ISCEV Standard for full-field clinical electroretinography (2008 update) von Marmor, M. F., Fulton, A. B., Holder, G. E., Miyake, Y., Brigell, M., Bach, M.

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Pattern ERGs suggest a possible retinal contribution to the visual acuity loss in acute optic neuritis von Kleerekooper, I., Del Porto, L., Dell’Arti, L., Guajardo, J., Leo, S., Robson, A. G., Trip, S. A., Petzold, A., Plant, G. T., Holder, G. E.

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Artificial scotoma estimation based on population receptive field mapping von Hummer, A., Ritter, M., Woletz, M., Ledolter, A.A., Tik, M., Dumoulin, S.O., Holder, G.E., Schmidt-Erfurth, U., Windischberger, C.

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Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity von Robson, A G, Saihan, Z, Jenkins, S A, Fitzke, F W, Bird, A C, Webster, A R, Holder, G E

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Eyetracker-based gaze correction for robust mapping of population receptive fields von Hummer, A., Ritter, M., Tik, M., Ledolter, A.A., Woletz, M., Holder, G.E., Dumoulin, S.O., Schmidt-Erfurth, U., Windischberger, C.

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Diagnostic features of the autoimmune retinopathies von Braithwaite, T, Holder, G.E, Lee, R.W.J, Plant, G.T, Tufail, A

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Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy von Holder, G E, Robson, A G, Pavesio, C, Graham, E M

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ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing von Burgess, R, MacLaren, R E, Davidson, A E, Urquhart, J E, Holder, G E, Robson, A G, Moore, A T, Keefe, R O’, Black, G C M, Manson, F D C

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Electrophysiological assessment of optic nerve disease von Holder, G E

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A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D gene von Mukherjee, R, Robson, A G, Holder, G E, Stockman, A, Egan, C A, Moore, A T, Webster, A R

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ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull’s-eye maculopathy von Michaelides, M, Chen, L L, Brantley, M A, Andorf, J L, Isaak, E M, Jenkins, S A, Holder, G E, Bird, A C, Stone, E M, Webster, A R

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Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone–rod dystrophy von Robson, A G, Michaelides, M, Luong, V A, Holder, G E, Bird, A C, Webster, A R, Moore, A T, Fitzke, F W

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RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections von Zito, I, Downes, S M, Patel, R J, Cheetham, M E, Ebenezer, N D, Jenkins, S A, Bhattacharya, S S, Webster, A R, Holder, G E, Bird, A C, Bamiou, D E, Hardcastle, A J

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Batten disease: features to facilitate early diagnosis von Collins, J, Holder, G E, Herbert, H, Adams, G G W

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Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene von Tschernutter, M, Jenkins, S A, Waseem, N H, Saihan, Z, Holder, G E, Bird, A C, Bhattacharya, S S, Ali, R R, Webster, A R

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Acute zonal occult outer retinopathy: towards a set of diagnostic criteria von Francis, P J, Marinescu, A, Fitzke, F W, Bird, A C, Holder, G E

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The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy von Majander, A, Robson, A G, João, C, Holder, G E, Chinnery, P F, Moore, A T, Votruba, M, Stockman, A, Yu-Wai-Man, P

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Functional observations in vitamin A deficiency: diagnosis and time course of recovery von McBain, V A, Egan, C A, Pieris, S J, Supramaniam, G, Webster, A R, Bird, A C, Holder, G E

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A detailed phenotypic study of “cone dystrophy with supernormal rod ERG” von Michaelides, M, Holder, G E, Webster, A R, Hunt, D M, Bird, A C, Fitzke, F W, Mollon, J D, Moore, A T

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A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1 von Michaelides, M, Holder, G E, Hunt, D M, Fitzke, F W, Bird, A C, Moore, A T

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