Eduardo Jose Gil Duarte Silva
AuthID: R-000-4EZ
11
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
WOS12
TITLE: Genetically induced impairment of retinal ganglion cells at the axonal level is linked to extrastriate cortical plasticity Full Text
AUTHORS: Catarina Mateus; Otilia C d'Almeida; Aldina Reis; Eduardo Silva; Miguel Castelo Branco;
PUBLISHED: 2016, SOURCE: BRAIN STRUCTURE & FUNCTION, VOLUME: 221, ISSUE: 3
AUTHORS: Catarina Mateus; Otilia C d'Almeida; Aldina Reis; Eduardo Silva; Miguel Castelo Branco;
PUBLISHED: 2016, SOURCE: BRAIN STRUCTURE & FUNCTION, VOLUME: 221, ISSUE: 3
13
TITLE: Cultural Adaptation of the Portuguese Version of the "Sniffin' Sticks" Smell Test: Reliability, Validity, and Normative Data Full Text
AUTHORS: Joao Carlos Ribeiro; Joao Simoes; Filipe Silva; Eduardo D Silva; Cornelia Hummel; Thomas Hummel; Antonio Paiva;
PUBLISHED: 2016, SOURCE: PLOS ONE, VOLUME: 11, ISSUE: 2
AUTHORS: Joao Carlos Ribeiro; Joao Simoes; Filipe Silva; Eduardo D Silva; Cornelia Hummel; Thomas Hummel; Antonio Paiva;
PUBLISHED: 2016, SOURCE: PLOS ONE, VOLUME: 11, ISSUE: 2
14
TITLE: Accelerated age-related olfactory decline among type 1 Usher patients Full Text
AUTHORS: Joao Carlos Ribeiro; Barbara Oliveiros ; Paulo Pereira; Natalia Antonio; Thomas Hummel; Antonio Paiva; Eduardo D Silva;
PUBLISHED: 2016, SOURCE: SCIENTIFIC REPORTS, VOLUME: 6
AUTHORS: Joao Carlos Ribeiro; Barbara Oliveiros ; Paulo Pereira; Natalia Antonio; Thomas Hummel; Antonio Paiva; Eduardo D Silva;
PUBLISHED: 2016, SOURCE: SCIENTIFIC REPORTS, VOLUME: 6
15
TITLE: Possible Rare Congenital Dysinnervation Disorder: Congenital Ptosis Associated with Adduction Full Text
AUTHORS: Silvia Mendes; Diana Beselga; Sonia Campos; Arminda Neves; Joana Campos; Silvia Carvalho; Eduardo Silva; Joao P C Paulo Castro Sousa;
PUBLISHED: 2015, SOURCE: STRABISMUS, VOLUME: 23, ISSUE: 1
AUTHORS: Silvia Mendes; Diana Beselga; Sonia Campos; Arminda Neves; Joana Campos; Silvia Carvalho; Eduardo Silva; Joao P C Paulo Castro Sousa;
PUBLISHED: 2015, SOURCE: STRABISMUS, VOLUME: 23, ISSUE: 1
16
TITLE: Functional Reorganization of the Visual Dorsal Stream as Probed by 3-D Visual Coherence in Williams Syndrome Full Text
AUTHORS: Ines Bernardino; Jose Rebola; Reza Farivar; Eduardo Silva; Miguel Castelo Branco;
PUBLISHED: 2014, SOURCE: JOURNAL OF COGNITIVE NEUROSCIENCE, VOLUME: 26, ISSUE: 11
AUTHORS: Ines Bernardino; Jose Rebola; Reza Farivar; Eduardo Silva; Miguel Castelo Branco;
PUBLISHED: 2014, SOURCE: JOURNAL OF COGNITIVE NEUROSCIENCE, VOLUME: 26, ISSUE: 11
17
TITLE: GABA deficit in the visual cortex of patients with neurofibromatosis type 1: genotype-phenotype correlations and functional impact Full Text
AUTHORS: Ines R Violante ; Maria J Ribeiro ; Richard A E Edden; Pedro Guimarares; Ines Bernardino; Jose Rebola ; Gil Cunha; Eduardo Silva; Miguel Castelo Branco ;
PUBLISHED: 2013, SOURCE: BRAIN, VOLUME: 136, ISSUE: 3
AUTHORS: Ines R Violante ; Maria J Ribeiro ; Richard A E Edden; Pedro Guimarares; Ines Bernardino; Jose Rebola ; Gil Cunha; Eduardo Silva; Miguel Castelo Branco ;
PUBLISHED: 2013, SOURCE: BRAIN, VOLUME: 136, ISSUE: 3
18
TITLE: AAO Task Force on Genetic Testing Full Text
AUTHORS: Bronwyn Bateman; Eduardo Silva;
PUBLISHED: 2013, SOURCE: OPHTHALMOLOGY, VOLUME: 120, ISSUE: 10
AUTHORS: Bronwyn Bateman; Eduardo Silva;
PUBLISHED: 2013, SOURCE: OPHTHALMOLOGY, VOLUME: 120, ISSUE: 10
19
TITLE: ALDH1A3 Mutations Cause Recessive Anophthalmia and Microphthalmia
AUTHORS: Lucas Fares-Taie; Sylvie Gerber; Nicolas Chassaing; Jill Clayton-Smith; Sylvain Hanein; Eduardo Silva; Margaux Serey; Valérie Serre; Xavier Gérard; Clarisse Baumann; Ghislaine Plessis; Bénédicte Demeer; Lionel Brétillon; Christine Bole; Patrick Nitschke; Arnold Munnich; Stanislas Lyonnet; Patrick Calvas; Josseline Kaplan; Nicola Ragge; ...More
PUBLISHED: 2013, SOURCE: The American Journal of Human Genetics, VOLUME: 92, ISSUE: 2
AUTHORS: Lucas Fares-Taie; Sylvie Gerber; Nicolas Chassaing; Jill Clayton-Smith; Sylvain Hanein; Eduardo Silva; Margaux Serey; Valérie Serre; Xavier Gérard; Clarisse Baumann; Ghislaine Plessis; Bénédicte Demeer; Lionel Brétillon; Christine Bole; Patrick Nitschke; Arnold Munnich; Stanislas Lyonnet; Patrick Calvas; Josseline Kaplan; Nicola Ragge; ...More
PUBLISHED: 2013, SOURCE: The American Journal of Human Genetics, VOLUME: 92, ISSUE: 2
20
TITLE: Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations
AUTHORS: Isabelle Perrault; Sophie Saunier; Sylvain Hanein; Emilie Filhol; Albane A Bizet; Felicity Collins; Mustafa A M Salih; Sylvie Gerber; Nathalie Delphin; Karine Bigot; Christophe Orssaud; Eduardo Silva; Veronique Baudouin; Machteld M Oud; Nora Shannon; Martine Le Merrer; Olivier Roche; Christine Pietrement; Jamal Goumid; Clarisse Baumann; ...More
PUBLISHED: 2012, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 90, ISSUE: 5
AUTHORS: Isabelle Perrault; Sophie Saunier; Sylvain Hanein; Emilie Filhol; Albane A Bizet; Felicity Collins; Mustafa A M Salih; Sylvie Gerber; Nathalie Delphin; Karine Bigot; Christophe Orssaud; Eduardo Silva; Veronique Baudouin; Machteld M Oud; Nora Shannon; Martine Le Merrer; Olivier Roche; Christine Pietrement; Jamal Goumid; Clarisse Baumann; ...More
PUBLISHED: 2012, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 90, ISSUE: 5
