The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes von Motta, Fabiana Louise, Salles, Mariana Vallim, Costa, Karita Antunes, Filippelli-Silva, Rafael, Martin, Renan Paulo, Sallum, Juliana Maria Ferraz

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Synonymous Variant in the CHM Gene Causes Aberrant Splicing in Choroideremia von da Palma, Mariana Matioli, Motta, Fabiana Louise, Gomes, Caio Perez, Salles, Mariana Vallim, Pesquero, Joao Bosco, Ferraz Sallum, Juliana Maria

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Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2 von Rezende Filho, Flávio Moura, Jurkute, Neringa, Andrade, João Brainer Clares, Marianelli, Bruna Ferraço, Lima, Fabrício Diniz, França, Marcondes Cavalcante, Sallum, Juliana Maria Ferraz, Yu‐Wai‐Man, Patrick, Barsottini, Orlando G.P., Pedroso, José Luiz

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Unusual case of double anterior segment with two lenses and double cataract in a 6-month child von Ohara de Oliveira Junior, Elder, Fernandes, Arthur Gustavo, Nakanami, Celia Regina, Nakayama, Simone Akiko, Sallum, Juliana Maria Ferraz, Allemann, Norma, Brant Fernandes, Rodrigo Antonio

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A needle in a haystack? The impact of a targeted epilepsy gene panel in the identification of a treatable but rapidly progressive metabolic epilepsy: CLN2 disease von Lourenço, Charles Marques, Sallum, Juliana Maria Ferraz, Pereira, Alessandra Marques, Girotto, Paula Natale, Kok, Fernando, Vilela, Daniel Reda Fenga, Barron, Erika, Pessoa, André, Oliveira, Bibiana Mello de

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A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7 von Marianelli, Bruna Ferraço, Filho, Flávio Moura Rezende, Salles, Mariana Vallim, de Andrade, João Brainer Clares, Pedroso, José Luiz, Sallum, Juliana Maria Ferraz, Barsottini, Orlando Graziani P.

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Novel Complex ABCA4 Alleles in Brazilian Patients With Stargardt Disease: Genotype-Phenotype Correlation von Salles, Mariana Vallim, Motta, Fabiana Louise, Dias da Silva, Elton, Varela, Patricia, Costa, Kárita Antunes, Filippelli-Silva, Rafael, Martin, Renan Paulo, Chiang, John Pei-Wen, Pesquero, João Bosco, Sallum, Juliana Maria Ferraz

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Autoimmune retinopathy: A Review von Canamary, Jr, Aristófanes Mendonça, Takahashi, Walter Yukihiko, Sallum, Juliana Maria Ferraz

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Rare disease day and Ophthalmology von da Palma, Mariana Matioli, Cabral de Vasconcellos, Cecilia Francini, Ferraz Sallum, Juliana Maria

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Rheumatic fever and long-term use of benzathine penicillin as possible risk factors for extensive macular atrophy with pseudodrusen in a Brazilian cohort von Moreira-Neto, Carlos Augusto, Schmidt Andujar, Rafaella Atherino, Chao, John Chii Tyng, Vasconcelos, Huber, Alves, Fábio Eduardo Eberhardt, Rodrigues, Gabriela Doná, Hirt, Bruno, Arana, Jayme, Souza, Eduardo Cunha, Maia, André, Sallum, Juliana Maria Ferraz, Moreira, Jr, Carlos Augusto

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ATP8A2‐Related Disorder: Beyond Cerebellar Ataxia von Alves Corazza, Luíza, Lopes Braga, Vinícius, Yoshinaga Tonholo Silva, Thiago, Moura Rezende Filho, Flávio, Ferraz Sallum, Juliana Maria, Graziani Povoas Barsottini, Orlando, Pedroso, José Luiz

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Retinal function in patients treated with tamoxifen von Watanabe, Sung Eun Song, Berezovsky, Adriana, Motono, Márcia, Sacai, Paula Yuri, Pereira, Josenilson Martins, Sallum, Juliana Maria Ferraz, Gebrim, Luiz Henrique, Salomão, Solange Rios

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Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy von Magrinelli, Francesca, Cali, Elisa, Braga, Vinícius Lopes, Yis, Uluç, Tomoum, Hoda, Shamseldin, Hanan, Raiman, Julian, Kernstock, Christoph, Rezende Filho, Flávio Moura, Barsottini, Orlando Graziani Povoas, Taylor, Robert W., Østergaard, Elsebet, Tamim, Abdullah, Schäferhoff, Karin, Sallum, Juliana Maria Ferraz, Zaki, Maha S., Kok, Fernando, Bhatia, Kailash P., Wissinger, Bernd, Sergeant, Kate, Haack, Tobias B., Horvath, Rita, Hiz, Semra, Alkuraya, Fowzan S., Houlden, Henry, Pedroso, José Luiz, Maroofian, Reza

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Vision-related quality of life in children with retinopathy of prematurity von Messa, Alcione Aparecida, Mattos, Ricardo Belfort, Areco, Kelsy Catherina Nema, Sallum, Juliana Maria Ferraz

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Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report von Takitani, Guilherme Eiichi da Silva, Azevedo, Alexandre Gomes Bortoloti de, Motta, Fabiana Louise, Teixeira, Sérgio Henrique, Sallum, Juliana Maria Ferraz, Vessani, Roberto Murad

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A Vivência de Mães e Pais de Bebês Prematuros com Doença Ocular von Messa, Alcione Aparecida, Mattos, Ricardo Belfort, Sallum, Juliana Maria Ferraz

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Screening for Autism Spectrum Disorder in Children and Adolescents With Leber's Congenital Amaurosis von Sallum, Juliana Maria Ferraz, Pellissari, Marina Cruz, Carreiro, Luiz Renato, de Vasconcellos, Cecília Francini Cabral

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Comparison of anti-angiogenic effect in vitro between ranibizumab and bevacizumab von Souto, Alexandre Cupello, Maricato, Juliana Terzi, Denapoli, Priscila Martins Andrade, Sallum, Juliana Maria Ferraz, Han, Sang Won

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A Prospective, Observational, Non-interventional Clinical Study of Participants With Choroideremia: The NIGHT Study von MACLAREN, ROBERT E., LAM, BYRON L., FISCHER, M. DOMINIK, HOLZ, FRANK G., PENNESI, MARK E., BIRCH, DAVID G., SANKILA, EEVA-MARJA, MEUNIER, ISABELLE ANNE, STEPIEN, KIMBERLY E., SALLUM, JULIANA MARIA FERRAZ, LI, JIANG, YOON, DAN, PANDA, SUSHIL, GOW, JAMES A.

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Rehabilitation for patients with retinal diseases in Brazil: An exploratory study von Vasconcellos, Cecília Francini Cabral de, Brandão, Marina Leite, Sallum, Juliana Maria Ferraz

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