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Investigative Ophthalmology & Visual Science|May 1, 1997
Evaluation of the gene encoding the tissue inhibitor of metalloproteinases-3 in various maculopathiesU Felbor, D Doepner, U Schneider, et al.The Journal of Physiology|December 1, 1988
Current source density analysis of linear and non-linear components of the primate electroretinogramC L Baker, R R Hess, B T Olsen, et al.Klinische Monatsblatter Fur Augenheilkunde|May 13, 1998
[Multifocal electroretinography in acquired macular dysfunction]U Kretschmann, T Schlote, N Stübiger, et al.Klinische Monatsblatter Fur Augenheilkunde|March 7, 2000
[Carcinoma-associated retinopathy: a review with clinical examples]B Sobottka, T Schlote, D Besch, et al.Klinische Monatsblatter Fur Augenheilkunde|January 1, 1993
[Clinical electroretinography: standard protocol and normal values]P C Jacobi, K Rüther, K D Miliczek, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 1, 1996
[Noise field screening. Results of a television field study for detection of visual field defects]U Schiefer, A C Gisolf, J Kirsch, et al.Documenta Ophthalmologica. Advances in Ophthalmology|April 5, 2019
Retinal dystrophies with bull's-eye maculopathy along with negative ERGsF Nasser, A Kurtenbach, S Kohl, et al.Klinische Monatsblatter Fur Augenheilkunde|February 28, 2001
[Automated swinging flashlight test in patients with optic nerve diseases]B Wilhelm, H Lüdtke, T Peters, et al.German Journal of Ophthalmology|July 1, 1996
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 geneB Leo-Kottler, M Christ-Adler, B Baumann, et al.Documenta Ophthalmologica. Advances in Ophthalmology|February 3, 2019
Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutationF Nasser, L Mulahasanovic, M Alkhateeb, et al.Pageof 30