Documenta Ophthalmologica

Displaying 1 - 5 of 5
Kong, M. D., Bailey, J. A., Exinor, A., Piamjitchol, C., Demirkol, A., & Tsang, S. H. (2025). SLC37A3-associated retinitis pigmentosa: a case report of clinical features and three-year follow up. Documenta Ophthalmologica. https://doi.org/10.1007/s10633-025-10013-6
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Brodie, S. E., Faruque, P., Pincay, J., Sylla, M., Cui, X., Choi, S., Holopigian, K., & Greenstein, V. (2025). Comparison of ERG signal-to-noise ratios in simultaneous recordings with skin electrodes and contact lens electrodes. Documenta Ophthalmologica. https://doi.org/10.1007/s10633-025-10003-8
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Pincay, J., Rodriguez, M., Kaushal, D., & Tsang, S. H. (2024). Rod-sparing in a bardet-biedl syndrome patient with mutations in the ARL6 gene. Documenta Ophthalmologica. https://doi.org/10.1007/s10633-024-09985-8
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Sylla, M. M., Kolesinkova, M., da Costa, B. L., Maumenee, I. H., Tsang, S. H., & Quinn, P. M. J. (2023). A novel pathogenic CRB1 variant presenting as Leber Congenital Amaurosis 8 and evaluation of gene editing feasibility. Documenta Ophthalmologica, 147(3), 217–224. https://doi.org/10.1007/s10633-023-09951-w
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Soucy, M., Kolesnikova, M., Kim, A. H., & Tsang, S. H. (2023). Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy. Documenta Ophthalmologica, 146(3), 267–272. https://doi.org/10.1007/s10633-022-09916-5
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