Congenital hereditary bilateral non-attachment of retina. A sibship of two

Altered photic and non-photic phase shifts in 5-HT(1A) receptor knockout mice.

Neuroscience·2008

Influence of dehydroepiandrosterone on rabbit intraocular pressure.

Ophthalmic research·2000

Some plasma constituents correlate with human cataract location and nuclear colour.

Ophthalmic research·1997

Skin disease and age-related cataract.

Acta dermato-venereologica·1996

Human cataract risk factors: significance of abstention from, and high consumption of, ethanol (U-curve) and non-significance of smoking.

Ophthalmic research·1996

Some blood plasma constituents correlate with human cataract.

The British journal of ophthalmology·1995

Higher plasma vitamin D levels are not causally associated with less age-related macular degeneration.

Acta ophthalmologica·2026

Low-level light therapy for dry eye disease and meibomian gland dysfunction: A systematic review and meta-analysis.

Acta ophthalmologica·2026

Insulin usage and glaucoma treatment associated with the incidence of surgically treated vision-threatening epiretinal membrane: Evidence from an epidemiological study.

Acta ophthalmologica·2026

Probability of myopic macular degeneration in dependence on axial length and age: The two-continent eye study.

Acta ophthalmologica·2026

Intravitreal faricimab in patients with nAMD: French data from the Fight Retinal Blindness! Registry.

Acta ophthalmologica·2026

Impact of retinal break location on surgical outcomes in primary uncomplicated rhegmatogenous retinal detachment: Superior versus inferior breaks.

Acta ophthalmologica·2026

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

International journal of reproductive biomedicine·2026

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

CNS neuroscience & therapeutics·2026

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Nature communications·2026

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Stem cell research·2026

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Diabetes, obesity & metabolism·2026

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

Related Experiment Videos

Congenital hereditary bilateral non-attachment of retina. A sibship of two

Related Concept Videos

Altered photic and non-photic phase shifts in 5-HT(1A) receptor knockout mice.

Influence of dehydroepiandrosterone on rabbit intraocular pressure.

Some plasma constituents correlate with human cataract location and nuclear colour.

Skin disease and age-related cataract.

Human cataract risk factors: significance of abstention from, and high consumption of, ethanol (U-curve) and non-significance of smoking.

Some blood plasma constituents correlate with human cataract.

Higher plasma vitamin D levels are not causally associated with less age-related macular degeneration.

Low-level light therapy for dry eye disease and meibomian gland dysfunction: A systematic review and meta-analysis.

Insulin usage and glaucoma treatment associated with the incidence of surgically treated vision-threatening epiretinal membrane: Evidence from an epidemiological study.

Probability of myopic macular degeneration in dependence on axial length and age: The two-continent eye study.

Intravitreal faricimab in patients with nAMD: French data from the Fight Retinal Blindness! Registry.

Impact of retinal break location on surgical outcomes in primary uncomplicated rhegmatogenous retinal detachment: Superior versus inferior breaks.

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

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Congenital hereditary bilateral non-attachment of retina. A sibship of two

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