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1 y of an isolate allows for strain typing and antimicrobial susceptibility testing).
2 sm identification and automated-system-based antimicrobial susceptibility testing.
3 quence typing (MLST), plasmid profiling, and antimicrobial susceptibility testing.
4 ted by the NCCLS Subcommittee for Veterinary Antimicrobial Susceptibility Testing.
5 nce of accurate organism identification, and antimicrobial susceptibility testing.
6 tion's External Quality Assurance System for Antimicrobial Susceptibility Testing.
7 bolic profiling provides an avenue for rapid antimicrobial susceptibility testing.
8 phoresis, extended virulence genotyping, and antimicrobial susceptibility testing.
9 demonstrated an added value for LC-MS/MS in antimicrobial susceptibility testing.
10 ria promulgated by the European Committee on Antimicrobial Susceptibility Testing.
11 for broad-based bacterial identification or antimicrobial susceptibility testing.
12 Antimicrobial susceptibility testing.
13 t bacilli smears, and microbial cultures and antimicrobial susceptibility testing.
14 nating the need for biochemical analysis and antimicrobial susceptibility testing.
15 ime needed for phenotypic identification and antimicrobial susceptibility testing.
16 gel electrophoresis (PFGE), serotyping, and antimicrobial susceptibility testing.
17 Typhi strains has emerged worldwide, making antimicrobial susceptibility testing an important functi
18 s of 2004 to 2005 and 2009 to 2010 underwent antimicrobial susceptibility testing and characterizatio
19 pulsed-field gel electrophoresis (PFGE) and antimicrobial susceptibility testing and examined for th
20 ne can expect to see changes in guidance for antimicrobial susceptibility testing and interpretation.
24 istance mechanisms in staphylococci, current antimicrobial susceptibility testing and reporting recom
26 ovides an effective quantitative measure for antimicrobial susceptibility testing, and determination
27 e now using WGS for pathogen identification, antimicrobial susceptibility testing, and epidemiologica
28 by the VITEK 2 system for identification and antimicrobial susceptibility testing, and the results we
29 In January 2015, the CLSI Subcommittee on Antimicrobial Susceptibility Testing approved these rang
30 which were outside of the United States, for antimicrobial susceptibility testing as part of the Worl
39 oenix system for the identification (ID) and antimicrobial susceptibility testing (AST) of 251 isolat
40 Sparks, MD) for the identification (ID) and antimicrobial susceptibility testing (AST) of challenge
42 signed for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically
45 rovide rapid species identification (ID) and antimicrobial susceptibility testing (AST) results for t
47 ast majority of bacterial identification and antimicrobial susceptibility testing (AST) results were
48 boring MRSA, including three (semi)automated antimicrobial susceptibility testing (AST) systems and f
49 sistant Klebsiella pneumoniae demands faster antimicrobial susceptibility testing (AST) to guide anti
50 atory practice in the preanalytical phase of antimicrobial susceptibility testing (AST) was evaluated
51 determining the optimal frequency of repeat antimicrobial susceptibility testing (AST) when an organ
54 ISA (hVISA) are pathogens for which accurate antimicrobial susceptibility testing (AST) would rule ou
55 harmacokinetics (PK), pharmacodynamics (PD), antimicrobial susceptibility testing (AST), and how thes
57 n and facilitates rapid bacterial growth for antimicrobial susceptibility testing at the point of car
58 large surface-to-volume ratio, toward rapid antimicrobial susceptibility testing at the point of car
59 dy were approved by the CLSI Subcommittee on Antimicrobial Susceptibility Testing at their June 2015
60 simple microfluidic device that can perform antimicrobial susceptibility testing automatically via a
62 through 10 May 2016 underwent routine Etest antimicrobial susceptibility testing by the Hawaii Depar
63 enotypic analysis, including biochemical and antimicrobial susceptibility testing, cellular fatty aci
64 em, were determined by the dielectrophoretic antimicrobial susceptibility testing (dAST) and by the c
66 or =1 microg/ml by the European Committee on Antimicrobial Susceptibility Testing]; disk diffusion br
67 tion's External Quality Assurance System for Antimicrobial Susceptibility Testing (EQAS-AST) from Jan
68 s Institute (CLSI) and European Committee on Antimicrobial Susceptibility Testing (EUCAST) broth micr
69 s Institute (CLSI) and European Committee of Antimicrobial Susceptibility Testing (EUCAST) methodolog
70 k breakpoints, and the European Committee on Antimicrobial Susceptibility Testing (EUCAST) S. pseudin
71 on (BMD) method of the European Committee on Antimicrobial Susceptibility Testing (EUCAST) was compar
75 enterococci following a laboratory change in antimicrobial susceptibility testing from disk diffusion
77 ofluidic device provides a simple method for antimicrobial susceptibility testing in an automated for
78 ds were approved by the CLSI Subcommittee on Antimicrobial Susceptibility Testing in January 2015 and
79 terobacteriaceae family poses a challenge to antimicrobial susceptibility testing in the clinical lab
81 tandards Institute and European Committee on Antimicrobial Susceptibility Testing interpretative stan
86 f identification to bacterial species level, antimicrobial susceptibility testing, macrolide resistan
87 atory Standards Institute (CLSI) revised the antimicrobial susceptibility testing method for telavanc
88 should consider using a second, independent antimicrobial susceptibility testing method to validate
92 up organisms on the selection of appropriate antimicrobial susceptibility testing methods and interpr
96 me geographic area using broth microdilution antimicrobial susceptibility testing, multilocus sequenc
99 uld be developed, and the optimal method for antimicrobial susceptibility testing of A. xylosoxidans
102 tion and the agar disk diffusion methods for antimicrobial susceptibility testing of Campylobacter we
104 as been used to reduce the time required for antimicrobial susceptibility testing of Mycobacterium tu
105 s for the performance and quality control of antimicrobial susceptibility testing of Mycoplasma pneum
106 methods decrease the time to identification/antimicrobial susceptibility testing of S. aureus and de
107 ods take several days for identification and antimicrobial susceptibility testing of staphylococcal i
108 It appears to be an acceptable method for antimicrobial susceptibility testing of staphylococci an
109 in S. aureus, Vitek 2 performed reliably for antimicrobial susceptibility testing of staphylococci an
111 control limits and interpretive criteria for antimicrobial susceptibility testing of Streptococcus pn
114 lity control (QC) standards for the in vitro antimicrobial susceptibility testing of two fastidious v
117 A bloodstream isolates were characterized by antimicrobial susceptibility testing, PCR analysis of vi
119 e isolates were characterized by serotyping, antimicrobial-susceptibility testing, phage typing, and
121 ble S. aureus isolates were characterized by antimicrobial-susceptibility testing, pulsed-field gel e
123 ysis interpretation, culture thresholds, and antimicrobial susceptibility testing, require special co
124 ) CD-ROM on AST, and (iv) the CDC Multilevel Antimicrobial Susceptibility Testing Resource website.
125 high degree of correlation of serotyping and antimicrobial susceptibility testing results between fou
126 increased the importance of having accurate antimicrobial susceptibility testing results for guiding
129 tant but clindamycin susceptible by in vitro antimicrobial susceptibility testing should be tested fo
130 ified selection for changes in motility, and antimicrobial susceptibility testing suggested that the
132 apid ID 32 Strep identification methods, and antimicrobial susceptibility testing to determine their
133 esis (PFGE) following SmaI macrorestriction, antimicrobial susceptibility testing, urease production,
134 human clinical specimens, were subjected to antimicrobial susceptibility testing using a MicroScan W
135 We present a method for rapid and scalable antimicrobial susceptibility testing using stationary na
137 lobacter spp. and E. coli were isolated, and antimicrobial susceptibility testing was conducted using
143 ngoing national surveillance, serotyping and antimicrobial susceptibility testing were done on all pn
144 culture, manual speciation, serotyping, and antimicrobial susceptibility testing were performed at M
146 apid ID 32 Strep identification methods; and antimicrobial susceptibility testing were performed on t
147 Culture-based identification methods and antimicrobial susceptibility testing were used as the re
148 od, Mo.), an established automated method of antimicrobial susceptibility testing with the ability to
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