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Retinal Cases & Brief Reports|May 2, 2025
Intrafamilial Variability of IMPG1-Associated Vitelliform DystrophyLilian Chan, Mattie Adams, Tomas S Aleman, et al.
Genes|October 23, 2021
WDR36-Associated Neurodegeneration: A Case Report Highlights Possible Mechanisms of Normal Tension GlaucomaElana Meer, Tomas S Aleman, Ahmara G Ross
American Journal of Ophthalmology Case Reports|February 7, 2022
Relative preservation of the extramacular retina in LCA5-associated Leber congenital amaurosisKeli O'Connor, Erin C O'Neil, Tomas S Aleman
Ophthalmic Genetics|April 29, 2022
RP1-associated recessive retinitis pigmentosa caused by paternal uniparental disomyEmma C Bedoukian, Erin C O'Neil, Tomas S Aleman
Documenta Ophthalmologica. Advances in Ophthalmology|August 1, 2013
Retinal structure in vitamin A deficiency as explored with multimodal imagingTomas S Aleman, Sean T Garrity, Alexander J Brucker
Retinal Cases & Brief Reports|May 18, 2021
ADULT-ONSET BEST1 -VITELLIFORM DYSTROPHY ASSOCIATED WITH ANGIOID STREAK-LIKE CHANGES IN TWO SIBLINGSYafeng Li, Peter Bracha, Tomas S Aleman, et al.
Translational Vision Science & Technology|August 5, 2025
Photoreceptor Disease at Ambiguous Transition Zones in Inherited Retinal DegenerationsAlexander Sumaroka, Malgorzata Swider, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 28, 2025
Location and Identity of Photoreceptors Contributing to the Full-Field Stimulus Test (FST)Artur V Cideciyan, Hongsong Neuhauser, Alejandro J Roman, et al.
Retinal Cases & Brief Reports|March 13, 2023
NPHP1 FULL DELETION CAUSES NEPHRONOPHTHISIS AND A CONE-ROD DYSTROPHYZujaja Tauqeer, Erin C O'Neil, Alexander J Brucker, et al.
Investigative Ophthalmology & Visual Science|December 3, 2024
Retinal Sensitivity in Comparison to Cone Density in ChoroideremiaNiamh Wynne, Yu You Jiang, Tomas S Aleman, et al.
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