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Salles, Mariana Vallim
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1

Expanding the Phenotypic and Genotypic Spectrum of Bietti C..:

da Palma, Mariana Matioli ; Motta, Fabiana Louise ; Salles, Mariana Vallim...
Genes.  12 (2021)  5 - p. 713 , 2021
Link: https://doi.org/10.3390/..
 
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2

Retinitis Pigmentosa Due to Rp1 Biallelic Variants:

Silva, Rita Sousa ; Salles, Mariana Vallim ; Motta, Fabiana Louise.
Scientific Reports.  10 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
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3

Synonymous Variant in the CHM Gene Causes Aberrant Splicing..:

da Palma, Mariana Matioli ; Motta, Fabiana Louise ; Gomes, Caio Perez...
Investigative Opthalmology & Visual Science.  61 (2020)  2 - p. 38 , 2020
Link: https://doi.org/10.1167/..
 
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4

A Proposal for Classification of Retinal Degeneration in Sp..:

Marianelli, Bruna Ferraço ; Filho, Flávio Moura Rezende ; Salles, Mariana Vallim...
The Cerebellum.  20 (2020)  3 - p. 384-391 , 2020
Link: https://doi.org/10.1007/..
 
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5

Relative frequency of inherited retinal dystrophies in Braz..:

Motta, Fabiana Louise ; Martin, Renan Paulo ; Filippelli-Silva, Rafael..
Scientific Reports.  8 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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6

The correlation between CRB1 variants and the clinical seve..:

Motta, Fabiana Louise ; Salles, Mariana Vallim ; Costa, Karita Antunes...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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7

Novel Complex ABCA4 Alleles in Brazilian Patients With Star..:

Salles, Mariana Vallim ; Motta, Fabiana Louise ; Dias da Silva, Elton...
Investigative Opthalmology & Visual Science.  58 (2017)  13 - p. 5723 , 2017
Link: https://doi.org/10.1167/..
 
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8

Gene panel sequencing in Brazilian patients with retinitis ..:

Costa, Kárita Antunes ; Salles, Mariana Vallim ; Whitebirch, Chris..
International Journal of Retina and Vitreous.  3 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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9

Expanding the Phenotypic and Genotypic Spectrum of Bietti C..:

da Palma, Mariana Matioli ; Motta, Fabiana Louise ; Salles, Mariana Vallim...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8151499/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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10

Expanding the phenotypic and genotypic spectrum of Bietti c..:

Matioli da Palma, Mariana ; Motta, Fabiana Bouise ; Salles, Mariana Vallim...
Reproducció del document publicat a: https://doi.org/10.3390/genes12050713.  , 2021
Link: http://hdl.handle.net/24..
 
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11

Retinitis Pigmentosa Due to Rp1 Biallelic Variants:

Silva, Rita Sousa ; Salles, Mariana Vallim ; Motta, Fabiana Louise.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994576/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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12

Synonymous Variant in the CHM Gene Causes Aberrant Splicing..:

da Palma, Mariana Matioli ; Motta, Fabiana Louise ; Gomes, Caio Perez...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329626/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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13

Retinal dystrophies and variants in PRPH2:

Palma, Mariana Matioli da ; Martin, Daniel ; Salles, Mariana Vallim...
10.5935/0004-2749.20190033.  , 2019
Link: http://www.scielo.br/sci..
 
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14

Relative frequency of inherited retinal dystrophies in Braz..:

Motta, Fabiana Louise ; Martin, Renan Paulo ; Filippelli-Silva, Rafael..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206004/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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15

Resolving the dark matter of ABCA4 for 1054 Stargardt disea..:

Khan, Mubeen ; Cornelis, Stéphanie S ; Del Pozo Valero, Marta...
info:eu-repo/semantics/altIdentifier/doi/.  ,
Link: http://hdl.handle.net/11..
 
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