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Number of items: 6.

Journal Article

Boon, C. J. F., van Dijk, E. H. C., Fauser, S., Breukink, M. D., Blanco-Garavito, R., Groenewoud, J. M. M., Keunen, J. E. E., Peters, P. J. H., Dijkman, G., Souied, E. H., MacLaren, R. E., Querques, G., Downes, S. M. and Hoyng, C. B. (2018). The PLACE trial: an open-label, multicenter, randomized controlled trial comparing half-dose photodynamic therapy with subthreshold micropulse laser for chronic central serous chorioretinopathy. Acta Ophthalmol., 96. S. 31 - 32. HOBOKEN: WILEY. ISSN 1755-3768

Chung, W. H., van Dijk, E. H. C., Mohabati, D., Dijkman, G., Yzer, S., de Jong, E. K., Fauser, S., Schlingemann, R. O., Hoyng, C. B. and Boon, C. J. F. (2017). Neovascular age-related macular degeneration without drusen in the fellow eye: clinical spectrum and therapeutic outcome. Acta Ophthalmol., 95. S. 23 - 24. HOBOKEN: WILEY. ISSN 1755-3768

Mohabati, D., van Dijk, E. H. C., van Rijssen, T. J., de Jong, E. K., Breukink, M. B., Martinez-Ciriano, J. P., Dijkman, G., Hoyng, C. B., Fauser, S., Yzer, S. and Boon, C. J. F. (2017). Severe phenotypes of chronic central serous chorioretinopathy: clinical characteristics and response to photodynamic therapy. Acta Ophthalmol., 95. S. 21 - 22. HOBOKEN: WILEY. ISSN 1755-3768

Schellevis, R. L., van Dijk, E. H. C., van Bergen, M. G. J. M., Breukink, M. B., Altay, L., Scholz, P., Fauser, S., Meijer, O. C., Hoyng, C. B., den Hollander, A. I., Boon, C. J. F. and de Jong, E. K. (2017). A genetic variant in the NR3C2 gene, encoding the mineralocorticoid receptor, is associated with chronic central serous chorioretinopathy. Acta Ophthalmol., 95. S. 21 - 22. HOBOKEN: WILEY. ISSN 1755-3768

van Dijk, E. H. C., Hahn, L., van Rijssen, T. J., Scholz, P., Breukin, M. B., Souied, E. H., MacLaren, R. E., Querques, G., Fauser, S., Downes, S. M., Hoyng, C. B. and Boon, C. J. F. (2020). Pigment epithelial detachments in chronic central serous chorioretinopathy: Effect of half-dose photodynamic therapy versus high-density subthreshold micropulse laser PLACE trial report No. 5. Acta Ophthalmol., 98. S. 40 - 42. HOBOKEN: WILEY. ISSN 1755-3768

van de Ven, J. P. H., Nilsson, S. C., Tan, P. L., Buitendijk, G., Ristau, T., Mohlin, F. C., Nabuurs, S. B., Schoenmaker-Koller, F. E., Smailhodzic, D., Campochiarro, P. A., Zack, D. J., Duvvari, M. R., Bakker, B., Paun, C. C., Boon, C. J. F., Uitterlinden, A. G., Liakopoulos, S., Klevering, B. J., Fauser, S., Daha, M. R., Katsanis, N., Klaver, C. C. W., Blom, A. M., Hoyng, C. B. and den Hollander, A. I. (2013). A functional variant in the CFI gene confers a high risk of age-related macular degeneration. Mol. Immunol., 56 (3). S. 247 - 249. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0161-5890

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