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The British Journal of Ophthalmology|January 21, 2021
Spatial and temporal resolution of the photoreceptors rescue dynamics after treatment with voretigene neparvovecKrunoslav Stingl, Melanie Kempf, Karl U Bartz-Schmidt, et al.
International Journal of Molecular Sciences|March 6, 2021
Clinical Phenotype of PDE6B-Associated Retinitis PigmentosaLaura Kuehlewein, Ditta Zobor, Katarina Stingl, et al.
Current Eye Research|July 18, 2018
Usher Syndrome and Color VisionAnne Kurtenbach, Gesa Hahn, Christoph Kernstock, et al.
Cell Death and Differentiation|November 7, 2020
HDAC inhibition ameliorates cone survival in retinitis pigmentosa miceMarijana Samardzija, Andrea Corna, Raquel Gomez-Sintes, et al.
Human Gene Therapy. Clinical Development|September 7, 2018
Development of Methodology and Study Protocol: Safety and Efficacy of a Single Subretinal Injection of rAAV.hCNGA3 in Patients with CNGA3-Linked Achromatopsia Investigated in an Exploratory Dose-Escalation TrialNadine A Kahle, Tobias Peters, Ditta Zobor, et al.
Ophthalmology. Retina|May 4, 2019
Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3Etienne M Schönbach, Mohamed A Ibrahim, Rupert W Strauss, et al.
Proceedings. Biological Sciences|February 22, 2013
Artificial vision with wirelessly powered subretinal electronic implant alpha-IMSKatarina Stingl, Karl Ulrich Bartz-Schmidt, Dorothea Besch, et al.
Ophthalmic Research|August 16, 2018
The Progression of the Stargardt Disease Type 4 (ProgStar-4) Study: Design and Baseline Characteristics (ProgStar-4 Report No. 1)Rupert W Strauss, Beatriz Muñoz, Mohamed I Ahmed, et al.
JACC. Cardiovascular Interventions|July 8, 2017
Neointimal Modification With Scoring Balloon and Efficacy of Drug-Coated Balloon Therapy in Patients With Restenosis in Drug-Eluting Coronary Stents: A Randomized Controlled TrialSebastian Kufner, Michael Joner, Simon Schneider, et al.
Investigative Ophthalmology & Visual Science|June 23, 2011
Spatial resolution and perception of patterns mediated by a subretinal 16-electrode array in patients blinded by hereditary retinal dystrophiesRobert Wilke, Veit-Peter Gabel, Helmut Sachs, et al.
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