Results 41 to 50 of about 22,111 (213)

Retroequatorial myopexy in the management of adult-onset cyclic esotropia

open access: yesIndian Journal of Ophthalmology, 2020
A 65-year-old otherwise healthy female, with bilateral normal visual acuity, presented with a unique pattern of strabismus. She complained of esotropia and diplopia occurring after every 24 h.
Gunjan Saluja, Pradeep Sharma
doaj   +1 more source

Shared decision making and patients satisfaction with strabismus care—a pilot study

open access: yesBMC Medical Informatics and Decision Making, 2021
Background Strabismus is a complex disease that has various treatment approaches each with its own advantages and drawbacks. In this context, shared decisions making (SDM) is a communication process with the provider sharing all the relevant treatment ...
Ala Paduca   +4 more
doaj   +1 more source

The Effect of Surgical Treatment of Horizontal Strabismus on Refractive Changes in Adult Patients

open access: yesOftalʹmologiâ, 2023
Concomitant strabismus and refractive anomalies are often common pathological conditions in adult patients. The patient’s desire to get rid of both problems poses a question to the surgeon about the order of surgical interventions. With non-accommodative
M. G. Kataev   +2 more
doaj   +1 more source

Visual pathway function and structure in Wolfram syndrome: Patient age, variation and progression [PDF]

open access: yes, 2018
Background/aimsTo report alterations in visual acuity and visual pathway structure over an interval of 1–3 years in a cohort of children, adolescents and young adults who have Wolfram syndrome (WFS) and to describe the range of disease severity evident ...
Al-Lozi, Amal   +6 more
core   +2 more sources

Amblyopia [PDF]

open access: yes, 2016
Amblyopia is, aside from refractive error, the most common cause of visual loss in children. Thus amblyopia is a serious public health issue. When diagnosed and treated early, the visual losses may be easily reversed.
Levi, DM
core  

Strabismus measurements with novel video goggles [PDF]

open access: yes, 2017
PURPOSE: To assess the validity of a novel, simplified, noninvasive test for strabismus using video goggles. DESIGN: Cross-sectional method comparison study in which the new test, the strabismus video goggles, is compared with the existing reference ...
Bockisch, Christopher J   +7 more
core   +1 more source

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

Dorsal visual pathway changes in patients with comitant extropia. [PDF]

open access: yesPLoS ONE, 2010
BACKGROUND: Strabismus is a disorder in which the eyes are misaligned. Persistent strabismus can lead to stereopsis impairment. The effect of strabismus on human brain is not unclear. The present study is to investigate whether the brain white structures
Xiaohe Yan   +6 more
doaj   +1 more source

A review of the role of ultrasound biomicroscopy in glaucoma associated with rare diseases of the anterior segment [PDF]

open access: yes, 2016
Ultrasound biomicroscopy is a non-invasive imaging technique, which allows high-resolution evaluation of the anatomical features of the anterior segment of the eye regardless of optical media transparency.
Abdolrahimzadeh, B   +5 more
core   +2 more sources

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina   +11 more
wiley   +1 more source

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