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Archives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1988
Histopathologic findings in Best's vitelliform macular dystrophyS O'Gorman, W A Flaherty, G A Fishman, et al.
Ophthalmology|July 6, 2015
Visual Function in Carriers of X-Linked Retinitis PigmentosaJason Comander, Carol Weigel-DiFranco, Michael A Sandberg, et al.
American Journal of Ophthalmology|August 29, 2006
Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR geneMichael Adamian, Basil S Pawlyk, Dong-Hyun Hong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 28, 1998
Histopathologic and immunohistochemical study of an autopsy eye with X-linked cone degenerationK W To, M Adamian, F A Jakobiec, et al.
American Journal of Human Genetics|April 25, 2000
Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing lossC Rivolta, E A Sweklo, E L Berson, et al.
American Journal of Ophthalmology|June 1, 1983
Color plates to help identify patients with blue cone monochromatismE L Berson, M A Sandberg, B Rosner, et al.
Investigative Ophthalmology & Visual Science|August 1, 1981
Retinal degeneration in cats fed casein. IV. The early receptor potentialE L Berson, G Watson, K L Grasse, et al.
Birth Defects Original Article Series|January 1, 1982
A two year trial of low protein, low arginine diets or vitamin B6 for patients with gyrate atrophyE L Berson, A H Hanson, B Rosner, et al.
American Journal of Human Genetics|March 1, 1978
Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retinaV E Shih, E L Berson, R Mandell, et al.
Investigative Ophthalmology & Visual Science|October 23, 1997
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosaT P Dryja, L B Hahn, K Kajiwara, et al.
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