Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families. by Caroline Van Cauwenbergh, Frauke Coppieters, Dimitri Roels, Sarah De Jaegere, Helena Flipts, Julie De Zaeytijd, Sophie Walraedt, Charlotte Claes, Erik Fransen, Guy Van Camp, Fanny Depasse, Ingele Casteels, Thomy de Ravel, Bart P Leroy, Elfride De Baere

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Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience by Hwei Wuen Chan, Hwei Wuen Chan, Filip Van den Broeck, Filip Van den Broeck, Axelle Cools, Sophie Walraedt, Inge Joniau, Hannah Verdin, Hannah Verdin, Irina Balikova, Stefaan Van Nuffel, Patricia Delbeke, Elfride De Baere, Elfride De Baere, Bart P. Leroy, Bart P. Leroy, Bart P. Leroy, Bart P. Leroy, Fanny Nerinckx

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The natural history of Leber congenital amaurosis and cone–rod dystrophy associated with variants in the GUCY2D gene by Hahn, LC, Georgiou, M, Almushattat, H, van Schooneveld, MJ, de Carvalho, ER, Wesseling, NL, Ten Brink, JB, Florijn, RJ, Lissenberg-Witte, BI, Strubbe, I, van Cauwenbergh, C, de Zaeytijd, J, Walraedt, S, de Baere, E, Mukherjee, R, McKibbin, M, Meester-Smoor, MA, Thiadens, AAHJ, Al-Khuzaei, S, Akyol, E, Lotery, AJ, van Genderen, MM, Norel, JO-V, Ingeborgh van den Born, L, Hoyng, CB, Klaver, CCW, Downes, SM, Bergen, AA, Leroy, BP, Michaelides, M, Boon, CJF