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Documenta Ophthalmologica. Advances in Ophthalmology|October 15, 2025
Chromatic pupil campimetry as objective diagnostic tool for progressive optic neuropathiesMárton Viktor Edelmayer, Torsten Strasser, Ronja Jung, et al.Mechanisms of Development|May 9, 2006
Impaired development of the Harderian gland in mutant protein phosphatase 2A transgenic miceAndreas Schild, Stefan Isenmann, Naoyuki Tanimoto, et al.Investigative Ophthalmology & Visual Science|June 3, 2024
Influencing Factors on Pupillary Light Responses as a Biomarker for Local Retinal Function in a Large Normative CohortRicarda Jendritza, Krunoslav Stingl, Torsten Strasser, et al.Radiation Oncology (London, England)|December 29, 2019
Retrospective analysis of fractionated intensity-modulated radiotherapy (IMRT) in the interdisciplinary management of primary optic nerve sheath meningiomasFranziska Eckert, Kerstin Clasen, Carina Kelbsch, et al.Radiation Oncology (London, England)|November 20, 2020
Correction to: Retrospective analysis of fractionated intensity-modulated radiotherapy (IMRT) in the interdisciplinary management of primary optic nerve sheath meningiomasFranziska Eckert, Kerstin Clasen, Carina Kelbsch, et al.Plos One|July 9, 2021
Mutation spectrum of the OPA1 gene in a large cohort of patients with suspected dominant optic atrophy: Identification and classification of 48 novel variantsNicole Weisschuh, Simone Schimpf-Linzenbold, Pascale Mazzola, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 20, 2007
A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1Serge A van de Pavert, Jan Meuleman, Anna Malysheva, et al.The Journal of Clinical Investigation|January 18, 2006
Independent degeneration of photoreceptors and retinal pigment epithelium in conditional knockout mouse models of choroideremiaTanya Tolmachova, Ross Anders, Magnus Abrink, et al.Journal of Medical Genetics|January 29, 2022
DNAJC30 disease-causing gene variants in a large Central European cohort of patients with suspected Leber's hereditary optic neuropathy and optic atrophySinja Kieninger, Ting Xiao, Nicole Weisschuh, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|July 20, 2005
Prolonged recovery of retinal structure/function after gene therapy in an Rs1h-deficient mouse model of x-linked juvenile retinoschisisSeok H Min, Laurie L Molday, Mathias W Seeliger, et al.Pageof 4