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1 rticipants were taken before the walk in the hospital laboratory.
2 2, which are potentially exploitable by any hospital laboratory.
3 f gram-negative organisms encountered in the hospital laboratory.
4 and with other HPLC assays currently used in hospital laboratories.
5 or HIV according to standard practice in the hospital laboratories.
6 logy laboratory and, in some cases, at local hospital laboratories.
7 tients and 12 environmental isolates from 24 hospital laboratories across the United Kingdom on an Il
9 rove the diagnostic accuracy and capacity of hospital laboratories, allowing for timely and appropria
10 e laboratory were compared with those of the hospital laboratories and risk of transfusion-associated
11 re cultured from patient infections in 71 US hospital laboratories and were submitted to a central re
12 rveillance in Baltimore and Atlanta and from hospital-laboratory-based sentinel surveillance of 12 ho
13 g a tightly clustered set of isolates from 3 hospital laboratories consistent with an outbreak from a
15 g conducted in 11 of the participating ICARE hospital laboratories failed to pinpoint the factors res
17 specimens collected from children at 11 U.S. hospital laboratories from November 1997 to March 1998 a
19 rent control measures; isolates from 7 other hospital laboratories in London and southeast England we
20 . soudanense that were processed in a single hospital laboratory in Baltimore, Maryland, between 1 Ja
22 heid, Sunnyvale, CA) performed at a district hospital laboratory or (2) POC Xpert MTB/RIF test perfor
23 r commercial HMO enrollees for professional, hospital, laboratory, pharmaceutical, and ancillary serv
24 dy investigators, paediatricians in referral hospitals, laboratory staff, and committee members were
26 consider the diagnosis on presentation, U.S. hospital laboratory technologists have very limited expe
27 emographics, physiologic variables, standard hospital laboratory tests, and circulating cytokine conc
28 gration of demographics, bedside physiology, hospital laboratory tests, and circulating cytokines pre
29 erial input, including patient demographics, hospital laboratory tests, and plasma concentrations of
33 h Cryptosporidium oocysts were recognized by hospital laboratories were collected from 218 patients w
34 s and drug susceptibility data directly from hospital laboratories, whereas the CDC-sponsored system
35 be due to the culturing methods employed in hospital laboratories, which are unable to detect the un
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