Résultats de la recherche - Webster, Andrew R.
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An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case report par Karampelas, Michael, Soumplis, Vasileios, Karagiannis, Dimitrios, Parikakis, Efstratios, Webster, Andrew R
Publié 2013Texte -
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Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness par Cammack, Jocelyn, Whight, John, Cross, Vinette, Rider, Andrew T, Webster, Andrew R, Stockman, Andrew
Publié 2016Texte -
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QUANTITATIVE ANALYSIS OF HYPERAUTOFLUORESCENT RINGS TO CHARACTERIZE THE NATURAL HISTORY AND PROGRESSION IN RPGR-ASSOCIATED RETINOPATHY par Tee, James J. L., Kalitzeos, Angelos, Webster, Andrew R., Peto, Tunde, Michaelides, Michel
Publié 2018Texte -
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Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated Retinopathy par Anikina, Evgenia, Georgiou, Michalis, Tee, James, Webster, Andrew R., Weleber, Richard G., Michaelides, Michel
Publié 2022Texte -
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Missense variants in the conserved transmembrane M2 protein domain of KCNJ13 associated with retinovascular changes in humans and zebrafish par Toms, Maria, Dubis, Adam M., Lim, Wei Sing, Webster, Andrew R., Gorin, Michael B., Moosajee, Mariya
Publié 2019Texte -
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Reanalysis of Association of Pro50Leu Substitution in Guanylate Cyclase Activating Protein-1 With Dominant Retinal Dystrophy par Mahroo, Omar A., Arno, Gavin, Ba-Abbad, Rola, Downes, Susan M., Bird, Alan, Webster, Andrew R.
Publié 2020Texte -
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Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia par Schiff, Elena R., Tailor, Vijay K., Chan, Hwei Wuen, Theodorou, Maria, Webster, Andrew R., Moosajee, Mariya
Publié 2021Texte -
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Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History par Georgiou, Michalis, Grewal, Parampal S., Narayan, Akshay, Alser, Muath, Ali, Naser, Fujinami, Kaoru, Webster, Andrew R., Michaelides, Michel
Publié 2021Texte -
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Prospective deep phenotyping of choroideremia patients using multimodal structure-function approaches par Hagag, Ahmed M., Mitsios, Andreas, Narayan, Akshay, Abbouda, Alessandro, Webster, Andrew R., Dubis, Adam M., Moosajee, Mariya
Publié 2020Texte -
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Investigation of SLA4A3 as a candidate gene for human retinal disease par Downs, Louise M., Webster, Andrew R., Moore, Anthony T., Michaelides, Michel, Ali, Robin R., Hardcastle, Alison J., Mellersh, Cathryn S.
Publié 2016Texte -
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Awareness of olfactory impairment in a cohort of patients with CNGB1-associated retinitis pigmentosa par Afshar, Farid, Arno, Gavin, Ba-Abbad, Rola, Esposti, Simona Degli, Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.
Publié 2019Texte -
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Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis par Sergouniotis, Panagiotis I., Davidson, Alice E., Mackay, Donna S., Li, Zheng, Yang, Xu, Plagnol, Vincent, Moore, Anthony T., Webster, Andrew R.
Publié 2011Texte -
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Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular Degeneration par Cipriani, Valentina, Hogg, Ruth E., Sofat, Reecha, Moore, Anthony T., Webster, Andrew R., Yates, John R. W., Fletcher, Astrid E.
Publié 2017Texte -
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Transcorneal electrical stimulation for the treatment of retinitis pigmentosa: results from the TESOLAUK trial par Wagner, Siegfried K, Jolly, Jasleen K, Pefkianaki, Maria, Gekeler, Florian, Webster, Andrew R, Downes, Susan M, Maclaren, Robert E
Publié 2017Texte