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1 Hg and he was found to have advanced primary open angle glaucoma.
2 linked directly to juvenile- and adult-onset open angle glaucoma.
3 ut there is no clear gender predilection for open angle glaucoma.
4 suggested to be important for progression of open angle glaucoma.
5 Genetics seem to play an important role in open angle glaucoma.
6 heir role in the management of patients with open angle glaucoma.
7 ar diseases, such as keratoconus and primary open angle glaucoma.
8 ent of patients with ocular hypertension and open-angle glaucoma.
9 in lowering intraocular pressure in primary open-angle glaucoma.
10 high prevalence of glaucoma which is largely open-angle glaucoma.
11 in the United States and had newly diagnosed open-angle glaucoma.
12 and 2012 and newly diagnosed and treated for open-angle glaucoma.
13 e the most common genetic factors of primary open-angle glaucoma.
14 set of the prevalent ocular disorder primary open-angle glaucoma.
15 have previously been associated with primary open-angle glaucoma.
16 myocilin, a protein associated with primary open-angle glaucoma.
17 etic retinopathy, uveoretinitis, and primary open-angle glaucoma.
18 (IOP)-lowering medications in patients with open-angle glaucoma.
19 to mutations in the MYOCILIN gene is primary open-angle glaucoma.
20 when selecting treatments for patients with open-angle glaucoma.
21 ay lead to juvenile- and adult-onset primary open-angle glaucoma.
22 a multiple topical drug regimen for primary open-angle glaucoma.
23 procedure for reducing IOP in patients with open-angle glaucoma.
24 at baseline; 68% were diagnosed with primary open-angle glaucoma.
25 rule has limited utility in the diagnosis of open-angle glaucoma.
26 sfunction results in ocular hypertension and open-angle glaucoma.
27 ar disease and 233 eyes of 163 patients with open-angle glaucoma.
28 because TGF-beta2 is associated with primary open-angle glaucoma.
29 ciated with juvenile and adult-onset primary open-angle glaucoma.
30 the most common identifiable risk factor for open-angle glaucoma.
31 d by cataract surgery, increases the risk of open-angle glaucoma.
32 ay lead to juvenile- and adult-onset primary open-angle glaucoma.
33 ix and the most common identifiable cause of open-angle glaucoma.
34 in 58 eyes of 58 patients with suspected or open-angle glaucoma.
35 transgenic mouse model of hereditary primary open-angle glaucoma.
36 6 had ocular hypertension and 14 had primary open-angle glaucoma.
37 be a new risk factor to consider in primary open-angle glaucoma.
38 ce to AH outflow, is a major risk factor for open-angle glaucoma.
39 ular-pressure-lowering drug in patients with open-angle glaucoma.
40 surgery was performed in adults with various open-angle glaucomas.
44 ed diabetic macular edema and no preexisting open-angle glaucoma, 260 were randomly assigned to recei
45 study included 122 eyes treated for primary open angle glaucoma, 50 eyes (study group) in which, aft
46 ed 354 eyes in 180 subjects (97 with primary open-angle glaucoma, 83 with glaucoma suspicion) who had
48 have identified novel loci for POAG (primary-open-angle glaucoma) (ABCA1, AFAP1, GMDS, PMM2, TGFBR3,
49 ree eyes of 2 patients who developed chronic open-angle glaucoma after Nd:YAG vitreolysis for symptom
52 2 eyes, comprising 38 glaucomatous eyes with open angle glaucoma and 24 healthy controls, were includ
53 s a highly heritable risk factor for primary open angle glaucoma and currently the only target for gl
57 Sixty-four patients at different stages of open-angle glaucoma and 26 patients with ocular hyperten
58 cts (48 male, 40 female) with a diagnosis of open-angle glaucoma and a median age of 67 years (interq
59 ere collected from 111 patients with primary open-angle glaucoma and an age-matched control group of
63 urgical algorithms for care in patients with open-angle glaucoma and coexistent cataract remain uncle
65 GN, SETTING, AND PARTICIPANTS: Patients with open-angle glaucoma and healthy controls were examined b
66 ntia, including Alzheimer's disease, primary open-angle glaucoma and Helicobacter pylori (H.pylori) i
69 NTG when compared with patients with primary open-angle glaucoma and nonglaucomatous control subjects
70 trabeculoplasty (SLT) as initial therapy for open-angle glaucoma and ocular hypertension and have dem
72 sc appearance used for the classification of open-angle glaucoma and ocular hypertension, significant
76 with an increased prevalence of all forms of open-angle glaucoma and OHTN, whereas hyperopia was asso
79 y 24-2 and 10-2 VFs in patients with primary open-angle glaucoma and to test the hypothesis that pati
80 aucoma Associates of Texas with uncontrolled open-angle glaucoma and underwent gonioscopy-assisted tr
82 is and pars plana vitrectomy, and 1 juvenile open-angle glaucoma) and 21 of 70 eyes with nonglaucomat
83 A total of 234 patients (104 with primary open angle glaucoma, and 130 control subjects without an
84 ntil death; 203 patients (65.7%) had primary open-angle glaucoma, and 106 patients (34.2%) had exfoli
85 entosa, while Bardet-Biedl syndrome, primary open-angle glaucoma, and tumor cell invasiveness are lin
86 le have a 2.5-fold increased risk of primary open-angle glaucoma as compared with those in the lowest
89 l, we enrolled patients with newly diagnosed open-angle glaucoma at ten UK centres (tertiary referral
90 essure in patients with primary or secondary open angle glaucomas, both as an initial therapy or in c
91 e uveitis, diabetic retinopathy, and primary open angle glaucoma, but its role in normal vision is la
93 en species play a pathogenic role in primary open angle glaucoma by fostering changes that reduce per
95 osterior sclera in a canine model of primary open-angle glaucoma caused by the G661R missense mutatio
96 s with a minimum 2-year diagnosis of primary open-angle glaucoma, chronic primary angle-closure glauc
97 in choroidal thickness of eyes with advanced open-angle glaucoma compared to that of fellow eyes with
98 In an institutional setting, a patient with open-angle glaucoma consented to be the recipient of the
99 with many ocular problems, such as secondary open angle glaucoma, corneal dysfunction, cataract, and
101 ERIA: participants with primary or secondary open-angle glaucoma (excluding uveitic) who had undergon
103 tively; by 30% and 22%, respectively, in the open-angle glaucoma group compared with the control grou
104 d mean amplitudes in ocular hypertension and open-angle glaucoma groups compared with the control gro
105 eculoplasty (LTP) is routinely used to treat open-angle glaucoma; hence, understanding variations in
106 rs investigated the genetic cause of primary open angle glaucoma in a large four-generation family wi
107 e was being followed and treated for primary open angle glaucoma in our tertiary referral center.
109 of LOXL1 play a significant role in primary open-angle glaucoma in the Caucasian, African-American,
110 specific risk factors and manifestations of open-angle glaucoma in this rapidly growing population.
111 contribute to the predisposition of primary open-angle glaucoma in various high-risk populations.
112 gle glaucoma (POAG) represent a continuum of open-angle glaucomas, in which a certain level of intrao
114 ed with progression of patients with primary open angle glaucoma is essential to our clinical practic
118 ar meshwork (TM) and the elevation of IOP in open-angle glaucoma is associated with dysfunction and l
123 llowing cataract surgery (GFCS) and juvenile open-angle glaucoma (JOAG) is variable and with relative
128 es with changing expression in this model of open-angle glaucoma may help elucidate the primary chang
129 < 0.001) in both eyes with incident primary open-angle glaucoma (mean, 10.6%; standard deviation, 22
131 umor samples were analyzed from 23 eyes with open angle glaucoma (OAG) undergoing glaucoma filtration
135 beculoplasty (SLT) on medically uncontrolled open-angle glaucoma (OAG) and to evaluate the effects of
136 d (VF) deterioration events in patients with open-angle glaucoma (OAG) by 50% over a 2-year period.
137 personalized forecasts of how patients with open-angle glaucoma (OAG) experience disease progression
139 This study determined the risk factors for open-angle glaucoma (OAG) in adults examined in the Nige
141 ice-daily timolol eye drops in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT) t
143 oprost ophthalmic solution, in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).
148 iagnosis; 20.0% (n = 330) were identified as open-angle glaucoma (OAG) suspects, 9.2% (n = 151) were
150 f Diseases (ICD-9-CM) diagnoses of cataract, open-angle glaucoma (OAG), nonexudative age-related macu
155 a major risk factor for the deterioration of open-angle glaucoma (OAG); medical IOP reduction is the
156 eroid use, myopia, socioeconomic status, and open-angle glaucoma (odds ratio [OR], 0.89; 95% confiden
157 ular hypertension, and patients with primary open angle glaucoma or primary angle closure glaucoma.
160 ication of Diseases, Ninth Revision, code of open-angle glaucoma or its related entities who underwen
162 tive cohort study of untreated patients with open-angle glaucoma or ocular hypertension at a hospital
163 l of 660 adults with a clinical diagnosis of open-angle glaucoma or ocular hypertension from a referr
166 eserved with PQ reduced IOP in patients with open-angle glaucoma or ocular hypertension who were into
169 y and effectively lower IOP in patients with open-angle glaucoma or ocular hypertension, showing sign
176 intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension; however, the
177 I, 1.31-10.13; P = .01), presence of primary open-angle glaucoma (OR, 3.82; 95% CI, 1.60-9.14; P = .0
178 beculectomy surgery in patients with primary open angle glaucoma over a 3-year period of follow-up.
179 ), more glaucoma suspects (p < 0.0001), more open angle glaucoma (p = 0.0006) and fewer other conditi
180 of glaucoma (P < .0001), and a diagnosis of open-angle glaucoma (P = .0003) were associated with inc
181 fold; n=20) in AH derived from human primary open angle glaucoma patients as compared to AH derived f
182 ve, observational cohort study that included open angle glaucoma patients with visually significant c
188 The study included patients with primary open angle glaucoma (POAG group, n = 30) and controls (n
189 12 normal controls, 7 patients with primary open angle glaucoma (POAG) and 9 patients with normal te
190 OPTN) are linked to the pathology of primary open angle glaucoma (POAG) and amyotrophic lateral scler
191 les frequencies in primary glaucoma [primary open angle glaucoma (POAG) and primary angle closure gla
192 changes of optic nerve in eyes with primary open angle glaucoma (POAG) by the joint use of optical c
193 tly associated with 6.0% of cases of primary open angle glaucoma (POAG) in patients from Oregon and G
194 oci have been associated with either primary open angle glaucoma (POAG) or heritable ocular quantitat
195 between groups of eyes differing in primary open angle glaucoma (POAG) outcome, how POAG was determi
196 (codon 72 Pro/Arg) and the subset of primary open angle glaucoma (POAG) patients with early loss of c
198 beagle model of autosomal recessive primary open angle glaucoma (POAG) to a 4-Mb interval on chromos
199 ns in the myocilin (MYOC) gene cause primary open angle glaucoma (POAG) with varying age-of-onset and
200 of 30.8 months, including 28 (4.4%) primary open angle glaucoma (POAG), 27 (4.2%) primary angle clos
201 jects were glaucomatous: (67 PXG, 42 Primary Open Angle Glaucoma (POAG), 28 PACG, 14 Normal Tension G
203 are the most common genetic cause of primary open angle glaucoma (POAG), but the mechanisms underlyin
204 defects also occur in patients with primary open angle glaucoma (POAG), in which there is specific R
205 netically complex disorders, such as primary open angle glaucoma (POAG), may include highly heritable
207 ic or glaucoma faculty patients with primary open angle glaucoma (POAG), ocular hypertension (OHTN),
208 n the aqueous humor of patients with primary open angle glaucoma (POAG), pseudoexfoliation syndrome (
211 cular meshwork (TM) of patients with primary open-angle glaucoma (POAG) and appears to contribute to
212 ssociation of known loci for IOP and primary open-angle glaucoma (POAG) and identify four new IOP-ass
214 ly examined the global prevalence of primary open-angle glaucoma (POAG) and primary angle-closure gla
215 meshwork (TM) height differs between primary open-angle glaucoma (POAG) and primary angle-closure gla
216 en implicated in the pathogenesis of primary open-angle glaucoma (POAG) based on elevated levels in g
217 age to the optic disc in humans with primary open-angle glaucoma (POAG) can be measured using a novel
218 s) endophthalmitis and risk of a new primary open-angle glaucoma (POAG) diagnosis within 365 days aft
219 ses (TIMPs) in the aqueous humour of primary open-angle glaucoma (POAG) eyes have been described.
220 a genome-wide association study for primary open-angle glaucoma (POAG) in 1,007 cases with high-pres
221 culoplasty (SLT) as sole therapy for primary open-angle glaucoma (POAG) in an Afro-Caribbean populati
222 k, CA) for treating mild-to-moderate primary open-angle glaucoma (POAG) in patients undergoing catara
223 DKN2B genes has been associated with primary open-angle glaucoma (POAG) in several independent studie
234 r for optic nerve damage in cases of primary open-angle glaucoma (POAG) is an increased intraocular p
235 The primary causative factor of primary open-angle glaucoma (POAG) is elevated intraocular press
237 venous pressure (RVP) in the eyes of primary open-angle glaucoma (POAG) patients and healthy subjects
238 difference in severity of disease in primary open-angle glaucoma (POAG) patients with a Myocilin (MYO
239 itary determination) was examined in primary open-angle glaucoma (POAG) patients with cataract and no
240 g can cause fibrosis of the TM as in primary open-angle glaucoma (POAG) patients, and is characterize
242 American Academy of Ophthalmology's Primary Open-angle Glaucoma (POAG) Preferred Practice Pattern (P
243 erature continues to be that NTG and primary open-angle glaucoma (POAG) represent a continuum of open
244 of aqueous humor from patients with primary open-angle glaucoma (POAG) revealed marked increases in
245 Economic viability of treatments for primary open-angle glaucoma (POAG) should be assessed objectivel
247 ce was 1.24% (95% CI, 1.14-1.34) for primary open-angle glaucoma (POAG), 0.39% (95% CI, 0.34-0.45) fo
249 egion previously was associated with primary open-angle glaucoma (POAG), although replication among i
250 the 4 forms of open-angle glaucoma: primary open-angle glaucoma (POAG), normal-tension glaucoma (NTG
261 pressure (IOP) in the evaluation of primary open-angle glaucoma (POAG); and to determine the feasibi
262 ODH) before and after development of primary open-angle glaucoma (POAG); determine the prognostic sig
263 ce interval, 3.3-5.4), consisting of primary open-angle glaucoma (POAG, 3.2%, including high-tension
265 ELINES: Evidence-based update of the Primary Open-Angle Glaucoma Preferred Practice Pattern(R) (PPP)
267 closure glaucoma (PACG); 1 of the 4 forms of open-angle glaucoma: primary open-angle glaucoma (POAG),
269 glandin analog eye drops in treating primary open-angle glaucoma, published between December 2000 and
270 0.77-0.80) and with increases in the odds of open-angle glaucoma ranging from 1.23 (95% CI, 1.20-1.26
271 involved diabetic macular edema and no prior open-angle glaucoma, repeated intravitreous injections o
275 osis and management of patients with primary open-angle glaucoma suspect with detailed recommendation
280 l-tension glaucoma (NTG) is a common form of open-angle glaucoma throughout the world, and yet there
281 etrospective case series of 81 patients with open-angle glaucoma undergoing 110 SLT procedures from N
284 mary glaucoma that had gonioscopy (n = 243), open-angle glaucoma was more common (86 %) than angle-cl
286 nical questions on the management of primary open-angle glaucoma were derived from practice guideline
289 study, healthy individuals and patients with open-angle glaucoma were prospectively enrolled between
290 itivity sometimes increases in patients with open-angle glaucoma when intraocular pressure (IOP) is d
291 ary 1, 2013, including patients with primary open-angle glaucoma who had a best-corrected visual acui
292 otal of 603 patients (603 eyes) with primary open-angle glaucoma who were using up to 3 glaucoma medi
293 ophotographs from 1 eye of 125 patients with open-angle glaucoma with >/=8 reliable Swedish interacti
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
299 posure is associated with increased risk for open angle glaucoma, yet population-based studies presen
300 as various ocular implications, most notably open angle glaucoma, zonular abnormalities, and cataract
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