Rod-cone interaction in patients with fundus flavimaculatus.

Por Schneider, T., Zrenner, E.
Publicado em 1987

Differences in adaptation between on- and off-centre ganglion cells and rod-mediated cone sensitization in cat retina.

Por Guenther, E, Zrenner, E
Publicado em 1993

Inter-individual variability in the dynamics of natural accommodation in humans: relation to age and refractive errors.

Por Schaeffel, F, Wilhelm, H, Zrenner, E
Publicado em 1993

Longitudinal chromatic aberration and emmetropization: results from the chicken eye.

Por Rohrer, B, Schaeffel, F, Zrenner, E
Publicado em 1992

Human photopic vision with only short wavelength cones: post-receptoral properties.

Por Hess, R F, Mullen, K T, Zrenner, E
Publicado em 1989

Preretinopic changes in the colour vision of juvenile diabetics

Por Kurtenbach, A., Schiefer, U., Neu, A., Zrenner, E.
Publicado em 1999

Modeling the response of ON and OFF retinal bipolar cells during electric stimulation

Por Werginz, P., Benav, H., Zrenner, E., Rattay, F.
Publicado no Vision Res (2015)

The photoreceptors in atypical achromatopsia.

Por Hess, R F, Mullen, K T, Sharpe, L T, Zrenner, E
Publicado em 1989

Current source density analysis of linear and non-linear components of the primate electroretinogram.

Por Baker, C L, Hess, R R, Olsen, B T, Zrenner, E
Publicado em 1988

Multifocal electroretinography in patients with Stargardt's macular dystrophy

Por Kretschmann, U, Seeliger, M, Ruether, K, Usui, T, Apfelstedt-Sylla, E, Zrenner, E
Publicado em 1998

Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene.

Por Apfelstedt-Sylla, E, Theischen, M, Rüther, K, Wedemann, H, Gal, A, Zrenner, E
Publicado em 1995

Stereotactic fractionated irradiation of optic nerve sheath meningioma: a new treatment alternative

Por Pitz, S, Becker, G, Schiefer, U, Wilhelm, H, Jeremic, B, Bamberg, M, Zrenner, E
Publicado em 2002

Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.

Por Apfelstedt-Sylla, E, Kunisch, M, Horn, M, Rüther, K, Gerding, H, Gal, A, Zrenner, E
Publicado em 1993

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.

Por Weber, B H, Sander, S, Kopp, C, Walker, D, Eckstein, A, Wissinger, B, Zrenner, E, Grimm, T
Publicado em 1996

RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.

Por Kohl, S, Christ-Adler, M, Apfelstedt-Sylla, E, Kellner, U, Eckstein, A, Zrenner, E, Wissinger, B
Publicado em 1997

A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosa

Por Dietrich, K, Jacobi, F K, Tippmann, S, Schmid, R, Zrenner, E, Wissinger, B, Apfelstedt-Sylla, E
Publicado em 2002

Efficacy of PARP inhibition in Pde6a mutant mouse models for retinitis pigmentosa depends on the quality and composition of individual human mutations

Por Jiao, K, Sahaboglu, A, Zrenner, E, Ueffing, M, Ekström, P A R, Paquet-Durand, F
Publicado no Cell Death Discov (2016)

Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.

Por Weitz, C J, Miyake, Y, Shinzato, K, Montag, E, Zrenner, E, Went, L N, Nathans, J
Publicado em 1992

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa

Por Schuster, A, Weisschuh, N, Jägle, H, Besch, D, Janecke, A R, Zierler, H, Tippmann, S, Zrenner, E, Wissinger, B
Publicado em 2005

Transfer characteristics of subretinal visual implants: corneally recorded implant responses

Por Stingl, K., Bartz-Schmidt, K. U., Braun, A., Gekeler, F., Greppmaier, U., Schatz, A., Stett, A., Strasser, T., Kitiratschky, V., Zrenner, E.
Publicado no Doc Ophthalmol (2016)