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Current and Future Landscape in Genetic Therapies for Leber Hereditary Optic Neuropathy.

Journal article

Shamsnajafabadi H. et al, (2023), Cells, 12

Microperimetry as an Outcome Measure in RPGR-associated Retinitis Pigmentosa Clinical Trials

Journal article

Taylor LJ. et al, (2023), Translational Vision Science & Technology, 12, 4 - 4

Choroideremia: Toward Regulatory Approval of Retinal Gene Therapy.

Journal article

Yusuf IH. and MacLaren RE., (2023), Cold Spring Harb Perspect Med, 13

Developmental Expression of the Cell Cycle Regulator p16INK4a in Retinal Glial Cells: A Novel Marker for Immature Ocular Astrocytes?

Journal article

Martinez-Fernandez de la Camara C. et al, (2023), Journal of Histochemistry & Cytochemistry, 71, 301 - 320

Programmable RNA editing with endogenous ADAR enzymes – a feasible option for the treatment of inherited retinal disease?

Journal article

Bellingrath J-S. et al, (2023), Frontiers in Molecular Neuroscience, 16

Microperimetry Reliability Assessed From Fixation Performance

Journal article

Josan AS. et al, (2023), Translational Vision Science & Technology, 12, 21 - 21

AAV2-Mediated Gene Therapy for Choroideremia: 5-Year Results and Alternate Anti-sense Oligonucleotide Therapy

Journal article

Zhai Y. et al, (2023), American Journal of Ophthalmology, 248, 145 - 156

Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations

Journal article

von Krusenstiern L. et al, (2023), JAMA Ophthalmology, 141, 275 - 275

Harnessing the potential of practice‐based clinical optometry research in the United Kingdom

Journal article

Taylor LJ. et al, (2023), Ophthalmic and Physiological Optics, 43, 239 - 243

Is RPGR-related retinal dystrophy associated with systemic disease? A case series

Journal article

Han RC. et al, (2023), Ophthalmic Genetics, 1 - 8

Clinical Research on the Leading Causes of Severe Sight Impairment in the UK General and Working Populations.

Journal article

Liu WJ. et al, (2023), Clin Ophthalmol, 17, 2729 - 2735

Impaired glutamylation of RPGR ORF15 underlies the cone-dominated phenotype associated with truncating distal ORF15 variants

Journal article

Cehajic-Kapetanovic J. et al, (2022), Proceedings of the National Academy of Sciences, 119

Compound dominant-null heterozygosity in a family with RP1-related retinal dystrophy

Journal article

Buckley TMW. et al, (2022), American Journal of Ophthalmology Case Reports, 28

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