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1 t of 3 consecutive abnormal visual fields on standard automated perimetry.
2 in optical coherence tomography (SD-OCT) and standard automated perimetry.
3 rimetric sensitivity for reliable testing by standard automated perimetry.
4 high-risk ocular hypertension and performed standard automated perimetry.
5 ent, gonioscopy, dilated ophthalmoscopy, and standard automated perimetry.
6 Visual fields were obtained with standard automated perimetry.
7 re evaluated by the mean deviation (MD) from standard automated perimetry.
8 ased on visual field index (VFI) values from standard automated perimetry.
9 d based on the visual field index (VFI) from standard automated perimetry.
10 ared against an existing standard technique--standard automated perimetry.
11 ices are available to summarize results from standard automated perimetry.
12 System and also by mean deviation (MD) from standard automated perimetry.
13 aluated with all three tests as well as with standard automated perimetry.
14 ather than based on isolated parameters from standard automated perimetry (8.5%) or optical coherence
16 coma were examined at 4-month intervals with standard automated perimetry and confocal scanning laser
18 Estimates of RGC counts were obtained from standard automated perimetry and optical coherence tomog
20 having repeatable visual field defects with standard automated perimetry) and 189 subjects without g
21 pants underwent a full clinical examination, standard automated perimetry, and imaging with time-doma
22 complete examination, including gonioscopy, standard automated perimetry, and stereoscopic optic dis
24 Algorithm is replacing Full-Threshold as the standard automated perimetry gold-standard strategy, and
25 ptic disc stereophotograph assessment and/or standard automated perimetry guided progression analysis
26 ten based on pointwise sensitivity data from standard automated perimetry; however, frequency-of seei
30 41 eyes with moderate to advanced glaucoma (standard automated perimetry mean deviation </=-8 dB) wa
31 The subjects were examined annually with standard automated perimetry, optic disc stereophotograp
32 HT with four or more visual field tests with standard automated perimetry over three or more years an
34 reliability indices to judge the quality of standard automated perimetry results are fixation losses
37 omplete ophthalmologic examination including standard automated perimetry, retinal nerve fiber layer
38 ely determine how the reliability indices in standard automated perimetry (SAP) affect the global ind
39 Subjects were longitudinally monitored with standard automated perimetry (SAP) and confocal scanning
40 nd intertest variability components for both standard automated perimetry (SAP) and frequency-doublin
42 (GAT; 45, 95% CrI 17-68), whereas threshold standard automated perimetry (SAP) and Heidelberg Retina
46 ionnaire (NEI VFQ-25) performed annually and standard automated perimetry (SAP) at 6-month intervals.
47 ionnaire (NEI VFQ)-25 performed annually and standard automated perimetry (SAP) at 6-month intervals.
50 were eligible, full threshold, pattern 24-2, standard automated perimetry (SAP) examinations (Humphre
51 was shown to segment clusters of patterns in standard automated perimetry (SAP) for glaucoma in previ
52 covariates TSS; disease severity, defined as standard automated perimetry (SAP) mean deviation [MD];
53 cal scanning laser ophthalmoscope (CSLO) and standard automated perimetry (SAP) measurements analyzed
54 cted to investigate the relationship between standard automated perimetry (SAP) measures of RGCs and
55 ified as glaucomatous by repeatable abnormal standard automated perimetry (SAP) or progressive glauco
58 participants underwent at least one reliable standard automated perimetry (SAP) test, while RNFL meas
59 oherence tomography (OCT) RNFL thickness and standard automated perimetry (SAP) visual field loss wer
65 r different rates of visual field loss using standard automated perimetry (SAP) when considering diff
67 ionship between visual function, measured by standard automated perimetry (SAP), and retinal nerve fi
70 ltifocal visual evoked potential (mfVEP) and standard automated perimetry (SAP), in eyes with high-ri
73 repeatable (either two or three consecutive) standard automated perimetry (SAP)-detected abnormalitie
79 Patients were examined every 4 months with standard automated perimetry (SAP, SITA Standard, 24-2 t
80 e tested on HRT II, StratusOCT, GDx VCC, and standard automated perimetry (SAP, with the Swedish Inte
81 esults in a Glaucoma Hemifield Test [GHT] on standard automated perimetry [SAP] 24-2 fields) and RNFL
82 the Guided Progression Analysis software for standard automated perimetry [SAP] and by masked assessm
83 rmalities (GS: mean age 56.6 +/- 13.8 years, standard automated perimetry [SAP] mean deviation [MD] -
84 retest variability of four perimetry tests: standard automated perimetry size III (SAP III), with th
85 cipate in a prospective evaluation including standard automated perimetry, spectral-domain optical co
86 pecific perimetry may be influenced by which standard automated perimetry technique is used as the re
87 pillary responses were evaluated relative to standard automated perimetry testing (Humphrey Visual Fi
88 coherence tomography (OCT) of the RNFL, and standard automated perimetry testing at 6-month interval
90 up for an average of 4.5 +/- 0.8 years with standard automated perimetry visual fields and optical c
91 y were consecutively recruited and underwent standard automated perimetry, visual acuity measurement,
94 n-EDI) and EDI modes, ultrasound B-scan, and standard automated perimetry were performed on both eyes
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