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B Wissinger

Showing results (31-40 of 61) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|August 21, 2012
Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophyIsaac Wang, Naheed W Khan, Kari Branham, et al.
Vision Research|July 20, 2002
M-cone opsin gene number does not correlate with variation in L/M-cone sensitivityH Knau, J Kremers, H-J Schmidt, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 22, 2019
A case of X-linked retinoschisis with atypical fundus appearanceF Nasser, S Kohl, L Kuehlewein, et al.
The European Journal of Neuroscience|March 28, 1998
Cloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptorsB Wissinger, F Müller, I Weyand, et al.
Investigative Ophthalmology & Visual Science|October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX geneH P Scholl, H Langrová, C M Pusch, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 14, 1999
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girlsH Thieme, B Wissinger, C Jandeck, 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.
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.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Documenta Ophthalmologica. Advances in Ophthalmology|August 21, 2012
Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophyIsaac Wang, Naheed W Khan, Kari Branham, et al.
Vision Research|July 20, 2002
M-cone opsin gene number does not correlate with variation in L/M-cone sensitivityH Knau, J Kremers, H-J Schmidt, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 22, 2019
A case of X-linked retinoschisis with atypical fundus appearanceF Nasser, S Kohl, L Kuehlewein, et al.
The European Journal of Neuroscience|March 28, 1998
Cloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptorsB Wissinger, F Müller, I Weyand, et al.
Investigative Ophthalmology & Visual Science|October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX geneH P Scholl, H Langrová, C M Pusch, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 14, 1999
A pedigree of Leber's hereditary optic neuropathy with visual loss in childhood, primarily in girlsH Thieme, B Wissinger, C Jandeck, 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.
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.
Pageof 7