Results 121 to 130 of about 32,629 (301)

Retinal biomarkers in cognitive impairment and dementia: Structural, functional, and molecular insights

open access: yesAlzheimer's &Dementia, Volume 21, Issue 9, September 2025.
Abstract Cognitive impairment and dementia, including Alzheimer's disease (AD), pose a global health crisis, necessitating non‐invasive biomarkers for early detection. This review highlights the retina, an accessible extension of the central nervous system (CNS), as a window to cerebral pathology through structural, functional, and molecular ...
Yan Min   +3 more
wiley   +1 more source

Retinal Angiomatous Proliferation in an Eye with Cuticular Drusen

open access: yesCase Reports in Ophthalmology, 2015
Purpose: To report the presence of retinal angiomatous proliferation (RAP) in an eye with cuticular drusen detected by fluorescein and indocyanine green angiography by confocal scanning laser ophthalmoscopy and by spectral-domain optical coherence ...
Atsuko Sato   +3 more
doaj   +1 more source

Optic disc drusen in children: morphologic features using EDI-OCT

open access: yesEye, 2019
This study aimed to investigate morphologic features of optic disc drusen (ODD) and peripapillary hyperreflective ovoid mass-like structures (PHOMS) in children, using enhanced depth imaging optical coherence tomography (EDI-OCT). It also assessed if the
F. Teixeira   +4 more
semanticscholar   +1 more source

Drusen drizzle

open access: yesIndian Journal of Ophthalmology, 2023
Praveena Venkatakrishnan   +2 more
openaire   +3 more sources

Association of Optic Nerve Head Drusen with Best Vitelliform Macular Dystrophy: A Case Series

open access: yesCase Reports in Ophthalmology, 2018
Purpose: To report the association of optic nerve head (ONH) drusen with Best vitelliform macular dystrophy (BVMD). Methods: Chart review. Patients: Five patients from 3 families.
Robert J. White   +3 more
doaj   +1 more source

Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers. [PDF]

open access: yes, 2016
PurposeWe determined the phenotypic variation, disease progression, and potential modifiers of autosomal dominant retinal dystrophies caused by a splice site founder mutation, c.828+3A>T, in the PRPH2 gene.MethodsA total of 62 individuals (19 families)
Birch, David G   +7 more
core  

INFLUENCE OF OPTIC NERVE DRUSEN ON VISUAL FUNCTIONS IN CHILDREN AND ADOLESCENTS WITH ESSENTIAL ARTERIAL HYPERTENSION

open access: yesActa Biomedica Scientifica, 2016
The article presents data examination of children and male adolescents, aged 8 to 17 years without eye pathologies, with primary hypertension diagnosis - established at the clinic of Scientific Centre for Family Health and Human Reproduction Problems ...
A. G. Shchuko   +3 more
doaj   +1 more source

Drusen Volume as a Predictor of Disease Progression in Patients With Late Age-Related Macular Degeneration in the Fellow Eye.

open access: yesInvestigative Ophthalmology and Visual Science, 2016
PURPOSE Increasing drusen volume was proposed to be a predictor of disease progression in age-related macular degeneration (AMD). In patients with late AMD in one eye, the fellow eyes without neovascularization are known to be at higher risk of ...
N. Abdelfattah   +6 more
semanticscholar   +1 more source

Peptide redesign for inhibition of the complement system: Targeting age-related macular degeneration. [PDF]

open access: yes, 2016
PurposeTo redesign a complement-inhibiting peptide with the potential to become a therapeutic for dry and wet age-related macular degeneration (AMD).MethodsWe present a new potent peptide (Peptide 2) of the compstatin family.
Cabrera, Andrea P   +6 more
core   +1 more source

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