Resultados da pesquisa - Webster, Andrew R.
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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 2013Text -
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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 em 2016Text -
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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 em 2018Text -
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Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated Retinopathy Por Anikina, Evgenia, Georgiou, Michalis, Tee, James, Webster, Andrew R., Weleber, Richard G., Michaelides, Michel
Publicado em 2022Text -
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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 em 2019Text -
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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 em 2020Text -
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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 em 2021Text -
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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 em 2021Text -
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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 em 2020Text -
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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 em 2016Text -
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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 em 2019Text -
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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 2011Text -
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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 em 2017Text -
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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 em 2017Text