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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.International Journal of Molecular Medicine|June 16, 2001
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disordersK Pesch, J Tomiuk, M Broghammer, et al.Proceedings of the National Academy of Sciences of the United States of America|June 23, 1999
Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3M Biel, M Seeliger, A Pfeifer, et al.Investigative Ophthalmology & Visual Science|February 7, 2001
Evaluation of the rhodopsin knockout mouse as a model of pure cone functionG B Jaissle, C A May, J Reinhard, et al.The British Journal of Ophthalmology|July 30, 2008
Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patientsD Besch, H Sachs, P Szurman, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 15, 2016
[Transcorneal electrical stimulation in primary open angle glaucoma]T Röck, L Naycheva, G Willmann, et al.Human Molecular Genetics|July 7, 2001
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritanceU E Pesch, B Leo-Kottler, S Mayer, et al.Pageof 30