S18-1 Clinical application of electroretinography (ERG) von Holder, G.E

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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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Somatosensory evoked potentials in children with dystonia help predict outcome from deep brain stimulation von McClelland, V.M, Fialho, D, Flexney-Briscoe, D, Holder, G.E, Elze, M.C, Gimeno, H, Siddiqui, A, Mills, K.R, Selway, R, Lin, J.P

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Proliferation of perivascular macrophages in macaque models of lentiviral encephalitis: a potential mechanism for HIV/SIV persistence in the brain von Kim, W.K., Filipowicz, A.R., McGary, C.M., Holder, G.E., Kuroda, M.J.

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Comparison of Multi-Focal ERG with pattern ERG and sensitivity loss in patients with retinitis pigmentosa (RP) and abnormal fundus autofluorescence (AF) von Robson, A.G, Bird, A.C, Fitzke, F.W, Holder, G.E

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Chromatic VEP and psychophysical assessment of normal and simulated macular pigment von Robson, A.G, Holder, G.E, Moreland, J.D, Kulikowski, J.J

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The role of pattern ERG and full-field ERG in the characterisation and management of birdshot chorioretinopathy von Robson, A.G, Pavesio, C, Graham, E.M, Holder, G.E

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Phenotypic variations in enhanced S-cone syndrome von Holder, G.E, Hogg, C.R, Neveu, M.M, Robson, A.G, Bird, A.C

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Age-related changes in the human albino uncrossed visual pathway von Neveu, M.M, Jeffery, G, Burton, L.C, Sloper, J.J, 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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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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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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The clinical features of albinism and their correlation with visual evoked potentials von Dorey, S E, Neveu, M M, Burton, L C, Sloper, J J, Holder, G E

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Abnormal visual projection in a human albino studied with functional magnetic resonance imaging and visual evoked potentials von Morland, A B, Hoffmann, M B, Neveu, M, Holder, G E

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Oligocone trichromacy: a rare and unusual cone dysfunction syndrome von Michaelides, M, Holder, G E, Bradshaw, K, Hunt, D M, Mollon, J D, Moore, A T

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Chromatic VEP assessment of human macular pigment: Comparison with minimum motion and minimum flicker profiles von ROBSON, A.G., HOLDER, G.E., MORELAND, J.D., KULIKOWSKI, J.J.

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An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene von Dandekar, S S, Ebenezer, N D, Grayson, C, Chapple, J P, Egan, C A, Holder, G E, Jenkins, S A, Fitzke, F W, Cheetham, M E, Webster, A R, Hardcastle, A J

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Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss von Francis, P J, Johnson, S, Edmunds, B, Kelsell, R E, Sheridan, E, Garrett, C, Holder, G E, Hunt, D M, Moore, A T

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Cone dystrophy phenotype associated with a frameshift mutation von Michaelides, M, Aligianis, I.A, Holder, G.E, Simunovic, M.P, Mollon, J D, Maher, E.R, Hunt, D.M, Moore, A.T

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141 Images d’autofluorescence dans la maculopathie polymorphe exsudative vitelliforme aiguë von Vaclavik, V., Ooi, K.G., Holder, G.E., Robson, A.G., Bird, A.C., Webster, A.R.

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