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Ophthalmology|March 17, 2004
Waldenström's macroglobulinemia-associated retinopathyH Nida Sen, Chi-Chao Chan, Rafael C Caruso, et al.
Retina (Philadelphia, Pa.)|March 13, 2010
Rapid vision loss associated with fludarabine administrationRachel J Bishop, Xiaoyan Ding, Charles K Heller, et al.
Human Mutation|September 3, 2010
Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) diseaseCamasamudram Vijayasarathy, Ruifang Sui, Yong Zeng, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 2006
Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implantsPaul A Sieving, Rafael C Caruso, Weng Tao, et al.
Retinal Cases & Brief Reports|November 13, 2014
Clinical and genetic heterogeneity of crystalline retinopathies: report of two families without bietti crystalline dystrophyO'Neil M Biscette, Rafael C Caruso, Nizar Smaoui, et al.
Ophthalmology|April 11, 2006
Nephropathic cystinosis: posterior segment manifestations and effects of cysteamine therapyEkaterini T Tsilou, Benjamin I Rubin, George Reed, et al.
American Journal of Ophthalmology|June 15, 2005
Central visual function and the NEI-VFQ-25 near and distance activities subscale scores in people with type 1 and 2 diabetesMichael Cusick, John Paul SanGiovanni, Emily Y Chew, et al.
Molecular Vision|March 30, 2007
Mutations in NYX of individuals with high myopia, but without night blindnessQingjiong Zhang, Xueshan Xiao, Shiqiang Li, et al.
Human Mutation|June 1, 2010
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRLLorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
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