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German Journal of Ophthalmology|November 1, 1995
Colour contrast sensitivity in patients with age-related Bruch's membrane changesF G Holz, M Gross-Jendroska, A Eckstein, et al.Eye (London, England)|January 1, 1996
Retinopathy in haemoglobin C traitM Hingorani, C R Bentley, H Jackson, et al.Eye (London, England)|January 1, 1993
Macular ischaemia in posterior uveitisC R Bentley, M R Stanford, J S Shilling, et al.Investigative Ophthalmology & Visual Science|May 11, 1999
Repeated injections of a ciliary neurotrophic factor analogue leading to long-term photoreceptor survival in hereditary retinal degenerationN H Chong, R A Alexander, L Waters, et al.Australian and New Zealand Journal of Ophthalmology|August 1, 1996
A randomised prospective study of outpatient haemodilution for central retinal vein obstructionA P Luckie, J J Wroblewski, P Hamilton, et al.Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.Ophthalmology|December 1, 1989
Sorsby's fundus dystrophy. A light and electron microscopic studyM R Capon, J Marshall, J I Krafft, et al.The British Journal of Ophthalmology|February 1, 1987
Ocular findings in a double-blind study of ivermectin versus diethylcarbamazine versus placebo in the treatment of onchocerciasisK Y Dadzie, A C Bird, K Awadzi, et al.The British Journal of Ophthalmology|January 25, 2005
A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1M Michaelides, G E Holder, D M Hunt, et al.The British Journal of Ophthalmology|September 1, 1994
New classification of peripheral retinal vascular changes in sickle cell diseaseA D Penman, J F Talbot, E L Chuang, et al.Pageof 33