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Ophthalmology|September 17, 2019
Highly Variable Disease Courses in Siblings with Stargardt DiseaseDyon Valkenburg, Esmee H Runhart, Nathalie M Bax, et al.Investigative Ophthalmology & Visual Science|August 10, 2019
Foveal Sparing in Central Retinal DystrophiesNathalie M Bax, Dyon Valkenburg, Stanley Lambertus, et al.American Journal of Ophthalmology|July 27, 2025
The Visual Acuity Course in Stargardt DiseaseJeroen A A H Pas, Dyon Valkenburg, Catherina H Z Li, et al.HGG Advances|January 20, 2022
Long-read technologies identify a hidden inverted duplication in a family with choroideremiaZeinab Fadaie, Kornelia Neveling, Tuomo Mantere, et al.Investigative Ophthalmology & Visual Science|October 17, 2019
Late-Onset Stargardt Disease Due to Mild, Deep-Intronic ABCA4 AllelesEsmee H Runhart, Dyon Valkenburg, Stéphanie S Cornelis, et al.Investigative Ophthalmology & Visual Science|September 8, 2018
Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290Dyon Valkenburg, Caroline van Cauwenbergh, Birgit Lorenz, et al.Pageof 1