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E Zrenner

Showing results (241-250 of 284) with videos related to

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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.
Biochemical and Biophysical Research Communications|May 19, 1997
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathyB Wissinger, D Besch, B Baumann, et al.
Neurology|May 1, 1997
Color vision tests for early detection of antiepileptic drug toxicityA U Bayer, H J Thiel, E Zrenner, et al.
Neuroreport|December 1, 2001
Presence of kynurenic acid and kynurenine aminotransferases in the inner retinaR Rejdak, T Zarnowski, W A Turski, et al.
The British Journal of Ophthalmology|September 20, 2005
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster, N Weisschuh, H Jägle, et al.
Pageof 29

Showing results (241-250 of 284) with videos related to

Sort By:
Pageof 29
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.
Biochemical and Biophysical Research Communications|May 19, 1997
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathyB Wissinger, D Besch, B Baumann, et al.
Neurology|May 1, 1997
Color vision tests for early detection of antiepileptic drug toxicityA U Bayer, H J Thiel, E Zrenner, et al.
Neuroreport|December 1, 2001
Presence of kynurenic acid and kynurenine aminotransferases in the inner retinaR Rejdak, T Zarnowski, W A Turski, et al.
The British Journal of Ophthalmology|September 20, 2005
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster, N Weisschuh, H Jägle, et al.
Pageof 29