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Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1985
The retinal manifestations of mitochondrial myopathy. A study of 22 casesM A Mullie, A E Harding, R K Petty, et al.Genomics|September 1, 1991
Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment siteT J Keen, C F Inglehearn, D H Lester, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.Human Mutation|June 22, 2000
Novel frameshift mutations in the RP2 gene and polymorphic variantsD L Thiselton, I Zito, C Plant, et al.Journal of Medical Genetics|June 5, 2001
Molecular genetic heterogeneity in autosomal dominant drusenE E Tarttelin, C Y Gregory-Evans, A C Bird, et al.Eye (London, England)|January 1, 1995
The role of molecular genetics in the prenatal diagnosis of retinal dystrophiesK Evans, C Y Gregory, A Fryer, et al.The British Journal of Ophthalmology|April 29, 2008
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescenceP P Rath, S Jenkins, M Michaelides, et al.Transactions of the Ophthalmological Societies of the United Kingdom|September 1, 1981
Autoimmunity and circulating immune complexes in retinal vasculitisE Kasp-Grochowska, E Graham, M D Sanders, et al.The British Journal of Ophthalmology|September 1, 1992
Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathyF X Borruat, W T Green, E M Graham, et al.AANA Journal|June 1, 1989
Arterial oxygen desaturation following intravenous injection of midazolamL D Curtis, M P Troop, M D Sanders, et al.Pageof 33