Showing results (81-90 of 436) with videos related to

Sort By:
Pageof 44
Investigative Ophthalmology & Visual Science|April 2, 2010
Altered expression of metallothionein-I and -II and their receptor megalin in inherited photoreceptor degenerationKirsten A Wunderlich, Thierry Leveillard, Milena Penkowa, et al.
Acta Ophthalmologica|October 4, 2019
Ophthalmic features of retinitis pigmentosa in Cohen syndrome caused by pathogenic variants in the VPS13B geneFadi Nasser, Anne Kurtenbach, Saskia Biskup, et al.
Molecular Vision|September 26, 2007
Two truncating USH3A mutations, including one novel, in a German family with Usher syndromeInga Ebermann, Robert Wilke, Thomas Lauhoff, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 16, 2004
Subretinal electrical stimulation of the rabbit retina with acutely implanted electrode arraysFlorian Gekeler, Karin Kobuch, Hartmut Normann Schwahn, et al.
Ocular Immunology and Inflammation|July 16, 2005
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndromeAndreas Schuster, Eckart Apfelstedt-Sylla, Carsten M Pusch, et al.
Vision Research|April 25, 2015
Oculomotor behavior of blind patients seeing with a subretinal visual implantZiad M Hafed, Katarina Stingl, Karl-Ulrich Bartz-Schmidt, et al.
The Journal of Comparative Neurology|July 2, 2010
cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retinaDragana Trifunović, Katja Dengler, Stylianos Michalakis, et al.
Plos One|July 21, 2017
Temporal progression of PARP activity in the Prph2 mutant rd2 mouse: Neuroprotective effects of the PARP inhibitor PJ34Ayse Sahaboglu, Alaa Sharif, Lili Feng, et al.
Investigative Ophthalmology & Visual Science|November 24, 2004
Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutationsThomas Rosenberg, Britta Baumann, Susanne Kohl, et al.
Vision Research|June 5, 2002
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein typeHana Langrová, Daphne Gamer, Christoph Friedburg, et al.
Pageof 44