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1 ence in rabbits (based on survival following ocular infection).
2 of infected mice between days 1 and 5 after ocular infection.
3 fic effector T (T(eff)) cells induced during ocular infection.
4 oss lymphoid and extralymphoid tissues after ocular infection.
5 mice than in BALB/c and CBA/J mice following ocular infection.
6 le of CXCL10 during the acute phase of HSV-1 ocular infection.
7 d disease occurs in humans following primary ocular infection.
8 imulation in susceptibility to P. aeruginosa ocular infection.
9 nd enteric washes and were protected against ocular infection.
10 ymphotropic dissemination of HSV-1 following ocular infection.
11 for the treatment of symptomatic adenoviral ocular infection.
12 ndicating the critical role of HVEM in HSV-1 ocular infection.
13 ding virulence and immune responses to viral ocular infection.
14 n models: mouse footpad infection and rabbit ocular infection.
15 s into immunopathological responses to viral ocular infection.
16 tics in order to gain effective control over ocular infection.
17 SE by acyclovir treatment provided 4 d after ocular infection.
18 of either receptor attenuates disease after ocular infection.
19 against herpes simplex virus type 1 (HSV-1) ocular infection.
20 ls of testican-1 after P. aeruginosa-induced ocular infection.
21 ratitis (AK) is a rare but sight-threatening ocular infection.
22 ne model of naturally-acquired P. aeruginosa ocular infection.
23 monas aeruginosa are the leading isolates in ocular infections.
24 therapy for the treatment of adenoviral (Ad) ocular infections.
25 teria are the major contributor of bacterial ocular infections.
26 ence showing excellent potency in the war on ocular infections.
27 was aimed to review the bacterial profile of ocular infections.
28 f this antiviral drug in treating adenoviral ocular infections.
29 ibility pattern among patients with external ocular infections.
30 s hospital infections and community-acquired ocular infections.
31 ibacterials used for empirical management of ocular infections.
32 marily on innate immunity to protect against ocular infections.
33 n be a vector for transmission of adenovirus ocular infections.
34 live attenuated vaccines against genital and ocular infections.
35 is known about the role of magA in secondary ocular infections.
36 lens could be used as a treatment for fungal ocular infections.
37 differentiate Fusarium spp. responsible for ocular infections.
38 al wild-type adenoviral serotypes that cause ocular infections.
39 unoglobulin for treatment and prophylaxis of ocular infections.
40 he role of NK cells in the modulation of CMV ocular infection, 9.0 x 10(2) plaque-forming units of th
42 simplex virus type 1 (HSV-1) during primary ocular infection and after reactivation of latent infect
45 Pneumococcus is also a major cause of human ocular infections and is commonly isolated in cases of b
47 ed in the eyes of control mice after primary ocular infection, and near-normal histology with few tac
48 s conducted among 160 patients with external ocular infections at Borumeda hospital, Northeast Ethiop
50 s latent HSV infection in the mouse model of ocular infection but has no impact on the maintenance of
52 ratory tract suspected to be responsible for ocular infections but no well-described case of D. pigru
54 are highly antibiotic resistant, and primary ocular infection by ESBL E coli has rarely been reported
55 ns of DCs to the protection afforded against ocular infection by immunization against HSV-1 and their
58 ion of neutrophils during primary chlamydial ocular infection by using the guinea pig model of Chlamy
59 -associated MRSA is an important pathogen of ocular infections; CA-MRSA and HA-MRSA ocular infections
60 arises during Pseudomonas aeruginosa-induced ocular infection can trigger tissue damage resulting in
63 y and duration of Chlamydia trachomatis (Ct) ocular infections decrease with age, suggesting developm
65 en of ocular infections; CA-MRSA and HA-MRSA ocular infections differ demographically and clinically,
66 The rare descriptions, in the literature, of ocular infections due to Pasteurella multocida include:
67 ch has targeted immune mechanisms in primary ocular infections, events that could impact chronic resp
80 he role of neutrophils in primary chlamydial ocular infection, indicates a previously unappreciated r
83 l as well as molecular investigation on HAdV ocular infections is rather absent in Greece, which has
84 ), a subgroup D virus associated with severe ocular infections, is unable to use CAR efficiently to i
85 icroflora isolates, 0.80 (CI, 0.54-0.94) for ocular infection isolates, and 1.0 (CI, 0.45-1.0) for st
87 ied a potential target for modulation during ocular infection, macrophage migration inhibitory factor
89 anti-HSV-1 mechanisms of murine IFN-beta in ocular infection, mice were transduced with an adenovira
91 st to provide evidence that in P. aeruginosa ocular infection, mouse strains favoring development of
94 ollowing herpes simplex virus type 1 (HSV-1) ocular infection of C57BL/6 mice, activated CD8(+) T cel
97 dministration begun at different times after ocular infection of mice with HSV could influence the se
100 lactic Delta41Delta29 vaccination on primary ocular infection of NIH inbred mice with HSV-1 McKrae, a
108 ing IL-18 to the cornea of mice before HSV-1 ocular infection resulted in reduced angiogenesis and di
109 IL-10(-/-) animals depleted of nTregs before ocular infection showed more severe SK lesions as compar
110 r System, Central Nervous System Infections, Ocular Infections, Soft Tissue Infections of the Head an
112 C. trachomatis infection causes trachoma, an ocular infection that leads to blindness, and sexually t
113 tible C57BL/6J (B6) mouse to resistant after ocular infection through modulation of the inflammatory
117 moral immunity in herpes simplex virus (HSV) ocular infections was studied in immunoglobulin mu chain
118 potheses, guinea pigs with primary C. caviae ocular infections were depleted of neutrophils by using
123 implex virus type 1 (HSV-1) during the acute ocular infection with and without AED treatment focusing
124 scertain the disease pattern of trachoma and ocular infection with C trachomatis in a trachoma hypere
125 ll households were examined for trachoma and ocular infection with C. trachomatis at baseline, and 6
126 s where trachoma is mesoendemic suggest that ocular infection with Chlamydia trachomatis can be elimi
129 tibiotic treatment could reduce trachoma and ocular infection with Chlamydia trachomatis in hyperende
130 reventable blindness, is produced by chronic ocular infection with Chlamydia trachomatis, an obligate
133 erpetic stromal keratitis (HSK) that follows ocular infection with herpes simplex virus (HSV) is sugg
139 f immunization strategies to protect against ocular infection with herpes simplex virus 1 (HSV-1) mus
145 plicated in the modulation of the outcome of ocular infection with herpes simplex virus type 1 (HSV-1
146 Treatment was begun at different times after ocular infection with HSV and the outcome was assessed c
151 sion was up-regulated (10- to 20-fold) after ocular infection with HSV, an event that involved the pr
152 e between VEGF-A and sVR-1 that occurs after ocular infection with HSV, which causes prominent neovas
157 e are highly susceptible to HSV-1 infection, ocular infection with HSV-IL-4 resulted in 100% survival
160 s potential importance, the role of IL-12 in ocular infection with P. aeruginosa remains unexplored a
163 study was conducted to determine whether the ocular infection with this recombinant virus induces opt
164 prevalent among staphylococcal isolates from ocular infections, with many strains demonstrating multi
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