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1 year, therapy significantly reduced the mean panretinal (3.9% vs. 5.8%; P = 0.002) and macular (6.2%
2 mean quantitative leakage index was 3.5% for panretinal, 6.6% for macular, 4.8% for posterior pole, 3
3 zonal sparing (grade 2), and 35% (12/34) had panretinal alterations (grade 3).
4                                              Panretinal analyses were not linked to DME as strongly.
5  count and ischemic index were quantified in panretinal and macular regions.
6 MD, supporting the claim that the disease is panretinal and not macula only.
7 pheral retinal NV severity and incidence and panretinal arteriole and venule tortuosity indexes (TI(a
8 the intent of generating a rapid noninvasive panretinal assessment of ocular inflammation.
9 mild, isolated macular involvement to severe panretinal degeneration with abnormal ERG.
10 the vascular arcades, and 4 patients (11.1%) panretinal degeneration.
11 entan admix both produced similar (P > 0.05) panretinal DeltaPo(2).
12                               On day 20, the panretinal deltaPO2 of the room air-recovered group (125
13                                          The panretinal deltaPO2 value for the SOR group (87 +/- 5 mm
14           Also, control and diabetic LEW rat panretinal DeltaPO2(t1-ra) were lower (P < 0.05) than in
15  diabetic LEW rats, a supernormal (P < 0.05) panretinal DeltaPO2(t2-t1) was found that could be corre
16  beyond the macula, suggesting that AMD is a panretinal disease.
17 ated a 63-year-old woman demonstrating acute panretinal dysfunction after intravitreous ocriplasmin i
18      Ocriplasmin injection may lead to acute panretinal dysfunction in some eyes, but the mechanism o
19 phy leakage was measured in 5 retinal zones: panretinal (entire retina), central macular (3-disc diam
20  oxygen physiopathology unfolds in eyes with panretinal hypoperfusion courtesy of the transparent ocu
21 .75%), and PDR (mean = 5.84%); P<2x10(-16)], panretinal ischemic index [mild NPDR (mean = 0.95%, mode
22                       A numeric reduction in panretinal ischemic index and area was noted.
23                                              Panretinal ischemic index decreased between baseline and
24                                     The mean panretinal ischemic index demonstrated a small but likel
25                                              Panretinal ischemic index did not demonstrate any signif
26                                              Panretinal ischemic index did not improve and trended to
27                    Panretinal leakage index, panretinal ischemic index, and panretinal microaneurysm
28 those with regressed ROP following bilateral panretinal laser photocoagulation (n = 37; median gestat
29 ive diabetic retinopathy has been managed by panretinal laser photocoagulation (PRP) for the past 40
30                                              Panretinal laser photocoagulation (PRP) was shown to be
31                                              Panretinal laser photocoagulation is the cornerstone of
32 ailable to all patients starting at month 3; panretinal laser was available as necessary.
33                                              Panretinal leakage index [mild NPDR (mean = 0.51%), mode
34 g-based qUWFA analysis platform was used for panretinal leakage index assessment and differentiation
35 The primary end point was the mean change in panretinal leakage index at month 12 from baseline as me
36                                         Mean panretinal leakage index improved significantly, decreas
37 tween both baseline macular leakage area and panretinal leakage index with IRF volume, SRF volume, an
38             Angiographic parameters included panretinal leakage index, ischemic index, and microaneur
39 rs demonstrates a significant improvement in panretinal leakage index, leakage area, and MA burden in
40                                              Panretinal leakage index, microaneurysm count, and ische
41                                              Panretinal leakage index, panretinal ischemic index, and
42                                         Mean panretinal leakage index, zonal leakage area, and panret
43 jections resulted in a dramatic reduction in panretinal leakage index.
44                                              Panretinal leakage was associated with DRSS (mean 2.2% f
45 tinal leakage index, zonal leakage area, and panretinal MA count improved significantly between basel
46 ), and PDR (mean = 9.53%); P<2x10(-16)], and panretinal microaneurysm count [mild NPDR (mean = 36), m
47 eakage index, panretinal ischemic index, and panretinal microaneurysm count are associated with DR se
48                                              Panretinal or focal endolaser photocoagulation was perfo
49 7D (MBDL) or 35B to 53E (MBCU), and no prior panretinal or focal photocoagulation in at least one eye
50 /cone/cone-rod dystrophy, "MCCRD group") and panretinal or peripheral dysfunction (retinitis pigmento
51 gly support an association between subnormal panretinal oxygenation ability and increased NV risk in
52  occurred but with an unexpected decrease in panretinal oxygenation ability.
53 ance imaging (MRI) was used to determine the panretinal oxygenation response (deltaPO2, mm Hg) to a c
54 ing the period when lesions are present, the panretinal oxygenation response remained significantly (
55 s, a significant (P < 0.05) reduction in the panretinal oxygenation response was observed in the gala
56 s exhibit a grainy retina that progresses to panretinal patches of depigmentation.
57  compared with baseline, as well as the mean panretinal perivascular leakage index (1.5% vs. 2.3%; P
58 ercept (100 participants) or vitrectomy with panretinal photocoagulation (105 participants).
59  bevacizumab, sub-Tenon's triamcinolone, and panretinal photocoagulation (PRP) after cataract surgery
60 termine the validity of self-report of prior panretinal photocoagulation (PRP) and focal photocoagula
61  diabetic retinopathy (PDR) interventions of panretinal photocoagulation (PRP) and intravitreal injec
62  clinical study was to compare the effect of panretinal photocoagulation (PRP) associated with intrav
63  retinopathy (PDR) treated to stability with panretinal photocoagulation (PRP) continue to lose visio
64                                              Panretinal photocoagulation (PRP) for proliferative diab
65 ate the efficacy and safety of anti-VEGF and panretinal photocoagulation (PRP) for the treatment of p
66                     Eyes without preexistent panretinal photocoagulation (PRP) had a higher risk to u
67 ing neovascularization (NV) before and after panretinal photocoagulation (PRP) in eyes with treatment
68 ges in retinal nonperfusion before and after panretinal photocoagulation (PRP) in treatment-naive eye
69 thelial growth factor (VEGF) injections plus panretinal photocoagulation (PRP) is a common approach f
70                                              Panretinal photocoagulation (PRP) is the standard treatm
71 y have a variable response to treatment with panretinal photocoagulation (PRP) or anti-vascular endot
72 betic retinopathy (PDR) in eyes treated with panretinal photocoagulation (PRP) or ranibizumab.
73 emorrhage on presentation (P = .001), and no panretinal photocoagulation (PRP) treatments (P < .001).
74 emorrhage on presentation (P = .001), and no panretinal photocoagulation (PRP) treatments (P < .001).
75 h newly diagnosed high-risk PDR treated with panretinal photocoagulation (PRP) using either argon gre
76 ntravitreal aflibercept (IVA) injection with panretinal photocoagulation (PRP) versus early vitrectom
77           Adjuvant preoperative therapy with panretinal photocoagulation (PRP) versus no PRP (0.95 vs
78 ity (VA) over 24 weeks after vitrectomy with panretinal photocoagulation (PRP) vs aflibercept in a ra
79 more common among eyes assigned initially to panretinal photocoagulation (PRP) vs anti-vascular endot
80 mab is a reasonable treatment alternative to panretinal photocoagulation (PRP) when managing prolifer
81 re recorded, including anti-VEGF injections, panretinal photocoagulation (PRP), and surgical interven
82 al treatments including PPV, injections, and panretinal photocoagulation (PRP), as well as visual acu
83  PDR based on graded fundus photographs, (2) panretinal photocoagulation (PRP), or (3) pars plana vit
84 rative DR (NPDR), proliferative DR (PDR) and panretinal photocoagulation (PRP).
85 erative diabetic retinopathy (PDR) following panretinal photocoagulation (PRP).
86 d, though somewhat disorganized, as in human panretinal photocoagulation (PRP).
87 c retinopathy (PDR), previously treated with panretinal photocoagulation (PRP).
88 (SS) OCT angiography (OCTA) before and after panretinal photocoagulation (PRP).
89                       All patients underwent panretinal photocoagulation (PRP).
90 ovascularization is best managed by applying panretinal photocoagulation after the first appearance o
91 s followed by immunosuppressants, along with panretinal photocoagulation and intravitreal ranibizumab
92 lar endothelial growth factor injections and panretinal photocoagulation are important to prevent neo
93 BCVA, early PPV, and absence of preoperative panretinal photocoagulation as significant predictors of
94 cluding visual acuity improvement, increased panretinal photocoagulation completion rates, and reduce
95  had vitreous hemorrhage from PDR precluding panretinal photocoagulation completion.
96                                              Panretinal photocoagulation could be initiated for failu
97 bercept, 2 mg, vs pars plana vitrectomy plus panretinal photocoagulation for nonclearing vitreous hem
98 ersus Intravitreal Ranibizumab With Deferred Panretinal Photocoagulation for Proliferative Diabetic R
99                        The patient underwent panretinal photocoagulation in both eyes with regression
100                                              Panretinal photocoagulation is designed to increase reti
101 n with intravitreal anti-VEGF medication and panretinal photocoagulation may help to prevent addition
102                                              Panretinal photocoagulation monotherapy was associated w
103 ween conversion to proliferative disease and panretinal photocoagulation or first treatment, and loss
104                                              Panretinal photocoagulation or intravitreous ranibizumab
105                                              Panretinal photocoagulation rates declined from 784/1000
106                                              Panretinal photocoagulation rates declined from 784/1000
107                                              Panretinal photocoagulation rates did not significantly
108                                              Panretinal photocoagulation rates in diabetic macular ed
109                                              Panretinal photocoagulation rates in diabetic macular ed
110 thy type, number of intravitreal injections, panretinal photocoagulation sessions, or photocoagulatio
111                 In case of retinal ischemia, panretinal photocoagulation should be initiated soon to
112 line visual acuity, baseline hemoglobin A1c, panretinal photocoagulation status, and cumulative anti-
113                                              Panretinal photocoagulation treatment patterns and clini
114                                              Panretinal photocoagulation treatments declined from 109
115  Diabetic Macular Edema), Protocol S (Prompt Panretinal Photocoagulation Versus Intravitreal Ranibizu
116                                              Panretinal photocoagulation was shown to be beneficial f
117                               The absence of panretinal photocoagulation was the primary significant
118  intravitreous injections of bevacizumab and panretinal photocoagulation were administered, the new v
119  acuity (VA) (P = 0.001), failure to receive panretinal photocoagulation within 2 weeks of surgery (P
120 nce, 4%; 95% CI, -4% to 13%) and of complete panretinal photocoagulation without vitrectomy by 16 wee
121  in eyes without PDR at baseline, (3) having panretinal photocoagulation, (4) experiencing vitreous h
122 rative diabetic retinopathy (PDR) usually is panretinal photocoagulation, an inherently destructive t
123                           Treatment for PDR, panretinal photocoagulation, is inherently destructive a
124 des for intravitreal injection, focal laser, panretinal photocoagulation, laterality of procedure, ra
125  endothelial growth factor (VEGF) injection, panretinal photocoagulation, or both for retinal ischemi
126                                       Before panretinal photocoagulation, patients received one of se
127                                    Following panretinal photocoagulation, subjective pain was assesse
128 iteria were previous intravitreal injection, panretinal photocoagulation, vitrectomy, central-involvi
129                          However, heightened panretinal photocoagulation-related pain in females, pat
130 algesic efficacy in nearly all patients with panretinal photocoagulation-related pain, while nepafena
131  benefit in favor of initial vitrectomy with panretinal photocoagulation.
132 teristics on pain perception associated with panretinal photocoagulation.
133 eloped in 4 patients, which was managed with panretinal photocoagulation.
134 especially in eyes that are nonresponsive to panretinal photocoagulation.
135 cludes placement or confirmation of complete panretinal photocoagulation.
136 intravitreous aflibercept vs vitrectomy with panretinal photocoagulation.
137 -enabled feature extraction system generated panretinal quantitative UWFA metrics, including leakage,
138                                              Panretinal TI(a) and TI(v) were increased over control v
139 y associated with peripheral NV severity and panretinal TI(a).
140 s associated with peripheral NV severity and panretinal TI(a).
141                                              Panretinal TI(v) was not correlated with intraretinal io

 
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