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1  coupling in a mouse model of oxygen-induced proliferative retinopathy.
2  declined for treatment of macular edema and proliferative retinopathy.
3 arization is a leading cause of blindness in proliferative retinopathy.
4 ially expressed sncRNAs in a murine model of proliferative retinopathy.
5 bfields of the deep plexus with sickle SC or proliferative retinopathy.
6  development of nephropathy, neuropathy, and proliferative retinopathy.
7 sed or considered at risk for progression to proliferative retinopathy.
8 utic target to inhibit neovascularization in proliferative retinopathy.
9 uced retinopathy (OIR), a postnatal model of proliferative retinopathy.
10 g in pathological retinal vascular growth in proliferative retinopathy.
11 arization in a mouse model of oxygen-induced proliferative retinopathy.
12 ss retinal neovascularization and to prevent proliferative retinopathy.
13 ful pharmaceutical intervention for treating proliferative retinopathy.
14 e data suggest that STAT3 may have a role in proliferative retinopathy.
15 may be an ideal target for the prevention of proliferative retinopathy.
16 ha-defensins were studied in hypoxia-induced proliferative retinopathy.
17 reatment with plasma of patients affected by proliferative retinopathy.
18 n to prevent retinal detachment in models of proliferative retinopathy.
19 ferable retinopathy, 97.9% (94.9%-99.1%) for proliferative retinopathy.
20  were preferentially transduced in eyes with proliferative retinopathy.
21 initiation of the angiogenesis that leads to proliferative retinopathy.
22 arization in a mouse model of oxygen-induced proliferative retinopathy.
23  but may be more extensive with sickle SC or proliferative retinopathy.
24 tion and VEGF synthesis in a murine model of proliferative retinopathy.
25  is crucial for pathological angiogenesis in proliferative retinopathies.
26 tions of ischemia-reperfusion encountered in proliferative retinopathies.
27 ic compounds for prevention and treatment of proliferative retinopathies.
28 neovascularization is a crucial component of proliferative retinopathies.
29 a potential clinical use of this compound in proliferative retinopathies.
30  pathological conditions, such as cancer and proliferative retinopathies.
31 tide may be a promising future treatment for proliferative retinopathies.
32 vide a clinically efficient strategy against proliferative retinopathies.
33 peutic role for 16K hPRL in the treatment of proliferative retinopathies.
34 K2 inhibitors may be useful for treatment of proliferative retinopathies.
35 tant therapeutic target in the management of proliferative retinopathies.
36 PDGF) is an important stimulatory factor for proliferative retinopathies.
37 c inflammatory response in arthritis and the proliferative retinopathies.
38  the possibility that PGs may play a role in proliferative retinopathies.
39  intravitreous injections in mouse eyes with proliferative retinopathies.
40 en implicated in vascular development and in proliferative retinopathies.
41 pharmacologic therapies for the treatment of proliferative retinopathies.
42 investigate new treatments for patients with proliferative retinopathies.
43  the exaggerated wound repair that occurs in proliferative retinopathies.
44 chments similar to those seen in humans with proliferative retinopathies.
45 an alternative approach in the management of proliferative retinopathies.
46 7 [0.07-1.00], p = 0.05), and progression to proliferative retinopathy (0.18 [0.04-0.82], p = 0.03).
47  nonproliferative retinopathy was 66% (75%); proliferative retinopathy, 24% (32%); maculopathy, 56% (
48 role for VEGF expression in ischemia-induced proliferative retinopathies and a potential therapeutic
49  as a therapeutic target in the treatment of proliferative retinopathies and other diseases dependent
50 ufficiency and retinal ischemia precede many proliferative retinopathies and stimulate secretion of v
51                       Ischemia then leads to proliferative retinopathy and blindness.
52 sm, rs161740, with the combined phenotype of proliferative retinopathy and end-stage renal disease in
53 demonstrate that SDF-1 plays a major role in proliferative retinopathy and may be an ideal target for
54 ips between this factor and the incidence of proliferative retinopathy and of macular edema, 2 import
55 otein to be associated with the incidence of proliferative retinopathy and other complications of typ
56                                              Proliferative retinopathy and overt nephropathy showed n
57   VEGF is involved pathologically in cancer, proliferative retinopathy and rheumatoid arthritis, and
58 retinal space of wild-type mice or mice with proliferative retinopathies, and quantitative comparison
59 01) more likely to develop microalbuminuria, proliferative retinopathy, and distal symmetrical polyne
60 c control and the onset of microalbuminuria, proliferative retinopathy, and DSP observed in the Diabe
61 g incidences in Europe of overt nephropathy, proliferative retinopathy, and mortality in type 1 diabe
62                           Overt nephropathy, proliferative retinopathy, and neuropathy were assessed
63                                              Proliferative retinopathy because of retinal neovascular
64  is a critical component of diseases such as proliferative retinopathies, cancer and rheumatoid arthr
65                                     Ischemic proliferative retinopathy, characterized by pathological
66 e an attractive target for the prevention of proliferative retinopathies, CNV, and cancer.
67  to 0.65; P = 0.59); and laser treatment for proliferative retinopathy elasticity, 0.05 (95% CI, -0.2
68  from eyes of patients with diabetes without proliferative retinopathy, eyes of patients without diab
69 a direct link between ATF4 and the degree of proliferative retinopathy has not been demonstrated to d
70 ed for treatment of vascular and nonvascular proliferative retinopathies in humans.
71 )-A and PDGF-B is increased in patients with proliferative retinopathies in which traction retinal de
72                 This case report describes a proliferative retinopathy in a 16 year-old patient with
73 ors of diabetic nephropathy, neuropathy, and proliferative retinopathy in a young population-based Da
74 a may have helped prevent complications from proliferative retinopathy in eyes clinically observed to
75 ect out individual contributions, a model of proliferative retinopathy in mice with attenuated ephrin
76 ed, as is a significantly prolonged phase of proliferative retinopathy in PWG pups (20 days) compared
77 vessels commonly causes vision impairment in proliferative retinopathies, including retinopathy of pr
78 t the levels of SDF-1 found in patients with proliferative retinopathy induce retinopathy in our muri
79                        A defining feature in proliferative retinopathies is the formation of patholog
80  angiogenesis in the pathological setting of proliferative retinopathy is a major cause of blindness
81 nificantly greater in mice with two types of proliferative retinopathy (ischemic retinopathy or trans
82 ither moderate-to-severe nonproliferative or proliferative retinopathy occurred on chromosomes 5 (2.5
83 n; (4) diabetic vitrectomy; (5) treatment of proliferative retinopathy of prematurity and (6) treatme
84 nnual dilated retinal examinations to detect proliferative retinopathy or clinically significant macu
85  was defined in FIELD as laser treatment for proliferative retinopathy or macular edema or increase b
86 lation therapy or vitrectomy, development of proliferative retinopathy, or progression of diabetic re
87 en precedes cerebral infarcts or hemorrhage, proliferative retinopathy prior to loss of eyesight, pul
88  oligodeoxynucleotides prior to the onset of proliferative retinopathy reduced new blood vessel growt
89                The associations of ERMs with proliferative retinopathy, retinal lesions, macular hole
90 , or proliferative), 99.6% (97.0%-99.9%) for proliferative retinopathy; Retmarker 73.0% (72.0 %-74.0%
91 clining, others (CAD, overt nephropathy, and proliferative retinopathy) show less favorable changes b
92         Compared with normal eyes, eyes with proliferative retinopathy showed increased transduction,
93 ovide a good strategy for acute treatment of proliferative retinopathies, such as diabetic retinopath
94 actor (PDGF) has been implicated in vascular proliferative retinopathies, such as diabetic retinopath
95                                              Proliferative retinopathies, such as those complicating
96 een the cornerstone of studies investigating proliferative retinopathies, there is currently no harmo
97 he eyes that developed SVLV before high-risk proliferative retinopathy was observed, baseline risk fa
98        Using a mouse model of oxygen-induced proliferative retinopathy, we showed that RORalpha expre
99                                     Ischemic proliferative retinopathy, which occurs as a complicatio
100 he potential increase in the HR for incident proliferative retinopathy, with an increase in oxidized

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