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The British Journal of Ophthalmology|December 20, 2005
Age related macular degeneration and sun exposure, iris colour, and skin sensitivity to sunlightJ C Khan, H Shahid, D A Thurlby, et al.
The British Journal of Ophthalmology|May 1, 1985
A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosaA L Lyness, W Ernst, M P Quinlan, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
The British Journal of Ophthalmology|June 27, 2002
Low vision services for vision rehabilitation in the United KingdomL E Culham, B Ryan, A J Jackson, et al.
The British Journal of Ophthalmology|May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding siteS L Owens, F W Fitzke, C F Inglehearn, et al.
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.
Eye (London, England)|January 1, 1995
Thrombophilic factors in ischaemic and non-ischaemic idiopathic retinal vasculitisH E Palmer, K M Jurd, B J Hunt, et al.
Neurology|March 1, 1989
Ptosis and supranuclear downgaze paralysisJ A Büttner-Ennever, J F Acheson, U Büttner, 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.
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