Retinal findings in a patient with mutations in ABCC6 and ABCA4

Por Mahroo, Omar A., Fujinami, Kaoru, Moore, Anthony T., Webster, Andrew R.
Publicado no Eye (Lond) (2018)

An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case report

Por Karampelas, Michael, Soumplis, Vasileios, Karagiannis, Dimitrios, Parikakis, Efstratios, Webster, Andrew R
Publicado em 2013

Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy

Por Tee, James J.L., Carroll, Joseph, Webster, Andrew R., Michaelides, Michel
Publicado no Am J Ophthalmol (2017)

The clinical features of retinal disease due to a dominant mutation in RPE65

Por Hull, Sarah, Mukherjee, Rajarshi, Holder, Graham E., Moore, Anthony T., Webster, Andrew R.
Publicado no Mol Vis (2016)

Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness

Por Cammack, Jocelyn, Whight, John, Cross, Vinette, Rider, Andrew T, Webster, Andrew R, Stockman, Andrew
Publicado no Clin Ophthalmol (2016)

QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY

Por Tee, James J. L., Kalitzeos, Angelos, Webster, Andrew R., Peto, Tunde, Michaelides, Michel
Publicado no Retina (2018)

Clinical utility gene card for: Choroideremia

Por Moosajee, Mariya, Ramsden, Simon C, Black, Graeme CM, Seabra, Miguel C, Webster, Andrew R
Publicado em 2014

Retinal detachment in retinitis pigmentosa

Por Chan, Weng Onn, Brennan, Nicholas, Webster, Andrew R, Michaelides, Michel, Muqit, Mahiul M K
Publicado no BMJ Open Ophthalmol (2020)

Reanalysis of Association of Pro50Leu Substitution in Guanylate Cyclase Activating Protein-1 With Dominant Retinal Dystrophy

Por Mahroo, Omar A., Arno, Gavin, Ba-Abbad, Rola, Downes, Susan M., Bird, Alan, Webster, Andrew R.
Publicado no JAMA Ophthalmol (2020)

Missense variants in the conserved transmembrane M2 protein domain of KCNJ13 associated with retinovascular changes in humans and zebrafish

Por Toms, Maria, Dubis, Adam M., Lim, Wei Sing, Webster, Andrew R., Gorin, Michael B., Moosajee, Mariya
Publicado no Exp Eye Res (2019)

Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia

Por Schiff, Elena R., Tailor, Vijay K., Chan, Hwei Wuen, Theodorou, Maria, Webster, Andrew R., Moosajee, Mariya
Publicado no Int J Mol Sci (2021)

Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History

Por Georgiou, Michalis, Grewal, Parampal S., Narayan, Akshay, Alser, Muath, Ali, Naser, Fujinami, Kaoru, Webster, Andrew R., Michaelides, Michel
Publicado no Am J Ophthalmol (2021)

Prospective deep phenotyping of choroideremia patients using multimodal structure-function approaches

Por Hagag, Ahmed M., Mitsios, Andreas, Narayan, Akshay, Abbouda, Alessandro, Webster, Andrew R., Dubis, Adam M., Moosajee, Mariya
Publicado no Eye (Lond) (2020)

Investigation of SLA4A3 as a candidate gene for human retinal disease

Por Downs, Louise M., Webster, Andrew R., Moore, Anthony T., Michaelides, Michel, Ali, Robin R., Hardcastle, Alison J., Mellersh, Cathryn S.
Publicado no J Negat Results Biomed (2016)

Awareness of olfactory impairment in a cohort of patients with CNGB1-associated retinitis pigmentosa

Por Afshar, Farid, Arno, Gavin, Ba-Abbad, Rola, Esposti, Simona Degli, Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.
Publicado no Eye (Lond) (2019)

Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis

Por Sergouniotis, Panagiotis I., Davidson, Alice E., Mackay, Donna S., Li, Zheng, Yang, Xu, Plagnol, Vincent, Moore, Anthony T., Webster, Andrew R.
Publicado em 2011

Clinical characteristics of early retinal disease due to CDHR1 mutation

Por Ba-Abbad, Rola, Sergouniotis, Panagiotis I., Plagnol, Vincent, Robson, Anthony G., Michaelides, Michel, Holder, Graham E., Webster, Andrew R.
Publicado em 2013

Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular Degeneration

Por Cipriani, Valentina, Hogg, Ruth E., Sofat, Reecha, Moore, Anthony T., Webster, Andrew R., Yates, John R. W., Fletcher, Astrid E.
Publicado no JAMA Ophthalmol (2017)

Transcorneal electrical stimulation for the treatment of retinitis pigmentosa: results from the TESOLAUK trial

Por Wagner, Siegfried K, Jolly, Jasleen K, Pefkianaki, Maria, Gekeler, Florian, Webster, Andrew R, Downes, Susan M, Maclaren, Robert E
Publicado no BMJ Open Ophthalmol (2017)

Phagosomal and mitochondrial alterations in RPE may contribute to KCNJ13 retinopathy

Por Toms, Maria, Burgoyne, Thomas, Tracey-White, Dhani, Richardson, Rose, Dubis, Adam M., Webster, Andrew R., Futter, Clare, Moosajee, Mariya
Publicado no Sci Rep (2019)