Eberhart Zrenner
Eberhart Zrenner
Professor of Ophthalmology, Univ. of Tuebingen - Germany, Instit. for Opht. Research, Retina Clinic
Bestätigte E-Mail-Adresse bei - Startseite
Zitiert von
Zitiert von
Will retinal implants restore vision?
E Zrenner
Science 295 (5557), 1022-1025, 2002
Subretinal electronic chips allow blind patients to read letters and combine them to words
E Zrenner, KU Bartz-Schmidt, H Benav, D Besch, A Bruckmann, VP Gabel, ...
Proceedings of the Royal Society B: Biological Sciences 278 (1711), 1489-1497, 2011
Mutations in RPE65 cause Leber's congenital amaurosis
F Marlhens, C Bareil, JM Griffoin, E Zrenner, P Amalric, C Eliaou, SY Liu, ...
Nature genetics 17 (2), 139-141, 1997
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
TM Strom, G Nyakatura, E Apfelstedt-Sylla, H Hellebrand, B Lorenz, ...
Nature genetics 19 (3), 260-263, 1998
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3)
A Meindl, K Dry, K Herrmann, E Manson, A Ciccodicola, A Edgar, ...
Nature genetics 13 (1), 35-42, 1996
Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS
K Stingl, KU Bartz-Schmidt, D Besch, A Braun, A Bruckmann, F Gekeler, ...
Proceedings of the Royal Society B: Biological Sciences 280 (1757), 20130077, 2013
Standard for clinical electroretinography (1999 update)
MF Marmor, E Zrenner
Documenta Ophthalmologica 97 (2), 143-156, 1998
Subretinal visual implant alpha IMS–clinical trial interim report
K Stingl, KU Bartz-Schmidt, D Besch, CK Chee, CL Cottriall, F Gekeler, ...
Vision research 111, 149-160, 2015
Can subretinal microphotodiodes successfully replace degenerated photoreceptors?
E Zrenner, A Stett, S Weiss, RB Aramant, E Guenther, K Kohler, ...
Vision research 39 (15), 2555-2567, 1999
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel
S Kohl, T Marx, I Giddings, H Jägle, SG Jacobson, E Apfelstedt-Sylla, ...
Nature genetics 19 (3), 257-259, 1998
Standard for clinical electroretinography: international standardization committee
MF Marmor, GB Arden, SEG Nilsson, E Zrenner
Archives of Ophthalmology 107 (6), 816-819, 1989
CNGA3 mutations in hereditary cone photoreceptor disorders
B Wissinger, D Gamer, H Jägle, R Giorda, T Marx, S Mayer, S Tippmann, ...
The American Journal of Human Genetics 69 (4), 722-737, 2001
Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to …
S Kohl, B Baumann, M Broghammer, H Jägle, P Sieving, U Kellner, ...
Human molecular genetics 9 (14), 2107-2116, 2000
Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3
M Biel, M Seeliger, A Pfeifer, K Kohler, A Gerstner, A Ludwig, G Jaissle, ...
Proceedings of the National Academy of Sciences 96 (13), 7553-7557, 1999
Electrical multisite stimulation of the isolated chicken retina
A Stett, W Barth, S Weiss, H Haemmerle, E Zrenner
Vision research 40 (13), 1785-1795, 2000
Photoreceptor cell death mechanisms in inherited retinal degeneration
J Sancho-Pelluz, B Arango-Gonzalez, S Kustermann, FJ Romero, ...
Molecular neurobiology 38, 253-269, 2008
Inter‐individual variability in the dynamics of natural accommodation in humans: relation to age and refractive errors.
F Schaeffel, H Wilhelm, E Zrenner
The Journal of Physiology 461 (1), 301-320, 1993
The development of subretinal microphotodiodes for replacement of degenerated photoreceptors
E Zrenner, KD Miliczek, VP Gabel, HG Graf, E Guenther, H Haemmerle, ...
Ophthalmic research 29 (5), 269-280, 1997
Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration
DA Thompson, P Gyürüs, LL Fleischer, EL Bingham, CL McHenry, ...
Investigative ophthalmology & visual science 41 (13), 4293-4299, 2000
Cataract prevalence and prevention in Europe: a literature review
E Prokofyeva, A Wegener, E Zrenner
Acta ophthalmologica 91 (5), 395-405, 2013
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