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Experimental Eye Research|April 1, 1994
Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistryZ Y Li, S G Jacobson, A H MilamBehavioural Brain Research|October 1, 1983
Psychophysical assessment of visual acuity in infants with visual disordersI Mohindra, S G Jacobson, J Zwaan, et al.Transactions of the Ophthalmological Societies of the United Kingdom|January 1, 1983
Visual pigment levels in retinitis pigmentosaC M Kemp, D J Faulkner, S G JacobsonExperimental Brain Research|August 1, 1979
Optic nerve fibre lesions in adult cats: pattern of recovery of spatial visionS G Jacobson, R A Eames, W I McDonaldInvestigative Ophthalmology & Visual Science|July 1, 1988
The distribution and kinetics of visual pigments in the cat retinaC M Kemp, D J Faulkner, S G JacobsonNature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.Documenta Ophthalmologica. Advances in Ophthalmology|June 1, 1988
Rod and cone psychophysics and electroretinography: methods for comparison in retinal degenerationsK Yagasaki, S G Jacobson, P P Apáthy, et al.American Journal of Ophthalmology|September 15, 1991
Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutationsS G Jacobson, C M Kemp, C H Sung, et al.Experimental Eye Research|May 1, 1989
Interocular asymmetry of visual function in heterozygotes of X-linked retinitis pigmentosaS G Jacobson, K Yagasaki, W J Feuer, et al.Experimental Eye Research|November 1, 1989
Rhodopsin levels and rod-mediated function in Abyssinian cats with hereditary retinal degenerationS G Jacobson, C M Kemp, K Narfström, et al.Pageof 13