Suchergebnisse - Webster, Andrew R.
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Retinal findings in a patient with mutations in ABCC6 and ABCA4 von Mahroo, Omar A., Fujinami, Kaoru, Moore, Anthony T., Webster, Andrew R.
Veröffentlicht 2018Text -
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An atypical case of choroidal neovascularization associated with pseudoxanthoma elasticum treated with intravitreal bevacizumab: a case report von Karampelas, Michael, Soumplis, Vasileios, Karagiannis, Dimitrios, Parikakis, Efstratios, Webster, Andrew R
Veröffentlicht 2013Text -
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Clinical utility gene card for: Choroideremia von Moosajee, Mariya, Ramsden, Simon C, Black, Graeme CM, Seabra, Miguel C, Webster, Andrew R
Veröffentlicht 2014Text -
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Retinal detachment in retinitis pigmentosa von Chan, Weng Onn, Brennan, Nicholas, Webster, Andrew R, Michaelides, Michel, Muqit, Mahiul M K
Veröffentlicht 2020Text -
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Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated Retinopathy von Anikina, Evgenia, Georgiou, Michalis, Tee, James, Webster, Andrew R., Weleber, Richard G., Michaelides, Michel
Veröffentlicht 2022Text -
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Sector Retinitis Pigmentosa: Extending the Molecular Genetics Basis and Elucidating the Natural History von Georgiou, Michalis, Grewal, Parampal S., Narayan, Akshay, Alser, Muath, Ali, Naser, Fujinami, Kaoru, Webster, Andrew R., Michaelides, Michel
Veröffentlicht 2021Text -
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Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis von Sergouniotis, Panagiotis I., Davidson, Alice E., Mackay, Donna S., Li, Zheng, Yang, Xu, Plagnol, Vincent, Moore, Anthony T., Webster, Andrew R.
Veröffentlicht 2011Text -
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