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The British Journal of Ophthalmology|October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophyA G Robson, M Michaelides, V A Luong, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.
The British Journal of Ophthalmology|August 1, 1992
Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutationA T Moore, F W Fitzke, C M Kemp, et al.
The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.
Journal of Environmental Pathology, Toxicology and Oncology : Official Organ of the International Society for Environmental Toxicology and Cancer|July 25, 2000
Cytotoxic effects of 5-fluorocytosine on melanoma cells transduced with cytosine deaminase geneH Lü, D Wu, Y Wan, et al.
Experimental Eye Research|August 2, 2005
High resolution imaging of fluorescein patterns in RCS rat retinae and their direct correlation with histologyH J Zambarakji, D J Keegan, T M Holmes, et al.
The British Journal of Ophthalmology|November 1, 1994
Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosaJ J Wroblewski, J A Wells, A Eckstein, et al.
Cell Death & Disease|March 3, 2011
Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivoM F Cordeiro, L Guo, K M Coxon, et al.
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