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Investigative Ophthalmology & Visual Science|January 22, 2015
Temporal summation in children with a history of retinopathy of prematurityRonald M Hansen, Anne Moskowitz, Jena L Tavormina, et al.Ophthalmic Genetics|June 25, 2026
Absent cone function and stable ophthalmic features in a non-syndromic woman with pathogenic variants in CEP290Samet Gulkas, Ines Fenniri, Hanna De Bruyn, et al.Epidemiology (Cambridge, Mass.)|October 31, 2000
A prospective study of the risk of congenital defects associated with maternal obesity and diabetes mellitusL L Moore, M R Singer, M L Bradlee, et al.Nephron|January 1, 1978
Accelerated atherosclerosis in chronic-dialysis patients--another lookJ F Burke, G C Francos, L L Moore, et al.Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosisH Morimura, G A Fishman, S A Grover, et al.Photochemistry and Photobiology|July 15, 2003
Does solvent influence the ground-state tautomeric population of hypericin?J Wen, P Chowdhury, D B Fulton, et al.Behavioural Brain Research|July 1, 1988
Visual fields of young childrenM F Cummings, J van Hof-van Duin, D L Mayer, et al.British Journal of Anaesthesia|April 8, 2019
Integrating basophil activation tests into evaluation of perioperative anaphylaxis to neuromuscular blocking agentsJamma Li, Oliver G Best, Michael A Rose, et al.Human Mutation|December 19, 2001
Novel frameshift mutations in CRX associated with Leber congenital amaurosisC Rivolta, N E Peck, A B Fulton, et al.Vision Research|May 1, 1995
The course of myopia in children with mild retinopathy of prematurityC L Lue, R M Hansen, D S Reisner, et al.Pageof 41