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The British Journal of Ophthalmology|August 1, 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 casesB H Weber, S Sander, C Kopp, et al.Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Ocular side effects of beta-pyridylcarbinol]P G Wolff-Kormann, B A Kormann, K G Riedel, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 25, 2006
[The European Vision Institute. Opening up new frontiers?]E Zrenner, J Cunha-Vaz, J A Sahel, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|May 26, 2001
[Physiological functional evaluation of retinal implants in animal models]R Eckhorn, A Stett, T Schanze, et al.Human Mutation|March 27, 1999
Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneityA R Janecke, M Meins, M Sadeghi, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, et al.Investigative Ophthalmology & Visual Science|May 31, 2001
Prevention of photoreceptor apoptosis by activation of the glucocorticoid receptorA Wenzel, C Grimm, M W Seeliger, et al.Current Molecular Medicine|April 21, 2012
Neuroprotective strategies for the treatment of inherited photoreceptor degenerationD Trifunović, A Sahaboglu, J Kaur, et al.Investigative Ophthalmology & Visual Science|January 15, 1999
Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesisM W Seeliger, H K Biesalski, B Wissinger, et al.Journal of Neuroscience Methods|November 16, 2010
A new DTL-electrode holder for recording of electroretinograms in animalsA Schatz, G Willmann, H Enderle, et al.Pageof 30