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Investigative Ophthalmology & Visual Science|July 1, 1996
The relationship between visual field size and electroretinogram amplitude in retinitis pigmentosaM A Sandberg, C Weigel-DiFranco, B Rosner, et al.Ophthalmology|January 1, 1993
Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigationK W To, M Adamian, F A Jakobiec, et al.Experimental Eye Research|August 1, 1997
Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosaS Yamamoto, S C Khani, E L Berson, et al.Nature Genetics|March 1, 1993
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescensK Kajiwara, M A Sandberg, E L Berson, et al.Nature Genetics|February 1, 1997
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindnessS Yamamoto, K C Sippel, E L Berson, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1996
Clinical and histopathologic findings in clumped pigmentary retinal degenerationK W To, M Adamian, F A Jakobiec, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His)E L Berson, B Rosner, M A Sandberg, et al.American Journal of Ophthalmology|November 15, 1989
An electroretinographic and molecular genetic study of X-linked cone degenerationE Reichel, A M Bruce, M A Sandberg, et al.Investigative Ophthalmology & Visual Science|July 7, 1999
Frequency of mutations in the gene encoding the alpha subunit of rod cGMP-phosphodiesterase in autosomal recessive retinitis pigmentosaT P Dryja, D E Rucinski, S H Chen, et al.Nature Genetics|June 1, 1993
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosaM E McLaughlin, M A Sandberg, E L Berson, et al.Pageof 22