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Annals of Neurology|August 29, 2012
Familial cortical myoclonus with a mutation in NOL3Jonathan F Russell, Jamie L Steckley, Giovanni Coppola, et al.Journal of Vitreoretinal Diseases|November 6, 2023
Unexplained Vision Loss Associated With Intraocular Silicone Oil Tamponade in Rhegmatogenous Retinal Detachment RepairParastou Pakravan, Abdulla Shaheen, Veshesh Patel, et al.Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degenerationGregory S Hageman, Don H Anderson, Lincoln V Johnson, et al.Investigative Ophthalmology & Visual Science|June 16, 2026
MMP9 Genotype and Systemic T-Cell Subsets Correlate With Structural and Functional Outcomes in Neovascular Age-Related Macular DegenerationThomas L Martinez, Zeb R Zacharias, Kyungmoo Lee, et al.Nature Medicine|December 19, 2018
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defectArtur V Cideciyan, Samuel G Jacobson, Arlene V Drack, et al.Nature Medicine|April 5, 2022
Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trialStephen R Russell, Arlene V Drack, Artur V Cideciyan, et al.Retina (Philadelphia, Pa.)|May 5, 2026
Surgical Management and Outcomes of Large High Myopic Macular Holes: Global Macular Hole Multicenter Study 3Tianyu Liu, Nassim A Abreu-Arbaje, Joana Andoh, et al.Pageof 14