Results 31 to 40 of about 2,486,595 (276)
Variability and systematic differences in normal, protan and deutan color naming
Congenital color vision deficients generally demonstrate difficulties in color naming tasks. In our study we investigated the color naming properties and uncertainties of a relatively large group of red-green color vision deficients using quasi ...
BALAZS VINCE NAGY +4 more
doaj +1 more source
Introduction: Colour of iris is associated with race and may show hereditary patterns. In this context it may be associated with colour vision defects and size of pupil.
Muhammad Rashid +5 more
doaj +1 more source
Color Vision Defects in School Going Children
Introduction: Color Vision defect can be observed in various diseases of optic nerve and retina and also a significant number of people suffer from the inherited condition of red and green color defect.
R K Shrestha +3 more
doaj +1 more source
Background: People with color vision deficiencies report numerous limitations in daily life. However, they use basic color terms systematically and in a similar manner as people with people with normal color vision.
Günter eKugler +12 more
doaj +1 more source
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru +13 more
wiley +1 more source
Natural Frequencies of Levodopa‐Induced Dyskinesia in Parkinson's Disease
ABSTRACT Objectives Abnormal involuntary movements, known as dyskinesias, are common complications of levodopa treatment in patients with Parkinson's disease and can significantly impair quality of life. The underlying pathophysiology remains unclear, and current therapeutic options are limited.
Ioannis U. Isaias +3 more
wiley +1 more source
Development and validation of a novel and graded colour saturation threshold test, the LSS-8
Colour vision changes are a key clinical feature of many acquired retinal and optic nerve disorders. Current clinical tests are often labour-intensive or designed for congenital defects. We introduce the novel LSS-8 test, which measures colour saturation
Kristyna Stepnicka +3 more
doaj +1 more source
Posterior Disconnection Syndrome in Early‐Stage Adult‐Onset Cerebral Adrenoleukodystrophy
ABSTRACT Adult‐onset cerebral adrenoleukodystrophy is potentially treatable but often difficult to recognize before advanced cerebral involvement. Herein, we describe three men with early‐stage disease who initially presented with subtle visual complaints rather than subcortical dementia. Targeted neuropsychological testing revealed higher‐order visual
Kazuto Katsuse +13 more
wiley +1 more source

