Browsing by Author Silva, Eduardo Duarte


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Issue DateTitleAuthor(s)TypeAccess
25-Jan-2012Abnormal achromatic and chromatic contrast sensitivity in neurofibromatosis type 1Ribeiro, Maria José ; Violante, Inês R ; Bernardino, Inês ; Ramos, Fabiana ; Saraiva, Jorge ; Reviriego, Pablo ; Upadhyaya, Meena ; Silva, Eduardo D. ; Castelo-Branco, Miguel articleopenAccess
2012Abnormal brain activation in neurofibromatosis type 1: a link between visual processing and the default mode networkViolante, Inês R. ; Ribeiro, Maria J. ; Cunha, Gil ; Bernardino, Inês ; Duarte, João V. ; Ramos, Fabiana ; Saraiva, Jorge ; Silva, Eduardo ; Castelo-Branco, Miguel articleopenAccess
21-Feb-2014Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficitsRibeiro, Maria J. ; Almeida, Otília C. d' ; Ramos, Fabiana ; Saraiva, Jorge ; Silva, Eduardo D. ; Castelo-Branco, Miguel articleopenAccess
22-Jun-2016Accelerated age-related olfactory decline among type 1 Usher patientsRibeiro, João Carlos; Oliveiros, Bárbara ; Pereira, Paulo ; António, Natália ; Hummel, Thomas; Paiva, António ; Silva, Eduardo D. articleopenAccess
2011Autosomal recessive nanophthalmos : MFRP mutation and phenotypical spectrumBreda, João Filipe Barbosa masterThesisopenAccess
17-Jul-2014Characterization of a portuguese LCA family secondary to homozygous RPE65 mutationQuintas, Bruna Filipa Gomes Botelho masterThesisopenAccess
2014Clinical and molecular characterization of infantile neuroaxonal dystrophy patientsSilva, Nuno Miguel Barata Gaião Cunha da masterThesisopenAccess
2011Clinical assessment of rod-cone dystrophy patients carrying rhodopsin mutationsBeato, João Nuno Bicho masterThesisopenAccess
2016Cultural Adaptation of the Portuguese Version of the "Sniffin' Sticks" Smell Test: Reliability, Validity, and Normative DataRibeiro, João Carlos ; Simões, João ; Silva, Filipe; Silva, Eduardo ; Hummel, Cornelia; Hummel, Thomas; Paiva, António articleopenAccess
2011CYPBI mutations in portuguese patients with primary congenital glaucomaCarvalho, Ana Rita Simões masterThesisopenAccess
Mar-2010A dinâmica do tecido ósseo : desenvolvimento, estrutura e funçãoSimões, Maria Luis Lucas dos Santos Cruz masterThesisopenAccess
2014O "Disease Mongering" no ensino superior : um estudo em alunos universitários de medicinaLinhares, Maria Inês Reis Carneiro Aroso masterThesisopenAccess
2014Displasia epimetadiafisária autossómica recessiva associada a surdez neurossensorial grave e displasia dos cones e bastonetes grave de inicio precoce : uma nova síndrome?Valente, Cátia Celina dos Santos masterThesisopenAccess
2011Doença de CoatsCarvalho, Ana Luísa Dias de masterThesisopenAccess
2019Enhanced Visual Attentional Modulation in Patients with Inherited Peripheral Retinal Degeneration in the Absence of Cortical DegenerationFerreira, Sónia ; Pereira, Andreia Carvalho ; Quendera, Bruno ; Reis, Aldina ; Silva, Eduardo Duarte ; Castelo-Branco, Miguel articleopenAccess
2008Evidence of widespread retinal dysfunction in patients with stargardt disease and morphologically unaffected carrier relativesMaia-Lopes, Susana ; Silva, Eduardo D. ; Silva, Maria Fátima ; Reis, Aldina ; Faria, Pedro ; Castelo-Branco, Miguel articleopenAccess
2010Gene therapy for Stargardt and other ABCA4-related diseases: lessons from RPE65-LCA trialsSilva, Nuno Filipe Aguiar masterThesisopenAccess
2011Genotype-phenotype correlations in CFEOM syndrome : studies in the portuguese populationGante, Inês Raquel Cardoso masterThesisopenAccess
2010Genotyphe-phenotype correlations in BEST1 associated diseasesFerreira, Cátia Marisa Alves masterThesisopenAccess
13-Feb-2013Gyrification, cortical and subcortical morphometry in neurofibromatosis type 1: an uneven profile of developmental abnormalitiesViolante, Inês R. ; Ribeiro, Maria J. ; Silva, Eduardo D. ; Castelo-Branco, Miguel articleopenAccess