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1 urinary oxalate excretion during the oxalate load tests.
2 confirmation, followed by HIV-1 plasma viral load testing.
3 iation of ART with targeted or routine viral load testing.
4 igital PCR (ddPCR) for cytomegalovirus (CMV) load testing.
5 an assay for the clinical application of HCV load testing.
6 onal reagents that can be used for CMV viral load testing.
7 y an attractive option for routine HCV viral load testing.
8 mmunosorbent assay and repeated plasma viral load testing.
9 ection was falsely diagnosed by plasma viral load testing.
10 ive human immunodeficiency virus (HIV) viral-load testing.
11 sessed with WHO criteria, confirmed by viral-load testing.
12 onism was confirmed by using the oral sodium-loading test.
13 ting and genotyping, and quantitative (viral load) testing.
14 ibody-reactive patients, 435 completed viral load testing (82%), of whom 301 (69%) were chronically i
15 well compared to a market-leading HCV viral load test and should be considered for instances where r
16 ines have been useful in ensuring that viral-load testing and combination therapy is widely available
18 d with standardization of quantitative viral load testing are discussed in relation to human cytomega
19 ounts and human immunodeficiency virus (HIV) load testing are essential components of HIV care, and m
20 g data of human immunodeficiency virus (HIV) load testing are pivotal to limiting the threat of HIV d
21 ettings where both CD4 cell counts and viral load testing are routinely available, countries should c
22 ients, which will be vital in ensuring viral load tests are appropriately used to improve the quality
24 e mode is not observed in comparative static loading tests, attesting to a strong mechanical componen
25 s been widely implemented for clinical viral load testing, but a lack of standardization and relative
27 tings, and there is no appropriate HIV viral load test currently available at the point-of-care in lo
28 ivity and specificity of the Xpert HCV Viral Load test for HCV RNA detection by venepuncture and fing
34 n BioRobot is described for performing viral load tests for human immunodeficiency virus (HIV) with t
38 improve interlaboratory agreement for viral load testing; however, insufficient data are available t
40 to the assessment of Epstein-Bar virus (EBV) load testing in four quantitative PCR assays, treating d
45 HIV-1 RNA quantitation in plasma, or virus load testing, is the primary method by which the respons
46 ies that have just started to scale up viral load testing, lessons can be learnt from countries such
47 to an oral glucose test (OGTT) and oral fat load test (OFTT) in the EARSII group of young, healthy m
48 r an overnight fast and after an acute water-load test performed before oxcarbazepine exposure and af
49 immunodeficiency virus type 1 (HIV-1) viral load testing, plasma HIV-1 RNA levels were quantitated w
51 e suppression of hyperglycaemia in a maltose loading test than miglitol, a drug presently used in the
54 ted risk for illness immediately after viral load testing; this predictive relation attenuated over t
56 aulter tracing and scale-up of routine viral load testing to identify patients failing first-line ART
57 sed dramatically over the past decade, viral load testing to monitor the response of patients receivi
58 eening and CD4 counts, and in-parallel viral load testing, to promote fast and complete diagnosis and
62 casions, a 9-h oral [(13)C]-labeled fructose loading test was performed on the fifth day to measure [
65 to uniaxial tensile, relaxation, and cyclic loading testing with the use of an automated load cell u
66 nd metabolic syndrome, underwent an oral fat load test, with measurement of plasma triglyceride-rich
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