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Molecular Therapy : the Journal of the American Society of Gene Therapy|November 16, 2001
Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosaF Q Liang, T S Aleman, N S Dejneka, et al.
Journal of Food Science|June 7, 2023
Reduced-sodium roasted chicken: Physical/technological characteristics, optimized KCl-seasoning mixture, consumer perception, liking, emotions, and purchase intentRicardo S Aleman, Franklin Delarca Ruiz, Shirin Kazemzadeh Pournaki, et al.
Human Brain Mapping|July 11, 2020
Structural correlates of atypical visual and motor cortical oscillations in pediatric-onset multiple sclerosisAmy T Waldman, John R Sollee, Ritobrato Datta, et al.
Ophthalmic Genetics|March 17, 2021
Bardet-Biedl syndrome-7 (<i>BBS7</i>) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate modelTomas S Aleman, Erin C O'Neil, Keli O'Connor, et al.
Investigative Ophthalmology & Visual Science|June 10, 2008
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaArtur V Cideciyan, Samuel G Jacobson, Tomas S Aleman, et al.
Ophthalmology|May 11, 2005
Macular degeneration in a patient with aceruloplasminemia, a disease associated with retinal iron overloadJoshua L Dunaief, Chimene Richa, Edward P Franks, et al.
Ophthalmic Genetics|March 31, 2016
Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularizationNicole M Fuerst, Leona Serrano, Grace Han, et al.
Ophthalmic Genetics|July 3, 2024
Detailed phenotype and long-term follow-up of <i>RAB28-</i>associated cone-rod dystrophyNitya T Rao, Alexander Sumaroka, Arlene J Santos, et al.
Ophthalmic Genetics|March 27, 2025
Detailed structural abnormalities associated with a novel <i>VCAN</i> variant in a family with versican vitreoretinopathyAnny Zhong, Alexander Sumaroka, Jonathan C Tsui, et al.
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