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American Journal of Ophthalmology|February 19, 1998
Multifocal electroretinography in retinitis pigmentosaM Seeliger, U Kretschmann, E Apfelstedt-Sylla, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 1, 1992
[Retinitis pigmentosa. Clinical findings, results of molecular genetic techniques and research perspectives]E Zrenner, K Rüther, E Apfelstedt-SyllaDer Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|August 1, 1997
[Juvenile neuronal ceroid lipofuscinosis (Batten-Mayou) disease. Ophthalmologic diagnosis and findings]M Seeliger, K Rüther, E Apfelstedt-Sylla, et al.Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|October 1, 1995
[Social ophthalmologic aspects of retinitis pigmentosa]K Rüther, F Banhart, S Kremmer, et al.The British Journal of Ophthalmology|May 29, 1998
Multifocal electroretinography in patients with Stargardt's macular dystrophyU Kretschmann, M W Seeliger, K Ruether, et al.The British Journal of Ophthalmology|January 1, 1995
Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin geneE Apfelstedt-Sylla, M Theischen, K Rüther, et al.German Journal of Ophthalmology|January 1, 1992
Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsinE Apfelstedt-Sylla, M Kunisch, M Horn, et al.Ophthalmic Research|January 1, 1996
ERG campimetry using a multi-input stimulation technique for mapping of retinal function in the central visual fieldU Kretschmann, K Rüther, T Usui, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 20, 1999
Familial macular cone dystrophy: diagnostic value of multifocal ERG and two-color threshold perimetryU Kretschmann, R Stilling, K Rüther, et al.German Journal of Ophthalmology|November 1, 1993
Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein typeK Ruether, E Apfelstedt-Sylla, E ZrennerPageof 30