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1 t, visibility on funduscopy, ultrasound, and fundus autofluorescence.
2 ation plots), SD-OCT, and sometimes mfERG or fundus autofluorescence.
3 ger wavelengths, a characteristic typical of fundus autofluorescence.
4 n retinal diseases characterized by aberrant fundus autofluorescence.
5 g the growth of atrophic lesions measured by fundus autofluorescence.
6 diameter of a paracentral ring of increased fundus autofluorescence.
7 cidence of atrophic lesions as determined by fundus autofluorescence.
8 ral-domain optical coherence tomography, and fundus autofluorescence.
12 visual acuity (BCVA), widefield angiography, fundus autofluorescence (AF), and wnt signaling pathway
13 surements using two techniques (2-wavelength fundus autofluorescence [AF] and heterochromatic flicker
14 main optical coherence tomography (OCT), and fundus autofluorescence analysis were performed in patie
16 and optical coherence tomography (along with fundus autofluorescence and multifocal electroretinograp
17 ence tomography features and staging system, fundus autofluorescence and near-infrared reflectance fe
20 derwent best-corrected visual acuity (BCVA), fundus autofluorescence and spectral domain-optical cohe
21 e evaluated the multimodal imaging including fundus autofluorescence and spectral-domain optical cohe
22 ed the foveal attenuation normally seen with fundus autofluorescence, and a concentric macular rings
23 infrared reflectance, hypoautofluorescent on fundus autofluorescence, and as subretinal deposits on s
24 ptic nerve head (ONH), infrared reflectance, fundus autofluorescence, and color fundus photographs (C
26 color photography, fluorescein angiography, fundus autofluorescence, and high-resolution optical coh
27 ncluding optical coherence tomography (OCT), fundus autofluorescence, and indocyanine green and fluor
28 l field, and full-field electroretinography, fundus autofluorescence, and optical coherence tomograph
30 color photography, fluorescein angiography, fundus autofluorescence, and optical coherence tomograph
32 ering) could produce a cross-shaped increase fundus autofluorescence artifact on subsequent imaging.
33 ral color fundus and optic disc photography, fundus autofluorescence, automated perimetry, and optica
36 visual acuity with ETDRS charts, blue-light fundus autofluorescence, (BL-FAF), near-infrared fundus
37 o short-wavelength light resulted in reduced fundus autofluorescence, decreased HPLC-quantified A2E,
41 he enlargement of the atrophic lesions using fundus autofluorescence (FAF) and color fundus photograp
42 coherence tomography (OCT), OCT-Angiography, fundus autofluorescence (FAF) and fluorescein-angiograph
43 almoscopy, and fundus photography, including fundus autofluorescence (FAF) and near-infrared reflecta
44 basis of full-field electroretinogram (ERG) Fundus autofluorescence (FAF) and spectral domain-optica
45 jective corroboration for visual fields, and fundus autofluorescence (FAF) can show damage topographi
52 s photography, optical coherence tomography, fundus autofluorescence (FAF) imaging, and audiologic an
53 l-domain optical coherence tomography (OCT), fundus autofluorescence (FAF) imaging, full-field electr
55 l-domain optical coherence tomography (OCT), fundus autofluorescence (FAF) imaging, Humphrey visual f
56 s photography, fluorescein angiography (FA), fundus autofluorescence (FAF) imaging, optical coherence
57 us photography, near-infrared (NIR) imaging, fundus autofluorescence (FAF) imaging, spectral domain o
58 logic examination, color fundus photography, fundus autofluorescence (FAF) imaging, spectral-domain (
60 thalmologic examination, fundus photography, fundus autofluorescence (FAF) imaging, spectral-domain o
67 contribution of retro-mode imaging (RMI) and fundus autofluorescence (FAF) to the characterization of
68 omain optical coherence tomography (SD OCT), fundus autofluorescence (FAF), and fluorescein angiograp
69 rimetry, optical coherence tomography (OCT), fundus autofluorescence (FAF), and fundus photography.
70 omain optical coherence tomography (SD-OCT), fundus autofluorescence (FAF), and infrared reflectance
71 with conventional multimodal imaging (color, fundus autofluorescence (FAF), and infrared reflectance
72 ear-infrared (NIR) and short-wavelength (SW) fundus autofluorescence (FAF), and NIR reflectance (REF)
73 ompared with automated visual fields (AVFs), fundus autofluorescence (FAF), and optical coherence tom
75 tion together with color fundus photography, fundus autofluorescence (FAF), and spectral-domain optic
76 ude color fundus photography (CFP), confocal fundus autofluorescence (FAF), confocal near-infrared re
77 plete ophthalmological examination including fundus autofluorescence (FAF), dynamic simultaneous fluo
78 undus examination, color fundus photographs, fundus autofluorescence (FAF), fluorescein angiography (
79 (BCVA), ophthalmoscopy, fundus photography, fundus autofluorescence (FAF), fluorescein angiography (
80 ct ophthalmoscopy, color fundus photography, fundus autofluorescence (FAF), high-resolution optical c
81 thalmologic examination, fundus photography, fundus autofluorescence (FAF), infrared imaging, and spe
82 chart, fundus photography, ultrasonography, fundus autofluorescence (FAF), infrared reflectance (IR)
83 ng best-corrected visual acuity (BCVA), blue fundus autofluorescence (FAF), near-infrared autofluores
84 uding color and red-free fundus photography, fundus autofluorescence (FAF), near-infrared reflectance
85 fundus photography, fluorescein angiography, fundus autofluorescence (FAF), near-infrared reflectance
86 omain optical coherence tomography (SD OCT), fundus autofluorescence (FAF), or multifocal electroreti
87 uscin accumulation, as measured by increased fundus autofluorescence (FAF), precedes progression or d
88 visits for at least 1 examination modality: fundus autofluorescence (FAF), spectral-domain (SD) opti
89 gment epithelium (RPE) is the main source of fundus autofluorescence (FAF), the target of an imaging
99 fundus imaging, including color photographs, fundus autofluorescence, fluorescein angiography, and in
100 r detachments based on clinical examination, fundus autofluorescence, fluorescein angiography, and op
101 ubmaculopathy based on clinical examination, fundus autofluorescence, fluorescein angiography, and sp
102 ation, fundus photography, infrared imaging, fundus autofluorescence, fluorescein angiography, and sp
105 reen angiography, near-infrared reflectance, fundus autofluorescence, high-resolution OCT, and ultraw
106 east 1 eye at the most recent visit, and (2) fundus autofluorescence images for at least 2 visits wit
109 these patients, 215 had at least 2 gradable fundus autofluorescence images with atrophic lesion(s) p
110 tofluorescent AZOOR line in short-wavelength fundus autofluorescence images, delineating the peripapi
111 fundus examination, Goldmann visual fields, fundus autofluorescence imaging (FAF), optical coherence
113 responded to hyperautofluorescent lesions on fundus autofluorescence imaging and subretinal hyperrefl
115 a normal retinal appearance, although their fundus autofluorescence imaging demonstrated foci of inc
121 elength reduced-illuminance and conventional fundus autofluorescence imaging showed good concordance
124 graphy (CFP), near-infrared reflectance, and fundus autofluorescence imaging were performed in all pa
125 uorescein and indocyanine green angiography, fundus autofluorescence imaging, and corresponding eye-t
126 l-domain optical coherence tomography (OCT), fundus autofluorescence imaging, and electroretinogram (
127 eld electroretinography, fundus photography, fundus autofluorescence imaging, and optical coherence t
128 clinically by wide-field color photography, fundus autofluorescence imaging, and spectral-domain opt
129 linical examination, fundus photography, and fundus autofluorescence imaging, and visual function was
130 and detailed retinal imaging was performed: fundus autofluorescence imaging, digital color fundoscop
131 tance, red-free images and blue reflectance, fundus autofluorescence imaging, indocyanine green angio
132 fundus examination, wide-field photography, fundus autofluorescence imaging, sedated electroretinogr
143 We assessed the utility of quantification of fundus autofluorescence in the evaluation and follow-up
144 Most importantly, we also observed reduced fundus autofluorescence in the eyes injected with NP and
145 chart, fundus photography, ultrasonography, fundus autofluorescence, infrared reflectance (IR) imagi
146 ield and pattern), visual evoked potentials, fundus autofluorescence IRR, and optical coherence tomog
150 In Stargardt disease with DDAF lesions, fundus autofluorescence may serve as a monitoring tool f
151 pectral-domain optical coherence tomography, fundus autofluorescence, multifocal electroretinography,
154 graphy (OCT), en face near-infrared imaging, fundus autofluorescence, optical coherence tomography an
157 length fundus autofluorescence (quantitative fundus autofluorescence [qAF]) and spectral-domain optic
158 ndus lesions by quantifying short-wavelength fundus autofluorescence (quantitative fundus autofluores
160 ite 10-2 visual field pattern density plots, fundus autofluorescence, spectral-density optical cohere
162 idenced by HPLC analysis and quantitation of fundus autofluorescence; this effect is consistent with
164 aluate the disease extent on ultra-widefield fundus autofluorescence (UWF-FAF) in patients with ABCA4
165 CI, 0.42-0.61 mm2/y), and of total decreased fundus autofluorescence was 0.35 mm2/y (95% CI, 0.28-0.4
166 f patients exhibiting annular RPE lesions on fundus autofluorescence was included for chart review an
170 uding optical coherence tomography (OCT) and fundus autofluorescence were evaluated at the baseline a
171 tients, and optical coherence tomography and fundus autofluorescence were performed in 4 patients.
172 ncluding near-infrared (NIR) reflectance and fundus autofluorescence with a confocal scanning laser o
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