Autoimmune retinopathy: A Review

por Canamary, Aristófanes Mendonça, Takahashi, Walter Yukihiko, Sallum, Juliana Maria Ferraz
Publicado 2018

Spectral-Domain Optical Coherence Tomography for Macular Edema

por Badaró, Emmerson, Novais, Eduardo, Prodocimo, Larissa Maria, Sallum, Juliana M. Ferraz
Publicado 2014

Retinitis Pigmentosa Due to Rp1 Biallelic Variants

por Silva, Rita Sousa, Salles, Mariana Vallim, Motta, Fabiana Louise, Sallum, Juliana Maria Ferraz
Publicado 2020

Gene panel sequencing in Brazilian patients with retinitis pigmentosa

por Costa, Kárita Antunes, Salles, Mariana Vallim, Whitebirch, Chris, Chiang, John, Sallum, Juliana Maria Ferraz
Publicado 2017

Relative frequency of inherited retinal dystrophies in Brazil

por Motta, Fabiana Louise, Martin, Renan Paulo, Filippelli-Silva, Rafael, Salles, Mariana Vallim, Sallum, Juliana Maria Ferraz
Publicado 2018

Novel codon 15 RHO gene mutation associated with retinitis pigmentosa

por Vilela, Manuel AP, Menna Barreto, Roberta K, Menna Barreto, Pedro K, Sallum, Juliana MF, Mattevi, Vanessa S
Publicado 2018

PRPS1 Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in Women

por Rezende Filho, Flávio M., Palma, Mariana M., Pedroso, José Luiz, Barsottini, Orlando G., Sallum, Juliana M.
Publicado 2021

Simultaneous Confocal Scanning Laser Ophthalmoscopy Combined with High-Resolution Spectral-Domain Optical Coherence Tomography: A Review

por Castro Lima, Verônica, Rodrigues, Eduardo B., Nunes, Renata P., Sallum, Juliana F., Farah, Michel E., Meyer, Carsten H.
Publicado 2011

Association of age and macular pigment optical density using dual-wavelength autofluorescence imaging

por Lima, Verônica Castro, Rosen, Richard B, Prata, Tiago Santos, Dorairaj, Syril, Spielberg, Leigh, Maia, Mauricio, Sallum, Juliana M
Publicado 2013

The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes

por Motta, Fabiana Louise, Salles, Mariana Vallim, Costa, Karita Antunes, Filippelli-Silva, Rafael, Martin, Renan Paulo, Sallum, Juliana Maria Ferraz
Publicado 2017

Molecular and Clinical Characterization of CNGA3 and CNGB3 Genes in Brazilian Patients Affected with Achromatopsia

por Amaral, Rebeca A. S., Motta, Fabiana L., Zin, Olivia A., da Palma, Mariana M., Rodrigues, Gabriela D., Sallum, Juliana M. F.
Publicado 2023

Synonymous Variant in the CHM Gene Causes Aberrant Splicing in Choroideremia

por da Palma, Mariana Matioli, Motta, Fabiana Louise, Gomes, Caio Perez, Salles, Mariana Vallim, Pesquero, João Bosco, Sallum, Juliana Maria Ferraz
Publicado 2020

Epidemiology of Mutations in the 65-kDa Retinal Pigment Epithelium (RPE65) Gene-Mediated Inherited Retinal Dystrophies: A Systematic Literature Review

por Sallum, Juliana M. F., Kaur, Vinay Preet, Shaikh, Javed, Banhazi, Judit, Spera, Claudio, Aouadj, Celia, Viriato, Daniel, Fischer, M. Dominik
Publicado 2022

Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline Dystrophy

por da Palma, Mariana Matioli, Motta, Fabiana Louise, Salles, Mariana Vallim, Texeira, Caio Henrique Marques, Gomes, André V., Casaroli-Marano, Ricardo, Sallum, Juliana Maria Ferraz
Publicado 2021

Pathogenicity Reclassification of RPE65 Missense Variants Related to Leber Congenital Amaurosis and Early-Onset Retinal Dystrophy

por Motta, Fabiana L., Martin, Renan P., Porto, Fernanda B. O., Wohler, Elizabeth S., Resende, Rosane G., Gomes, Caio P., Pesquero, João B., Sallum, Juliana M. F.
Publicado 2019

Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants

por Toulis, Vasileios, Cortés-González, Vianney, de Castro-Miró, Marta, Ferraz Sallum, Juliana, Català-Mora, Jaume, Villanueva-Mendoza, Cristina, Ciccioli, Marcela, Gonzàlez-Duarte, Roser, Valero, Rebeca, Marfany, Gemma
Publicado 2020

Variants in the ABCA4 gene in a Brazilian population with Stargardt disease

por Salles, Mariana Vallim, Motta, Fabiana Louise, Martin, Renan, Filippelli-Silva, Rafael, Dias da Silva, Elton, Varela, Patricia, Costa, Kárita Antunes, Chiang, John PeiWen, Pesquero, João Bosco, Sallum, Juliana-Maria Ferraz
Publicado 2018

RNA-based therapies in inherited retinal diseases

por Girach, Aniz, Audo, Isabelle, Birch, David G., Huckfeldt, Rachel M., Lam, Byron L., Leroy, Bart P., Michaelides, Michel, Russell, Stephen R., Sallum, Juliana M.F., Stingl, Katarina, Tsang, Stephen H., Yang, Paul
Publicado 2022

Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia

por Zin, Olivia A., Neves, Luiza M., Motta, Fabiana L., Horovitz, Dafne D. G., Guida, Leticia, Gomes, Leonardo H. F., Cunha, Daniela P., Rodrigues, Ana Paula S., Zin, Andrea A., Sallum, Juliana M. F., Vasconcelos, Zilton F. M.
Publicado 2021

Ceramidas Plasmáticas na Estratificação de Risco das Doenças Cardiovasculares

por Junqueira, Débora L. M., Stach, Alline, Caixeta, Adriano, Sallum, Juliana, Yasaki, Erika, Tsutsui, Jeane, Rizatti, Edgar, Rochitte, Carlos E., Ching-Jianhong, Kovalik, Jean-Paul, Krieger, José E., Richards, A. Mark, Chan, Mark Y., de Carvalho, Leonardo P.
Publicado 2022