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Dive into the research topics where Neuro-Ophthalmology is active. These topic labels come from the works of this organisation's members. Together they form a unique fingerprint.
Collaborations and top research areas from the last five years
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Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy
de Muijnck, C., Haer-Wigman, L., van Everdingen, J., Lushchyk, T., Heutinck, P. A. T., van Dooren, M. F., Kievit, A. J. A., Verhoeven, V. J. M., Simon, M. E. H., Wasmann, R. A., Notting, I. C., De Baere, E., Walraedt, S., de Zaeytijd, J., Van den Broeck, F., Leroy, B. P., Boon, C. J. F. & van Genderen, M. M., 3 Oct 2024, In: Scientific Reports.Research output: Contribution to journal › Article › Research › peer-review
Open Access -
Clinical outcomes of treatment with idebenone in Leber's hereditary optic neuropathy in the Netherlands: A national cohort study
van Everdingen, J. A. M., Pott, J. W. R., Bauer, N. J. C., Krijnen, A. M., Lushchyk, T. & Wubbels, R. J., Sept 2022, In: Acta Ophthalmologica. 100, 6, p. 700-706 7 p.Research output: Contribution to journal › Article › Research › peer-review
Open Access -
Nieuwe therapie voor hereditaire opticusneuropathie van Leber. Dat vereist wel een snellere diagnose.
van Everdingen, J. A. M., Tjon Fo Sang, M., van den Born, L. I. & Pott, J.-W. R., Nov 2021, In: Nederlands Tijdschrift voor Geneeskunde. 165, p. D5444 4 p.Translated title of the contribution :New treatment option for Leber hereditary optic neuropathy: early diagnosis is required. Research output: Contribution to journal › Letter › peer-review