Results 21 to 30 of about 12,355 (175)

Clinical, electroretinographic and histomorphometric evaluation of the retina in sheep with natural scrapie

open access: yesBMC Veterinary Research, 2011
Background The retina is part of the diencephalon in a peripheral location and may be involved in prion diseases. Retinal function and structural changes were assessed in naturally scrapie-affected red face Manech ewes presenting the classical signs of ...
Toutain Pierre-Louis   +5 more
doaj   +1 more source

Ophthalmic Bioengineering. Review

open access: yesOftalʹmologiâ, 2023
This article published the materials of the round table “Bioengineering in ophthalmology” (OphthalmicBioengineering), held on May 13, 2021 as part of the international conference Ural Symposium on Biomedical Engineering, Radioelectronics and Information ...
V. O. Ponomarev   +11 more
doaj   +1 more source

Comparison of structural and functional tests in primary open angle glaucoma

open access: yesIndian Journal of Ophthalmology, 2020
Purpose: To comparatively analyze the structural and functional tests used in the diagnosis and follow-up of glaucoma. Methods: Eighty eyes of 40 patients with primary open angle glaucoma (POAG) and 46 eyes of 23 healthy individuals were included in the ...
Umut Karaca   +4 more
doaj   +1 more source

Noninvasive Monitoring and Neurointerventional Management of Idiopathic Intracranial Hypertension

open access: yesJournal of Clinical Interventional Radiology ISVIR, 2020
Idiopathic intracranial hypertension (IIH) is characterized by isolated rise in intracranial pressure (ICP) leading to chronic, debilitating headaches, tinnitus, and vision loss.
Matthew Lang   +4 more
doaj   +1 more source

Role of Electrophysiologal Studies for Detection of Simulation and Aggravation in Ophthalmology

open access: yesActa Medica Bulgarica, 2023
To present the importance of the electrophysiological studies for detection of malingering and aggravation in ophthalmology.
Mermeklieva E.
doaj   +1 more source

Electrophysiological signs of retinal cone remodeling in geographic atrophy of the pigment epithelium in patients with non-exudative age-related macular degeneration

open access: yesРоссийский офтальмологический журнал, 2021
Testing patients with primary geographic atrophy (GA) requires a multimodal approach and identification of functional biomarkers characterizing retinal structural remodeling.Purpose: to identify the changes in the functional activity of the retinal cone ...
N. V. Neroeva   +6 more
doaj   +1 more source

Retinal Functional and Structural Changes in the 5xFAD Mouse Model of Alzheimer’s Disease

open access: yesFrontiers in Neuroscience, 2020
Alzheimer’s disease is characterized by the aberrant deposition of protein in the brain and is the leading cause of dementia worldwide. Increasingly, there have been reports of the presence of these protein hallmarks in the retina.
Jeremiah K. H. Lim   +8 more
doaj   +1 more source

Useful Role of a New Generation of Dexamethasone, Vitamin E and Human Serum Albumin Microparticles in the Prevention of Excitotoxicity Injury in Retinal Ocular Diseases

open access: yesPharmaceutics
Excitotoxicity has been linked to the pathogenesis of several serious degenerative ocular diseases. Long-term overactivation of the NMDA receptor by glutamate in retinal ganglion cells (RGCs) results in degeneration, apoptosis and loss of function ...
Javier Rodríguez Villanueva   +4 more
doaj   +1 more source

GHRHR Deficiency Enhances Retinal Ganglion Cell Survival and Visual Functions in Experimental Glaucoma by Inhibiting Ferroptosis

open access: yesAdvanced Science, EarlyView.
Glaucoma, a major cause of blindness, involves retinal ganglion cell (RGC) degeneration. This study shows growth hormone‐releasing hormone receptor (GHRHR) deficiency preserves RGC survival and restores vision, unlike activation which only aids survival.
Yan Tong   +24 more
wiley   +1 more source

Improved electroretinographic responses following dietary intervention in a patient with Refsum disease

open access: yesJIMD Reports, 2020
Refsum disease is a rare inherited metabolic disorder arising from a defect in peroxisomal metabolism. Patients lack the functional enzyme phytanoyl‐CoA hydroxylase, resulting in perturbed alpha oxidation of fatty acids.
Matthew D. Benson   +3 more
doaj   +1 more source

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