Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy ; volume:12 ; number:1 ; day:21 ; month:10 ; year:2022 ; pages:1-9 ; date:12.2022
Scientific reports ; 12, Heft 1 (21.10.2022), 1-9, 12.2022
- Creator
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Testa, Francesco
Melillo, Paolo
Di Iorio, Valentina
Iovino, Claudio
Farinaro, Francesco
Karali, Marianthi
Banfi, Sandro
Rossi, Settimio
Della Corte, Michele
Simonelli, Francesca
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-022-22180-6
- URN
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urn:nbn:de:101:1-2023010709125837638856
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:29 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Testa, Francesco
- Melillo, Paolo
- Di Iorio, Valentina
- Iovino, Claudio
- Farinaro, Francesco
- Karali, Marianthi
- Banfi, Sandro
- Rossi, Settimio
- Della Corte, Michele
- Simonelli, Francesca
- SpringerLink (Online service)
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Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Retinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerations
Consanguinity-based analysis of exome sequencing yields likely genetic causes in patients with inherited retinal dystrophy
Relative frequency of inherited retinal dystrophies in Brazil
Genetic testing and diagnosis of inherited retinal diseases
An Economic Evaluation of Voretigene Neparvovec for the Treatment of Biallelic RPE65-Mediated Inherited Retinal Dystrophies in the UK
Long-term experience with gene augmentation therapy in patients with inherited retinal disease associated with biallelic mutations in RPE65
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Cellular imaging of inherited retinal diseases using adaptive optics
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