Birgit Lorenz
Giessen, HE, Germany
Last Updated: 09/26/2026
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Found 166 publications
Evaluation of aggressive posterior retinopathy of prematurity (AP-ROP) in the German Retina.net ROP registry.
Journal: Frontiers in medicine
Published: December 20, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.
Journal: medRxiv : the preprint server for health sciences
Published: July 09, 2025
Multicenter Retrospective Study of Spiroplasma ixodetis Infantile Cataract in 8 Countries in Europe.
Multicenter Retrospective Study of Spiroplasma ixodetis Infantile Cataract in 8 Countries in Europe.
Journal: Emerging infectious diseases
Published: May 29, 2025
Correction: Letter to the editor relating to Stingl K, Priglinger C, Herrmann P. "RPE65-Associated Retinal Dystrophies: Phenotypes and Treatment Effects with Voretigene Neparvovec" Klin Monbl Augenheilkd 2024; 241(03): 259-265. DOI: 10.1055/a-2227-3671.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: May 07, 2025
Corrigendum to: Long-term experience with gene augmentation therapy in patients with inherited retinal disease associated with biallelic mutations in RPE65.
Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
Published: April 10, 2025
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
Letter to the Editor, Klinische Monatsblätter für Augenheilkunde.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: April 02, 2025
Addressing unmet needs in pregnancy and family planning of people living with rare and low-prevalence diseases: results of the "ERN transversal working group on pregnancy and family planning" survey.
Journal: Reproductive health
Published: February 26, 2025
Long-term experience with gene augmentation therapy in patients with inherited retinal disease associated with biallelic mutations in RPE65.
Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
Published: February 13, 2025
Deep Learning-Based SD-OCT Layer Segmentation Quantifies Outer Retina Changes in Patients With Biallelic RPE65 Mutations Undergoing Gene Therapy.
Journal: Investigative ophthalmology & visual science
Published: January 02, 2025
CACNB3 defects are associated with infantile idiopathic nystagmus.
Journal: Brain communications
Published: November 07, 2024
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene.
Journal: Nature machine intelligence
Published: September 09, 2024
Last Updated: 09/26/2026