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Klinische Monatsblatter Fur Augenheilkunde|March 24, 2025
Enzyme Replacement Therapy in CLN2-Associated RetinopathyClaudia Priglinger, Carolina Courage, Esther M MaierMMW Fortschritte Der Medizin|February 28, 2023
[Considering Leber´s hereditary optic neuropathy]Claudia PriglingerNeuropediatrics|January 8, 2025
Intravitreal Enzyme Replacement Therapy Slows Retinopathy in Late Infantile Ceroid Lipofuscinosis Type 2Claudia S Priglinger, Carolina Courage, Amelie S Lotz-Havla, et al.Methods in Molecular Biology (Clifton, N.J.)|October 17, 2018
Induction and Readout of Oxygen-Induced RetinopathyRaffael Liegl, Claudia Priglinger, Andreas OhlmannKlinische Monatsblatter Fur Augenheilkunde|March 20, 2024
RPE65-Associated Retinal Dystrophies: Phenotypes and Treatment Effects with Voretigene NeparvovecKatarina Stingl, Claudia Priglinger, Philipp HerrmannMedizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 18, 2025
Leber's hereditary optic neuropathy - current status of idebenone and gene replacement therapiesThomas Klopstock, Leopold H Zeng, Claudia PriglingerEuropean Journal of Medical Genetics|June 17, 2014
15q26.1 microdeletion encompassing only CHD2 and RGMA in two adults with moderate intellectual disability, epilepsy and truncal obesityCarolina Courage, Gunnar Houge, Sabina Gallati, et al.Clinical Case Reports|February 16, 2018
Prenatal diagnosis of diaphanospondylodysostosis (DSD): a case reportCornelia Hofstaetter, Carolina Courage, Deborah Bartholdi, et al.Klinische Monatsblatter Fur Augenheilkunde|October 23, 2019
[Leber's Hereditary Optic Neuropathy]Claudia Priglinger, Thomas Klopstock, Günter Rudolph, et al.Molecular Diagnosis & Therapy|December 3, 2021
Achromatopsia: Genetics and Gene TherapyStylianos Michalakis, Maximilian Gerhardt, Günther Rudolph, et al.Pageof 13