Results 111 to 120 of about 42,373 (278)

Altered Spontaneous Brain Activity of Children with Unilateral Amblyopia: A Resting State fMRI Study

open access: yesJournal of Neural Transplantation and Plasticity, 2019
Objective This study is aimed at investigating differences in local brain activity and functional connectivity (FC) between children with unilateral amblyopia and healthy controls (HCs) by using resting state functional magnetic resonance imaging (rs ...
Peishan Dai   +7 more
semanticscholar   +1 more source

Severe Nerve Enlargement in SOS2‐Related Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Noonan syndrome is a genetic multisystem congenital disorder, caused by pathogenic variants in genes that encode components of the RAS/MAPK signaling pathway. Pathogenic variants in SOS2 represent less than 2% of cases with NS. The phenotype includes a particularly high prevalence (65%) of lymphatic disease. Recently, severe nerve enlargements
Erika Leenders   +11 more
wiley   +1 more source

INFLUENCE OF CHOLINE ALFOSCERATE ON VISUAL PERCEPTION IN PATIENTS WITH AMBLYOPIA

open access: yesПедиатрическая фармакология, 2006
Amblyopia is a frequent disorder in pediatric ophthalmology. The term of amblyopia refers to reduced vision caused by limited visual sensory stimulation (visual deprivation) at a time of visual system development, so the vision can not be improved by ...
I.E. Aznauryan, I.S. Bagrova
doaj   +2 more sources

Fixational Eye Movement Waveforms in Amblyopia: Characteristics of Fast and Slow Eye Movements

open access: yesJournal of Eye Movement Research, 2019
Fixational eye movements comprise of fast microsaccades alternating with slow intersaccadic drifts. These physiologic eye movements play an important role in visual perception.
Sarah L. Kang   +4 more
semanticscholar   +1 more source

Identification of Genetic Variants Causing Paediatric Cataract in Myanmar

open access: yesClinical Genetics, Volume 108, Issue 4, Page 457-462, October 2025.
Up to 60% of children with cataract in Myanmar have a causative variant in a known cataract gene. This is a similar rate to other populations screened to date, but highlights that there are more cataract genes left to identify. ABSTRACT Genetic testing for paediatric cataract detects a cause in 50%–70% of affected children but is as low as 20% in some ...
Johanna L. Jones   +16 more
wiley   +1 more source

Associations between the cause of amblyopia and pre-treatment contrast sensitivity, stereoacuity, fixation, and nystagmus

open access: yesHeliyon
Purpose: To explore the association between the cause of amblyopia and pre-treatment contrast sensitivity, stereoacuity, fixation and nystagmus. Design: Retrospective cohort study.
Yu Jia   +10 more
doaj   +1 more source

Amblyopia Affects the ON Visual Pathway More than the OFF

open access: yesJournal of Neuroscience, 2019
Visual information reaches the cerebral cortex through parallel ON and OFF pathways that signal the presence of light and dark stimuli in visual scenes.
Carmen Pons   +5 more
semanticscholar   +1 more source

A Practical Guide to Genetic Eye Conditions for Paediatricians

open access: yesJournal of Paediatrics and Child Health, Volume 61, Issue 10, Page 1538-1548, October 2025.
ABSTRACT Introduction Inherited eye disorders, though individually rare, are a collectively common cause of paediatric vision impairment. Many occur as part of a syndrome, in association with congenital anomalies and/or growth/developmental disorders.
Richard Lin   +5 more
wiley   +1 more source

Amblyopia [PDF]

open access: yesInternational Ophthalmology Clinics, 1992
S E, Navon, C A, McKeown
openaire   +4 more sources

TYPES OF CONGENITAL SYMBOL AMBLYOPIA. [PDF]

open access: green, 1906
J. Herbert Claiborne
openalex   +1 more source

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