Renato Emílio Santos Silva


AuthID: R-002-R2A

Confirmed Publications: 16



1
TITLE: Advancement of the muscle insertion toward the limbus as an alternative or adjunct to resection  Full Text
AUTHORS: Breda, Jorge; Magalhaes, Augusto; Faria, Olinda; Silva, Renato ; Freitas da Costa, Paulo;
PUBLISHED: 2022, SOURCE: JOURNAL OF AAPOS, VOLUME: 26, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
2
TITLE: Role of the haematological phenotype as a predictive biomarker of retinopathy of prematurity development  Full Text
AUTHORS: Mariza Fevereiro Martins; Ana Carolina Santos; Filipa Teixeira; Rita Rosa; Pedro Barros; Ricardo Parreira; Susana Teixeira; Mafalda Mota; Madalena Monteiro; Mário Alfaiate; Renato Silva ; Jorge Breda; Hercília Guimarães; Carlos Marques‐Neves; Manuel Bicho;
PUBLISHED: 2022, SOURCE: Acta Ophthalmologica, VOLUME: 100, ISSUE: S275
INDEXED IN: CrossRef
IN MY: ORCID
3
TITLE: A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 (RLBP1) gene causes retinitis punctata albescens
AUTHORS: Torres Costa, S; Ferreira, CS; Grangeia, A ; Santos Silva, R ; Brandao, E; Estrela Silva, S; Falcao Reis, F ;
PUBLISHED: 2021, SOURCE: EUROPEAN JOURNAL OF OPHTHALMOLOGY, VOLUME: 31, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
4
TITLE: Child with a mild phenotype of Incontinentia Pigmenti and inner retinal dysfunction  Full Text
AUTHORS: Cunha, AM ; Breda, J; Rocha Sousa, A ; Falcao Reis, F ; Santos Silva, R ;
PUBLISHED: 2021, SOURCE: DOCUMENTA OPHTHALMOLOGICA, VOLUME: 143, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID
5
TITLE: Cone dystrophy with supernormal rod responses: A rare KCNV2 gene variant
AUTHORS: Esteves Leandro, J; Torres Costa, S; Estrela Silva, S; Santos Silva, R ; Brandão, E; Grangeia, A ; Fernandes, S; Oliveira, R; Falcão Reis, F; Rocha Sousa, A ;
PUBLISHED: 2021, SOURCE: European Journal of Ophthalmology
INDEXED IN: Scopus CrossRef: 1
IN MY: ORCID
6
TITLE: Longitudinal Retinal Changes Induced by Hydroxychloroquine in Eyes without Retinal Toxicity
AUTHORS: Godinho, G; Madeira, C; Falcao, M ; Penas, S; Dinah Braganca, T; Brandao, E; Carneiro, A ; Santos Silva, R ; Falcao Reis, F; Beato, J;
PUBLISHED: 2021, SOURCE: OPHTHALMIC RESEARCH, VOLUME: 64, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 3
IN MY: ORCID
7
TITLE: Two Novel Disease-Causing Variants in the PDE6C Gene Underlying Achromatopsia  Full Text
AUTHORS: Madeira, Carolina; Godinho, Goncalo; Grangeia, Ana ; Falcao, Manuel ; Silva, Renato ; Carneiro, Angela ; Brandao, Elisete; Magalhaes, Augusto; Falcao Reis, Fernando ; Estrela Silva, Sergio ;
PUBLISHED: 2021, SOURCE: CASE REPORTS IN OPHTHALMOLOGY, VOLUME: 12, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
8
TITLE: A novel MFRP gene variant in a family with posterior microphthalmos, retinitis pigmentosa, foveoschisis, and foveal hypoplasia  Full Text
AUTHORS: Godinho, G; Madeira, C; Grangeia, A ; Neves Cardoso, P; Santos Silva, R ; Brandao, E; Carneiro, A ; Falcao Reis, F; Estrela Silva, S;
PUBLISHED: 2020, SOURCE: OPHTHALMIC GENETICS, VOLUME: 41, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
9
TITLE: Idiopathic Acute Exudative Polymorphous Vitelliform Maculopathy: Insight into Imaging Features and Outcomes  Full Text
AUTHORS: Torres Costa, S; Penas, S ; Carneiro, A ; Santos Silva, R ; Moura, R; Brandao, E; Falcao Reis, F ; Figueira, L ;
PUBLISHED: 2020, SOURCE: CASE REPORTS IN OPHTHALMOLOGICAL MEDICINE, VOLUME: 2020
INDEXED IN: WOS CrossRef
IN MY: ORCID
10
TITLE: Adequacy of the Fogging Test in the Detection of Clinically Significant Hyperopia in School-Aged Children  Full Text
AUTHORS: Joao Esteves Leandro; Jorge Meira; Carla Sofia Ferreira; Renato Santos Silva ; Paulo Freitas Costa; Augusto Magalhaes; Jorge Breda; Fernando Falcao Reis ;
PUBLISHED: 2019, SOURCE: JOURNAL OF OPHTHALMOLOGY, VOLUME: 2019
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID
Page 1 of 2. Total results: 16.

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