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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 mutation in gene CNGA3 is associated with day blindness in sheep.
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… 
Review
2003
Review
2003
Inherited multifocal RPE-diseases: mechanisms for local dysfunction in global retinoid cycle gene defects
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.
1992
1992
Changes in the DC electroretinogram in Briard dogs with hereditary congenital night blindness and partial day blindness.
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… 
Highly Cited
1965
Highly Cited
1965
Genetic and epidemiological investigations on pigmentary degeneration of the retina and allied disorders in Switzerland.
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