Inflammation after Voretigene Neparvovec Administration in Patients with RPE65-Related Retinal Dystrophy

Author:

Kessel LineORCID,Christensen Ulrik Correll,Klemp Kristian

Publisher

Elsevier BV

Subject

Ophthalmology

Reference12 articles.

1. Genetic basis of inherited retinal disease in a molecularly characterized cohort of more than 3000 families from the United Kingdom;Pontikos;Ophthalmology,2020

2. Inherited retinal diseases: therapeutics, clinical trials and end points—A review;Georgiou;Clin Exp Ophthalmol,2021

3. The natural history of inherited retinal dystrophy due to biallelic mutations in the RPE65 gene;Chung;Am J Ophthalmol,2019

4. Voretigene neparvovec in patients with RPE65 mutation-associated inherited retinal dystrophy: baseline characteristics from the real-world, prospective, observational PERCEIVE study;Fischer;Invest Ophthalmol Vis Sci,2021

5. Perifoveal chorioretinal atrophy after subretinal Voretigene Neparvovec-rzyl for RPE65-mediated Leber congenital amaurosis;Gange;Ophthalmol Retina,2022

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