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Ditta Zobor

Showing results (21-30 of 54) with videos related to

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Investigative Ophthalmology & Visual Science|July 20, 2018
Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German CohortDitta Zobor, Gergely Zobor, Stephanie Hipp, et al.
American Journal of Ophthalmology|November 18, 2019
CEP290 Mutation Spectrum and Delineation of the Associated Phenotype in a Large German Cohort: A Monocentric StudyBritta Feldhaus, Nicole Weisschuh, Fadi Nasser, et al.
The European Journal of Neuroscience|September 17, 2013
Visual cortex organisation in a macaque monkey with macular degenerationYibin Shao, Georgios A Keliris, Amalia Papanikolaou, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 28, 2012
Detailed functional and structural characterization of a macular lesion in a rhesus macaqueM Dominik Fischer, Ditta Zobor, Georgios A Keliris, et al.
Investigative Ophthalmology & Visual Science|May 9, 2022
Central Visual Function and Genotype-Phenotype Correlations in PDE6A-Associated Retinitis PigmentosaLaura Kuehlewein, Torsten Straßer, Gunnar Blumenstock, et al.
Genes|June 24, 2017
Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular LesionsCaroline Brandl, Heidi L Schulz, Peter Charbel Issa, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian AuthorityAnja K Mayer, Ghassan Balousha, Rajech Sharkia, et al.
Genes|January 28, 2026
<i>CDHR1</i>-Associated Retinal Dystrophies: Expanding the Clinical and Genetic Spectrum with a Hungarian CohortÁgnes Takács, Balázs Varsányi, Mirella Barboni, et al.
Genes|October 29, 2025
Cystoid Macular Lesions in Inherited Retinal Diseases: Prevalence, Characteristics, and Genetic Associations in a Hungarian CohortBarbara Asboth, Alessandra Sanrocco, Barbara Besztercei, 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.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Investigative Ophthalmology & Visual Science|July 20, 2018
Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German CohortDitta Zobor, Gergely Zobor, Stephanie Hipp, et al.
American Journal of Ophthalmology|November 18, 2019
CEP290 Mutation Spectrum and Delineation of the Associated Phenotype in a Large German Cohort: A Monocentric StudyBritta Feldhaus, Nicole Weisschuh, Fadi Nasser, et al.
The European Journal of Neuroscience|September 17, 2013
Visual cortex organisation in a macaque monkey with macular degenerationYibin Shao, Georgios A Keliris, Amalia Papanikolaou, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 28, 2012
Detailed functional and structural characterization of a macular lesion in a rhesus macaqueM Dominik Fischer, Ditta Zobor, Georgios A Keliris, et al.
Investigative Ophthalmology & Visual Science|May 9, 2022
Central Visual Function and Genotype-Phenotype Correlations in PDE6A-Associated Retinitis PigmentosaLaura Kuehlewein, Torsten Straßer, Gunnar Blumenstock, et al.
Genes|June 24, 2017
Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular LesionsCaroline Brandl, Heidi L Schulz, Peter Charbel Issa, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian AuthorityAnja K Mayer, Ghassan Balousha, Rajech Sharkia, et al.
Genes|January 28, 2026
<i>CDHR1</i>-Associated Retinal Dystrophies: Expanding the Clinical and Genetic Spectrum with a Hungarian CohortÁgnes Takács, Balázs Varsányi, Mirella Barboni, et al.
Genes|October 29, 2025
Cystoid Macular Lesions in Inherited Retinal Diseases: Prevalence, Characteristics, and Genetic Associations in a Hungarian CohortBarbara Asboth, Alessandra Sanrocco, Barbara Besztercei, 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.
Pageof 6