Results 21 to 30 of about 12,477 (204)

Near-infrared fundus autofluorescence-visualized melanin in the choroidal abnormalities of neurofibromatosis type 1 [PDF]

open access: yesClinical Ophthalmology, 2012
Tomoko Ueda-Consolvo, Akio Miyakoshi, Hironori Ozaki, Satoshi Houki, Atsushi HayashiDepartment of Ophthalmology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, JapanPurpose: To report a series of three cases of ...
Ueda-Consolvo T   +4 more
doaj   +1 more source

A review of fundus autofluorescence imaging [PDF]

open access: yesAfrican Vision and Eye Health, 2013
Autofluorscence photography of the retina provides important diagnostic information about diseases that affect the outer retina; more specifically the retinal pigment epithelium and photoreceptors.
D. J. Booysen
doaj   +3 more sources

Fundus autofluorescence in detection of embolus in retinal artery occlusion

open access: yesIndian Journal of Ophthalmology. Case Reports, 2022
Fundus autofluorescence (FAF) is a noninvasive imaging tool helpful in various retinal and choroidal diseases. In this series, we report the utility of FAF in two cases of retinal artery occlusion (RAO).
Pradeep Sagar   +2 more
doaj   +1 more source

The Diagnostic Role of Multimodal Imaging Techniques in Isolated Foveal Hypoplasia [PDF]

open access: yesTürk Oftalmoloji Dergisi, 2017
To report a case of bilateral isolated foveal hypoplasia in which multimodal imaging was used to confirm the diagnosis. Fundus autofluorescence imaging, optical coherence tomography (OCT), and fundus fluorescein angiography were used to describe the ...
Figen Batıoğlu   +4 more
doaj   +1 more source

The Use of Fundus Autofluorescence in Dry Age-Related Macular Degeneration [PDF]

open access: yes, 2021
Fundus autofluorescence (FAF) has been a well-known imaging method for quite some time. However, with developing technologies and novel imaging devices, FAF is being used more often to diagnose and monitor retinal diseases. The density of lipofuscin (LF)
Nedime Şahinoğlu Keşkek   +1 more
core   +1 more source

Frequency and risk factors for hydroxychloroquine retinopathy among patients with systemic lupus erythematosus

open access: yesThe Egyptian Journal of Internal Medicine, 2021
Background Hydroxychloroquine (HCQ) is an antimalarial drug, recently used in COVID-19 treatment. Also it is considered over many years the cornerstone in treating systemic lupus erythematosus (SLE) in adults and children.
Mohammed Salah Eldin Abdelbaky   +3 more
doaj   +1 more source

Autofluorescence indexes as biomarkers for antiangiogenic loading dose outcome in diabetic macular edema

open access: yesTherapeutic Advances in Ophthalmology, 2020
Purpose: To evaluate the combination of fundus autofluorescence results with several clinical and structural variables into mathematical indexes to enhance their ability to predict visual and anatomical changes after the antivascular endothelial growth ...
Sergio E. Hernández Da Mota   +6 more
doaj   +1 more source

Bilateral pigmented paravenous chorioretinal atrophy in a patient with tuberculosis – A case report

open access: yesTNOA Journal of Ophthalmic Science and Research, 2022
Pigmented paravenous chorioretinal atrophy (PPCRA) refers to unilateral or bilateral pigmentation along retinal veins with changes on fundus autofluorescence and electroretinography (ERG).
Sanyukta Joshi   +2 more
doaj   +1 more source

Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence

open access: yesMolecular Genetics & Genomic Medicine, 2022
Introduction Leber congenital amaurosis (LCA) type 2, due to disease‐causing variants in RPE65, is characterized by severe visual loss in early infancy. Current treatments include voretigene neparvovec‐rzyl (VN) for RPE65‐associated LCA.
Masha Kolesnikova   +6 more
doaj   +1 more source

CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD. [PDF]

open access: yes, 2009
Age-related macular degeneration (AMD) is a prevalent cause of blindness in Western societies. Variants in the genes encoding complement factor H (CFH), complement component 3 (C3) and age-related maculopathy susceptibility 2 (ARMS2) have repeatedly been
Weber, Bernhard H. F.   +68 more
core   +1 more source

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