Hakutulokset - Webster, Andrew R.
- Näytetään 1 - 20 yhteensä 135 tuloksesta
- Siirry seuraavalle sivulle
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An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case report Tekijä Karampelas, Michael, Soumplis, Vasileios, Karagiannis, Dimitrios, Parikakis, Efstratios, Webster, Andrew R
Julkaistu 2013Teksti -
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Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness Tekijä Cammack, Jocelyn, Whight, John, Cross, Vinette, Rider, Andrew T, Webster, Andrew R, Stockman, Andrew
Julkaistu 2016Teksti -
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Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated Retinopathy Tekijä Anikina, Evgenia, Georgiou, Michalis, Tee, James, Webster, Andrew R., Weleber, Richard G., Michaelides, Michel
Julkaistu 2022Teksti -
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Missense variants in the conserved transmembrane M2 protein domain of KCNJ13 associated with retinovascular changes in humans and zebrafish Tekijä Toms, Maria, Dubis, Adam M., Lim, Wei Sing, Webster, Andrew R., Gorin, Michael B., Moosajee, Mariya
Julkaistu 2019Teksti -
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Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History Tekijä Georgiou, Michalis, Grewal, Parampal S., Narayan, Akshay, Alser, Muath, Ali, Naser, Fujinami, Kaoru, Webster, Andrew R., Michaelides, Michel
Julkaistu 2021Teksti -
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Prospective deep phenotyping of choroideremia patients using multimodal structure-function approaches Tekijä Hagag, Ahmed M., Mitsios, Andreas, Narayan, Akshay, Abbouda, Alessandro, Webster, Andrew R., Dubis, Adam M., Moosajee, Mariya
Julkaistu 2020Teksti -
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Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis Tekijä Sergouniotis, Panagiotis I., Davidson, Alice E., Mackay, Donna S., Li, Zheng, Yang, Xu, Plagnol, Vincent, Moore, Anthony T., Webster, Andrew R.
Julkaistu 2011Teksti -
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Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular Degeneration Tekijä Cipriani, Valentina, Hogg, Ruth E., Sofat, Reecha, Moore, Anthony T., Webster, Andrew R., Yates, John R. W., Fletcher, Astrid E.
Julkaistu 2017Teksti -
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Transcorneal electrical stimulation for the treatment of retinitis pigmentosa: results from the TESOLAUK trial Tekijä Wagner, Siegfried K, Jolly, Jasleen K, Pefkianaki, Maria, Gekeler, Florian, Webster, Andrew R, Downes, Susan M, Maclaren, Robert E
Julkaistu 2017Teksti