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Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Translational Vision Science & Technology|May 23, 2022
Restoration of Vision and Retinal Responses After Adeno-Associated Virus-Mediated Optogenetic Therapy in Blind DogsSergei Nikonov, Puya Aravand, Arkady Lyubarsky, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 18, 2005
Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindnessGregory M Acland, Gustavo D Aguirre, Jean Bennett, et al.
JAMA Ophthalmology|February 28, 2017
Evaluation of Optical Coherence Tomography to Detect Elevated Intracranial Pressure in ChildrenJordan W Swanson, Tomas S Aleman, Wen Xu, et al.
Experimental Eye Research|January 27, 2005
Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measuresAlejandro J Roman, Sharon B Schwartz, Tomas S Aleman, et al.
Retinal Cases & Brief Reports|January 27, 2026
A Spectrum of Severity of a Unifying Retinal Phenotype in TUBB4B-Associated Inherited Retinal DegenerationSophia Zhang, Robert A Avery, Vivian Wu, et al.
Nature Genetics|April 28, 2001
Gene therapy restores vision in a canine model of childhood blindnessG M Acland, G D Aguirre, J Ray, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
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