Skip to search formSkip to main contentSkip to account menu

Hemeralopia

Known as: Day Blindness, Hemeralopias, Blindness, Day 
A visual defect characterized by the inability to see as clearly in bright light as in dim light. The word hemeralopia literally means day blindness… 
National Institutes of Health

Related topics

Related topics

7 relations
Achromatopsia 2MetamorphopsiaMicropsiaNIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2

Broader (1)

Eyelid Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Flicker cone function in normal and day blind sheep: a large animal model for human achromatopsia caused by CNGA3 mutation
PurposeRecently we reported on day blindness in sheep caused by a mutation in the CNGA3 gene, thus making affected sheep a… 
2010
2010
A novel day blindness in sheep: epidemiological, behavioural, electrophysiological and histopathological studies.
Highly Cited
2005
Highly Cited
2005
A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD).
PURPOSE To elucidate the phenotypic and biochemical characteristics of a novel mutation associated with autosomal dominant cone… 
Highly Cited
1999
Highly Cited
1999
Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14.
1995
1995
Foveal densitometry and color matching in oligocone trichromacy
Oligocone trichromacy (a subtype of incomplete achromatopsia) is a congenital and stationary cone dysfunction with trichromatism… 
1988
1988
Progressive peripheral cone dysfunction.
1986
1986
Usher syndrome in four Norwegian counties
Among 89 probands selected for tapeto‐retinal degeneration, 18 (20%) were given the diagnosis of Usher syndrome. Among the… 
1973
1973
Slow Potentials of ERG in Hemeralopia Congenita
Since 1952, when Schubert & Bornschein published the electroretinographic results of a subject with congenital night blindness… 
1965
1965
REFSUM'S SYNDROME: REPORT OF A CASE INCLUDING ELECTRON MICROSCOPIC STUDIES OF THE LIVER.
REFSUM'S syndrome, a hereditary disorder of the nervous system, was first described under the title of "Heredopathia Atactica… 
1931
1931
The Sedimentation Velocity of Blood Cells in Eye Diseases Caused by Vitamin A Deficiency
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)