Juliana M. Sallum-Ferraz
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 11 publications
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 2025
Clinical trials to gene therapy development and production in Brazil: a review.
Journal: Lancet regional health. Americas
Published: July 02, 2024
Clinical and Genetic Characterization of RDH12-Retinal Dystrophy in a South American Cohort.
Journal: Ophthalmology. Retina
Published: June 27, 2023
ATP8A2-Related Disorder: Beyond Cerebellar Ataxia.
Journal: Movement disorders clinical practice
Published: April 10, 2023
TRANSPLANTATION OF SUBRETINAL STEM CELL-DERIVED RETINAL PIGMENT EPITHELIUM FOR STARGARDT DISEASE: A Phase I Clinical Trial.
Journal: Retina (Philadelphia, Pa.)
Published: October 12, 2022
The first gene therapy for RPE65 biallelic dystrophy with voretigene neparvovec-rzyl in Brazil.
Journal: Ophthalmic genetics
Published: April 13, 2022
Characterization of Retinal Architecture in Spinocerebellar Ataxia Type 3 and Correlation with Disease Severity.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 27, 2021
Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis.
Journal: Ophthalmic genetics
Published: June 23, 2021
TUBGCP4 - associated microcephaly and chorioretinopathy.
Journal: Ophthalmic genetics
Published: April 10, 2020
PROM1 gene variations in Brazilian patients with macular dystrophy.
Journal: Ophthalmic genetics
Published: January 18, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026