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Publications by Apfelstedt-Sylla, E.

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Number of items: 6.


Reinhard, J., Messias, A., Dietz, K., Mackeben, M., Lakmann, R., Scholl, H. P., Apfelstedt-Sylla, E., Weber, Bernhard H. F. , Seeliger, M. W., Zrenner, E. and Trauzettel-Klosinski, S. (2007) Quantifying fixation in patients with Stargardt disease. Vision Research 47 (15), pp. 2076-2085. Fulltext not available.


Scholl, H. P. N., Besch, D., Vonthein, R., Weber, Bernhard H. F. and Apfelstedt-Sylla, E. (2002) Alterations of slow and fast rod ERG signals in patients with molecularly confirmed Stargardt disease type 1 (STGD1). Investigative ophthalmology and visual science 43 (4), pp. 1248-1256.


Scholl, H. P. N., Langrova, H., Weber, Bernhard H. F. , Zrenner, E. and Apfelstedt-Sylla, E. (2001) Clinical electrophysiology of two rod pathways: normative values and clinical application. Graefe's Archive for Clinical and Experimental Ophthalmology 239 (2), pp. 71-80. Fulltext not available.


Rivera, A., White, K., Stöhr, H., Steiner, K., Hemmrich, N., Grimm, T., Jurklies, B., Lorenz, B., Scholl, H. P. N., Apfelstedt-Sylla, E. and Weber, Bernhard H. F. (2000) A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration. The American Journal of Human Genetics 67 (4), pp. 800-813. Fulltext not available.


Strom, T. M., Nyakatura, G., Apfelstedt-Sylla, E., Hellebrand, H., Lorenz, B., Weber, Bernhard H. F. , Wutz, K., Gutwillinger, N., Rüther, K., Drescher, B., Sauer, C. G., Zrenner, E., Meitinger, T., Rosenthal, A. and Meindl, A. (1998) An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nature Genetics 19, pp. 260-263. Fulltext not available.


Felbor, U., Stöhr, H., Amann, T., Schönherr, U., Apfelstedt-Sylla, E. and Weber, Bernhard H. F. (1996) A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy. Journal of Medical Genetics 33 (3), pp. 233-236. Fulltext not available.

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