Novel codon 15 RHO gene mutation associated with retinitis pigmentosa von Vilela, Manuel Ap, Menna Barreto, Roberta K, Menna Barreto, Pedro K, Sallum, Juliana Mf, Mattevi, Vanessa S

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Clinical and molecular findings in a cohort of 152 Brazilian severe early onset inherited retinal dystrophy patients von Sallum, JMF, Motta, FL, Arno, G, Porto, FBO, Resende, RG, Belfort, R

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Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome von Igelman, AD, Ku, C, da Palma, MM, Georgiou, M, Schiff, ER, Lam, BL, Sankila, E-M, Ahn, J, Pyers, L, Vincent, A, Sallum, JMF, Zein, WM, Oh, JK, Maldonado, RS, Ryu, J, Tsang, SH, Gorin, MB, Webster, AR, Michaelides, M, Yang, P, Pennesi, ME

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Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS von Rezende Filho, FM, Parkinson, MH, Pedroso, JL, Poh, R, Faber, I, Lourenço, CM, Júnior, WM, França Junior, MC, Kok, F, Sallum, JMF, Giunti, P, Barsottini, OGP

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Giant annular posttraumatic choroidal rupture von Unonius, Nichard, MD, Araújo, Jodeilson, MD, Farah, Michel E., MD, Ferraz Sallum, Juliana M., MD, Calucci, Daniela, COMT

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Genetic Heterogeneity of Dominant Optic Atrophy, Kjer Type: Identification of a Second Locus on Chromosome 18q12.2-12.3 von Kerrison, John B, Arnould, Veronique J, Ferraz Sallum, Juliana M, Vagefi, M. Reza, Barmada, M. Michael, Li, Yingying, Zhu, Danping, Maumenee, Irene H

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