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1 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus.
2 sistant Staphylococcus aureus infections and vancomycin-resistant enterococcus.
3 ction was masked by the prior isolation of a vancomycin-resistant enterococcus.
4 osa, 15 of 86 (17.4%; 95% CI 9.4% to 25.4%), vancomycin-resistant Enterococcus, 25 of 180 (13.9%, 95%
5  to appropriate antibiotic for patients with vancomycin-resistant Enterococcus (4.2 versus 43.7 h; P=
6                                          For vancomycin-resistant Enterococcus, a four-variable class
7 thicillin-resistant Staphylococcus aureus or vancomycin-resistant Enterococcus admission surveillance
8 hicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococcus are inconsistent with
9 nterococcal domination increased the risk of Vancomycin-resistant Enterococcus bacteremia 9-fold, and
10                            For patients with vancomycin-resistant Enterococcus bacteremia, the mean t
11                                              Vancomycin-resistant Enterococcus bloodstream infections
12                                              Vancomycin-resistant Enterococcus bloodstream infections
13 ancomycin on susceptibility to C. difficile, vancomycin-resistant Enterococcus, carbapenem-resistant
14 proof of concept, wild-type (ATCC 29212) and vancomycin-resistant Enterococcus cells were incubated a
15 methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococcus, Clostridium difficile
16                       There were no cases of vancomycin-resistant Enterococcus colonization in patien
17 e detected, including increased incidence of vancomycin-resistant Enterococcus colonization or diseas
18 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus colonization were intr
19 cility in the past year were associated with vancomycin-resistant Enterococcus colonization.
20  relatedness, including the first known U.S. vancomycin-resistant enterococcus (E. faecalis strain V5
21 ses consisted of 1 patient with recalcitrant vancomycin-resistant Enterococcus faecalis (VRE) and 2 p
22 against vancomycin-susceptible organisms and vancomycin-resistant Enterococcus faecalis (VRE) of VanB
23 . aureus (MRSA), Streptococcus pyogenes, and vancomycin-resistant Enterococcus faecalis (VRE).
24 eus (MSSA, MRSA, and TRSA, respectively) and vancomycin-resistant Enterococcus faecalis (VRE).
25 sistant Streptococcus pneumoniae (PRSP), and vancomycin-resistant Enterococcus faecalis (VRE).
26                                              Vancomycin-resistant Enterococcus faecalis (VREfs) is an
27                                              Vancomycin-resistant Enterococcus faecalis (VREfs) is an
28   A chromogenic medium for identification of vancomycin-resistant Enterococcus faecalis and Enterococ
29 investigate the changes to PG composition in vancomycin-resistant Enterococcus faecalis following the
30 n of the cell envelope of a clinical pair of vancomycin-resistant Enterococcus faecalis isolates from
31 and January 1995, we identified a cluster of vancomycin-resistant Enterococcus faecalis isolates invo
32       We found that GML suppresses growth of vancomycin-resistant Enterococcus faecalis on plates wit
33 rains carry transposon Tn1546, acquired from vancomycin-resistant Enterococcus faecalis, which is kno
34 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecalis.
35 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecalis.
36 rst clinical isolate of linezolid-resistant, vancomycin-resistant Enterococcus faecium (LRVRE).
37 stant S. aureus (1.3 +/- 0.4 microg/mL), and vancomycin-resistant Enterococcus faecium (MIC(50) 2.9 +
38 tbreaks involving three important pathogens: vancomycin-resistant Enterococcus faecium (n=19), methic
39 sus group (1), Streptococcus pneumoniae (6), vancomycin-resistant Enterococcus faecium (VRE FCM) (16)
40 onization of the gastrointestinal tract with vancomycin-resistant Enterococcus faecium (VRE) has beco
41                             A mouse model of vancomycin-resistant Enterococcus faecium (VRE) intestin
42                Genomic DNA extracted from 45 vancomycin-resistant Enterococcus faecium (VRE) isolates
43 REA), and epidemiological data for typing 45 vancomycin-resistant Enterococcus faecium (VRE) isolates
44                       Thirty-two isolates of vancomycin-resistant Enterococcus faecium (VRE) recovere
45 llin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococcus faecium (VRE), and bet
46 llin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococcus faecium (VRE), Escheri
47          To investigate the dissemination of vancomycin-resistant Enterococcus faecium (VREF) in a 72
48                                              Vancomycin-resistant Enterococcus faecium (VREF) was iso
49 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecium (VREF) with MI
50 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecium (VREF).
51                                              Vancomycin-resistant Enterococcus faecium (VREfm) is a l
52                                              Vancomycin-resistant Enterococcus faecium (VREfm) is an
53 mia, 54 (19.6%) were due to rESKAPE strains (vancomycin-resistant Enterococcus faecium [0], methicill
54 medium designed to recover and differentiate vancomycin-resistant Enterococcus faecium and Enterococc
55  Gram-positive bacteria (high priority) were vancomycin-resistant Enterococcus faecium and meticillin
56 rointestinal colonization by ampicillin- and vancomycin-resistant Enterococcus faecium C68 in a mouse
57 lishment of gastrointestinal colonization by vancomycin-resistant Enterococcus faecium C68 in a mouse
58 OG1RF and against two serologically related, vancomycin-resistant Enterococcus faecium clinical isola
59        The patient remained febrile and grew vancomycin-resistant Enterococcus faecium from the cereb
60                               In particular, vancomycin-resistant Enterococcus faecium infections hav
61 ons; lower respiratory tract infections; and vancomycin-resistant Enterococcus faecium infections, in
62 ted States in late 1999 for the treatment of vancomycin-resistant Enterococcus faecium infections.
63 an also identify isolated colonies as either vancomycin-resistant Enterococcus faecium or Enterococcu
64 dition, this serum killed two (28%) of seven vancomycin-resistant Enterococcus faecium strains.
65 methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus faecium, and beta-lact
66 fied that both inhibited and dispersed MRSA, vancomycin-resistant Enterococcus faecium, and Staphyloc
67 e may find future use as antibiotics against vancomycin-resistant Enterococcus faecium, methicillin-r
68 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecium.
69 S), we identified one neonate colonized with vancomycin-resistant Enterococcus faecium.
70 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecium.
71 reus, vancomycin-intermediate S. aureus, and vancomycin-resistant Enterococcus faecium.
72 ately controlled and powered, infection with vancomycin-resistant enterococcus has had more of an eff
73 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus in a neurocritical car
74 k we analyzed data observed on the spread of vancomycin-resistant Enterococcus in an intensive care u
75 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus in neurocritical care
76 46 has only been described in human clinical vancomycin-resistant enterococcus isolates unique to the
77 ifficile infection and dense colonization by vancomycin-resistant Enterococcus, K. pneumoniae, and E.
78 pears to be a safe and effective therapy for vancomycin-resistant enterococcus meningitis.
79 im-sulfamethoxazole-resistant MRSA (n = 10), vancomycin-resistant Enterococcus (n = 37), high-level g
80 ria monocytogenes, Bacillus anthracis, and a vancomycin-resistant Enterococcus sp. with MIC or IC50 v
81 d for detection of Staphylococcus aureus and vancomycin-resistant Enterococcus species (VRE) using a
82 istance to colonization by clinically vexing vancomycin-resistant Enterococcus species.
83 ation of methicillin resistant S. aureus and vancomycin resistant Enterococcus spp. was completed an
84 y detecting and discriminating genotypes for vancomycin-resistant Enterococcus spp. in the clinical l
85 icillin-resistant Staphylococcus aureus, and vancomycin-resistant Enterococcus spp. in the environmen
86 ncept, amplification of a gene specific to a vancomycin-resistant Enterococcus strain was performed o
87 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus surveillance cultures.
88                            Indeed, a delayed vancomycin-resistant Enterococcus transmission component
89 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) among ICU patien
90 by the highly antibiotic-resistant bacterium vancomycin-resistant Enterococcus (VRE) can exceed 10(9)
91 lin azide agar plus vancomycin to screen for vancomycin-resistant enterococcus (VRE) colonization.
92                                              Vancomycin-resistant Enterococcus (VRE) has become a sig
93 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococcus (VRE) have achieved si
94 -resistant Staphylococcus aureus (MRSA), and vancomycin-resistant Enterococcus (VRE) in patients with
95                                   Nosocomial vancomycin-resistant Enterococcus (VRE) infections have
96                                 Treatment of vancomycin-resistant Enterococcus (VRE) infections is li
97           Bloodstream infection (BSI) to due vancomycin-resistant Enterococcus (VRE) is an important
98 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE) is driving the d
99                   Infections attributable to vancomycin-resistant Enterococcus (VRE) strains have bec
100 ecovered from perirectal swabs collected for vancomycin-resistant Enterococcus (VRE) surveillance as
101 llin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococcus (VRE), and MDR Enterob
102 erior to direct plating for the detection of vancomycin-resistant enterococcus (VRE), but vancomycin
103  with antibiotic-resistant bacteria, such as vancomycin-resistant Enterococcus (VRE), is a dangerous
104 ighly antibiotic-resistant bacteria, such as vancomycin-resistant Enterococcus (VRE), is a growing cl
105 nce can result in intestinal domination with vancomycin-resistant Enterococcus (VRE), leading to bloo
106 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE), while also exhi
107 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococcus (VRE).
108 sistant S. aureus (MRSA), S. pneumoniae, and vancomycin-resistant Enterococcus (VRE).
109 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococcus (VRE).
110 al of 142 stool specimens were evaluated for vancomycin-resistant enterococcus (VRE).
111                           An adolescent with vancomycin-resistant Enterococcus was given standard dos
112 thicillin-resistant Staphylococcus aureus or vancomycin-resistant Enterococcus) was constructed.

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