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Publications by Zrenner, E.

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Number of items: 8.


Zhour, A., Bolz, S., Grimm, C., Willmann, G., Schatz, A., Weber, Bernhard H. F. , Zrenner, E. and Fischer, M. D. (2012) In vivo imaging reveals novel aspects of retinal disease progression in Rs1h(-/Y) mice but no therapeutic effect of carbonic anhydrase inhibition. Veterinary Ophthalmology 15 (Suppl2), pp. 123-133. Fulltext not available.


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.


Seeliger, M. W., Weber, Bernhard H. F. , Besch, D., Zrenner, E., Schrewe, H. and Mayser, H. (2003) mfERG waveform characteristics in the RS1h mouse model featuring a `negative' ERG. Documenta Ophthalmologica 107 (1), pp. 37-44. Fulltext not available.


Wutz, K., Sauer, C., Zrenner, E., Lorenz, B., Alitalo, T., Broghammer, M., Hergersberg, M., de La Chapelle, A., Weber, Bernhard H. F. , Wissinger, B., Meindl, A. and Pusch, C. M. (2002) Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina. European Journal of Human Genetics 10 (8), pp. 449-456. Fulltext not available.


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.


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., Doepner, D., Schneider, U., Zrenner, E. and Weber, Bernhard H. F. (1997) Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathies. Investigative ophthalmology & visual science 38 (6), pp. 1054-1059.


Weber, Bernhard H. F. , Sander, S., Kopp, C., Walker, D., Eckstein, A., Wissinger, B., Zrenner, E. and Grimm, T. (1996) Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases. British Journal of Ophthalmology 80 (8), pp. 745-749. Fulltext not available.

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