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Zobor, Ditta
82
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Online (82)
Mediatypes
Articles (Online) (31)
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1
A contrast sensitivity model of the human visual system in ..:
Mozhaeva, Anastasia
;
Cree, Michael J.
;
Durrant, Robert J.
...
PLOS ONE. 19 (2024) 5 - p. e0303987 , 2024
Link:
https://doi.org/10.1371/..
?
2
Genetic and Clinical Profile of Retinopathies Due to Diseas..:
Zobor, Ditta
;
Brühwiler, Britta
;
Zrenner, Eberhart
..
International Journal of Molecular Sciences. 24 (2023) 10 - p. 8915 , 2023
Link:
https://doi.org/10.3390/..
?
3
The impact of display saturation on visual search performan..:
Hathibelagal, Amithavikram R.
;
Zobor, Ditta
PLOS ONE. 18 (2023) 9 - p. e0290782 , 2023
Link:
https://doi.org/10.1371/..
?
4
Central Visual Function and Genotype–Phenotype Correlations..:
Kuehlewein, Laura
;
Straßer, Torsten
;
Blumenstock, Gunnar
...
Investigative Opthalmology & Visual Science. 63 (2022) 5 - p. 9 , 2022
Link:
https://doi.org/10.1167/..
?
5
Comparison of CRT and LCD monitors for objective estimation..:
Straßer, Torsten
;
Leinberger, Denise Tara
;
Hillerkuss, Dominic
..
Documenta Ophthalmologica. 145 (2022) 2 - p. 133-145 , 2022
Link:
https://doi.org/10.1007/..
?
6
Characteristics of Retinitis Pigmentosa Associated with ADG..:
Fakin, Ana
;
Bonnet, Crystel
;
Kurtenbach, Anne
...
International Journal of Molecular Sciences. 22 (2021) 19 - p. 10352 , 2021
Link:
https://doi.org/10.3390/..
?
7
Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa:
Kuehlewein, Laura
;
Zobor, Ditta
;
Stingl, Katarina
...
International Journal of Molecular Sciences. 22 (2021) 5 - p. 2374 , 2021
Link:
https://doi.org/10.3390/..
?
8
Genetic architecture of inherited retinal degeneration in G..:
Weisschuh, Nicole
;
Obermaier, Carolin D.
;
Battke, Florian
...
Human Mutation. 41 (2020) 9 - p. 1514-1527 , 2020
Link:
https://doi.org/10.1002/..
?
9
CEP290 Mutation Spectrum and Delineation of the Associated ..:
Feldhaus, Britta
;
Weisschuh, Nicole
;
Nasser, Fadi
...
American Journal of Ophthalmology. 211 (2020) - p. 142-150 , 2020
Link:
https://doi.org/10.1016/..
?
10
Unraveling the genetic cause of hereditary ophthalmic disor..:
Mayer, Anja K.
;
Balousha, Ghassan
;
Sharkia, Rajech
...
European Journal of Human Genetics. 28 (2020) 6 - p. 742-753 , 2020
Link:
https://doi.org/10.1038/..
?
11
Objective assessment of visual acuity: a refined model for ..:
Strasser, Torsten
;
Nasser, Fadi
;
Langrová, Hana
...
Documenta Ophthalmologica. 138 (2019) 2 - p. 97-116 , 2019
Link:
https://doi.org/10.1007/..
?
12
Full-field electroretinography, visual acuity and visual fi..:
Stingl, Katarina
;
Kurtenbach, Anne
;
Hahn, Gesa
...
Documenta Ophthalmologica. 139 (2019) 2 - p. 151-160 , 2019
Link:
https://doi.org/10.1007/..
?
13
Molecular and clinical analysis of 27 German patients with ..:
Weisschuh, Nicole
;
Feldhaus, Britta
;
Khan, Muhammad Imran
...
PLOS ONE. 13 (2018) 12 - p. e0205380 , 2018
Link:
https://doi.org/10.1371/..
?
14
Phenotype Variations Caused by Mutations in theRP1L1Gene in..:
Zobor, Ditta
;
Zobor, Gergely
;
Hipp, Stephanie
...
Investigative Opthalmology & Visual Science. 59 (2018) 7 - p. 3041 , 2018
Link:
https://doi.org/10.1167/..
?
15
The Clinical Phenotype of CNGA3-Related Achromatopsia: Pret..:
Zobor, Ditta
;
Werner, Annette
;
Stanzial, Franco
...
Investigative Opthalmology & Visual Science. 58 (2017) 2 - p. 821 , 2017
Link:
https://doi.org/10.1167/..
1-15