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    Wyświetlanie 1-14 z 14
    Tytuł:
    Cohen Syndrome: Novel VPS13B Genetic Variants in a Male Portuguese Patient with Pigmentary Retinopathy.
    Autorzy:
    Vilares-Morgado R; Department of Ophthalmology, Centro Hospitalar Universitário de S. João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
    Ferreira AM; Department of Ophthalmology, Centro Hospitalar Universitário de S. João, Porto, Portugal.
    Santos-Silva R; Department of Ophthalmology, Centro Hospitalar Universitário de S. João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
    Quental R; Department of Human Genetics, Centro Hospitalar Universitário de S. João, Porto, Portugal.
    Carneiro Â; Department of Ophthalmology, Centro Hospitalar Universitário de S. João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
    Estrela-Silva S; Department of Ophthalmology, Centro Hospitalar Universitário de S. João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine, University of Porto, Porto, Portugal.
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    Źródło:
    Case reports in ophthalmology [Case Rep Ophthalmol] 2023 Oct 06; Vol. 14 (1), pp. 519-527. Date of Electronic Publication: 2023 Oct 06 (Print Publication: 2023).
    Typ publikacji:
    Case Reports
    Raport
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Prevalence and Area of Retinal Pigment Epithelium and Outer Retinal Atrophy in Eyes with Non-Exudative Macular Neovascularization.
    Autorzy:
    Vilares-Morgado R; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.; Faculty of Medicine, University of Porto, Porto, Portugal.
    Silva I; Faculty of Medicine, University of Porto, Porto, Portugal.
    Cunha AM; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Carneiro Â; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.; Faculty of Medicine, University of Porto, Porto, Portugal.
    Falcão-Reis F; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.; Faculty of Medicine, University of Porto, Porto, Portugal.
    Falcão M; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.; Faculty of Medicine, University of Porto, Porto, Portugal.
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    Źródło:
    Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde [Ophthalmologica] 2022; Vol. 245 (6), pp. 528-537. Date of Electronic Publication: 2022 Jul 19.
    Typ publikacji:
    Observational Study; Journal Article
    MeSH Terms:
    Retinal Pigment Epithelium*/pathology
    Geographic Atrophy*/diagnosis
    Geographic Atrophy*/epidemiology
    Humans ; Prevalence ; Cross-Sectional Studies ; Fluorescein Angiography/methods ; Tomography, Optical Coherence/methods ; Atrophy/diagnosis
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Macular Changes in a Mucopolysaccharidosis Type I Patient with Earlier Systemic Therapies.
    Autorzy:
    Magalhães A; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Cunha AM; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Vilares-Morgado R; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Leão-Teles E; Pediatric Department, Reference Centre of Inherited Metabolic Diseases, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Rodrigues E; Pediatric Department, Reference Centre of Inherited Metabolic Diseases, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Falcão M; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.
    Carneiro Â; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.
    Breda J; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.
    Falcão-Reis F; Department of Ophthalmology, Centro Hospitalar Universitário de São João, Porto, Portugal.; Department of Surgery and Physiology, Faculty of Medicine of University of Porto, Porto, Portugal.
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    Źródło:
    Case reports in ophthalmological medicine [Case Rep Ophthalmol Med] 2021 Apr 12; Vol. 2021, pp. 8866837. Date of Electronic Publication: 2021 Apr 12 (Print Publication: 2021).
    Typ publikacji:
    Case Reports
    Raport
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
      Wyświetlanie 1-14 z 14

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