Grey Filter Contact Lens as Therapeutic Option for Acquired Reduced Binocular Visual Performance

por van Vliet, Hans, Jellema, Hinke Marijke, Nieuwendaal, Carla, Lapid-Gortzak, Ruthie, Riemslag, Frans, van der Meulen, Ivanka
Publicado 2021

Cone-rod dystrophy can be a manifestation of Danon disease

por Thiadens, Alberta A. H. J., Slingerland, Niki W. R., Florijn, Ralph J., Visser, Gerhard H., Riemslag, Frans C., Klaver, Caroline C. W.
Publicado 2012

Assessment of Night Vision Problems in Patients with Congenital Stationary Night Blindness

por Bijveld, Mieke M. C., van Genderen, Maria M., Hoeben, Frank P., Katzin, Amir A., van Nispen, Ruth M. A., Riemslag, Frans C. C., Kappers, Astrid M. L.
Publicado 2013

Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome

por Littink, Karin W., Stappers, Patricia T. Y., Riemslag, Frans C. C., Talsma, Herman E., van Genderen, Maria M., Cremers, Frans P. M., Collin, Rob W. J., van den Born, L. Ingeborgh
Publicado 2018

A Rare Form of Retinal Dystrophy Caused by Hypomorphic Nonsense Mutations in CEP290

por Roosing, Susanne, Cremers, Frans P. M., Riemslag, Frans C. C., Zonneveld-Vrieling, Marijke N., Talsma, Herman E., Klessens-Godfroy, Francoise J. M., den Hollander, Anneke I., van den Born, L. Ingeborgh
Publicado 2017

Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68

por Littink, Karin W., Stappers, Patricia T.Y., Riemslag, Frans C.C., Talsma, Herman E., van Genderen, Maria M., Cremers, Frans P.M., Collin, Rob W.J., van den Born, L. Ingeborgh
Publicado 2018

Clinical course of cone dystrophy caused by mutations in the RPGR gene

por Thiadens, Alberta A. H. J., Soerjoesing, Gyan G., Florijn, Ralph J., Tjiam, A. G., den Hollander, Anneke I., van den Born, L. Ingeborgh, Riemslag, Frans C., Bergen, Arthur A. B., Klaver, Caroline C. W.
Publicado 2011