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Eye (London, England)|March 2, 2013
Ranibizumab for the treatment of choroidal neovascularisation secondary to pathological myopia: interim analysis of the REPAIR studyA Tufail, P J Patel, S Sivaprasad, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.Investigative Ophthalmology & Visual Science|May 1, 2001
An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000
Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.Human Molecular Genetics|March 30, 2021
The rare C9 P167S risk variant for age-related macular degeneration increases polymerization of the terminal component of the complement cascadeO McMahon, T M Hallam, S Patel, et al.Pageof 5