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Retina (Philadelphia, Pa.)|March 11, 2014
Prph2 mutations as a cause of electronegative ERGRola Ba-Abbad, Anthony G Robson, Yew C Yap, et al.
The European Journal of Neuroscience|July 6, 2006
Early midline interactions are important in mouse optic chiasm formation but are not critical in man: a significant distinction between man and mouseMagella M Neveu, Graham E Holder, Nicola K Ragge, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Differential changes of magnocellular and parvocellular visual function in early- and late-onset strabismic amblyopiaAlison R Davis, John J Sloper, Magella M Neveu, et al.
Investigative Ophthalmology & Visual Science|October 27, 2004
Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Catherine A Egan, Vy A Luong, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 5, 2011
Electroretinogram measures in a septuagenarian populationMagella M Neveu, Alan Dangour, Elizabeth Allen, et al.
American Journal of Ophthalmology|February 7, 2006
Evidence of genetic heterogeneity in MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndromeMichel Michaelides, Jill Urquhart, Graham E Holder, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 11, 2003
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL geneDavid A R Bessant, Graham E Holder, Frederick W Fitzke, et al.
American Journal of Ophthalmology Case Reports|April 13, 2019
Isolated rod dysfunction associated with a novel genotype of CNGB1Rola Ba-Abbad, Graham E Holder, Anthony G Robson, et al.
Brain and Cognition|June 19, 2003
Cerebral blood flow and anxiety in older men: an analysis of resting anterior asymmetry and prefrontal regionsCarol F Tankard, Shari R Waldstein, Eliot L Siegel, et al.
Ophthalmology|June 15, 2005
Mutation in the gene GUCA1A, encoding guanylate cyclase-activating protein 1, causes cone, cone-rod, and macular dystrophyMichel Michaelides, Susan E Wilkie, Sharon Jenkins, et al.
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