Loading... 2 0 5 0 false
 
Full Name
Silva, Eduardo
 
Main Affiliation
 
 
 
Loading... 3 0 5 0 false

Publications
(All)

Results 1-28 of 28 (Search time: 0.038 seconds).

Issue DateTitleAuthor(s)TypeAccess
125-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
22012Abnormal 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
321-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
42011Autosomal recessive nanophthalmos : MFRP mutation and phenotypical spectrumBreda, João Filipe Barbosa masterThesisopenAccess
517-Jul-2014Characterization of a portuguese LCA family secondary to homozygous RPE65 mutationQuintas, Bruna Filipa Gomes Botelho masterThesisopenAccess
62014Clinical and molecular characterization of infantile neuroaxonal dystrophy patientsSilva, Nuno Miguel Barata Gaião Cunha da masterThesisopenAccess
72011Clinical assessment of rod-cone dystrophy patients carrying rhodopsin mutationsBeato, João Nuno Bicho masterThesisopenAccess
82011CYPBI mutations in portuguese patients with primary congenital glaucomaCarvalho, Ana Rita Simões masterThesisopenAccess
9Mar-2010A dinâmica do tecido ósseo : desenvolvimento, estrutura e funçãoSimões, Maria Luis Lucas dos Santos Cruz masterThesisopenAccess
102014O "Disease Mongering" no ensino superior : um estudo em alunos universitários de medicinaLinhares, Maria Inês Reis Carneiro Aroso masterThesisopenAccess
112014Displasia 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
122011Doença de CoatsCarvalho, Ana Luísa Dias de masterThesisopenAccess
132008Evidence 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
142010Gene therapy for Stargardt and other ABCA4-related diseases: lessons from RPE65-LCA trialsSilva, Nuno Filipe Aguiar masterThesisopenAccess
152011Genotype-phenotype correlations in CFEOM syndrome : studies in the portuguese populationGante, Inês Raquel Cardoso masterThesisopenAccess
162010Genotyphe-phenotype correlations in BEST1 associated diseasesFerreira, Cátia Marisa Alves masterThesisopenAccess
1713-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
181-Jun-2017Identification of candidate genes associated with primary congenital glaucoma in patients negative for CYP1B1 mutationsCarmona, Susana Margarida Martins doctoralThesisembargoedAccess
1917-Mar-2016A new and integrative multisensory approach to Usher Syndrome: from genotypes towards an improved characterization of phenotypesRibeiro, João Carlos Gomes Silva doctoralThesisembargoedAccess
202003O papel dos factores de transcrição no desenvolvimento ocular : estudos do SIX6 e de outras moléculas reguladoras.Silva, Eduardo José Gil Duarte doctoralThesisembargoedAccess
21Mar-2012Phenotypical and molecular characterization of portuguese leber congenital amaurosis patientsProença, Ana Rita Pinto Barreiros masterThesisopenAccess
222015Phenotypical and molecular characterization of portuguese usher syndrome patientsNunes, Jóni Luís Soares masterThesisopenAccess
23Mar-2011Querotopatia em doentes com mieloma múltiploPaiva, Ana Raquel de Freitas Rodrigues masterThesisopenAccess
24Dec-2008Retinal function in best macular dystrophy: relationship between electrophysiological, psychophysical, and structural measures of damageMaia-Lopes, Susana ; Silva, Eduardo Duarte ; Reis, Aldina ; Silva, Maria Fátima ; Mateus, Catarina ; Castelo-Branco, Miguel articleopenAccess
252010Síndrome de blefarofimose-ptose-epicantus inversusPereira, Daniel Alexandre da Conceição masterThesisopenAccess
262014Spastic paraplegia with juvenile onset optic neuropathy|Pacheco, Mariana Teixeira Pinto Ferreira masterThesisopenAccess
2731-May-2017Spectrum of Ophthalmological Manifestations of Early-Onset Cobalamin C DeficiencyBarão, Rafael Correia masterThesisembargoedAccess
282007Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disordersCastelo-Branco, Miguel ; Mendes, Mafalda ; Sebastião, Ana Raquel ; Reis, Aldina ; Soares, Mário ; Saraiva, Jorge ; Bernardes, Rui ; Flores, Raquel ; Pérez-Jurado, Luis ; Silva, Eduardo articleopenAccess