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Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C > A p.(Pro188Thr) in the C1QTNF5 gene
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Une enquête de l’utilisation en Belgique de la radiothérapie pour des affections bénignes, non-tumorales
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Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease
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Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity
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Advancing Therapeutic Strategies for Inherited Retinal Degeneration: Recommendations From the Monaciano Symposium
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Complement C3 and its polymorphism: biological and clinical consequences
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Mechanisms and functions of inflammasomes
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Generation of hESC-derived retinal pigment epithelium on biopolymer coated polyimide membranes
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- Journal Article
- A1
- open access
The human visual cortex responds to gene therapy-mediated recovery of retinal function
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- Journal Article
- A1
- open access
Depressive symptoms and quality of life in people with age-related macular degeneration