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Ophthalmology|July 1, 1993
Hyperopia and neovascularization in age-related macular degenerationM A Sandberg, M J Tolentino, S Miller, et al.American Journal of Ophthalmology|March 15, 1985
Natural course of retinitis pigmentosa over a three-year intervalE L Berson, M A Sandberg, B Rosner, et al.American Journal of Ophthalmology|May 15, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucineE L Berson, B Rosner, M A Sandberg, et al.American Journal of Ophthalmology|November 15, 1991
Hydroxychloroquine retinopathyA Weiner, M A Sandberg, A R Gaudio, et al.Vision Research|January 1, 1987
Effects of IBMX on the ERG of the isolated perfused cat eyeM A Sandberg, B S Pawlyk, W G Crane, et al.Investigative Ophthalmology & Visual Science|October 1, 1995
Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutationP J Rosenfeld, L B Hahn, M A Sandberg, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|July 31, 1998
Rod and cone function in the Nougaret form of stationary night blindnessM A Sandberg, B S Pawlyk, J Dan, et al.Proceedings of the National Academy of Sciences of the United States of America|March 22, 2000
A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)D H Hong, B S Pawlyk, J Shang, et al.Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.Nature Genetics|June 1, 1992
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaP J Rosenfeld, G S Cowley, T L McGee, et al.Pageof 16