A Comprehensive Study of the Retinal Phenotype of Rpe65-Deficient Dogs

Gelijkaardige items

• First results of long-term follow-up of children in Russia after gene therapy for hereditary retinal dystrophies associated with biallelic mutations in the RPE65 gene
  door: V. V. Neroev, et al.
  Gepubliceerd in: (2023-12-01)
• Early experiences with voretigene neparvovec (Luxturna) gene therapy in Poland: an analysis of four patients with biallelic RPE65 gene mutations
  door: Marcin Stopa, et al.
  Gepubliceerd in: (2025-06-01)
• A decision making algorithm for inherited retinal dystrophies, caused by biallelic mutations in the RPE65 gene, in the clinical practice of an ophthalmologist
  door: E. I. Saidasheva, et al.
  Gepubliceerd in: (2022-03-01)
• Multi-Luminance Mobility Test (MLMT) as a tool for assessing functional vision in patients with RPE65 gene mutations following gene therapy (voretigene neparvovec)
  door: Martyna Mieszczak, et al.
  Gepubliceerd in: (2025-06-01)
• Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis
  door: Maximilian J. Gerhardt, et al.
  Gepubliceerd in: (2022-12-01)