RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy ; volume:16 ; number:1 ; day:4 ; month:6 ; year:2021 ; pages:1-11 ; date:12.2021
Orphanet journal of rare diseases ; 16, Heft 1 (4.6.2021), 1-11, 12.2021
- Urheber
-
Sodi, Andrea
Banfi, Sandro
Testa, Francesco
Della Corte, Michele
Passerini, Ilaria
Pelo, Elisabetta
Rossi, Settimio
Simonelli, Francesca
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-021-01868-4
- URN
-
urn:nbn:de:101:1-2021092819341159107018
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:38 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Sodi, Andrea
- Banfi, Sandro
- Testa, Francesco
- Della Corte, Michele
- Passerini, Ilaria
- Pelo, Elisabetta
- Rossi, Settimio
- Simonelli, Francesca
- SpringerLink (Online service)
Ähnliche Objekte (12)
Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders
Retinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerations
Relative frequency of inherited retinal dystrophies in Brazil
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Genetic testing and diagnosis of inherited retinal diseases
Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders
The socioeconomic epidemiology of inherited retinal diseases in Portugal
Systemic inflammation induced by lipopolysaccharide aggravates inherited retinal dystrophy
Gene Editing in pig models of inherited retinal diseases
Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders
Retinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerations
Relative frequency of inherited retinal dystrophies in Brazil
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Genetic testing and diagnosis of inherited retinal diseases
Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders
The socioeconomic epidemiology of inherited retinal diseases in Portugal
Systemic inflammation induced by lipopolysaccharide aggravates inherited retinal dystrophy
Gene Editing in pig models of inherited retinal diseases
Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders
Retinal prolactin isoform PRLΔE1 sustains rod disease in inherited retinal degenerations
Relative frequency of inherited retinal dystrophies in Brazil
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
Genetic testing and diagnosis of inherited retinal diseases
Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders
The socioeconomic epidemiology of inherited retinal diseases in Portugal
Systemic inflammation induced by lipopolysaccharide aggravates inherited retinal dystrophy