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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.
41          The 5 most prevalent diagnoses were open-angle glaucoma (1.61%), exfoliation glaucoma (0.20%
42                          In 30 patients with open-angle glaucoma, 1 eye (median mean deviation [MD],
43          Thirty subjects under treatment for open-angle glaucoma, 23 subjects with ocular hypertensio
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
47 ecular meshwork is a primary risk factor for open-angle glaucoma, a leading cause of blindness.
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
50                      Inclusion criteria were open-angle glaucoma, age >/= 40 years, and uncontrolled
51                               Treatments for open-angle glaucoma aim to prevent vision loss through l
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
54 h Weill-Marchesani-like syndrome and primary open angle glaucoma and ectopia lentis in dogs.
55 e patient with choroidal infarction, primary open angle glaucoma and Flammer syndrome.
56                                 29 eyes with open angle glaucoma and visual field defects, as well as
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
60 anuary 2000 and September 2013 on the topics open-angle glaucoma and angle-closure glaucoma.
61 otal of 609 patients (609 eyes) with primary open-angle glaucoma and cataract were included.
62 rther suggest a lack of relationship between open-angle glaucoma and choroidal thickness.
63 urgical algorithms for care in patients with open-angle glaucoma and coexistent cataract remain uncle
64          A 75-year-old pseudophakic man with open-angle glaucoma and diabetic retinopathy developed n
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
67 h CCT has been implicated, including primary open-angle glaucoma and keratoconus.
68        Consecutive trabeculectomy cases with open-angle glaucoma and no previous incisional glaucoma
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
71            All patients with newly diagnosed open-angle glaucoma and ocular hypertension were include
72 sc appearance used for the classification of open-angle glaucoma and ocular hypertension, significant
73 rine transporter inhibitor, in patients with open-angle glaucoma and ocular hypertension.
74 he diurnal, but not the nocturnal, period in open-angle glaucoma and ocular hypertension.
75 r lens implantation in patients with primary open-angle glaucoma and ocular hypertension.
76 with an increased prevalence of all forms of open-angle glaucoma and OHTN, whereas hyperopia was asso
77             One eye per patient with primary open-angle glaucoma and stable intraocular pressure (IOP
78           Glaucoma surveillance in eyes with open-angle glaucoma and statistically normal IOP should
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
81                                Patients with open-angle glaucoma and VFs obtained from reliable exami
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
87      These mice may be useful as a model for open-angle glaucoma, as well as for assessing the relati
88            To determine the stage of primary open angle glaucoma at presentation at a tertiary eye un
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
92      Genetic studies have linked myocilin to open angle glaucoma, but the functions of the protein in
93 en species play a pathogenic role in primary open angle glaucoma by fostering changes that reduce per
94                        However, in eyes with open angle glaucoma, cataract surgery alone may be of li
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
100               Myocilin, a causative gene for open angle glaucoma, encodes a secreted glycoprotein wit
101 ERIA: participants with primary or secondary open-angle glaucoma (excluding uveitic) who had undergon
102  hundred seven patients with newly diagnosed open-angle glaucoma from the CIGTS.
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.
108  benefits and harms of screening for primary open-angle glaucoma in adults.
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
113          It may also be important in primary open angle glaucoma influencing aqueous outflow.
114 ed with progression of patients with primary open angle glaucoma is essential to our clinical practic
115 1 single-nucleotide polymorphism and primary open angle glaucoma is found.
116                                      Primary open angle glaucoma is the most prevalent type of glauco
117                                    Secondary open-angle glaucoma is a complication of Nd:YAG vitreoly
118 ar meshwork (TM) and the elevation of IOP in open-angle glaucoma is associated with dysfunction and l
119                                      Primary open-angle glaucoma is characterized by increased resist
120                                      Primary open-angle glaucoma is the second leading cause of blind
121 14 Normal Tension Glaucoma (NTG), 5 Juvenile Open Angle Glaucoma (JOAG) and 6 (OHT).
122                                     Juvenile open-angle glaucoma (JOAG) is a severe neurodegenerative
123 llowing cataract surgery (GFCS) and juvenile open-angle glaucoma (JOAG) is variable and with relative
124 ntain any of the previously reported primary open angle glaucoma loci.
125          This study identifies a new primary open angle glaucoma locus, GLC1Q, in a region on chromos
126          Medical and surgical treatments for open-angle glaucoma lower intraocular pressure and reduc
127 ollowing cataract surgery alone in eyes with open angle glaucoma may be limited and transient.
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
130 (MetS) with intraocular pressure and primary open angle glaucoma (OAG) have been reported.
131 umor samples were analyzed from 23 eyes with open angle glaucoma (OAG) undergoing glaucoma filtration
132                         However, the risk of open-angle glaucoma (OAG) among patients with OSA remain
133 aluate the longitudinal relationship between open-angle glaucoma (OAG) and incident dementia.
134                                        Coded open-angle glaucoma (OAG) and OAG suspects accounted for
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
138 ection between ocular perfusion pressure and open-angle glaucoma (OAG) has been hypothesized.
139   This study determined the risk factors for open-angle glaucoma (OAG) in adults examined in the Nige
140                                              Open-angle glaucoma (OAG) is associated with systemic me
141 ice-daily timolol eye drops in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT) t
142          In randomized, controlled trials of open-angle glaucoma (OAG) or ocular hypertension (OHT),
143 oprost ophthalmic solution, in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).
144        Sequential surgical cases of juvenile open-angle glaucoma (OAG) or primary congenital glaucoma
145      Nine patients had previous diagnoses of open-angle glaucoma (OAG) or suspected glaucoma.
146 lective laser trabeculoplasty (SLT) in early open-angle glaucoma (OAG) patients.
147 iciary person-years and per 10,000 diagnosed open-angle glaucoma (OAG) person-years.
148 iagnosis; 20.0% (n = 330) were identified as open-angle glaucoma (OAG) suspects, 9.2% (n = 151) were
149 or visual field progression in patients with open-angle glaucoma (OAG) were eligible.
150 f Diseases (ICD-9-CM) diagnoses of cataract, open-angle glaucoma (OAG), nonexudative age-related macu
151 ty affect receipt of common tests to monitor open-angle glaucoma (OAG).
152 tect against the development or worsening of open-angle glaucoma (OAG).
153  coherence tomography (OCT) volume scans for open-angle glaucoma (OAG).
154 is an alternative to topical medications for open-angle glaucoma (OAG).
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.
158 s who have one of the two forms of glaucoma: open-angle glaucoma or angle-closure glaucoma.
159 were obtained in 57 eyes of 57 subjects with open-angle glaucoma or glaucoma suspicion.
160 ication of Diseases, Ninth Revision, code of open-angle glaucoma or its related entities who underwen
161                   Total of 233 patients with open-angle glaucoma or ocular hypertension and with mean
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
164                          Forty subjects with open-angle glaucoma or ocular hypertension were admitted
165         A total of 560 patients with primary open-angle glaucoma or ocular hypertension who had insuf
166 eserved with PQ reduced IOP in patients with open-angle glaucoma or ocular hypertension who were into
167                                Patients with open-angle glaucoma or ocular hypertension who were into
168                             In patients with open-angle glaucoma or ocular hypertension, polyquaterni
169 y and effectively lower IOP in patients with open-angle glaucoma or ocular hypertension, showing sign
170 rz/brim/tim in Mexican patients with primary open-angle glaucoma or ocular hypertension.
171 during late-day time points in patients with open-angle glaucoma or ocular hypertension.
172 ts of glaucoma, but also in individuals with open-angle glaucoma or ocular hypertension.
173 Eligible patients were adults diagnosed with open-angle glaucoma or ocular hypertension.
174  0.005% (50 mug/mL) in patients with primary open-angle glaucoma or ocular hypertension.
175                          Adult patients with open-angle glaucoma or ocular hypertension.
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
183               At baseline following washout, open-angle glaucoma patients (n = 75) were administered
184                                              Open-angle glaucoma patients without prior incisional gl
185  of TGF-beta2 has been found in many primary open-angle glaucoma patients.
186  paracentral visual field defects in primary open-angle glaucoma patients.
187 rgets after a first failed trabeculectomy in open-angle glaucoma patients.
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
197                  Control TM and most primary open angle glaucoma (POAG) TM were collected from cadave
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
202                                      Primary open angle glaucoma (POAG), a major cause of blindness w
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
206                     The mean IOP for primary open angle glaucoma (POAG), ocular hypertension (OHT), n
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 (
209  several characteristics observed in primary open angle glaucoma (POAG).
210 ied 61 patients (80 procedures) with primary open angle glaucoma (POAG).
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
213 ize the role of osteopontin (OPN) in primary open-angle glaucoma (POAG) and normal eyes.
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
224                                      Primary open-angle glaucoma (POAG) is a blinding disease.
225                                      Primary open-angle glaucoma (POAG) is a complex disease with a g
226                                      Primary open-angle glaucoma (POAG) is a genetically complex comm
227                                      Primary open-angle glaucoma (POAG) is a genetically complex neur
228                                      Primary open-angle glaucoma (POAG) is a highly prevalent conditi
229                                      Primary open-angle glaucoma (POAG) is a leading cause of blindne
230                                      Primary open-angle glaucoma (POAG) is a leading cause of irrever
231                                      Primary open-angle glaucoma (POAG) is a leading cause of irrever
232                                      Primary open-angle glaucoma (POAG) is a major cause of blindness
233                                      Primary open-angle glaucoma (POAG) is a major cause of irreversi
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
236                                      Primary open-angle glaucoma (POAG) is the second leading cause o
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
241 s in ocular hypertensive (OH) and in primary open-angle glaucoma (POAG) patients.
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
246                  The beagle model of primary open-angle glaucoma (POAG) was used to correlate ANGPTL7
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
248               We studied 1 eye of 63 primary open-angle glaucoma (POAG), 30 ocular hypertension (OH),
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
251                                      Primary open-angle glaucoma (POAG), the most common optic neurop
252                 In cadaver eyes with primary open-angle glaucoma (POAG), TSP1 is increased in one thi
253  a secondary glaucoma that resembles primary open-angle glaucoma (POAG).
254 at PMH use may decrease the risk for primary open-angle glaucoma (POAG).
255 TM, similar to those associated with primary open-angle glaucoma (POAG).
256 e most common known genetic cause of primary open-angle glaucoma (POAG).
257 orders of blindness, with a focus on primary open-angle glaucoma (POAG).
258  population-specific genetic risk of primary open-angle glaucoma (POAG).
259 nction, which has been implicated in primary open-angle glaucoma (POAG).
260 low autoregulation are implicated in primary open-angle glaucoma (POAG).
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
264 -2013) to estimate effects of T2D on primary open-angle glaucoma (POAG; 3,554 cases).
265 ELINES: Evidence-based update of the Primary Open-Angle Glaucoma Preferred Practice Pattern(R) (PPP)
266                                      PRIMARY OPEN-ANGLE GLAUCOMA PREFERRED PRACTICE PATTERN(R) GUIDEL
267 closure glaucoma (PACG); 1 of the 4 forms of open-angle glaucoma: primary open-angle glaucoma (POAG),
268 ify possible risk factors leading to primary open angle glaucoma progression and blindness.
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
272                                Patients with open-angle glaucoma (Shaffer Grade 3 and 4) and uncontro
273                                           In open-angle glaucoma, substantial RNFL thinning or struct
274                                      PRIMARY OPEN-ANGLE GLAUCOMA SUSPECT PREFERRED PRACTICE PATTERN(R
275 osis and management of patients with primary open-angle glaucoma suspect with detailed recommendation
276                  In 57 patients with primary open-angle glaucoma, the IOP decreased by 7.7 mmHg (stan
277                         In the subjects with open-angle glaucoma, the pattern ERG P50-N95 was found t
278                     Risk factors for primary open-angle glaucoma-the most common form of glaucoma-inc
279 or cataract surgery is 4500% and for medical open-angle glaucoma therapy is 4000%.
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
282         Lucia with medically treated primary open-angle glaucoma underwent a 30-day washout, followed
283                    The prevalence of primary open-angle glaucoma was 6.8% overall, increasing from 3.
284 mary glaucoma that had gonioscopy (n = 243), open-angle glaucoma was more common (86 %) than angle-cl
285                                      Primary open-angle glaucoma was the underlying diagnosis in 342
286 nical questions on the management of primary open-angle glaucoma were derived from practice guideline
287 s) with ocular hypertension or early primary open-angle glaucoma were enrolled.
288            Two hundred and six patients with open-angle glaucoma were examined at 4-month intervals w
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
298 FS) is the most common recognizable cause of open-angle glaucoma worldwide.
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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