Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Sérgio Estrela Silva"'
Autor:
Lara Queirós, Patrícia Redondo, M. França, Sérgio Estrela Silva, Pedro Borges, António Benevides de Melo, Nuno Pereira, Paulo Freitas da Costa, Nazaré Carvalho, Marina Borges, Isabel Sequeira, Francisco Nuno Rocha Gonçalves, José Lemos
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background This paper fills a gap in the applied research field, for a local context, by addressing the topics of describing cataract surgery’ clinical outcomes; quality of life (QoL); and costs of the patients treated after the implementa
Externí odkaz:
https://doaj.org/article/cf066db01b6849d68a2418385a015144
Autor:
Ana Catarina Pedrosa, Joana Rodrigues Araújo, João Paulo Macedo, Sérgio Estrela Silva, António Melo, Fernando Falcão-Reis
Publikováno v:
Case Reports in Ophthalmological Medicine, Vol 2018 (2018)
Purpose. To describe a clinical case of indapamide induced bilateral angle narrowing and acute myopia. Materials and Methods. Clinical case report. Results. A 37-year-old Caucasian emmetropic man presented to the Emergency Department with complaints
Externí odkaz:
https://doaj.org/article/f0275fbd6c96402296b7f43fca762d2c
Autor:
Till M. Schneider, Joana M. Afonso, Manuel Falcão, Frank Schlichtenbrede, Fernando Falcão-Reis, Sérgio Estrela Silva
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
PurposeCharacterized by a progressive onset of gait disturbances, dementia, and urinary incontinence, idiopathic normal pressure hydrocephalus (iNPH) is considered a rare, but under-diagnosed disease. Non-invasive diagnostic markers are still insuffi
Externí odkaz:
https://doaj.org/article/ed3f7d4991164fa8b1037c3c9be37362
Autor:
Mário Lima-Fontes, Ana Faria-Pereira, Mariana Leuzinger-Dias, Marta Inês Silva, João Barbosa-Breda, Joana Araújo, Sérgio Estrela-Silva, António Benevides-Melo, Flávio Alves, João Tavares-Ferreira
Publikováno v:
Journal of Glaucoma. 32:320-326
Autor:
Sónia Torres-Costa, António Benevides Melo, Sérgio Estrela-Silva, Fernando Falcão-Reis, João Barbosa-Breda
Publikováno v:
Clinical Ophthalmology, Vol Volume 16, Pp 357-367 (2022)
Sónia Torres-Costa,1 António Benevides Melo,1,2 Sérgio Estrela-Silva,1,2 Fernando Falcão-Reis,1,2 João Barbosa-Breda1â 4 1Department of Ophthalmology, Centro Hospitalar e Universitário São João, Porto, Portugal; 2Departme
Autor:
Sérgio Estrela-Silva, Manuel Falcão, Elisete Brandão, Augusto Magalhães, Ângela Carneiro, Gonçalo Godinho, Fernando Falcão-Reis, Ana Grangeia, Carolina Madeira, Renato Silva
Publikováno v:
Case Reports in Ophthalmology
Case Reports in Ophthalmology, Vol 12, Iss 3, Pp 749-760 (2021)
Case Reports in Ophthalmology, Vol 12, Iss 3, Pp 749-760 (2021)
We report the clinical phenotype and genetic findings of two variants in PDE6C underlying achromatopsia (ACHM). Four patients with the variant c.1670G>A in exon 13 of the PDE6C gene were identified. Additionally, one had compound heterozygous genotyp
Autor:
Sérgio Estrela-Silva, Ana Maria Cunha, Daniela Teixeira, Ângela Carneiro, Diogo Cabral, Fernando Falcão-Reis
Publikováno v:
Ophthalmologica. 245:41-48
Purpose: The aim of this study was to evaluate microvascular abnormalities of patients with Alport syndrome (AS) using optical coherence tomography angiography (OCT-A) quantitative biomarkers. Methods: This was cross sectional, prospective evaluation
Autor:
Ana Filipa Moleiro, Joana Santos Oliveira, Ana Grangeia, Pedro Faria, Fernando Falcão-Reis, Augusto Magalhães, Sérgio Estrela Silva
Publikováno v:
European Journal of Ophthalmology. :112067212311704
Background Oculofaciocardiodental (OFCD) syndrome is a rare genetic disorder affecting ocular, facial, dental, and cardiac systems, being an X-linked condition caused by pathogenic variants in the BCL-6 corepressor gene ( BCOR). We report a case seri
Autor:
Sónia Torres-Costa, Carla Sofia Ferreira, Renato Santos-Silva, Sérgio Estrela-Silva, Fernando Falcão-Reis, Elisete Brandão, Ana Grangeia
Publikováno v:
European Journal of Ophthalmology. 31:NP74-NP80
Background Retinitis punctata albescens is a form of retinitis pigmentosa characterized by white fleck-like deposits in the fundus, in most cases caused by pathogenic variants in RLBP1 gene. The purpose of this work is to report the phenotypic and ge
Autor:
Ana Maria Cunha, João Barbosa‐Breda, Ana Grangeia, Sérgio Estrela‐Silva, Ângela Carneiro, Fernando Falcão‐Reis, Olinda Faria
Publikováno v:
Acta Ophthalmologica. 100