abrupt drop in cell quot
18 chastic IBM model fails the steady chemostat culture test, because it produces excessive numerical ra
19 tumor cell cultures, and normal ectocervical cultures tested, but no IGF-1 transcripts were detected.
20 istome test and VERIGENE gram-negative blood culture test) could identify susceptibility to 2 newer b
21 ta revealed that the KeyPath MRSA/MSSA blood culture test delivered results a median of 30 h sooner t
22 tandard methods, the KeyPath MRSA/MSSA blood culture test demonstrated a sensitivity, specificity, po
23                                         Cell culture tests exhibited no significant cytotoxicity of t
24 ithout PD, as well as in interference tissue culture tests followed by multiple in-house and web-avai
25 xamine the incidence of urinalysis and urine culture testing for select diagnoses and patient factors
26 ual microwell AMPLICOR (Roche) (MWA), and by culture; testing for N. gonorrhoeae was done by CA and c
27                                              Culture testing identified the organism in 12 of the 23
28                                For the 1,389 cultures tested in phase 1, conducted to evaluate cutoff
29                Simulated body fluid and cell culture tests indicated favorable bioactivity and biocom
30 andard for diagnosis of typhoid fever, where culture testing is available, but novel diagnostic modal
31  and has the possibility to impact how blood culture testing is performed.
32 entation of the Verigene Gram-positive blood culture test led to reductions in time to acceptable ant
33 ed active case-finding with sputum smear and culture testing monthly for 6 months and then once every
34                                   Of the 314 cultures tested, multiplex, real-time PCR produced congr
35 site and five rural sites, we combined blood-culture testing of hospitalized patients who had a fever
36  by the reference standard method with rapid culture testing on saliva or urine.
37                                  Of 77 blood cultures tested, only 7 yielded results inconsistent wit
38 ysis yields positive results, but subsequent culture testing produces a negative result.
39                                Blood and CSF culture testing rates during the pandemic were comparabl
40 l admission consistently predicted increased culture testing, regardless of principal diagnosis or ag
41 Xpert MTB/RIF Ultra (Xpert Ultra) and liquid culture testing, respectively.
42 orting included influenza molecular or viral culture test result.
43 f septic arthritis before the Gram stain and culture test results are known.
44                    As inferred from positive culture test results, 106 cases had active PTB, the rema
45                                   Of the 244 cultures tested retrospectively, 226 (92.6%) had concord
46  1 to 2 days, and based on results from cell culture tests, the probe correctly detected the presence
47                                        Urine culture testing varied by principal diagnosis.
48 ce of the MicroPhage KeyPath MRSA/MSSA blood culture test was compared to conventional identification
49 s with a sample; on the other hand, when its culture test was negative it was 66.66-100% efficient fo
50                                     When its culture test was positive, the HRCT test was 69.56-92.85
51           The most accurate catheter segment culture test was quantitative culture (Q* = 0.87 [CI, 0.
52                                              Culture tests were positive for tuberculosis in 12% (420
53 of tuberculosis underwent sputum testing and culture testing (when available).
54  of low shedding animals (based on the fecal culture test) will be necessary.
55 omes of patients with GNB BSIs who had blood culture testing with standard-of-care (SOC) culture and
56                     All the patients had >=1 culture test within 7 days following admission.