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The British Journal of Ophthalmology|August 1, 1993
Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsinE Apfelstedt-Sylla, M Kunisch, M Horn, et al.American Journal of Human Genetics|March 1, 1992
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinC J Weitz, Y Miyake, K Shinzato, et al.Human Genetics|September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1F K Jacobi, M Broghammer, K Pesch, et al.The British Journal of Ophthalmology|July 26, 2008
Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutationV B D Kitiratschky, D Nagy, T Zabel, et al.The British Journal of Ophthalmology|February 28, 2002
A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosaK Dietrich, F K Jacobi, S Tippmann, et al.Annals of Neurology|October 1, 1993
Impairment of retinal increment thresholds in Huntington's diseaseW Paulus, G Schwarz, A Werner, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1991
Mizuo phenomenon in X-linked retinoschisis. Pathogenesis of the Mizuo phenomenonP T de Jong, E Zrenner, G J van Meel, et al.Journal of Medical Genetics|August 1, 1997
RDS/peripherin gene mutations are frequent causes of central retinal dystrophiesS Kohl, M Christ-Adler, E Apfelstedt-Sylla, et al.Investigative Ophthalmology & Visual Science|May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathyF K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 9, 2006
Kynurenic acid synthesis in bovine retinal slices--effect of glutamate agonistsT Zarnowski, M Bialek, R Rejdak, et al.Pageof 30