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2. Development of a genotyping microarray for Usher syndrome. Issue 2 (8th September 2006)

3. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial. Issue 10097 (26th August 2017)

5. Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsia. Issue 10 (22nd August 2018)

6. Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial. Issue 10045 (13th August 2016)

7. Study design and baseline characteristics for the reflect gene therapy trial ofm.11778g>A/ND4-LHON. Issue 1 (15th November 2022)