Eye Diseases, Hereditary

Displaying 1 - 3 of 3CSV
Tsai, A. S. H., Kang, E. Y. C., Wang, N.-K., Lee, H., Seo, G. H., Khang, R., & Wu, W.-C. (2023). LONG-TERM CLINICAL OUTCOMES AND GENOTYPE–PHENOTYPE CORRELATION IN FAMILIAL EXUDATIVE VITREORETINOPATHY IN A TERTIARY REFERRAL CENTER. Retina, 43(11), 1945–1950. https://doi.org/10.1097/iae.0000000000003868
Publication Date
Zeitz, C., Roger, J. E., Audo, I., Michiels, C., Sánchez-Farías, N., Varin, J., Frederiksen, H., Wilmet, B., Callebert, J., Gimenez, M.-L., Bouzidi, N., Blond, F., Guilllonneau, X., Fouquet, S., Léveillard, T., Smirnov, V., Vincent, A., Héon, E., Sahel, J.-A., … Picaud, S. (2023). Shedding light on myopia by studying complete congenital stationary night blindness. Progress in Retinal and Eye Research, 93, 101155. https://doi.org/10.1016/j.preteyeres.2022.101155
Publication Date
Kim, A. H., Liu, P.-K., Chang, Y.-H., Kang, E. Y.-C., Wang, H.-H., Chen, N., Tseng, Y.-J., Seo, G. H., Lee, H., Liu, L., Chao, A.-N., Chen, K.-J., Hwang, Y.-S., Wu, W.-C., Lai, C.-C., Tsang, S. H., Hsiao, M.-C., & Wang, N.-K. (2022). Congenital Stationary Night Blindness: Clinical and Genetic Features. International Journal of Molecular Sciences, 23(23), 14965. https://doi.org/10.3390/ijms232314965
Publication Date