Markus N. Preising
Giessen, HE, Germany
Last Updated: 09/26/2026
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Found 49 publications
Chorioretinal Atrophy after Voretigene Neparvovec Therapy in RPE65 Mutation-Associated Inherited Retinal Disease: Longitudinal Characterization in Multimodal Imaging.
Journal: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde
Published: April 02, 2025
CACNB3 defects are associated with infantile idiopathic nystagmus.
Journal: Brain communications
Published: November 07, 2024
Single Center Experience with Voretigene Neparvovec Gene Augmentation Therapy in RPE65 Mutation-Associated Inherited Retinal Degeneration in a Clinical Setting.
Journal: Ophthalmology
Published: April 20, 2023
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study.
Journal: The British journal of ophthalmology
Published: April 12, 2023
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 27, 2022
Reduced Visual Acuity at the Age of 3 Years and Flat Unilateral Retinal Detachment at the Age of 9 Years - History of a Child with Compound Heterozygous RP1 Mutations
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: March 22, 2019
The Phenotypic Spectrum of Ophthalmic Changes in CEP290 Mutations
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: March 22, 2019
Splitting of the lateral rectus muscle with medial transposition to treat oculomotor palsy: a retrospective analysis of 29 consecutive cases.
Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
Published: December 18, 2018
Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290.
Journal: Investigative ophthalmology & visual science
Published: September 08, 2018
The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene.
Journal: American journal of ophthalmology
Published: April 03, 2018
Overview of Congenital Stationary Night Blindness with Predominantly Normal Fundus Appearance
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: February 02, 2018
Last Updated: 09/26/2026