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Search results (482)

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Investigating ethnicity-related variability in the human L-cone spectral sensitivity function

Schneider AC. et al, (2026), Vision Research, 243, 108769 - 108769

Cataract surgery with autosomal recessive cornea plana caused by a novel KERA mutation.

Abdalla Elsayed MEA. and MacLaren RE., (2026), Am J Ophthalmol Case Rep, 41

Geographic atrophy in age-related macular degeneration: phenotypic characterisation for clinical trial consideration.

Borchert GA. et al, (2026), Graefes Arch Clin Exp Ophthalmol

A literature review of macular holes in age-related macular degeneration: insights into the pathogenesis, prognosis and surgical outcomes.

Christou EE. et al, (2026), Graefes Arch Clin Exp Ophthalmol

Central Retinal Sensitivity Decline in RPGR-Related Retinal Phenotypes

Josan AS. et al, (2026), American Journal of Ophthalmology, 282, 154 - 161

DIRECT POSTERIOR RETINAL INJURY CAUSED BY INTRAVITREAL INJECTIONS: Management and Outcomes From a Vitreoretinal Perspective.

Christou EE. et al, (2026), Retina, 46, 272 - 280

Multimodal imaging and electrophysiological features in bradyopsia associated with homozygous variants (c.895T>C) in Regulator of G-protein Signaling 9 (RGS9).

Borchert GA. et al, (2026), Ophthalmic Genet, 47, 14 - 21

A novel EYS c.6192-1G>A variant presents ideal base editing therapeutic opportunities.

Kaukonen M. et al, (2026), Ophthalmic Genet, 1 - 4

ABCA4-associated maculopathy suspected to be ocular toxoplasmosis.

Elsayed MEAA. et al, (2026), BMC Ophthalmol, 26

Low-luminance visual acuity and low-luminance deficit: optimising measurement and analysis

Forte G. et al, (2026), Clinical and Experimental Optometry, 109, 53 - 59

IMPG2-associated retinal dystrophy with a novel missense variant and therapeutic options via adenine base editing

Abdalla Elsayed MEA. et al, (2026), Ophthalmic Genetics, 1 - 7

Expanding the Genetic Spectrum in IMPG1 and IMPG2 Retinopathy

Al-Khuzaei S. et al, (2025), Genes, 16, 1474 - 1474

Gene Therapy Strategies for the Treatment of Bestrophinopathies.

Haldrup SB. et al, (2025), Int J Mol Sci, 26

Genotype–Phenotype Correlations in PRPH2 Retinopathies: A Comprehensive Analysis of 36 Patients from the Oxford Eye Hospital, UK

Al-Khuzaei S. et al, (2025), Genes, 16, 1016 - 1016

Single-cell and spatial transcriptomic analyses of gene therapy-associated retinal inflammation in non-human primates

Sourd C. et al, (2025)

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