ISCEV standard for clinical pattern electroretinography (2024 update) von Thompson, D. A., Bach, M., McAnany, J. J., Šuštar Habjan, M., Viswanathan, S., Robson, A. G.

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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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ISCEV and IPS guideline for the full-field stimulus test (FST) von Jolly, J. K., Grigg, J. R., McKendrick, A. M., Fujinami, K., Cideciyan, A. V., Thompson, D. A., Matsumoto, C., Asaoka, R., Johnson, C., Dul, M. W., Artes, P. H., Robson, A. G.

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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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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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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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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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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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Mizuo-Nakamura phenomenon in Oguchi disease due to a homozygous nonsense mutation in the SAG gene von Sergouniotis, P I, Davidson, A E, Sehmi, K, Webster, A R, Robson, A G, Moore, A T

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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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Structural evolution of a gravitationally detached normal fault array: analysis of 3D seismic data from the Ceduna Sub‐Basin, Great Australian Bight von Robson, A. G., King, R. C., Holford, S. P.

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Using laboratory measurements to predict in-flight desaturation in respiratory patients: Are current guidelines appropriate? von Robson, A.G, Lenney, J, Innes, J.A

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The Macular Assessment Profile test - a new VDU-based technique for measuring the spatial distribution of the macular pigment, lens density and rapid flicker sensitivity von Barbur, J. L., Konstantakopoulou, E., Rodriguez-Carmona, M., Harlow, J. A., Robson, A. G., Moreland, J. D.

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Unilateral electronegative ERG of non-vascular aetiology von Robson, A G, Richardson, E C, Koh, A H C, Pavesio, C E, Hykin, P G, Calcagni, A, Graham, E M, Holder, G E

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Retinal dysfunction and refractive errors: an electrophysiological study of children von Flitcroft, D I, Adams, G G W, Robson, A G, Holder, G E

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Short term variability of single breath carbon monoxide transfer factor von Robson, A G, Innes, J A

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Laboratory assessment of fitness to fly in patients with lung disease: a practical approach von Robson, AG, Hartung, TK, Innes, JA

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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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Congenital high myopia and central macular atrophy: a report of 3 families von Hull, S, Kalhoro, A, Marr, J, Thompson, D A, Holder, G E, Robson, A G, Moore, A T

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Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy von HOLDER, G. E, ROBSON, A. G, HOGG, C. R, KURZ-LEVIN, M, LOIS, N, BIRD, A. C

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