Results 151 to 160 of about 14,255 (204)

Lateral Transorbital Approach for Lateral Sphenoid Defects: Anatomy, Surgery, Nasoseptal Flap Use, and a 4‐Case Series

open access: yesLaryngoscope Investigative Otolaryngology, Volume 10, Issue 2, April 2025.
In this case series, we assess the effectiveness and anatomical advantages of the lateral transorbital approach for complex skull base repairs in the lateral recess of a pneumatized sphenoid sinus and compare it to standard transnasal methods. We conclude that the lateral transorbital approach enhances visualization, reduces nerve injury risk, and ...
Darlene Lubbe   +2 more
wiley   +1 more source

Scleral rupture during intraoperative silicone oil injection in pars plana vitrectomy

open access: yesAmerican Journal of Ophthalmology Case Reports, 2019
Purpose: To report a single case history of scleral rupture (SR) during silicone oil injection in a pars plana vitrectomy. Observations: A 60-year-old woman with a history of pathological myopia presented with acute vision loss in her right eye.
Ana Laura Domínguez Yates   +2 more
doaj  

CeViT: Copula-Enhanced Vision Transformer in multi-task learning and bi-group image covariates with an application to myopia screening [PDF]

open access: yesarXiv
We aim to assist image-based myopia screening by resolving two longstanding problems, "how to integrate the information of ocular images of a pair of eyes" and "how to incorporate the inherent dependence among high-myopia status and axial length for both eyes." The classification-regression task is modeled as a novel 4-dimensional muti-response ...
arxiv  

CSNK2B Mutation: A Rare Cause of IGHD

open access: yesClinical Endocrinology, Volume 102, Issue 4, Page 421-426, April 2025.
ABSTRACT Objective Poirier‐Bienvenu neurodevelopmental syndrome (POBINDS) is a rare neurodevelopmental syndrome, resulting from germline heterozygous CSNKB2 pathogenic variants. The main presentations are severe epilepsy, delayed psychomotor development, and/or profound intellectual disability.
Karine Aouchiche   +6 more
wiley   +1 more source

Hereditary Vitreoretinopathies: Molecular Diagnosis, Clinical Presentation and Management

open access: yesClinical &Experimental Ophthalmology, Volume 53, Issue 3, Page 281-291, April 2025.
ABSTRACT Hereditary vitreoretinopathies (HVRs), also known as hereditary vitreoretinal degenerations comprise a heterogeneous group of inherited disorders of the retina and vitreous, collectively and variably characterised by vitreal abnormalities, such as fibrillary condensations, liquefaction or membranes, as well as peripheral retinal abnormalities,
Hashem H. Ghoraba   +2 more
wiley   +1 more source

Refractive outcomes of implantation of an implantable phakic copolymer lens with peripheral holes in the intraocular posterior chamber in moderate to high myopia patients: a single-surgeon series

open access: yesClinical Ophthalmology, 2019
Praveen Subudhi,1,2 Sweta Patro,1 Zahiruddin Khan,2 B Nageswar Rao Subudhi,3 Silla Sitaram4 1Department of Cornea and Refractive Surgery, Ruby Eye Hospital, Berhampur, Odisha, India; 2Ophthalmology Department, Hitech Medical College, Bhubaneswar, India ...
Subudhi P   +4 more
doaj  

Monogenic Retinal Diseases Associated With Genes Encoding Phototransduction Proteins: A Review

open access: yesClinical &Experimental Ophthalmology, Volume 53, Issue 3, Page 260-280, April 2025.
ABSTRACT Phototransduction, the process by which captured photons elicit electrical changes in retinal rod and cone cells, represents the first neuronal step in vision and involves interactions between several highly specialised proteins. Pathogenic variants in genes encoding many of these proteins can give rise to significant vision impairment ...
Wendy M. Wong, Omar A. Mahroo
wiley   +1 more source

Home - About - Disclaimer - Privacy