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Juliana Maria Ferraz Sallum (Juliana Sallum, Olivia A Zin, Juliana M Ferraz Sallum, Juliana M F Sallum)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 17

Top Venues

Genes

Ophthalmic genetics

Arquivos brasileiros de oftalmologia

Arquivos brasileiros de cardiologia

Universidade Federal de Sao Paulo

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universidade Federal de Sao Paulo

Brazil

Afiliate Professor in Ophthalmology :: Ophthalmology

Publications

Olivia Araujo Zin, Luiza M Neves, Daniela P Cunha, Fabiana Louise Motta, Bruna N S Agonigi, Dafne D G Horovitz, Daltro C Almeida, Jocieli Malacarne, Ana Paula S Rodrigues, Adriana B Carvalho, Cinthia A Rivello, Rita Espariz, Andrea Araujo Zin, Juliana Maria Ferraz Sallum, Zilton Farias Meira de Vasconcelos
Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families. International journal of molecular sciences 24 (15) (2023)
Rebeca A S Amaral, Juliana Maria Ferraz Sallum, Mariana V Salles, Fabiana L Motta, Juliana Maria Ferraz Sallum
Macular dystrophies associated with Stargardt-like phenotypes. Arquivos brasileiros de oftalmologia (2023)
Rebeca A S Amaral, Fabiana Louise Motta, Olivia Araujo Zin, Mariana M da Palma, Gabriela D Rodrigues, Juliana Maria Ferraz Sallum
Molecular and Clinical Characterization of CNGA3 and CNGB3 Genes in Brazilian Patients Affected with Achromatopsia. Genes 14 (6) (2023)
Rebeca A S Amaral, Fabiana Louise Motta, Olivia Araujo Zin, Mariana M da Palma, Gabriela D Rodrigues, Juliana Maria Ferraz Sallum
Molecular and Clinical Characterization of CNGA3 and CNGB3 Genes in Brazilian Patients Affected with Achromatopsia. Genes 14 (6) (2023)
Mariana Matioli da Palma, Molly Marra, Austin D Igelman, Cristy A Ku, Amanda Burr, Katherine Andersen, Lesley A Everett, Fernanda Belga Ottoni Porto, Juliana Maria Ferraz Sallum, Paul Yang, Mark E Pennesi
Expanding the phenotypic and genotypic spectrum of patients with HGSNAT -related retinopathy. Ophthalmic genetics (2023)
Rebeca A S Amaral, Fabiana Louise Motta, Olivia Araujo Zin, Mariana M da Palma, Gabriela D Rodrigues, Juliana Maria Ferraz Sallum
Molecular and Clinical Characterization of CNGA3 and CNGB3 Genes in Brazilian Patients Affected with Achromatopsia. Genes 14 (6) (2023)
Juliana Maria Ferraz Sallum, Juliana Aparecida Preto de Godoy, Andrea Tiemi Kondo, José Mauro Kutner, Huber Martins Vasconcelos, André Maia
The first gene therapy for RPE65 biallelic dystrophy with voretigene neparvovec-rzyl in Brazil. Ophthalmic genetics 43 (4) (2022)
Débora L M Junqueira, Alline Stach, Adriano Caixeta, Juliana Maria Ferraz Sallum, Erika Yasaki, Jeane Tsutsui, Edgar Rizatti, Carlos E Rochitte, null Ching-Jianhong, Jean-Paul Kovalik, Jose Eduardo Krieger, A Mark Richards, Mark Y Chan, Leonardo P de Carvalho
Plasma Ceramides in Cardiovascular Disease Risk Stratification. Arquivos brasileiros de cardiologia 118 (4) (2022)
Cecília Francini Cabral de Vasconcellos, Marina Cruz Pellissari, Olivia Araujo Zin, Mariana Vallim Salles, Juliana Maria Ferraz Sallum, José Paulo Cabral de Vasconcelos
Breaking bad news in ophthalmology: a literature review. Arquivos brasileiros de oftalmologia (2022)
Olivia A Zin, Luiza M Neves, Fabiana Louise Motta, Dafne D G Horovitz, Leticia Guida, Leonardo Henrique Ferreira Gomes, Daniela P Cunha, Ana Paula S Rodrigues, Andrea A Zin, Juliana Maria Ferraz Sallum, Zilton Farias Meira de Vasconcelos
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia. Genes 12 (7) (2021)
Mariana Matioli da Palma, Fabiana Louise Motta, Mariana Vallim Salles, Caio Henrique Marques Texeira, André V Gomes, Ricardo-Pedro Casaroli-Marano, Juliana Maria Ferraz Sallum
Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline Dystrophy. Genes 12 (5) (2021)
Austin D Igelman, Cristy Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena R Schiff, Byron L Lam, Eeva-Marja Sankila, Jeeyun Ahn, Lindsey Pyers, Ajoy Vincent, Juliana Maria Ferraz Sallum, Wadih M Zein, Jin Kyun Oh, Maldonado Ramiro S, Joseph Ryu, Stephen H Tsang, Michael B Gorin, Andrew R Webster, Michel Michaelides, Paul Yang, Mark E Pennesi
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic genetics 42 (6) (2021)
Mariana Matioli da Palma, Cecilia Francini Cabral de Vasconcellos, Juliana Maria Ferraz Sallum
Rare disease day and Ophthalmology. Arquivos brasileiros de oftalmologia 84 (4) (2021)
Fabiana Louise Motta, Rafael Filippelli-Silva, Joao Paulo Kitajima, Denise A Batista, Elizabeth S Wohler, Nara L Sobreira, Renan Paulo Martin, Juliana Maria Ferraz Sallum
Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis. Ophthalmic genetics 42 (5) (2021)
Juliana Maria Ferraz Sallum, Fabiana Louise Motta, Gavin Arno, Fernanda Belga Ottoni Porto, Rosane Guazi Resende, Rubens Belfort
Clinical and molecular findings in a cohort of 152 Brazilian severe early onset inherited retinal dystrophy patients. American journal of medical genetics. Part C, Seminars in medical genetics 184 (3) (2020)
Mariana Matioli da Palma, Fabiana Louise Motta, Guilherme Eiichi Da Silva Takitani, Mariana Vallim Salles, Luiz Henrique Lima, Juliana Maria Ferraz Sallum
TUBGCP4 - associated microcephaly and chorioretinopathy. Ophthalmic genetics 41 (2) (2020)
Fabiana Louise Motta, Renan P Martin, Fernanda Belga Ottoni Porto, Elizabeth S Wohler, Rosane G Resende, Caio P Gomes, João B Pesquero, Juliana Maria Ferraz Sallum
Pathogenicity Reclasssification of RPE65 Missense Variants Related to Leber Congenital Amaurosis and Early-Onset Retinal Dystrophy. Genes 11 (1) (2019)

Juliana Maria Ferraz Sallum.css-eqlu8i{font-size:small;padding-left:4px;} (Juliana Sallum, Olivia A Zin, Juliana M Ferraz Sallum, Juliana M F Sallum)

Publication Activity (10 Years)

Top Topics

Top Venues

Juliana Maria Ferraz Sallum (Juliana Sallum, Olivia A Zin, Juliana M Ferraz Sallum, Juliana M F Sallum)