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BMC Medical Genetics|June 27, 2018
A 73,128 bp de novo deletion encompassing the OPN1LW/OPN1MW gene cluster in sporadic Blue Cone Monochromacy: a case reportElena Buena-Atienza, Fadi Nasser, Susanne Kohl, et al.Retinal Cases & Brief Reports|September 15, 2016
FUNDUS ALBIPUNCTATUS ASSOCIATED WITH CONE DYSFUNCTIONLaura Kuehlewein, Fadi Nasser, Nicola Gloeckle, et al.Ophthalmic Research|January 12, 2023
Elaborate Evaluation of Farnsworth Dichotomous D-15 Panel Test Can Help Differentiate between Best Vitelliform Macular Dystrophy and Autosomal Recessive BestrophinopathyKatarzyna Nowomiejska, Fadi Nasser, Agnieszka Brzozowska, et al.Acta Ophthalmologica|October 4, 2019
Ophthalmic features of retinitis pigmentosa in Cohen syndrome caused by pathogenic variants in the VPS13B geneFadi Nasser, Anne Kurtenbach, Saskia Biskup, et al.Frontiers in Ophthalmology|July 10, 2024
Adaptive optics retinal imaging in patients with usher syndromeMelanie Kempf, Susanne Kohl, Krunoslav Stingl, et al.Documenta Ophthalmologica. Advances in Ophthalmology|September 9, 2024
Age-dependencies of the electroretinogram in healthy subjectsRonja Jung, Melanie Kempf, Giulia Righetti, et al.Acta Ophthalmologica|December 2, 2017
Ophthalmic features of cone-rod dystrophy caused by pathogenic variants in the ALMS1 geneFadi Nasser, Nicole Weisschuh, Pietro Maffei, et al.Documenta Ophthalmologica. Advances in Ophthalmology|January 30, 2019
Objective assessment of visual acuity: a refined model for analyzing the sweep VEPTorsten Strasser, Fadi Nasser, Hana Langrová, et al.Ophthalmic Research|January 14, 2020
Correlating Adaptive Optics Images to Clinical Findings in Juvenile Macular Dystrophy with Hypotrichosis in Siblings with Homozygous CDH3 Pathogenic VariationFadi Nasser, Melanie Kempf, Anne Kurtenbach, et al.Acta Ophthalmologica|July 30, 2021
Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathiesKatarzyna Nowomiejska, Fadi Nasser, Katarina Stingl, et al.Pageof 3