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1 ar diseases, such as keratoconus and primary open angle glaucoma.
2 ion (ECP) surgeries in patients with primary open angle glaucoma.
3 in different types of primary and secondary open angle glaucoma.
4 Hg and he was found to have advanced primary open angle glaucoma.
5 s were mostly pseudo-exfoliative and primary open angle glaucoma.
6 M may be possible in human eyes with primary open angle glaucoma.
7 atients with coexisting cataract and primary open angle glaucoma.
8 transgenic mouse model of hereditary primary open-angle glaucoma.
9 ce to AH outflow, is a major risk factor for open-angle glaucoma.
10 in the United States and had newly diagnosed open-angle glaucoma.
11 myocilin, a protein associated with primary open-angle glaucoma.
12 6 had ocular hypertension and 14 had primary open-angle glaucoma.
13 be a new risk factor to consider in primary open-angle glaucoma.
14 ular-pressure-lowering drug in patients with open-angle glaucoma.
15 in lowering intraocular pressure in primary open-angle glaucoma.
16 high prevalence of glaucoma which is largely open-angle glaucoma.
17 and 2012 and newly diagnosed and treated for open-angle glaucoma.
18 e the most common genetic factors of primary open-angle glaucoma.
19 set of the prevalent ocular disorder primary open-angle glaucoma.
20 have previously been associated with primary open-angle glaucoma.
21 etic retinopathy, uveoretinitis, and primary open-angle glaucoma.
22 (IOP)-lowering medications in patients with open-angle glaucoma.
23 to mutations in the MYOCILIN gene is primary open-angle glaucoma.
24 when selecting treatments for patients with open-angle glaucoma.
25 ay lead to juvenile- and adult-onset primary open-angle glaucoma.
26 a multiple topical drug regimen for primary open-angle glaucoma.
27 procedure for reducing IOP in patients with open-angle glaucoma.
28 ic CPAMD8 variants to childhood and juvenile open-angle glaucoma.
29 pseudophakic patients with mild to moderate open-angle glaucoma.
30 n ethnicity, higher intraocular pressure and open-angle glaucoma.
31 ma and 2.1% (2/96) of probands with juvenile open-angle glaucoma.
32 and 2121 control individuals without primary open-angle glaucoma.
33 Genetic variants associated with primary open-angle glaucoma.
34 ellular matrix and frequent cause of chronic open-angle glaucoma.
35 Presence of primary open-angle glaucoma.
36 ent of patients with ocular hypertension and open-angle glaucoma.
37 surgery was performed in adults with various open-angle glaucomas.
40 tients were pseudophakic, with mild/moderate open-angle glaucoma, 12-month follow-up, and medicated i
41 ed diabetic macular edema and no preexisting open-angle glaucoma, 260 were randomly assigned to recei
42 study included 122 eyes treated for primary open angle glaucoma, 50 eyes (study group) in which, aft
43 gnoses in descending prevalence were primary open-angle glaucoma (55.9%), chronic angle-closure glauc
44 ed 354 eyes in 180 subjects (97 with primary open-angle glaucoma, 83 with glaucoma suspicion) who had
46 have identified novel loci for POAG (primary-open-angle glaucoma) (ABCA1, AFAP1, GMDS, PMM2, TGFBR3,
48 ree eyes of 2 patients who developed chronic open-angle glaucoma after Nd:YAG vitreolysis for symptom
51 2 eyes, comprising 38 glaucomatous eyes with open angle glaucoma and 24 healthy controls, were includ
52 s a highly heritable risk factor for primary open angle glaucoma and currently the only target for gl
55 r the development and progression of primary open angle glaucoma and is due to trabecular meshwork (T
57 uld be offered as a first-line treatment for open angle glaucoma and ocular hypertension, supporting
58 ry data set of 2320 individuals with primary open-angle glaucoma and 2121 control individuals without
59 cts (48 male, 40 female) with a diagnosis of open-angle glaucoma and a median age of 67 years (interq
63 GN, SETTING, AND PARTICIPANTS: Patients with open-angle glaucoma and healthy controls were examined b
64 ntia, including Alzheimer's disease, primary open-angle glaucoma and Helicobacter pylori (H.pylori) i
66 NTG when compared with patients with primary open-angle glaucoma and nonglaucomatous control subjects
70 with an increased prevalence of all forms of open-angle glaucoma and OHTN, whereas hyperopia was asso
72 y 24-2 and 10-2 VFs in patients with primary open-angle glaucoma and to test the hypothesis that pati
73 aucoma Associates of Texas with uncontrolled open-angle glaucoma and underwent gonioscopy-assisted tr
75 is and pars plana vitrectomy, and 1 juvenile open-angle glaucoma) and 21 of 70 eyes with nonglaucomat
76 A total of 234 patients (104 with primary open angle glaucoma, and 130 control subjects without an
77 ntil death; 203 patients (65.7%) had primary open-angle glaucoma, and 106 patients (34.2%) had exfoli
79 le have a 2.5-fold increased risk of primary open-angle glaucoma as compared with those in the lowest
81 l, we enrolled patients with newly diagnosed open-angle glaucoma at ten UK centres (tertiary referral
83 osterior sclera in a canine model of primary open-angle glaucoma caused by the G661R missense mutatio
84 s with a minimum 2-year diagnosis of primary open-angle glaucoma, chronic primary angle-closure glauc
85 In an institutional setting, a patient with open-angle glaucoma consented to be the recipient of the
86 with many ocular problems, such as secondary open angle glaucoma, corneal dysfunction, cataract, and
88 ERIA: participants with primary or secondary open-angle glaucoma (excluding uveitic) who had undergon
89 h patients diagnosed with moderate to severe open-angle glaucoma, focusing on outcomes they prioritiz
94 ined IOP reduction for patients with primary open-angle glaucoma (hazard ratio [HR], 1.19; 95% confid
95 eculoplasty (LTP) is routinely used to treat open-angle glaucoma; hence, understanding variations in
96 ncluding glaucoma suspect [GS], high-tension open-angle glaucoma [HTG], and normal-tension glaucoma [
97 tments for patients presenting with advanced open angle glaucoma in a publicly funded health service.
98 eyes of 72 participants with a diagnosis of open angle glaucoma in one or both eyes and a visual acu
99 e was being followed and treated for primary open angle glaucoma in our tertiary referral center.
101 al success, the pathophysiologic features of open-angle glaucoma in younger patients may be more loca
105 ar meshwork (TM) and the elevation of IOP in open-angle glaucoma is associated with dysfunction and l
106 y congenital glaucoma (PCG n = 22), juvenile open angle glaucoma (JOAG n = 16), glaucoma following ca
110 llowing cataract surgery (GFCS) and juvenile open-angle glaucoma (JOAG) is variable and with relative
112 women) and 2121 individuals without primary open-angle glaucoma (mean [interquartile range] age, 63.
113 A total of 2320 individuals with primary open-angle glaucoma (mean [interquartile range] age, 64.
114 < 0.001) in both eyes with incident primary open-angle glaucoma (mean, 10.6%; standard deviation, 22
115 iris; MPS type IV patients are vulnerable to open-angle glaucoma; MPS type VI patients have narrow an
117 present study, we investigated the risk for open angle glaucoma (OAG) in migraineurs using a 10-year
123 beculoplasty (SLT) on medically uncontrolled open-angle glaucoma (OAG) and to evaluate the effects of
124 d (VF) deterioration events in patients with open-angle glaucoma (OAG) by 50% over a 2-year period.
125 personalized forecasts of how patients with open-angle glaucoma (OAG) experience disease progression
126 surgery (medical group), while 32 eyes with open-angle glaucoma (OAG) had previously undergone glauc
127 This study determined the risk factors for open-angle glaucoma (OAG) in adults examined in the Nige
128 ice-daily timolol eye drops in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT) t
130 oprost ophthalmic solution, in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).
131 intraocular pressure (IOP) in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).
136 iagnosis; 20.0% (n = 330) were identified as open-angle glaucoma (OAG) suspects, 9.2% (n = 151) were
144 a major risk factor for the deterioration of open-angle glaucoma (OAG); medical IOP reduction is the
145 eroid use, myopia, socioeconomic status, and open-angle glaucoma (odds ratio [OR], 0.89; 95% confiden
146 2; chromosome 4, rs59892895T>C) with primary open-angle glaucoma (odds ratio [OR], 1.32 [95% CI, 1.20
147 cifically HiFU in patients with uncontrolled open-angle glaucoma on maximum tolerated medical therapy
148 ntrolled trial treatment-naive patients with open angle glaucoma or ocular hypertension and no ocular
149 ular hypertension, and patients with primary open angle glaucoma or primary angle closure glaucoma.
153 tive cohort study of untreated patients with open-angle glaucoma or ocular hypertension at a hospital
154 l of 660 adults with a clinical diagnosis of open-angle glaucoma or ocular hypertension from a referr
157 eserved with PQ reduced IOP in patients with open-angle glaucoma or ocular hypertension who were into
160 y and effectively lower IOP in patients with open-angle glaucoma or ocular hypertension, showing sign
166 intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension; however, the
167 r results suggest that patients with primary open-angle glaucoma or with narrow angles or chronic ang
169 I, 2.09-1.11;P = 0.02), higher prevalence of open-angle glaucoma (OR, 2.40; 95% CI, 1.36-4.23;P = 0.0
170 I, 1.31-10.13; P = .01), presence of primary open-angle glaucoma (OR, 3.82; 95% CI, 1.60-9.14; P = .0
171 beculectomy surgery in patients with primary open angle glaucoma over a 3-year period of follow-up.
172 ), more glaucoma suspects (p < 0.0001), more open angle glaucoma (p = 0.0006) and fewer other conditi
173 of glaucoma (P < .0001), and a diagnosis of open-angle glaucoma (P = .0003) were associated with inc
174 ithin different types of glaucoma, including open-angle glaucoma (P = 0.36), chronic angle closure gl
175 investigation of both childhood and juvenile open-angle glaucoma, particularly when associated with i
176 ve, observational cohort study that included open angle glaucoma patients with visually significant c
179 olled and treated more strictly than primary open-angle glaucoma patients to avoid visual field deter
180 erived from non-glaucomatous donors and from open-angle glaucoma patients were used to determine the
187 The study included patients with primary open angle glaucoma (POAG group, n = 30) and controls (n
188 12 normal controls, 7 patients with primary open angle glaucoma (POAG) and 9 patients with normal te
189 OPTN) are linked to the pathology of primary open angle glaucoma (POAG) and amyotrophic lateral scler
190 is study was designed to evaluate if primary open angle glaucoma (POAG) and its severity are associat
191 les frequencies in primary glaucoma [primary open angle glaucoma (POAG) and primary angle closure gla
192 oci have been associated with either primary open angle glaucoma (POAG) or heritable ocular quantitat
196 beagle model of autosomal recessive primary open angle glaucoma (POAG) to a 4-Mb interval on chromos
197 and combined screening for PACG and primary open angle glaucoma (POAG) to evaluate costs and benefit
198 of 30.8 months, including 28 (4.4%) primary open angle glaucoma (POAG), 27 (4.2%) primary angle clos
199 jects were glaucomatous: (67 PXG, 42 Primary Open Angle Glaucoma (POAG), 28 PACG, 14 Normal Tension G
201 defects also occur in patients with primary open angle glaucoma (POAG), in which there is specific R
202 ic or glaucoma faculty patients with primary open angle glaucoma (POAG), ocular hypertension (OHTN),
203 n the aqueous humor of patients with primary open angle glaucoma (POAG), pseudoexfoliation syndrome (
208 yes of 75 patients with uncontrolled primary open-angle glaucoma (POAG) and cataract who underwent PK
209 med on 27 consecutive eyes with both primary open-angle glaucoma (POAG) and cataract; each eye was tr
210 (AD) and European descent (ED) with primary open-angle glaucoma (POAG) and control participants comp
211 ssociation of known loci for IOP and primary open-angle glaucoma (POAG) and identify four new IOP-ass
212 meshwork (TM) height differs between primary open-angle glaucoma (POAG) and primary angle-closure gla
213 ly examined the global prevalence of primary open-angle glaucoma (POAG) and primary angle-closure gla
214 s) endophthalmitis and risk of a new primary open-angle glaucoma (POAG) diagnosis within 365 days aft
215 ses (TIMPs) in the aqueous humour of primary open-angle glaucoma (POAG) eyes have been described.
216 a genome-wide association study for primary open-angle glaucoma (POAG) in 1,007 cases with high-pres
217 culoplasty (SLT) as sole therapy for primary open-angle glaucoma (POAG) in an Afro-Caribbean populati
218 k, CA) for treating mild-to-moderate primary open-angle glaucoma (POAG) in patients undergoing catara
229 ctive cross-sectional study: 68 mild primary open-angle glaucoma (POAG) patients according to the Hod
230 venous pressure (RVP) in the eyes of primary open-angle glaucoma (POAG) patients and healthy subjects
231 difference in severity of disease in primary open-angle glaucoma (POAG) patients with a Myocilin (MYO
232 itary determination) was examined in primary open-angle glaucoma (POAG) patients with cataract and no
233 g can cause fibrosis of the TM as in primary open-angle glaucoma (POAG) patients, and is characterize
235 American Academy of Ophthalmology's Primary Open-angle Glaucoma (POAG) Preferred Practice Pattern (P
237 egion previously was associated with primary open-angle glaucoma (POAG), although replication among i
238 the 4 forms of open-angle glaucoma: primary open-angle glaucoma (POAG), normal-tension glaucoma (NTG
239 stent was implanted in patients with primary open-angle glaucoma (POAG), normal-tension glaucoma (NTG
248 ODH) before and after development of primary open-angle glaucoma (POAG); determine the prognostic sig
249 ce interval, 3.3-5.4), consisting of primary open-angle glaucoma (POAG, 3.2%, including high-tension
252 ELINES: Evidence-based update of the Primary Open-Angle Glaucoma Preferred Practice Pattern(R) (PPP)
256 closure glaucoma (PACG); 1 of the 4 forms of open-angle glaucoma: primary open-angle glaucoma (POAG),
257 he OMNI system in pseudophakic patients with open-angle glaucoma provides effective IOP reduction or
258 glandin analog eye drops in treating primary open-angle glaucoma, published between December 2000 and
259 0.77-0.80) and with increases in the odds of open-angle glaucoma ranging from 1.23 (95% CI, 1.20-1.26
260 involved diabetic macular edema and no prior open-angle glaucoma, repeated intravitreous injections o
261 PEX glaucoma is a common, aggressive form of open-angle glaucoma resulting from the deposition of fib
263 and primary open-angle glaucoma vs secondary open-angle glaucoma (SOAG) (HR 2.51; 95% CI 1.01-6.23) r
266 osis and management of patients with primary open-angle glaucoma suspect with detailed recommendation
267 h age, and particularly in eyes with primary open angle glaucoma, the number of cells residing within
272 etrospective case series of 81 patients with open-angle glaucoma undergoing 110 SLT procedures from N
274 tio [HR] 2.51; 95% CI 1.12-5.65) and primary open-angle glaucoma vs secondary open-angle glaucoma (SO
276 mary glaucoma that had gonioscopy (n = 243), open-angle glaucoma was more common (86 %) than angle-cl
278 ation number, ISRCTN96423140), patients with open-angle glaucoma were allocated to receive latanopros
280 tal of 607 participants with newly diagnosed open-angle glaucoma were enrolled at 14 clinical centers
284 study, healthy individuals and patients with open-angle glaucoma were prospectively enrolled between
285 as associated with increased risk of primary open-angle glaucoma when all data were included in a met
286 itivity sometimes increases in patients with open-angle glaucoma when intraocular pressure (IOP) is d
287 ary 1, 2013, including patients with primary open-angle glaucoma who had a best-corrected visual acui
288 ial for patients with medically uncontrolled open-angle glaucoma who have previously received 360 deg
290 tudy of the Cypass micro-stent) with primary open-angle glaucoma who were using 0-4 classes of topica
291 otal of 603 patients (603 eyes) with primary open-angle glaucoma who were using up to 3 glaucoma medi
292 ophotographs from 1 eye of 125 patients with open-angle glaucoma with >/=8 reliable Swedish interacti
293 The second cohort included all stages of open-angle glaucoma with >=5 OCT retinal nerve fiber lay
294 analysis included 186 patients with primary open-angle glaucoma with a mean age of 59.1 years (range
295 g was performed in 117 patients with primary open-angle glaucoma with a minimum treatment duration of
296 osis and management of patients with primary open-angle glaucoma with an algorithm for patient manage
297 quality of life among patients with primary open-angle glaucoma with structural macular retinal gang
298 (XFS), the most common recognizable cause of open-angle glaucoma worldwide, is a systemic disorder wi
300 as various ocular implications, most notably open angle glaucoma, zonular abnormalities, and cataract