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E Zrenner

Showing results (231-240 of 284) with videos related to

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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.
The British Journal of Ophthalmology|August 1, 1996
Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of casesB H Weber, S Sander, C Kopp, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Ocular side effects of beta-pyridylcarbinol]P G Wolff-Kormann, B A Kormann, K G Riedel, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 25, 2006
[The European Vision Institute. Opening up new frontiers?]E Zrenner, J Cunha-Vaz, J A Sahel, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|May 26, 2001
[Physiological functional evaluation of retinal implants in animal models]R Eckhorn, A Stett, T Schanze, et al.
Pageof 29

Showing results (231-240 of 284) with videos related to

Sort By:
Pageof 29
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.
The British Journal of Ophthalmology|August 1, 1996
Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of casesB H Weber, S Sander, C Kopp, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Ocular side effects of beta-pyridylcarbinol]P G Wolff-Kormann, B A Kormann, K G Riedel, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 25, 2006
[The European Vision Institute. Opening up new frontiers?]E Zrenner, J Cunha-Vaz, J A Sahel, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|May 26, 2001
[Physiological functional evaluation of retinal implants in animal models]R Eckhorn, A Stett, T Schanze, et al.
Pageof 29