Kristina Hess

Latest

• Supernormal foveal photoreceptor density in Alport syndrome: A case report
• Inner retinal degeneration associated with optic nerve head drusen in pseudoxanthoma elasticum
• Tamoxifen retinopathy and macular telangiectasia type 2: Similarities and differences on multimodal retinal imaging
• Evaluation of cone- and rod-mediated parameters in dark adaptation testing as outcome measures in age-related macular degeneration
• Investigations of renal function and age-related macular degeneration phenotypes
• Morphological characteristics preceding exudative neovascularisation secondary to macular telangiectasia type 2
• Deep learning-based modeling of the dark adaptation curve for robust parameter estimation
• Dark adaptation and its role in age-related macular degeneration
• Visual dysfunction and structural correlates in Sorsby fundus dystrophy
• Choriocapillaris flow signal impairment in Sorsby fundus dystrophy
• Analysis of imaging biomarkers and retinal nerve fiber layer thickness in RPGR-associated retinitis pigmentosa
• Hyperreflectivity on optical coherence tomography in macular telangiectasia Type 2
• Optical coherence tomography-angiography for monitoring neovascularisations in macular telangiectasia type 2
• Mesopic and scotopic light sensitivity and its microstructural correlates in pseudoxanthoma elasticum
• Spectral fundus autofluorescence excitation and emission in abca4-related retinopathy
• WITHDRAWN: Hyper-reflectivity on optical coherence tomography in macular telangiectasia type 2
• Dark adaptation in macular telangiectasia Type 2
• Impaired dark adaptation associated with a diseased Bruch membrane in pseudoxanthoma elasticum
• Phenotypic spectrum of the foveal configuration and foveal avascular zone in patients with Alport syndrome
• Comprehensive Geno- and phenotyping in a complex pedigree including four different inherited retinal dystrophies