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Ophthalmology|November 5, 2002
Lymphoma-associated retinopathyKing W To, Charles E Thirkill, Frederick A Jakobiec, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|February 15, 2012
ω-3 intake and visual acuity in patients with retinitis pigmentosa receiving vitamin AEliot L Berson, Bernard Rosner, Michael A Sandberg, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2003
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degenerationDror Sharon, Michael A Sandberg, Rafael C Caruso, et al.Foot & Ankle International|March 10, 2000
Growth disturbances after distal tibial physeal fracturesL Berson, R S Davidson, J P Dormans, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1996
Evaluation of patients with retinitis pigmentosa receiving electric stimulation, ozonated blood, and ocular surgery in CubaE L Berson, J F Remulla, B Rosner, et al.Human Mutation|February 16, 2005
Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseasesKoji M Nishiguchi, Michael A Sandberg, Nasim Gorji, et al.JAMA Ophthalmology|March 30, 2018
Association of Vitamin A Supplementation With Disease Course in Children With Retinitis PigmentosaEliot L Berson, Carol Weigel-DiFranco, Bernard Rosner, et al.Experimental Eye Research|August 10, 2000
Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type IA K Bharadwaj, J P Kasztejna, S Huq, et al.Investigative Ophthalmology & Visual Science|August 31, 2002
Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutationsEliot L Berson, Bernard Rosner, Carol Weigel-DiFranco, et al.Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degenerationT Li, W K Franson, J W Gordon, et al.Pageof 22