Results 31 to 40 of about 2,091 (202)

DOTATATE Scan in Meningiomatosis in a Patient With Ophthalmoplegia

open access: yesCase Reports in Ophthalmological Medicine, Volume 2026, Issue 1, 2026.
DOTATATE (1,4,7,10‐tetraazacyclododecane‐1,4,7,10‐tetraacetic acid [DOTA]‐octreotate) is a compound that binds somatostatin receptors seen in tumors such as meningiomas. Here, we present a case of a patient with progressive bilateral ophthalmoplegia due to meningiomatosis involving both cavernous sinuses, which was highlighted by DOTATATE imaging. Some
Joshua Pasol   +3 more
wiley   +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  

Nonmydriatic Fundus Photography: A Practical Review for the Neurologist [PDF]

open access: yes, 2016
Declining proficiency in direct ophthalmoscopy by non-ophthalmologists has spurred a search for alternative methods of ocular fundus examination. Recent technological advances have improved the ease of use and quality of non-mydriatic fundus photography,
Bruce, Beau B., Mackay, Devin D.
core   +1 more source

Mainstream Artificial Intelligence Technologies in Contemporary Ophthalmology

open access: yesAdvanced Intelligent Systems, Volume 7, Issue 12, December 2025.
This review explores the latest artificial intelligence (AI) technologies in ophthalmology, focusing on four key data types: medical imaging, electronic health records, robotic‐assisted surgery, and genomics. It examines the structural features, use cases, clinical goals, and evaluation metrics of various AI algorithms, while also introducing emerging ...
Shiqi Yin   +9 more
wiley   +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  

Effects of Hypercholesterolaemia in the Retina [PDF]

open access: yes, 2012
© 2012 Triviño et al., licensee InTech. This is an open access chapter distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in
Gallego Collado, Beatriz Isabel   +6 more
core   +2 more sources

Automated registration of multimodal optic disc images: clinical assessment of alignment accuracy [PDF]

open access: yes, 2016
Purpose: To determine the accuracy of automated alignment algorithms for the registration of optic disc images obtained by 2 different modalities: fundus photography and scanning laser tomography.
Avadhanam, Venkat   +8 more
core   +1 more source

The rs10191329 Risk Allele Is Associated With Pronounced Retinal Layer Atrophy in Multiple Sclerosis

open access: yesAnnals of Clinical and Translational Neurology, Volume 12, Issue 11, Page 2226-2234, November 2025.
ABSTRACT Objective To investigate whether the rs10191329 risk allele in the DYSF–ZNF638 locus, which is implicated in central nervous system resilience rather than immune‐mediated pathology, is associated with retinal layer thinning, a biomarker of neuroaxonal damage in relapsing multiple sclerosis (RMS). Methods From a prospective observational study,
Gabriel Bsteh   +22 more
wiley   +1 more source

Proposal of a Simpler Eye‐Level Risk Model Incorporating Reticular Pseudodrusen for the Clinical Prediction of Late Age‐Related Macular Degeneration

open access: yesClinical &Experimental Ophthalmology, Volume 53, Issue 8, Page 936-945, November 2025.
ABSTRACT Background The updated simplified AREDS risk model predicts progression to late age‐related macular degeneration (AMD) by person, describing up to nine observations across both eyes and 10 annual risk scores (0–4, with/without reticular pseudodrusen [RPD]).
Matt Trinh   +8 more
wiley   +1 more source

Fundus wide subretinal and pigment epithelial abnormalities in macular telangiectasia type 2 [PDF]

open access: yes, 2017
Purpose: Macular telangiectasia Type 2 (MacTel) causes glial and photoreceptor cell death in a small, oval patch in the central retina. Beyond this oval area, no disease manifestations have been described so far.
Arnold   +21 more
core   +1 more source

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