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Ophthalmology|February 1, 1985
Retinal histopathology of a carrier of X-chromosome-linked retinitis pigmentosaR B Szamier, E L BersonAmerican Journal of Ophthalmology|June 1, 1980
Risk factors for genetic typing and detection in retinitis pigmentosaE L Berson, B Rosner, E SimonoffHuman Mutation|December 19, 2001
Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRXC Rivolta, E L Berson, T P DryjaClinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1981
Reduction of hyperornithinemia with a low protein, low arginine diet and pyridoxine in patients with a deficiency of ornithine-ketoacid transaminase (OKT) activity and gyrate atrophy of the choroid and retinaV E Shih, E L Berson, M GargiuloInvestigative Ophthalmology & Visual Science|November 1, 1990
Rod electroretinograms in an elevated cyclic guanosine monophosphate-type human retinal degeneration. Comparison with retinitis pigmentosaM A Sandberg, S Miller, E L BersonScience (New York, N.Y.)|May 15, 1981
Rod-cone interaction in the distal human retinaM A Sandberg, E L Berson, M EffronInvestigative Ophthalmology & Visual Science|April 2, 1999
Recessive mutations in the RLBP1 gene encoding cellular retinaldehyde-binding protein in a form of retinitis punctata albescensH Morimura, E L Berson, T P DryjaArchives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1977
Visually evoked response testing with a stimulator-ophthalmoscope. Macular scars, hereditary macular degenerations, and retinitis pigmentosaM A Sandberg, E L Berson, M ArielOphthalmology|November 1, 1986
Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotypeJ F Rizzo, E L Berson, S LessellPageof 19