Search Results - "Zobor, Ditta"

Altered Ocular Surface Temperature in Congenital Aniridia with PAX6 Pathogenic Variants: Impact of Age, Salzmann Nodules and Ocular Surgery.

Authors: Németh, Orsolya Náray, Annamária Csidey, Mária et al.

Source: Life (2075-1729). Feb2026, Vol. 16 Issue 2, p238. 17p.

DR-GPT: A large language model for medical report analysis of diabetic retinopathy patients.

Authors: Jaskari, Joel Sahlsten, Jaakko Summanen, Paula et al.

Source: PLoS ONE. 10/11/2024, Vol. 19 Issue 10, p1-14. 14p.

Genetic and Clinical Profile of Retinopathies Due to Disease-Causing Variants in Leber Congenital Amaurosis (LCA)-Associated Genes in a Large German Cohort.

Authors: Zobor, Ditta Brühwiler, Britta Zrenner, Eberhart et al.

Source: International Journal of Molecular Sciences. May2023, Vol. 24 Issue 10, p8915. 16p.

A contrast sensitivity model of the human visual system in modern conditions for presenting video content.

Authors: Mozhaeva, Anastasia Cree, Michael J. Durrant, Robert J. et al.

Source: PLoS ONE. 5/30/2024, Vol. 19 Issue 5, p1-19. 19p.

Cone-rod dystrophy associated with amelogenesis imperfecta in a child with neurofibromatosis type 1.

Authors: Zobor, Ditta Kaufmann, Dieter H. Weckerle, Petra et al.

Source: Ophthalmic Genetics. Mar2012, Vol. 33 Issue 1, p34-38. 5p. 2 Color Photographs, 1 Chart.

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia.

Authors: Kohl, Susanne Zobor, Ditta Weisschuh, Nicole et al.

Source: Nature Genetics. Jul2015, Vol. 47 Issue 7, p757-765. 9p. 4 Color Photographs, 2 Black and White Photographs, 1 Graph.

Oscillatory Potential-based Characterization of the Human Light-adapted Electroretinogram Using Discrete Wavelet Transform.

Authors: Min Gao Barboni, Mirella Telles Salgueiro Szabó, Viktória et al.

Source: Periodica Polytechnica: Mechanical Engineering. 2024, Vol. 68 Issue 3, p187-195. 9p.

Visual cortex organisation in a macaque monkey with macular degeneration.

Authors: Shao, Yibin Keliris, Georgios A. Papanikolaou, Amalia et al.

Source: European Journal of Neuroscience. Nov2013, Vol. 38 Issue 10, p3456-3464. 9p.

Subjects: Visual cortex, Macaques, Retinal degeneration, Visual fields, Functional magnetic resonance imaging, Receptive fields (Neurology), Neurosciences

Rod and Cone Function in Patients with KCNV2 Retinopathy.

Authors: Zobor, Ditta Kohl, Susanne Wissinger, Bernd et al.

Source: PLoS ONE. Oct2012, Vol. 7 Issue 10, Special section p1-13. 13p.

Novel homozygous mutation in the SPATA7 gene causes autosomal recessive retinal degeneration in a consanguineous German family.

Authors: Feldhaus, Britta Kohl, Susanne Hörtnagel, Konstanze et al.

Source: Ophthalmic Genetics. Jan/Feb2018, Vol. 39 Issue 1, p131-134. 4p.

Clinical Phenotype of PDE6B -Associated Retinitis Pigmentosa.

Authors: Kuehlewein, Laura Zobor, Ditta Stingl, Katarina et al.

Source: International Journal of Molecular Sciences. Mar2021, Vol. 22 Issue 5, p2374-2374. 1p.

Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush.

Authors: Fakin, Ana Bonnet, Crystel Kurtenbach, Anne et al.

Source: International Journal of Molecular Sciences. Oct2021, Vol. 22 Issue 19, p10352. 1p.

Usher Syndrome and Color Vision.

Authors: Kurtenbach, Anne Hahn, Gesa Kernstock, Christoph et al.

Source: Current Eye Research. Oct2018, Vol. 43 Issue 10, p1295-1301. 7p.

Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT).

Authors: Scholl, Hendrik P. N. Moore, Anthony T. Koenekoop, Robert K. et al.

Source: PLoS ONE. 12/10/2015, Vol. 10 Issue 12, p1-16. 16p.

Phenotype variations of retinal dystrophies caused by mutations in the RLBP1 gene.

Authors: Hipp, Stephanie Zobor, Gergely Glöckle, Nicola et al.

Source: Acta Ophthalmologica (1755375X). Jun2015, Vol. 93 Issue 4, pe281-e286. 6p.

Novel insights into the molecular pathogenesis of CYP4V2-associated Bietti's retinal dystrophy.

Authors: Astuti, Galuh D. N. Sun, Vincent Bauwens, Miriam et al.

Source: Molecular Genetics & Genomic Medicine. Jan2015, Vol. 3 Issue 1, p14-29. 16p.

De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy.

Authors: Buena-Atienza, Elena Rüther, Klaus Baumann, Britta et al.

Source: Scientific Reports. 6/24/2016, p28253. 1p.