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Scientific Reports|February 2, 2020
Retinitis Pigmentosa Due to Rp1 Biallelic VariantsRita Sousa Silva, Mariana Vallim Salles, Fabiana Louise Motta, et al.
International Journal of Retina and Vitreous|September 16, 2017
Gene panel sequencing in Brazilian patients with retinitis pigmentosaKárita Antunes Costa, Mariana Vallim Salles, Chris Whitebirch, et al.
Scientific Reports|October 31, 2018
Relative frequency of inherited retinal dystrophies in BrazilFabiana Louise Motta, Renan Paulo Martin, Rafael Filippelli-Silva, et al.
Arquivos Brasileiros De Oftalmologia|February 7, 2019
Retinal dystrophies and variants in PRPH2Mariana Matioli da Palma, Daniel Martin, Mariana Vallim Salles, et al.
Scientific Reports|August 19, 2017
The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypesFabiana Louise Motta, Mariana Vallim Salles, Karita Antunes Costa, et al.
Investigative Ophthalmology & Visual Science|February 26, 2020
Synonymous Variant in the CHM Gene Causes Aberrant Splicing in ChoroideremiaMariana Matioli da Palma, Fabiana Louise Motta, Caio Perez Gomes, et al.
Arquivos Brasileiros De Oftalmologia|February 26, 2025
Retinal degeneration in spinocerebellar ataxia type 7: an overview of the current knowledgeBruna Ferraço Marianelli, Flávio Moura Rezende Filho, Mariana Vallim Salles, et al.
Ophthalmic Genetics|April 10, 2020
TUBGCP4 - associated microcephaly and chorioretinopathyMariana Matioli Da Palma, Fabiana Louise Motta, Guilherme Eiichi Da Silva Takitani, et al.
Genes|June 2, 2021
Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline DystrophyMariana Matioli da Palma, Fabiana Louise Motta, Mariana Vallim Salles, et al.
Cerebellum (London, England)|November 16, 2020
A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7Bruna Ferraço Marianelli, Flávio Moura Rezende Filho, Mariana Vallim Salles, et al.
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