- ORCID iD
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0009-0007-0647-672X
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- Conference Paper
- C3
- open access
In-depth phenotypic study of a Novel Autosomal Dominant RPE65-related Retinal Dystrophy
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- Journal Article
- A1
- open access
Short-term outcomes of pediatric patients with mild autosomal recessive RPE65-associated retinal dystrophy treated with voretigene neparvovec
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- Conference Paper
- C3
- open access
Phenotypic variability and evolution of MFSD8-related retinal disease
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- Conference Paper
- C3
- open access
Results of Belgian patients with RPE65-related inherited retinal dystrophy 6 months after treatment with voretigene neparvovec