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1 after birth and evaluated them regularly for middle-ear effusion.
2 days of age and evaluated them regularly for middle-ear effusion.
3 days of age and evaluated them regularly for middle-ear effusion.
4 Gly-Gly peptide-encoding gene in chinchilla middle ear effusions.
5 ET) in infants limits or delays clearance of middle ear effusions.
6 y culture, may be the source of endotoxin in middle-ear effusions.
7 o and persistence in the planktonic phase in middle-ear effusions.
9 genetic component to the amount of time with middle ear effusion and episodes of middle ear effusion
10 bacteria exist in culture-negative pediatric middle-ear effusions and that experimental infection wit
11 of MGAS5005 Deltasrv were isolated from the middle ear effusion, and MGAS5005 Deltasrv was found ran
12 e healthy young children who have persistent middle-ear effusion, as defined in our study, prompt ins
14 significant percentage of culturally sterile middle ear effusions, establishing the presence of viabl
16 from the nasopharynx of healthy children or middle ear effusions from patients with otitis media, re
17 raxella catarrhalis (detected by PCR) in 106 middle-ear effusions from pediatric patients with chroni
18 ients still have persistent symptoms such as middle ear effusion in COME after intensive antibiotic t
20 f antimicrobial treatment on the duration of middle ear effusion (MEE) and concomitant hearing impair
21 hamella) catarrhalis, which were detected in middle-ear effusion (MEE) samples taken from children wi
22 low-passage NTHi clinical isolates from the middle ear effusions of patients with chronic otitis med
23 f AOM; the estimated proportion of time with middle ear effusion; or the utilization of selected heal
24 younger than 3 years of age with persistent middle-ear effusion, prompt as compared with delayed ins
25 to explain the failure to culture NTHi from middle-ear effusions, recalcitrance to antibiotics and i
27 tes of discordance for 3 or more episodes of middle ear effusion were 0.04 for monozygotic twins and
30 e years of age, 429 children with persistent middle-ear effusion were randomly assigned to have tympa
31 in the chinchilla, inducing culture-positive middle ear effusions, whereas pgm and siaB mutants were
32 than three years of age who have persistent middle-ear effusion within the duration of effusion that
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