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Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1995
Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS geneR Y Kim, H Dollfus, T J Keen, et al.The British Journal of Ophthalmology|March 21, 2006
Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuityA G Robson, Z Saihan, S A Jenkins, et al.Eye (London, England)|December 13, 2005
Functional observations in vitamin A deficiency: diagnosis and time course of recoveryV A McBain, C A Egan, S J Pieris, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1997
Age-related macular disease in rural southern ItalyS Pagliarini, A Moramarco, R P Wormald, et al.Investigative Ophthalmology & Visual Science|August 1, 1994
Membrane-bound carbonic anhydrase in human retinal pigment epitheliumT J Wolfensberger, I Mahieu, J Jarvis-Evans, et al.Eye (London, England)|January 1, 1994
Acute zonal occult outer retinopathy (AZOOR) associated with multifocal choroidopathyF G Holz, R Y Kim, S D Schwartz, et al.Experimental Eye Research|February 1, 1987
Comparative biochemical analysis of purified S-antigen from human, bovine, porcine and rat retinaJ P Banga, E Kasp, S Suleyman, et al.Brain : a Journal of Neurology|April 1, 1995
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutationP Riordan-Eva, M D Sanders, G G Govan, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5R Y Kim, M al-Maghtheh, F W Fitzke, et al.Investigative Ophthalmology & Visual Science|February 9, 1999
The relationships of age changes in retinal pigment epithelium and Bruch's membraneA Okubo, R H Rosa, C V Bunce, et al.Pageof 33