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Bernd Wissinger

Showing results (101-110 of 196) with videos related to

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JAMA Ophthalmology|February 8, 2014
Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsiaJonathan P Greenberg, Jerome Sherman, Sandrine A Zweifel, et al.
Human Mutation|June 13, 2020
Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9-year periodNicole Weisschuh, Carolin D Obermaier, Florian Battke, et al.
Acta Ophthalmologica|June 26, 2026
Clinical manifestations of dual-gene variants in retinitis pigmentosaLasse Wolfram, Jan-Philipp Bodenbender, David A Merle, et al.
BMC Ophthalmology|April 24, 2025
Clinical manifestations of dual-gene variants involving ABCA4 in retinal dystrophiesLasse Wolfram, David A Merle, Laura Kühlewein, et al.
Investigative Ophthalmology & Visual Science|September 10, 2009
In vivo analysis of cone survival in miceSusanne C Beck, Karin Schaeferhoff, Stylianos Michalakis, et al.
International Journal of Molecular Sciences|June 24, 2022
Novel <i>OPN1LW/OPN1MW</i> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone DysfunctionKatarina Stingl, Britta Baumann, Pietro De Angeli, et al.
Annals of Neurology|October 27, 2004
Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophyRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, et al.
Journal of Medical Genetics|October 19, 2013
A novel heterozygous OPA3 mutation located in the mitochondrial target sequence results in altered steady-state levels and fragmented mitochondrial networkTanja Grau, Lena F Burbulla, Gertraud Engl, et al.
Molecular Vision|May 18, 2018
Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophyAnna Wawrocka, Anna Skorczyk-Werner, Katarzyna Wicher, et al.
Investigative Ophthalmology & Visual Science|June 11, 2025
Investigating the Immunogenic Potential of Variations in Host Cell Protein Levels in Clinical-Grade AAV8 ProductsImmanuel P Seitz, Eduardo Rodríguez-Bocanegra, Kirsten Bucher, et al.
Pageof 20

Showing results (101-110 of 196) with videos related to

Sort By:
Pageof 20
JAMA Ophthalmology|February 8, 2014
Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsiaJonathan P Greenberg, Jerome Sherman, Sandrine A Zweifel, et al.
Human Mutation|June 13, 2020
Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9-year periodNicole Weisschuh, Carolin D Obermaier, Florian Battke, et al.
Acta Ophthalmologica|June 26, 2026
Clinical manifestations of dual-gene variants in retinitis pigmentosaLasse Wolfram, Jan-Philipp Bodenbender, David A Merle, et al.
BMC Ophthalmology|April 24, 2025
Clinical manifestations of dual-gene variants involving ABCA4 in retinal dystrophiesLasse Wolfram, David A Merle, Laura Kühlewein, et al.
Investigative Ophthalmology & Visual Science|September 10, 2009
In vivo analysis of cone survival in miceSusanne C Beck, Karin Schaeferhoff, Stylianos Michalakis, et al.
International Journal of Molecular Sciences|June 24, 2022
Novel <i>OPN1LW/OPN1MW</i> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone DysfunctionKatarina Stingl, Britta Baumann, Pietro De Angeli, et al.
Annals of Neurology|October 27, 2004
Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophyRaffaele Lodi, Caterina Tonon, Maria Lucia Valentino, et al.
Journal of Medical Genetics|October 19, 2013
A novel heterozygous OPA3 mutation located in the mitochondrial target sequence results in altered steady-state levels and fragmented mitochondrial networkTanja Grau, Lena F Burbulla, Gertraud Engl, et al.
Molecular Vision|May 18, 2018
Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophyAnna Wawrocka, Anna Skorczyk-Werner, Katarzyna Wicher, et al.
Investigative Ophthalmology & Visual Science|June 11, 2025
Investigating the Immunogenic Potential of Variations in Host Cell Protein Levels in Clinical-Grade AAV8 ProductsImmanuel P Seitz, Eduardo Rodríguez-Bocanegra, Kirsten Bucher, et al.
Pageof 20