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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.
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.
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.
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