Publications by Zrenner, E

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.