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Documenta Ophthalmologica. Advances in Ophthalmology|July 4, 2020
Misaligned foveal morphology and sector retinal dysfunction in AKT1-mosaic Proteus syndromeOliver R Marmoy, Veronica A Kinsler, Robert H Henderson, et al.Ophthalmology Science|February 2, 2026
Novel Genotype-Phenotype Correlations in CRB1-Retinopathies: Insights from Isoforms and Protein Domains Linked to Disease SeverityAna Catalina Rodriguez-Martinez, Cécile Méjécase, Vijay K Tailor-Hamblin, et al.International Journal of Molecular Sciences|April 17, 2025
Expanding the Clinical Spectrum of CRB1-Retinopathies: A Novel Genotype-Phenotype Correlation with Macular Dystrophy and Elevated Intraocular PressureAna Catalina Rodriguez-Martinez, Oliver R Marmoy, Katrina L Prise, et al.Clinical & Experimental Ophthalmology|February 18, 2015
Wound-related complications and clinical outcomes following open globe injury repairGeorge Y X Kong, Robert H Henderson, Sukhpal S Sandhu, et al.Biomedicines|March 28, 2025
Assessment of CRB1-Associated Retinopathies Using the S-MAIA Fast Protocol and Spectral-Domain Optical Coherence TomographyBethany E Higgins, Ana Catalina Rodriguez-Martinez, Giovanni Montesano, et al.Ophthalmic Genetics|May 22, 2025
DYRK1A syndrome presenting with a familial exudative vitreoretinopathy (FEVR)-like retinovascular phenotypeSiying Lin, Eleanor Hay, Dorothy A Thompson, et al.Journal of Medical Genetics|December 18, 2025
Analysis of familial exudative vitreoretinopathy (FEVR) cases in the UK 100 000 genomes project increases diagnostic rate and implicates heterozygous CTNND1 mutations in FEVRDong Sun, Robert H Henderson, Emma Clement, et al.Ophthalmic Genetics|January 5, 2023
Is RPGR-related retinal dystrophy associated with systemic disease? A case seriesRuofan Connie Han, Laura J Taylor, Cristina Martinez-Fernandez de la Camara, et al.Clinical Genetics|June 13, 2020
Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variantsEleanor Hay, Robert H Henderson, Sahar Mansour, et al.Eye (London, England)|December 4, 2023
First in man study of intravitreal tripeptidyl peptidase 1 for CLN2 retinopathyJames Wawrzynski, Ana Rodriguez Martinez, Dorothy Ann Thompson, et al.Pageof 4