Eduardo Jose Gil Duarte Silva
AuthID: R-000-4EZ
1
TITLE: Vestibulo-ocular reflex dynamics with head-impulses discriminates Usher patients type 1 and 2 Full Text
AUTHORS: Amorim, Ana Margarida; Ramada, Ana Beatriz; Lopes, Ana Cristina; Duarte Silva, Eduardo; Lemos, Joao; Ribeiro, Joao Carlos;
PUBLISHED: 2024, SOURCE: SCIENTIFIC REPORTS, VOLUME: 14, ISSUE: 1
AUTHORS: Amorim, Ana Margarida; Ramada, Ana Beatriz; Lopes, Ana Cristina; Duarte Silva, Eduardo; Lemos, Joao; Ribeiro, Joao Carlos;
PUBLISHED: 2024, SOURCE: SCIENTIFIC REPORTS, VOLUME: 14, ISSUE: 1
2
TITLE: Novel Insights in the Management of Vernal Keratoconjunctivitis (VKC): European Expert Consensus Using a Modified Nominal Group Technique
AUTHORS: Dahlmann Noor, A; Bonini, S; Bremond Gignac, D; Heegaard, S; Leonardi, A; Montero, J; Silva, ED; EUR-VKC Group The;
PUBLISHED: 2023, SOURCE: Ophthalmology and Therapy, VOLUME: 12, ISSUE: 2
AUTHORS: Dahlmann Noor, A; Bonini, S; Bremond Gignac, D; Heegaard, S; Leonardi, A; Montero, J; Silva, ED; EUR-VKC Group The;
PUBLISHED: 2023, SOURCE: Ophthalmology and Therapy, VOLUME: 12, ISSUE: 2
3
TITLE: Myopia control: short-term effect of 0.01% atropine vs. defocus incorporated multiple segment lenses—a retrospective study in European children Full Text
AUTHORS: Sandra Guimarães; Patrícia Barros da Silva; Bárbara Oliveiros; Eduardo Silva;
PUBLISHED: 2023, SOURCE: International Ophthalmology, VOLUME: 43, ISSUE: 10
AUTHORS: Sandra Guimarães; Patrícia Barros da Silva; Bárbara Oliveiros; Eduardo Silva;
PUBLISHED: 2023, SOURCE: International Ophthalmology, VOLUME: 43, ISSUE: 10
5
TITLE: SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma
AUTHORS: Terri L Young; Kristina N Whisenhunt; Jing Jin; Sarah M LaMartina; Sean M Martin; Tomokazu Souma; Vachiranee Limviphuvadh; Fatemeh Suri; Emmanuelle Souzeau; Xue Zhang; Yongwook Dan; Evie Anagnos; Susana Carmona; Nicole M Jody; Nickie Stangel; Emily C Higuchi; Samuel J Huang; Owen M Siggs; Maria Jose Simoes; Brendan M Lawson; ...More
PUBLISHED: 2020, SOURCE: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, VOLUME: 61, ISSUE: 12
AUTHORS: Terri L Young; Kristina N Whisenhunt; Jing Jin; Sarah M LaMartina; Sean M Martin; Tomokazu Souma; Vachiranee Limviphuvadh; Fatemeh Suri; Emmanuelle Souzeau; Xue Zhang; Yongwook Dan; Evie Anagnos; Susana Carmona; Nicole M Jody; Nickie Stangel; Emily C Higuchi; Samuel J Huang; Owen M Siggs; Maria Jose Simoes; Brendan M Lawson; ...More
PUBLISHED: 2020, SOURCE: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, VOLUME: 61, ISSUE: 12
INDEXED IN: 
Scopus 
WOS
Scopus WOS6
TITLE: The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene
AUTHORS: Virginie G Peter; Mathieu Quinodoz; Jorge Pinto Basto; Sergio B Sousa; Silvio Alessandro Di Gioia; Gabriela Soares; Gabriela Ferraz Leal; Eduardo D Silva; Rosanna Pescini Gobert; Noriko Miyake; Naomichi Matsumoto; Elizabeth C Engle; Sheila Unger; Frederic Shapiro; Andrea Superti Furga; Carlo Rivolta; Belinda Campos Xavier;
PUBLISHED: 2019, SOURCE: GENETICS IN MEDICINE, VOLUME: 21, ISSUE: 12
AUTHORS: Virginie G Peter; Mathieu Quinodoz; Jorge Pinto Basto; Sergio B Sousa; Silvio Alessandro Di Gioia; Gabriela Soares; Gabriela Ferraz Leal; Eduardo D Silva; Rosanna Pescini Gobert; Noriko Miyake; Naomichi Matsumoto; Elizabeth C Engle; Sheila Unger; Frederic Shapiro; Andrea Superti Furga; Carlo Rivolta; Belinda Campos Xavier;
PUBLISHED: 2019, SOURCE: GENETICS IN MEDICINE, VOLUME: 21, ISSUE: 12
INDEXED IN: Scopus WOS
Scopus WOS7
TITLE: The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene
AUTHORS: Virginie G Peter; Mathieu Quinodoz; Jorge Pinto Basto; Sergio B Sousa; Silvio Alessandro Di Gioia; Gabriela Soares; Gabriela Ferraz Leal; Eduardo D Silva; Rosanna Pescini Gobert; Noriko Miyake; Naomichi Matsumoto; Elizabeth C Engle; Sheila Unger; Frederic Shapiro; Andrea Superti Furga; Carlo Rivolta; Belinda Campos Xavier;
PUBLISHED: 2019, SOURCE: GENETICS IN MEDICINE, VOLUME: 21, ISSUE: 12
AUTHORS: Virginie G Peter; Mathieu Quinodoz; Jorge Pinto Basto; Sergio B Sousa; Silvio Alessandro Di Gioia; Gabriela Soares; Gabriela Ferraz Leal; Eduardo D Silva; Rosanna Pescini Gobert; Noriko Miyake; Naomichi Matsumoto; Elizabeth C Engle; Sheila Unger; Frederic Shapiro; Andrea Superti Furga; Carlo Rivolta; Belinda Campos Xavier;
PUBLISHED: 2019, SOURCE: GENETICS IN MEDICINE, VOLUME: 21, ISSUE: 12
INDEXED IN: WOS
WOS8
TITLE: Diagnosis and Treatment Options for Achromatopsia: A Review of the Literature
AUTHORS: Isabel Pascual Camps; Honorio Barranco Gonzalez; Juan Avino Martinez; Eduardo Silva; Miguel Harto Castano;
PUBLISHED: 2018, SOURCE: JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS, VOLUME: 55, ISSUE: 2
AUTHORS: Isabel Pascual Camps; Honorio Barranco Gonzalez; Juan Avino Martinez; Eduardo Silva; Miguel Harto Castano;
PUBLISHED: 2018, SOURCE: JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS, VOLUME: 55, ISSUE: 2
INDEXED IN: Scopus WOS
Scopus WOS9
TITLE: Cytotoxicity of doxorubicin-loaded PLGA and PLGA-PEI nanoparticles: relevance for anti-tumor effects and cardiotoxicity Full Text
AUTHORS: Candido, C; Ferreira, L; Silva, E; Junior, AJ; Peccinini, R; Oliveira, P;
PUBLISHED: 2018, SOURCE: EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, VOLUME: 48
AUTHORS: Candido, C; Ferreira, L; Silva, E; Junior, AJ; Peccinini, R; Oliveira, P;
PUBLISHED: 2018, SOURCE: EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, VOLUME: 48
INDEXED IN: WOS
WOS10
TITLE: CYP1B1 mutational screening in a Portuguese cohort of primary congenital glaucoma patients Full Text
AUTHORS: Simoes, MJ; Carmona, S; Roberts, R; Wainwright, G; Faro, C; Silva, E; Egas, C;
PUBLISHED: 2017, SOURCE: OPHTHALMIC GENETICS, VOLUME: 38, ISSUE: 2
AUTHORS: Simoes, MJ; Carmona, S; Roberts, R; Wainwright, G; Faro, C; Silva, E; Egas, C;
PUBLISHED: 2017, SOURCE: OPHTHALMIC GENETICS, VOLUME: 38, ISSUE: 2
INDEXED IN: WOS
WOS