Bilaketaren emaitzak - Webster, Andrew R.

Retinal findings in a patient with mutations in ABCC6 and ABCA4 nork Mahroo, Omar A., Fujinami, Kaoru, Moore, Anthony T., Webster, Andrew R.

Testu osoa Testu osoa Testu osoa

An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case report nork Karampelas, Michael, Soumplis, Vasileios, Karagiannis, Dimitrios, Parikakis, Efstratios, Webster, Andrew R

Testu osoa Testu osoa Testu osoa

Quantitative Analysis of Retinal Structure Using Spectral-Domain Optical Coherence Tomography in RPGR-Associated Retinopathy nork Tee, James J.L., Carroll, Joseph, Webster, Andrew R., Michaelides, Michel

Testu osoa Testu osoa Testu osoa

The clinical features of retinal disease due to a dominant mutation in RPE65 nork Hull, Sarah, Mukherjee, Rajarshi, Holder, Graham E., Moore, Anthony T., Webster, Andrew R.

Testu osoa Testu osoa

Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness nork Cammack, Jocelyn, Whight, John, Cross, Vinette, Rider, Andrew T, Webster, Andrew R, Stockman, Andrew

Testu osoa Testu osoa Testu osoa

QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY nork Tee, James J. L., Kalitzeos, Angelos, Webster, Andrew R., Peto, Tunde, Michaelides, Michel

Testu osoa Testu osoa Testu osoa

Clinical utility gene card for: Choroideremia nork Moosajee, Mariya, Ramsden, Simon C, Black, Graeme CM, Seabra, Miguel C, Webster, Andrew R

Testu osoa Testu osoa Testu osoa

Retinal detachment in retinitis pigmentosa nork Chan, Weng Onn, Brennan, Nicholas, Webster, Andrew R, Michaelides, Michel, Muqit, Mahiul M K

Testu osoa Testu osoa Testu osoa

Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated Retinopathy nork Anikina, Evgenia, Georgiou, Michalis, Tee, James, Webster, Andrew R., Weleber, Richard G., Michaelides, Michel

Testu osoa Testu osoa Testu osoa

Missense variants in the conserved transmembrane M2 protein domain of KCNJ13 associated with retinovascular changes in humans and zebrafish nork Toms, Maria, Dubis, Adam M., Lim, Wei Sing, Webster, Andrew R., Gorin, Michael B., Moosajee, Mariya

Testu osoa Testu osoa Testu osoa

Reanalysis of Association of Pro50Leu Substitution in Guanylate Cyclase Activating Protein-1 With Dominant Retinal Dystrophy nork Mahroo, Omar A., Arno, Gavin, Ba-Abbad, Rola, Downes, Susan M., Bird, Alan, Webster, Andrew R.

Testu osoa Testu osoa Testu osoa

Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia nork Schiff, Elena R., Tailor, Vijay K., Chan, Hwei Wuen, Theodorou, Maria, Webster, Andrew R., Moosajee, Mariya

Testu osoa Testu osoa Testu osoa

Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History nork Georgiou, Michalis, Grewal, Parampal S., Narayan, Akshay, Alser, Muath, Ali, Naser, Fujinami, Kaoru, Webster, Andrew R., Michaelides, Michel

Testu osoa Testu osoa Testu osoa

Prospective deep phenotyping of choroideremia patients using multimodal structure-function approaches nork Hagag, Ahmed M., Mitsios, Andreas, Narayan, Akshay, Abbouda, Alessandro, Webster, Andrew R., Dubis, Adam M., Moosajee, Mariya

Testu osoa Testu osoa Testu osoa

Investigation of SLA4A3 as a candidate gene for human retinal disease nork Downs, Louise M., Webster, Andrew R., Moore, Anthony T., Michaelides, Michel, Ali, Robin R., Hardcastle, Alison J., Mellersh, Cathryn S.

Testu osoa Testu osoa Testu osoa

Awareness of olfactory impairment in a cohort of patients with CNGB1-associated retinitis pigmentosa nork Afshar, Farid, Arno, Gavin, Ba-Abbad, Rola, Esposti, Simona Degli, Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.

Testu osoa Testu osoa Testu osoa

Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis nork Sergouniotis, Panagiotis I., Davidson, Alice E., Mackay, Donna S., Li, Zheng, Yang, Xu, Plagnol, Vincent, Moore, Anthony T., Webster, Andrew R.

Testu osoa Testu osoa Testu osoa

Clinical characteristics of early retinal disease due to CDHR1 mutation nork Ba-Abbad, Rola, Sergouniotis, Panagiotis I., Plagnol, Vincent, Robson, Anthony G., Michaelides, Michel, Holder, Graham E., Webster, Andrew R.

Testu osoa Testu osoa

Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular Degeneration nork Cipriani, Valentina, Hogg, Ruth E., Sofat, Reecha, Moore, Anthony T., Webster, Andrew R., Yates, John R. W., Fletcher, Astrid E.

Testu osoa Testu osoa Testu osoa

Transcorneal electrical stimulation for the treatment of retinitis pigmentosa: results from the TESOLAUK trial nork Wagner, Siegfried K, Jolly, Jasleen K, Pefkianaki, Maria, Gekeler, Florian, Webster, Andrew R, Downes, Susan M, Maclaren, Robert E

Testu osoa Testu osoa Testu osoa