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1 ed identical antibiotic resistance profiles (antibiogram).
2 d gel electrophoresis, plasmid analysis, and antibiogram.
3 CLSI guidelines was observed in only 3 (9%) antibiograms.
4 nths to analyze data from urine cultures and antibiograms.
5 17.8]) compared with isolates with identical antibiograms (12.7 SNVs [95% CI, 12.5 to 12.8]) (P < 0.0
6 Thirty-two of 37 (86%) hospitals provided antibiograms; 26 of 37 (70%) also provided survey respon
10 tle had indistinguishable or closely related antibiograms and pulsed-field gel electrophoresis patter
11 ysis, biochemical profiles, protein spectra, antibiogram, and pathogenicity) properties, we classify
12 thods: (i) determination of a combination of antibiogram, auxotype, serovar, Lip type, and patterns o
19 s in vitro using a chemogram, similar to the antibiogram for microorganisms, establishing an individu
22 h 5 of the remaining 24 strains exhibited an antibiogram identical to those of the NICU isolates, all
27 this study were identified by evaluating the antibiograms of Enterobacteriaceae isolated in the UCLA
30 triction endonuclease analysis and taxonomic antibiograms of strains causing the outbreak demonstrate
37 y several different typing methods including antibiograms, pulsed-field gel gel electrophoresis, and
44 uated, unexpected results included the 7% of antibiograms that reported <100% vancomycin susceptibili
45 ed NCCLS M39-A guidelines for preparation of antibiograms to identify areas for improvement in the re
49 e combination of the results of capsular and antibiogram typing can be used as a useful epidemiologic
51 jective of this study was to analyze current antibiograms using the recently published NCCLS M39-A gu
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