Results 91 to 100 of about 22,596 (200)

Drusen drizzle

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

Quantum Machine Learning Applications to Medical Images: A Survey

open access: yesIET Quantum Communication, Volume 7, Issue 1, January/December 2026.
In this review paper, we provide an outline of quantum neural networks (QNNs), quantum convolution neural networks (QCNNs) and various hybrid models. We also explore human brain‐inspired quantum neuromorphic computing by the quantum spiking neural networks (QSNN).
Mahua Nandy Pal   +2 more
wiley   +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

Enhanced Depth Imaging Optical Coherence Tomography of Optic Nerve Head Drusen: A Comparison of Cases with and without Visual Field Loss [PDF]

open access: yes, 2017
PURPOSE: Enhanced depth imaging (EDI) spectral-domain optical coherence tomography (SD OCT) has been recognized as the most sensitive tool to diagnose optic nerve head drusen (ONHD).
Keane, PA   +4 more
core  

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

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  

Subthreshold Nanosecond Laser, from Trials to Real-Life Clinical Practice: A Cohort Study

open access: yesClinical Ophthalmology, 2021
Hasan Chichan,1,2 Matthias Maus,2,* Ludwig M Heindl1,3,* 1Department of Ophthalmology, University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, 50923, Germany; 2Sehkraft Eye Center, Cologne, 50667, Germany; 3Center for ...
Chichan H, Maus M, Heindl LM
doaj  

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

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

Spectral-Domain and Swept-Source OCT Angiographic Scans Yield Similar Drusen Measurements When Processed with the Same Algorithm

open access: yesOphthalmology Science
Purpose: An algorithm developed to obtain drusen area and volume measurements using swept-source OCT angiography (SS-OCTA) scans was tested on spectral-domain OCT angiography (SD-OCTA) scans. Design: Retrospective study.
Farhan E. Hiya, MD   +9 more
doaj   +1 more source

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