Einträge von Zrenner, Eberhart auf dem Publikationsserver

Nasser, Fadi, Kempf, Melanie, Kurtenbach, Anne, Stöhr, Heidi, Weber, Bernhard H. F., Neuhaus, Christine, Rating, Philipp und Zrenner, Eberhart (2020) Correlating Adaptive Optics Images to Clinical Findings in Juvenile Macular Dystrophy with Hypotrichosis in Siblings with Homozygous <b><i>CDH3</i></b> Pathogenic Variation. Ophthalmic Research 63 (2), S. 141-151. Volltext nicht vorhanden.

Jolly, Jasleen K. , Wagner, Siegfried K., Martus, Peter, MacLaren, Robert E., Wilhelm, Barbara, Webster, Andrew R., Downes, Susan M., Charbel Issa, Peter, Kellner, Ulrich, Jägle, Herbert, Rüther, Klaus, Bertelsen, Mette, Bragadóttir, Ragnheiður, Prener Holtan, Josephine, van den Born, L. Ingeborgh, Sodi, Andrea, Virgili, Gianni, Gosheva, Mariya, Pach, Johanna, Zündorf, Ida, Zrenner, Eberhart und Gekeler, Florian (2019) Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim® System (TESOLA-Study). Ophthalmic Research 63 (3), S. 234-243. Volltext nicht vorhanden.

Strasser, Torsten , Peters, Tobias, Jägle, Herbert und Zrenner, Eberhart (2018) ElVisML: an open data format for the exchange and storage of electrophysiological data in ophthalmology. Documenta Ophthalmologica 136 (1), S. 75-92. Volltext nicht vorhanden.

Bellingrath, Julia-Sophia, Ochakovski, G. Alex, Seitz, Immanuel P., Kohl, Susanne , Zrenner, Eberhart, Hanig, Nicola, Prokisch, Holger , Weber, Bernhard H., Downes, Susan M., Ramsden, Simon, MacLaren, Robert E. und Fischer, M. Dominik (2017) High Symmetry of Visual Acuity and Visual Fields in RPGR-Linked Retinitis Pigmentosa. Investigative Opthalmology & Visual Science 58 (11), S. 4457. Volltext nicht vorhanden.

Wunderlich, Kirsten A., Tanimoto, Naoyuki, Grosche, Antje , Zrenner, Eberhart, Pekny, Milos, Reichenbach, Andreas, Seeliger, Mathias W., Pannicke, Thomas und Perez, Maria‐Thereza (2015) Retinal functional alterations in mice lacking intermediate filament proteins glial fibrillary acidic protein and vimentin. The FASEB Journal 29 (12), S. 4815-4828. Volltext nicht vorhanden.

Zobor, Ditta, Zrenner, Eberhart, Wissinger, Bernd, Kohl, Susanne und Jägle, Herbert (2014) GUCY2D- OR GUCA1A-RELATED AUTOSOMAL DOMINANT CONE–ROD DYSTROPHY. Retina 34 (8), S. 1576-1587. Volltext nicht vorhanden.

Kurtenbach, Anne , Langrová, Hana , Messias, Andre , Zrenner, Eberhart und Jägle, Herbert (2013) A comparison of the performance of three visual evoked potential-based methods to estimate visual acuity. Documenta Ophthalmologica 126 (1), S. 45-56. Volltext nicht vorhanden.

den Hollander, Anneke I., Zobor, Ditta , Kohl, Susanne, Wissinger, Bernd, Zrenner, Eberhart und Jägle, Herbert (2012) Rod and Cone Function in Patients with KCNV2 Retinopathy. PLoS ONE 7 (10), e46762. Volltext nicht vorhanden.

Audo, Isabelle , Bujakowska, Kinga , Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne , Luu, Tien D., Lecompte, Odile , Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride , Sharon, Dror , Banin, Eyal, Jacobson, Samuel G. , Bonneau, Dominique , Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim , Sahel, José-Alain , Bhattacharya, Shomi S. und Zeitz, Christina (2012) Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness. The American Journal of Human Genetics 90 (2), S. 321-330. Volltext nicht vorhanden.

Wilke, Robert, Gabel, Veit-Peter, Sachs, Helmut, Bartz Schmidt, Karl-Ulrich, Gekeler, Florian, Besch, Dorothea, Szurman, Peter, Stett, Alfred , Wilhelm, Barbara, Peters, Tobias, Harscher, Alex, Greppmaier, Udo, Kibbel, Steffen, Benav, Heval, Bruckmann, Anna, Stingl, Katarina, Kusnyerik, Akos und Zrenner, Eberhart (2011) Spatial Resolution and Perception of Patterns Mediated by a Subretinal 16-Electrode Array in Patients Blinded by Hereditary Retinal Dystrophies. Investigative Opthalmology & Visual Science 52 (8), S. 5995. Volltext nicht vorhanden.

Zrenner, Eberhart, Bartz-Schmidt, Karl Ulrich, Benav, Heval, Besch, Dorothea, Bruckmann, Anna, Gabel, Veit-Peter, Gekeler, Florian, Greppmaier, Udo, Harscher, Alex, Kibbel, Steffen, Koch, Johannes, Kusnyerik, Akos, Peters, Tobias, Stingl, Katarina, Sachs, Helmut, Stett, Alfred , Szurman, Peter, Wilhelm, Barbara und Wilke, Robert (2011) Subretinal electronic chips allow blind patients to read letters and combine them to words. Proceedings of the Royal Society B: Biological Sciences 278 (1711), S. 1489-1497. Volltext nicht vorhanden.

Langmann, Thomas, Di Gioia, S. A., Rau, I., Stöhr, Heidi, Maksimovic, N. S., Corbo, J. C. , Renner, Agnes B., Zrenner, Eberhart, Kumaramanickavel, G., Karlstetter, Marcus, Arsenijevic, Y., Weber, Bernhard H. F. , make_name_string expected hash reference und make_name_string expected hash reference (2010) Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa. American Journal of Human Genetics 87, S. 376-381. Volltext nicht vorhanden.

Gekeler, Florian, Kobuch, Karin, Blatsios, Georgios, Zrenner, Eberhart und Shinoda, Kei (2010) Repeated transchoroidal implantation and explantation of compound subretinal prostheses: An exploratory study in rabbits. Japanese Journal of Ophthalmology 54 (5), S. 467-475. Volltext nicht vorhanden.

Audo, Isabelle, Kohl, Susanne , Leroy, Bart P., Munier, Francis L., Guillonneau, Xavier , Mohand-Saïd, Saddek, Bujakowska, Kinga , Nandrot, Emeline F., Lorenz, Birgit, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Bernd, Antje, Antonio, Aline, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Poloschek, Charlotte M., Drumare, Isabelle, Defoort-Dhellemmes, Sabine, Wissinger, Bernd, Léveillard, Thierry, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride , Berger, Wolfgang, Jacobson, Samuel G. , Zrenner, Eberhart, Sahel, José-Alain , Bhattacharya, Shomi S. und Zeitz, Christina (2009) TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness. The American Journal of Human Genetics 85 (5), S. 720-729. Volltext nicht vorhanden.

Eckhorn, Reinhard, Wilms, Marcus , Schanze, Thomas, Eger, Marcus, Hesse, Lutz, Eysel, Ulf T. , Kisvárday, Zoltán F., Zrenner, Eberhart, Gekeler, Florian, Schwahn, Helmut, Shinoda, Keisuke, Sachs, Helmut und Walter, Peter (2006) Visual resolution with retinal implants estimated from recordings in cat visual cortex. Vision research 46 (17), S. 2675-2690. Zugang zum Volltext eingeschränkt.

Kohl, Susanne , Varsanyi, Balazs, Antunes, Gesine Abadin, Baumann, Britta, Hoyng, Carel B, Jägle, Herbert, Rosenberg, Thomas, Kellner, Ulrich, Lorenz, Birgit, Salati, Roberto, Jurklies, Bernhard, Farkas, Agnes, Andreasson, Sten, Weleber, Richard G, Jacobson, Samuel G , Rudolph, Günther, Castellan, Claudio, Dollfus, Helene, Legius, Eric, Anastasi, Mario, Bitoun, Pierre , Lev, Dorit, Sieving, Paul A, Munier, Francis L, Zrenner, Eberhart, Sharpe, Lindsay T, Cremers, Frans P M und Wissinger, Bernd (2005) CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia. European Journal of Human Genetics 13 (3), S. 302-308. Volltext nicht vorhanden.

Ohlmann, Andreas, Scholz, Michael , Goldwich, Andreas, Chauhan, Bharesh K. , Hudl, Kristiane, Ohlmann, Anne V., Zrenner, Eberhart, Berger, Wolfgang, Cvekl, Aleš, Seeliger, Mathias W. und Tamm, Ernst R. (2005) Ectopic Norrin Induces Growth of Ocular Capillaries and Restores Normal Retinal Angiogenesis in Norrie Disease Mutant Mice. The Journal of Neuroscience 25 (7), S. 1701-1710. Volltext nicht vorhanden.

Völker, Michael, Shinoda, Kei, Sachs, Helmut, Gmeiner, Helmut, Schwarz, Thorsten, Kohler, Konrad, Inhoffen, Werner, Bartz-Schmidt, Karl Ulrich, Zrenner, Eberhart und Gekeler, Florian (2004) In vivo assessment of subretinally implanted microphotodiode arrays in cats by optical coherence tomography and fluorescein angiography. Graefe's Archive for Clinical and Experimental Ophthalmology 242 (9), S. 792-799. Volltext nicht vorhanden.

Gekeler, Florian, Kobuch, Karin, Schwahn, Hartmut Normann, Stett, Alfred , Shinoda, Kei und Zrenner, Eberhart (2004) Subretinal electrical stimulation of the rabbit retina with acutely implanted electrode arrays. Graefe's Archive for Clinical and Experimental Ophthalmology 242 (7), S. 587-596. Volltext nicht vorhanden.

Wissinger, Bernd, Gamer, Daphne, Jägle, Herbert, Giorda, Roberto , Marx, Tim, Mayer, Simone, Tippmann, Sabine, Broghammer, Martina, Jurklies, Bernhard, Rosenberg, Thomas, Jacobson, Samuel G. , Sener, E. Cumhur, Tatlipinar, Sinan, Hoyng, Carel B., Castellan, Claudio, Bitoun, Pierre , Andreasson, Sten, Rudolph, Günter, Kellner, Ulrich, Lorenz, Birgit, Wolff, Gerhard, Verellen-Dumoulin, Christine, Schwartz, Marianne, Cremers, Frans P.M. , Apfelstedt-Sylla, Eckart, Zrenner, Eberhart, Salati, Roberto, Sharpe, Lindsay T. und Kohl, Susanne (2001) CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders. The American Journal of Human Genetics 69 (4), S. 722-737. Volltext nicht vorhanden.

Schwahn, Hartmut N., Gekeler, Florian, Kohler, Konrad, Kobuch, Karin, Sachs, Helmut G., Schulmeyer, Frank, Jakob, Wolfgang, Gabel, Veit-Peter und Zrenner, Eberhart (2001) Studies on the feasibility of a subretinal visual prosthesis: data from Yucatan micropig and rabbit. Graefe's Archive for Clinical and Experimental Ophthalmology 239 (12), S. 961-967. Volltext nicht vorhanden.