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1 d by Gram stain showed large aggregations of Gram positive cocci.
2 identified as potent adhesins in pathogenic Gram-positive cocci.
3 shes it from other staphylococci and related Gram-positive cocci.
4 are key enzymes in vancomycin resistance of Gram-positive cocci.
5 d by MSSA and MRSA from that caused by other gram-positive cocci.
6 ococci in blood cultures growing clusters of gram-positive cocci.
7 of the 29 different bacteria identified were Gram-positive cocci.
8 ly collected blood culture broths containing Gram-positive cocci.
9 or difficult-to-identify catalase-negative, gram-positive cocci.
10 rate recognition by the secretion pathway of gram-positive cocci.
11 ology of nonpathogenic as well as pathogenic gram-positive cocci.
12 abases to include newly described species of gram-positive cocci.
13 in the pathogenicity of clinically important Gram-positive cocci.
14 otential antibacterial target in the low-G+C gram-positive cocci.
15 agents directed against multidrug-resistant gram-positive cocci.
16 of study animals with massive deposition of gram-positive cocci.
17 in three cultures heavily contaminated with gram-positive cocci.
18 organism for studying cell wall synthesis in Gram-positive cocci.
20 The most common causative pathogens included gram-positive cocci (45%), predominantly staphylococci,
22 comprising 10 Enterobacteriaceae isolates, 5 Gram-positive cocci, 5 Gram-negative nonfermenting speci
24 the molecular basis for a reaction by which Gram-positive cocci acquire resistance to a last resort
26 existent infection with antibiotic-resistant Gram-positive cocci and fungi, and high mortality (27.1%
27 otic with concentration-dependent killing of Gram-positive cocci and pharmacokinetics characterized b
28 he predominance of atypical mycobacteria and Gram-positive cocci and the growing number of other rare
29 PS) (Gram-negative rods), lipoteichoic acid (Gram-positive cocci), and lipoarabinomannan (Mycobacteri
30 caused by any organism, gram-negative rods, gram-positive cocci, and fungal bloodstream infection.
32 e catalase-negative, vancomycin-susceptible, gram-positive cocci arranged in clusters and tetrads, as
33 capable of providing rapid identification of Gram-positive cocci as well as detection of resistance m
34 osed that isoprenoid biosynthesis in several gram-positive cocci depends on the mevalonate pathway fo
35 suggest that multidrug-resistant strains of gram-positive cocci employ exclusively the mevalonate pa
38 lase-negative staphylococci (CoNS) and other Gram-positive cocci (GPC) directly from VersaTREK blood
39 g both on timely identification of clustered Gram-positive cocci (GPC) in blood cultures and on appro
40 Most DFIs are polymicrobial, with aerobic gram-positive cocci (GPC), and especially staphylococci,
41 olar lavage (BAL) fluid was notable for many Gram-positive cocci (GPC), but cultures of BAL fluid and
42 s: overall growth, pathogens, septic events, gram-positive cocci, gram-negative rods, Staphylococcus
43 ine its methicillin resistance directly from gram-positive cocci in cluster-containing blood culture
44 tly from positive blood culture bottles with gram-positive cocci in clusters (GPCC) and provides resu
45 ity testing of staphylococcal isolates after gram-positive cocci in clusters (GPCC) are observed in p
47 d culture instruments and demonstrating only Gram-positive cocci in clusters on Gram stain were teste
48 red BacT/ALERT blood culture bottles growing gram-positive cocci in clusters were cultured and studie
49 s from one hundred blood cultures containing gram-positive cocci in clusters were identified by conve
52 ive blood cultures (containing predominantly gram-positive cocci in clusters) were subcultured on 5%
55 t blood cultures with a Gram stain result of Gram-positive cocci in pairs and/or chains were evaluate
56 A total of 765 Bactec bottles demonstrating Gram-positive cocci in singles or clusters were tested d
57 to a class of surface-associated proteins of gram-positive cocci involved in virulence and immunity.
58 rebrospinal fluid (CSF) in order to identify Gram-positive cocci noted on a Gram stain of CSF from a
59 ood cultures (in BacT/Alert FA bottles) with Gram-positive cocci observed with Gram staining were ana
60 species of enteric gram-negative bacilli and gram-positive cocci, only Lactococcus lactis subspecies
61 P < .001) pathogens, 136 of 345 (39%) of the gram-positive cocci (P < .001), 48 of 175 (27%; P = .02)
62 aerobic bottle recovered significantly more gram-positive cocci (P < 0.001), S. aureus isolates (P <
63 naerobic bottle recovered significantly more gram-positive cocci (P < 0.001), S. aureus isolates (P <
64 The FAN bottles recovered significantly more gram-positive cocci (P < 0.001), Staphylococcus aureus (
65 nificantly more total organisms (P = 0.002), gram-positive cocci (P = 0.03), Staphylococcus aureus (P
68 re of an infected abdominal aortic aneurysm; gram-positive cocci resembling S. pneumoniae were detect
69 genes) were identified and sequenced in two gram-positive cocci, Staphylococcus aureus and Enterococ
70 p distinguish the alloiococci from the other gram-positive cocci that are facultatively anaerobic.
74 dentification of a substantial proportion of Gram-positive cocci using the Biotyper method according
75 sequence similarities when the genes of the gram-positive cocci were translated and compared to bact
76 quinolones, 24% of anaerobes, especially the gram-positive cocci, were resistant to moxifloxacin; 27%
77 hat the genes for mevalonate biosynthesis in gram-positive cocci, which are highly divergent from tho
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