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1 te detection of patients at risk for primary angle closure glaucoma.
2 with primary open angle glaucoma or primary angle closure glaucoma.
3 omy should be considered in the treatment of angle closure glaucoma.
4 ns/eye volume ratio, and a high incidence of angle-closure glaucoma.
5 nd hypermetropic refractive error on primary angle-closure glaucoma.
6 hway might be involved in biology of primary angle-closure glaucoma.
7 tive effect for both open-angle glaucoma and angle-closure glaucoma.
8 broad categories of glaucoma, open-angle and angle-closure glaucoma.
9 rter of 2023, which included 1629 reports of angle-closure glaucoma.
10 is and hypermetropia confer risk for primary angle-closure glaucoma.
11 origin are the main risk factors for primary angle-closure glaucoma.
12 55 had primary angle closure and 263 primary angle-closure glaucoma.
13 ular pressure 30 mm Hg or greater or primary angle-closure glaucoma.
14 0% (n = 148) with OAG and 1.0% (n = 16) with angle-closure glaucoma.
15 hat antidepressants may increase the risk of angle-closure glaucoma.
16 il dilation is a known risk factor for acute angle-closure glaucoma.
17 re defined according to the first coding for angle-closure glaucoma.
18 ain complications being severe hyperopia and angle-closure glaucoma.
19 r 2013 on the topics open-angle glaucoma and angle-closure glaucoma.
20 rior chamber angles that predisposed them to angle-closure glaucoma.
21 subjects (0.3%, 95% CI, 0.1-0.4) had primary angle-closure glaucoma.
22 utic strategy for certain types of secondary angle-closure glaucoma.
23 eliminate any pupillary block due to primary angle-closure glaucoma.
24 wo forms of glaucoma: open-angle glaucoma or angle-closure glaucoma.
25 NNia substrain of mouse (DBA) with inherited angle-closure glaucoma.
26 omic variations and underlying mechanisms in angle-closure glaucoma.
27 primary open-angle glaucoma (55.9%), chronic angle-closure glaucoma (10.8%), neovascular glaucoma (9.
28 spondents (14.6%; 95% CI, 9.9%-19.3%), acute angle-closure glaucoma; 11 of 216 respondents (5.1%; 95%
30 4%), failure to diagnose or mismanagement of angle-closure glaucoma (18.5%), adverse drug effects (14
32 e Lymphoblastic Leukemia who developed acute angle closure glaucoma (AACG) following daratumumab infu
33 eyes of 154 patients consisting of 40 acute angle-closure glaucoma (AACG) eyes, 40 fellow eyes of AA
36 Recent studies underscore the importance of angle-closure glaucoma (ACG) as a cause of world blindne
37 gnosed in 3.1% (95% CI = 2.5, 3.8%), primary angle-closure glaucoma (ACG) in 0.59% (95% CI = 0.35, 0.
38 nterior chamber (AC) depth and the attack of angle-closure glaucoma (ACG) in eyes with the recent ons
44 may present at an early age with features of angle closure glaucoma and a Thr518Met mutation in MYRF
46 ase represents the first report of worsening angle closure glaucoma and choroidal detachments over an
47 old Chinese female was diagnosed of primary angle closure glaucoma and had bilateral laser periphera
48 anophthalmos and pigmentary retinopathy with angle closure glaucoma and optic disc pit in one eye.
49 Clinically there was presence of bilateral angle closure glaucoma and peripheral choroidal detachme
52 udies reporting on the prevalence of primary angle-closure glaucoma and other precursor forms of the
54 pressure (IOP) in patients with PAC, primary angle closure glaucoma, and acute angle closure crisis.
56 syndrome predisposes to both open-angle and angle-closure glaucoma, and to capsular rupture, zonular
57 The IOP reductions obtained in patients with angle closure glaucoma are often more pronounced than th
60 CG) eyes, 40 fellow eyes of AACG, 42 chronic angle-closure glaucoma (CACG) eyes, 40 primary angle-clo
61 of glaucoma reside in Asia, and with primary angle-closure glaucoma carrying a higher rate of visual
62 an origin have a higher frequency of primary angle-closure glaucoma compared with those of European o
64 nd significant visual comorbidities, such as angle closure glaucoma, cystic macular edema, and exudat
67 The DBA/2J mouse is a model for secondary angle-closure glaucoma, due to iris atrophy and pigment
69 , GAS7, FOXC1, ATXN2, TXNRD2); PACG (primary angle-closure glaucoma (EPDR1, CHAT, GLIS3, FERMT2, DPM2
71 ulcers of 1 year's duration developed acute angle-closure glaucoma following the appearance of new m
73 s and knowledge of retinal detachment, acute angle-closure glaucoma, giant cell arteritis, and centra
74 d definitions to detect and diagnose primary angle-closure glaucoma has resulted in difficulties in i
75 t surgery in patients with acute and chronic angle-closure glaucoma have been well studied and are ge
76 International investigations into primary angle-closure glaucoma have demonstrated reproducible ev
78 oma--primary open-angle glaucoma and primary angle-closure glaucoma--have different risk factors.
79 ary glaucoma (HR = 1.641, P = .004), primary angle closure glaucoma (HR = 1.611, P < .001), and previ
80 (HR 0.755, 95% CI 0.729, 0.781) and primary angle-closure glaucoma (HR 0.702, 95% CI 0.636, 0.781).
81 removal surgery included presence of chronic angle-closure glaucoma (HR = 1.32; P < .001) and dry eye
82 e glaucoma (HR, 1.33; 95% CI, 1.16-1.52) and angle-closure glaucoma (HR, 1.66; 95% CI, 1.20-2.30).
83 ngs into discussion a new clinical entity of angle closure glaucoma in nanophthalmos accompanied by o
84 lmos with Optic Disc pit, with an associated angle closure glaucoma in the same eye, an association w
85 To report clinical features of bilateral angle-closure glaucoma in a patient with nanophthalmic e
88 pheral iridotomy prophylaxis against primary angle-closure glaucoma in Chinese people classified as p
90 ere, we present a discovery GWAS for primary angle-closure glaucoma in Europeans using the UK Biobank
101 tumumab use with ocular events such as acute angle-closure glaucoma, myopic shift, and choroidal effu
102 NTG: aHR, 1.87, 95% CI, 1.09-3.18), whereas angle-closure glaucoma (N = 3150) showed no significant
103 2 with IOP higher than 35 mm Hg, and 1 with angle-closure glaucoma not attributed to the study drug
105 primary open-angle glaucoma, chronic primary angle-closure glaucoma or pseudoexfoliation glaucoma wer
108 ding open-angle glaucoma (P = 0.36), chronic angle closure glaucoma (P = 0.85) and OHT (P = 0.42).
109 pseudoexfoliative glaucoma (PXG) and Primary Angle Closure Glaucoma (PACG) are scarce in the Sub-Saha
110 imary open angle glaucoma (POAG) and primary angle closure glaucoma (PACG) in a North Indian Punjabi
111 on the morbidity and progression to primary angle closure glaucoma (PACG) in White Caucasian individ
114 mary open angle glaucoma (POAG), 132 primary angle closure glaucoma (PACG) patients and 424 matched c
115 pen angle glaucoma (POAG), 27 (4.2%) primary angle closure glaucoma (PACG), and 5 (0.8%) normal tensi
116 with primary angle closure (PAC) and primary angle closure glaucoma (PACG), and to compare their diag
118 investigate whether the addition of primary angle closure glaucoma (PACG)-associated genetic loci al
119 imary open angle glaucoma (POAG) and primary angle closure glaucoma (PACG)] patients and matched heal
120 low-up examination, 5298 at risk for primary angle-closure glaucoma (PACG) and 5060 at risk for PACD
121 s and TIMPs in the aqueous humour of primary angle-closure glaucoma (PACG) eyes were measured and com
125 laucomatous VF loss in patients with primary angle-closure glaucoma (PACG) using pointwise linear reg
126 POAG), 0.39% (95% CI, 0.34-0.45) for primary angle-closure glaucoma (PACG), and 0.15% (95% CI, 0.07-0
127 imary open-angle glaucoma (POAG) and primary angle-closure glaucoma (PACG), and projected the number
128 s of visual field (VF) defects among primary angle-closure glaucoma (PACG), high-tension glaucoma (HT
130 Glaucoma cases were classified as primary angle-closure glaucoma (PACG); 1 of the 4 forms of open-
131 rmal-tension glaucoma [NTG], 1.5%]), primary angle-closure glaucoma (PACG, 0.4%), pseudoexfoliation g
133 foliative glaucoma (PXG) and primary chronic angle closure glaucoma (PCAG) patients was 19.22 mmHg, 2
134 itional features can include microphthalmia, angle-closure glaucoma, persistent hyperplastic primary
135 cus associated with nanophthalmos or with an angle-closure glaucoma phenotype, and the identification
136 our understanding of the pathophysiology of angle-closure glaucoma, pigmentary glaucoma, and a varie
137 g a higher rate of visual morbidity, primary angle-closure glaucoma poses an important public health
138 70-year-old female with a history of primary angle closure glaucoma presented with 4 mm of proptosis,
139 spectrum of RP by presenting with bilateral angle-closure glaucoma prior to typical cartilage involv
140 ts with primary open-angle glaucoma, primary angle-closure glaucoma, pseudoexfoliative glaucoma, and
141 eful in the clinical management of eyes with angle closure glaucoma, recent studies show that the dec
142 f the first reported cases of severe chronic angle- closure glaucoma secondary to ciliary body cysts
143 ic and surgical management of severe chronic angle- closure glaucoma secondary to ciliary body cysts
144 odigital dysplasia, with progressive chronic angle- closure glaucoma secondary to ciliary body cysts
145 primary open-angle glaucoma (POAG), primary angle-closure-glaucoma, secondary glaucoma, or a combina
146 the development of angle-closure and primary angle-closure glaucoma should also be investigated.
147 mice develop a progressive form of secondary angle-closure glaucoma that appears to be initiated by i
148 suspect, primary angle closure, and primary angle closure glaucoma was 8.8 (8.4, 9.2), 6.2 (5.9, 6.6
150 9; 1.28-1.50, respectively), whereas primary angle-closure glaucoma was associated with VaD (1.26; 1.
153 Eligible patients had primary open-angle or angle-closure glaucoma, were aged >=18 years, and underw
154 he highest cost category among patients with angle-closure glaucoma, whereas office visits was the hi
156 erfluoropropene (C3F8) may produce secondary angle-closure glaucoma with or without pupillary block.