Eduardo Jose Gil Duarte Silva
AuthID: R-000-4EZ
1
TITLE: Portuguese Society of Ophthalmology and Portuguese Society of Human Genetics Joint Clinical Practice Guidelines for Genetic Testing in Inherited Retinal Dystrophies Full Text
AUTHORS: Marques, Joao Pedro; Soares, Celia Azevedo ; Carvalho, Ana Luisa; Estrela Silva, Sergio; Santos, Luisa Coutinho; Ramos, Lina; Silva, Eduardo;
PUBLISHED: 2025, SOURCE: CLINICAL GENETICS
AUTHORS: Marques, Joao Pedro; Soares, Celia Azevedo ; Carvalho, Ana Luisa; Estrela Silva, Sergio; Santos, Luisa Coutinho; Ramos, Lina; Silva, Eduardo;
PUBLISHED: 2025, SOURCE: CLINICAL GENETICS
2
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
3
TITLE: Suture-Induced Allergic Contact Dermatitis to Polypropylene
AUTHORS: Pereira, Helena Pires; Silva, Eduardo; Lopes, Joao Cardoso; Carvalho, Joni Costa; Todo Bom, Ana;
PUBLISHED: 2024, SOURCE: DERMATITIS, VOLUME: 35, ISSUE: 6
AUTHORS: Pereira, Helena Pires; Silva, Eduardo; Lopes, Joao Cardoso; Carvalho, Joni Costa; Todo Bom, Ana;
PUBLISHED: 2024, SOURCE: DERMATITIS, VOLUME: 35, ISSUE: 6
INDEXED IN:
Scopus
WOS


4
TITLE: Rivaroxaban-Induced Symmetrical Drug-Related Intertriginous and Flexural Exanthema
AUTHORS: Pereira, Helena Pires; Silva, Eduardo; Moreira, Joana; Carrapatoso, Isabel; Todo Bom, Ana;
PUBLISHED: 2024, SOURCE: DERMATITIS
AUTHORS: Pereira, Helena Pires; Silva, Eduardo; Moreira, Joana; Carrapatoso, Isabel; Todo Bom, Ana;
PUBLISHED: 2024, SOURCE: DERMATITIS
INDEXED IN:
Scopus
WOS


5
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
6
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
8
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


9
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


10
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
