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1 n several fibrotic diseases, in RPE cells in proliferative vitreoretinopathy.
2 g this pathway could be useful in preventing proliferative vitreoretinopathy.
3 s that involve RPE dedifferentiation such as proliferative vitreoretinopathy.
4 l diseases, such as diabetic retinopathy and proliferative vitreoretinopathy.
5 ation of fibroproliferative diseases such as proliferative vitreoretinopathy.
6 ted disease progression in a rabbit model of proliferative vitreoretinopathy.
7 l therapy for related human diseases such as proliferative vitreoretinopathy.
8 t of endophthalmitis, retinal detachment and proliferative vitreoretinopathy.
9 atment of retinal detachment associated with proliferative vitreoretinopathy.
10 inopathies, such as diabetic retinopathy and proliferative vitreoretinopathy.
11 y, and in nonvascular retinopathies, such as proliferative vitreoretinopathy.
12 lications for proliferative diseases such as proliferative vitreoretinopathy.
13 uld have implications in the pathogenesis of proliferative vitreoretinopathy.
15 ual failure of surgery is the development of proliferative vitreoretinopathy, accounting for the fail
16 ogic characteristics of patients who develop proliferative vitreoretinopathy after retinoblastoma tre
17 in pathogenesis of such retinal disorders as proliferative vitreoretinopathy and age-related macular
18 on in anomalous reparative processes such as proliferative vitreoretinopathy and as a laboratory tool
19 several epiretinal membranes associated with proliferative vitreoretinopathy and idiopathic epiretina
20 NF-kappaB may be a useful strategy to treat proliferative vitreoretinopathy and uveitis, ocular dise
21 inal breaks, failure to reattach the retina, proliferative vitreoretinopathy, and delayed reabsorptio
22 the rate of retinal redetachment by limiting proliferative vitreoretinopathy, and protect against pho
23 ns include antimetabolites for modulation of proliferative vitreoretinopathy, antimicrobial agents fo
26 repair recurrent retinal detachments due to proliferative vitreoretinopathy, focusing on the most re
27 ature of recurrent retinal detachment due to proliferative vitreoretinopathy has grown concomitantly
29 tro model of the later contractile stages of proliferative vitreoretinopathy, interleukin-1 beta (IL-
31 Recurrent retinal detachment complicated by proliferative vitreoretinopathy is now most frequently t
33 lens status, tamponading agent, preoperative proliferative vitreoretinopathy (PVR) and axial length (
34 several epiretinal membranes associated with proliferative vitreoretinopathy (PVR) and idiopathic epi
35 ival, and contraction) that are intrinsic to proliferative vitreoretinopathy (PVR) and induce the dis
36 in vitro and in vivo models for experimental proliferative vitreoretinopathy (PVR) and provide a deta
38 t-derived growth factor (PDGF) contribute to proliferative vitreoretinopathy (PVR) in experimental mo
54 us from patients with retinal detachment and proliferative vitreoretinopathy (PVR) plus vitreous from
58 gher level 1 failure rates when grade 0 or B proliferative vitreoretinopathy (PVR) was present and hi
59 ibozyme to prevent or inhibit development of proliferative vitreoretinopathy (PVR) was tested in a di
60 h factor (PDGF) isoforms are associated with proliferative vitreoretinopathy (PVR), a sight-threateni
61 traction by ARPE-19 is an in vitro model for proliferative vitreoretinopathy (PVR), an aberrant wound
62 ermine the role of NF-kappaB in experimental proliferative vitreoretinopathy (PVR), and may offer a n
64 the environment that drives RPE responses in proliferative vitreoretinopathy (PVR), suggesting that t
65 l detachment with (n = 7) or without (n = 9) proliferative vitreoretinopathy (PVR), vitreous hemorrha
66 l-thickness macular hole (n = 33), recurrent proliferative vitreoretinopathy (PVR)-related retinal de
82 ated in this investigation were: (1) grade B proliferative vitreoretinopathy (PVR; n = 917), (2) grad
83 io [OR], 7.0), CNV recurrence (OR, 2.6), and proliferative vitreoretinopathy (PVR; OR, 17.6) were sta
85 patients with retinal detachment (3.65) and proliferative vitreoretinopathy stages A, B, and C (2.06
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