Casamento entre cegos: atrofia óptica congênita x síndrome de Rieger

by Juliana Maria Ferraz, Décio Brunoni, Clélia Maria Erwenne

Terapia gênica em distrofias hereditárias de retina Gene therapy for inherited retinal dystrophies

by Monique Côco, Sang Won Han, Juliana Maria Ferraz Sallum
Published 2009-08-01

Avaliação da autofluorescência do fundo de olho nas distrofias de retina com o aparelho Heidelberg Retina Angiograph2 Evaluation of fundus autofluorescence in hereditary retinal di...

by Monique Côco, Natalia Tamie Baba, Juliana Maria Ferraz Sallum
Published 2007-10-01

Anomalias oculares e características genéticas na síndrome de Marfan

by Sallum Juliana Maria Ferraz, Chen Jane, Perez Ana Beatriz Alvarez
Published 2002-01-01

Autoimmune retinopathy: A Review

by Aristófanes Mendonça Canamary, Walter Yukihiko Takahashi, Juliana Maria Ferraz Sallum
Published 2018-01-01

Anomalias oculares em pacientes portadores de deficiência auditiva genética Ocular abnormalities in genetically deaf people

by Jane Chen, Juliana Maria Ferraz Sallum, Silvia Bragagnolo Longhitano, Décio Brunoni
Published 2000-12-01

Ectopia Lentis et Pupillae

by Márcia Beatriz Tartarella, Arnaud Araújo Filho, Juliana Maria Ferraz Sallum, Clélia Maria Erwenne

Vision-related quality of life in children with retinopathy of prematurity

by Alcione Aparecida Messa, Ricardo Belfort Mattos, Kelsy Catherina Nema Areco, Juliana Maria Ferraz Sallum
Published 2015-08-01

Gene panel sequencing in Brazilian patients with retinitis pigmentosa

by Kárita Antunes Costa, Mariana Vallim Salles, Chris Whitebirch, John Chiang, Juliana Maria Ferraz Sallum
Published 2017-09-01

Relative frequency of inherited retinal dystrophies in Brazil

by Fabiana Louise Motta, Renan Paulo Martin, Rafael Filippelli-Silva, Mariana Vallim Salles, Juliana Maria Ferraz Sallum
Published 2018-10-01

Transplante terapêutico em úlceras de córnea bacterianas ativas

by Seiji Hayashi, Élcio Hideo Sato, Denise de Freitas, Cláudio Luís Lottenberg, Juliana Maria Ferraz, Walton Nose

Retinitis pigmentosa in pantothenate kinase-associated neurodegeneration

by José Luiz Pedroso, Priscilla Proveti, Luiz Fernando Teixeira, Juliana Maria Ferraz Sallum, Orlando G. P. Barsottini
Published 2014-10-01

Avaliação da tomografia de coerência óptica em pacientes portadores de degeneração macular relacionada à idade tratada com terapia fotodinâmica com verteporfina Ocular coherence to...

by Arnaldo Furman Bordon, Akioshi Oshima, Tércio Alves Guia, Daniela Calucci, Juliana Maria Ferraz Sallum, Michel Eid Farah
Published 2008-12-01

Comparação do efeito antiangiogênico do ranibizumab e do bevacizumab in vitro

by Alexandre Cupello Souto, Juliana Terzi Maricato, Priscila Martins Andrade Denapoli, Juliana Maria Ferraz Sallum, Sang Won Han
Published 2011-10-01

Retinose pigmentada unilateral secundária a trauma: relato de caso

by Alexandre Tagliari Cestari, Juliana Maria Ferraz Sallum, Marina Lourenço De Conti, Thiago Iorio Tagliari, Marcello Novoa Colombo Barboza
Published 2012-06-01

Aspectos da tomografia de coerência óptica na doença de Stargardt: relato de caso Optical coherence tomography aspects of Stargardt's disease: case report

by Enéias Bezerra Gouveia, Maira Saad de Ávila Morales, Norma Allemann, Guilherme Matte, Adriana Berezovsky, Juliana Maria Ferraz Sallum
Published 2006-08-01

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

by Fabiana Louise Motta, Mariana Vallim Salles, Karita Antunes Costa, Rafael Filippelli-Silva, Renan Paulo Martin, Juliana Maria Ferraz Sallum
Published 2017-08-01

Retinal dystrophies and variants in PRPH2

by Mariana Matioli da Palma, Daniel Martin, Mariana Vallim Salles, Fabiana Louise Teixeira Motta, Suel Abujamra, Juliana Maria Ferraz Sallum

Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report

by Guilherme Eiichi da Silva Takitani, Alexandre Gomes Bortoloti de Azevedo, Fabiana Louise Motta, Sérgio Henrique Teixeira, Juliana Maria Ferraz Sallum, Roberto Murad Vessani

Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline Dystrophy

by Mariana Matioli da Palma, Fabiana Louise Motta, Mariana Vallim Salles, Caio Henrique Marques Texeira, André V. Gomes, Ricardo Casaroli-Marano, Juliana Maria Ferraz Sallum
Published 2021-05-01