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Novartis Foundation Symposium|January 31, 2004
The expanding roles of ABCA4 and CRB1 in inherited blindnessF P M Cremers, A Maugeri, A I den Hollander, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 16, 2000
Relationship between anticoagulant medication and massive intraocular hemorrhage in age-related macular degenerationM A Tilanus, W Vaandrager, M H Cuypers, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 13, 2002
[From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa]F P M Cremers, A Maugeri, B J Klevering, et al.
American Journal of Ophthalmology|June 1, 1996
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS geneC B Hoyng, P Heutink, L Testers, et al.
Ophthalmic Genetics|November 12, 1998
ABCR unites what ophthalmologists divide(s)M A van Driel, A Maugeri, B J Klevering, et al.
Acta Ophthalmologica|May 3, 2025
Effectiveness and safety of repeated photodynamic therapy in recurrent central serous chorioretinopathyF M van den Tillaart, A Komrojan, C B Hoyng, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 8, 2007
[The Dutch version of the Radner Reading Chart for assessing vision function]K J M Maaijwee, C F M Meulendijks, W Radner, et al.
Experimental Eye Research|December 22, 2007
Analysis of visual pigment by fundus autofluorescenceT Theelen, T T J M Berendschot, C J F Boon, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 1, 1996
Visual acuity and scar size in eyes with age-related subfoveal choroidal neovascular lesions, 30 months after radiation therapyG J Bergnik, C B Hoyng, R W van der Maazen, et al.
The British Journal of Ophthalmology|July 22, 1999
Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR geneB J Klevering, M van Driel, D J van de Pol, et al.
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