Age-related decline in function of ON and OFF visual pathways. [PDF]
Hathibelagal AR +4 more
europepmc +1 more source
Why do albinos and other hypopigmented mutants lack normal binocular vision, and what else is abnormal in their central visual pathways? [PDF]
R. W. Guillery
openalex +1 more source
ABSTRACT Objective Natalizumab (NTZ) is a highly effective therapy for multiple sclerosis (MS); however, its use is limited by the risk of a rare potentially severe opportunistic brain infection, progressive multifocal leukoencephalopathy (PML). Alternative dosing strategies are evaluated to reduce PML risk while still maintaining efficacy, which ...
Regina Berkovich +10 more
wiley +1 more source
Exploring neural architectures for simultaneously recognizing multiple visual attributes
Much experimental evidence in neuroscience has suggested a division of higher visual processing into a ventral pathway specialized for object recognition and a dorsal pathway specialized for spatial recognition.
Zhixian Han, Anne B. Sereno
doaj +1 more source
Functional maturation in visual pathways predicts attention to the eyes in infant rhesus macaques: Effects of social status. [PDF]
Ford A +11 more
europepmc +1 more source
Functional morphology of the feedback pathway from area 17 of the cat visual cortex to the lateral geniculate nucleus [PDF]
P.N. Murphy, AM Sillito
openalex +1 more source
Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam +6 more
wiley +1 more source
Morpho-Functional Assessment of Retinal Ganglion Cells and Visual Pathways in Patients with Optic Disc Drusen: Superficial Drusen Visible Height as a Marker of Impairment. [PDF]
Antonelli G +4 more
europepmc +1 more source
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source
The impact of low birth weight on the visual pathway [PDF]
A R Fielder
openalex +1 more source

