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1 bliteration of vessels with stabilization of corneal scar.
2 ncluding corneal erosion, corneal ulcers, or corneal scars.
3 one of the alternatives for the treatment of corneal scars.
4 ages, 3 had post-herpetic leukoma, and 5 had corneal scars.
5 with postinfectious, full-thickness, central corneal scars.
6 source of fibrotic tissue in nontransparent corneal scars.
7 including steroids, have been used to treat corneal scarring.
8 h persistent visual impairment due to severe corneal scarring.
9 t virus that can cause recurrent disease and corneal scarring.
10 active outcome while eliminating or reducing corneal scarring.
11 n, PAI-1R may be a useful agent in combating corneal scarring.
12 ation of vision in patients with significant corneal scarring.
13 surgery, recent rigid contact lens wear, and corneal scarring.
14 ology and for cell-based therapies targeting corneal scarring.
15 anglion and reduced herpetic blepharitis and corneal scarring.
16 action may be an important goal for reducing corneal scarring.
17 ly protected against HSV-1-induced death and corneal scarring.
18 rimary genes involved in the pathobiology of corneal scarring.
19 nse leading to exacerbation of HSV-1-induced corneal scarring.
20 ice are normally refractory to HSV-1-induced corneal scarring.
21 spite the fact that KOS normally produces no corneal scarring.
22 te or severe vision loss, primarily owing to corneal scarring.
23 l decompensation from increased IOP (3), and corneal scar (1) underwent combined endoscopic vitrectom
24 included partial-thickness anterior stromal corneal scars (15 eyes), Descemet membrane ruptures (6 e
25 causes of vision loss were cataract (19.7%), corneal scars (15.7%), refractive error and amblyopia (1
27 eal neovascularization (44%), dry eye (38%), corneal scarring (26%), ectropion (25%), blepharitis (23
28 0.13 years; indications for PK were herpetic corneal scar (53.3%), corneal stromal dystrophy (23.3%),
29 or keratoconus (8), microbial keratitis (6), corneal scar (6), corneal keloid (3), chemical injury wi
32 from in vivo experiments suggest that in old corneal scars, a nonkeratocyte phenotype persists in an
33 s for MK in high-risk, vascularized herpetic corneal scars achieves clinical outcomes that remain sta
36 s to naive mice, resulted in exacerbation of corneal scarring after HSV-1 challenge (P < 0.0001).
37 dividually to naive mice, and the affects on corneal scarring after HSV-1 challenge were determined.
38 atitis can cause serious problems, including corneal scar and perforation, which can cause vision los
39 -nine percent of patients with keratitis had corneal scarring and 26% had vision of 20/40 or worse at
49 dophakic bullous keratopathy, postinfectious corneal scarring and thinning and keratoconus were the m
50 he patient had already developed significant corneal scarring and visual debilitation by the time top
52 D), Ninth and Tenth Revisions, codes of 371 (corneal scar) and H17 (corneal opacity), respectively.
55 ial basement membrane dystrophy, superficial corneal scars, and previous radial keratotomy will have
56 ce interval [CI]: 2.61-59.99; P = 0.002) and corneal scarring (aOR: 3.06; 95% CI, 1.15-8.14; P = 0.02
57 Current treatment options for controlling corneal scarring are limited, and outcomes are typically
58 lindness and visual impairment, particularly corneal scarring as a result of vitamin A deficiency, co
59 able refractive outcomes in the treatment of corneal scarring associated with Bowman layer irregulari
65 iece microkeratome-assisted MK for traumatic corneal scars can allow excellent visual rehabilitation
69 ected mouse strains had significantly higher corneal scarring (CS) than did McKrae-infected mice.
70 in KOS or McKrae, and the relative amount of corneal scarring determined 28 days after challenge.
72 (n = 15), corneal perforation (n = 11), and corneal scar following treated infectious keratitis (n =
73 ta support the hypothesis that CTGF promotes corneal scar formation and imply that regulating CTGF sy
75 brane pemphigoid presenting with HR-EOMs and corneal scarring has an increased risk of stage progress
80 Here, we demonstrate increased latency and corneal scarring in LTalpha(-/-) infected mice, independ
81 ls, increased 50% lethal dose, and decreased corneal scarring in ocularly infected mice compared to t
85 t pachymetry, corneal transplantation rates, corneal scarring incidence, and patient-reported outcome
87 However, the ability of steroids to reduce corneal scarring is limited and associated with numerous
89 of virus replication in the eyes, levels of corneal scarring, latency-reactivation in the trigeminal
91 expression of CD80 has a detrimental role in corneal scarring, likely by increasing CD8(+) T cell rec
92 herpetic episodes is high, and the resultant corneal scarring may require penetrating keratoplasty fo
94 s, including moderate or severe vision loss, corneal scarring, neurotrophic keratitis, band keratopat
95 Gonococcal ophthalmia neonatorum can cause corneal scarring, ocular perforation, and blindness as e
96 ficant corneal irregularities and/or central corneal scarring often secondary to long-standing preope
97 elate with any subset of BKC diagnoses (e.g. corneal scar or ulcer, chalazion, marginal or superficia
99 ervous system involvement, acral mutilation, corneal scarring or ulceration, liver failure, and metab
100 eal involvement without scarring), moderate (corneal scarring), or severe (corneal scarring with thin
103 cinated C57BL/6 mice resulted in significant corneal scarring (P < 0.0001), despite the fact that C57
104 ccinated BALB/c mice resulted in significant corneal scarring (P = 0.0003), despite the fact that KOS
105 conjunctival corkscrew vessels (P < 0.001), corneal scarring (P = 0.01) and pingueculae under the ag
106 ous corneal disorders including keratoconus, corneal scarring, post-corneal transplant, and post-refr
110 d LTalpha(-/-) mice had significantly higher corneal scarring than WT mice, and adoptive T cell trans
111 er study, 41 consecutive eyes with traumatic corneal scars that underwent 2-piece microkeratome-assis
113 ntibody titers (approximately 1:800-1:1200), corneal scarring (trace) and survival (100%) were simila
115 s with vascularized (>=2 quadrants) herpetic corneal scars underwent 2-piece microkeratome-assisted M
116 5 (AAV5)-mediated Id3 gene therapy to treat corneal scarring using an established rabbit in vivo dis
122 f gK vaccination to exacerbate HSV-1-induced corneal scarring was not mouse strain or HSV-1 strain sp
126 ng), moderate (corneal scarring), or severe (corneal scarring with thinning or perforation) disease b