Cortical Visual Impairment in Childhood: ‘Blindsight’ and the Sprague Effect Revisited [PDF]
Gerry Leisman +2 more
exaly +2 more sources
Cerebral/Cortical Visual Impairment Classification and Categorization Using Eye Tracking Measures of Oculomotor Function [PDF]
Melinda Y Chang, Mark S Borchert
exaly +2 more sources
Cortical Visual Impairment Across a Range of Neurodevelopmental Disorders: Clinical Characterization, Diagnostic Tool Evaluation, and Association with Developmental Outcomes [PDF]
Megan Abbott +2 more
exaly +2 more sources
Implications of cerebral/cortical visual impairment on life and learning: insights and strategies from lived experiences [PDF]
Bennett RG, Tibaudo ME, Mazel EC, Y N.
exaly +2 more sources
Method for assessing visual saliency in children with cerebral/cortical visual impairment using generative artificial intelligence [PDF]
Mark S Borchert +2 more
exaly +2 more sources
CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development [PDF]
Scott Demarest +2 more
exaly +2 more sources
Modulation of Homer1 EVH1 domain internal dynamics by putative autism‐associated mutations
The putative autism‐associated M65I and S97L variants of the EVH1 domain of the postsynaptic scaffold protein Homer1 do not exhibit substantial changes in their overall structure or partner binding. Both of them, but especially the M65I variant, show altered internal dynamics relative to the wild‐type domain on the μs‐ms timescale, indicated by the ...
Fanni Farkas +6 more
wiley +1 more source
The cytoskeleton‐mediated transport of mitochondria via tunnelling nanotubes restores respiration, increases ATP production, rescues cells from apoptosis, activates the AKT/mTOR signalling pathway, promotes cell migration and invasiveness, contributes to cancer progression and treatment resistance.
Stanislava Martínková, Jan Trnka
wiley +1 more source
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
ABSTRACT Introduction Progressive Supranuclear Palsy (PSP) is a neurodegenerative ‘tauopathy’ with predominating pathology in the basal ganglia and midbrain. Caudal tau spread frequently implicates the cerebellum; however, the pattern of atrophy remains equivocal.
Chloe Spiegel +8 more
wiley +1 more source

