Zoekresultaten - Francesca Simonelli
- Toon 1 - 20 resultaten van 53
- Ga naar de volgende pagina
-
1
-
2
Gene Therapy of Inherited Retinal Degenerations: Prospects and Challenges door Ivana Trapani, Sandro Banfi, Francesca Simonelli, Enrico Maria Surace, Alberto Auricchio
Gepubliceerd in 2015Revisão -
3
-
4
-
5
-
6
Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linking door Settimio Rossi, Ada Orrico, Carmine Santamaria, Vito Romano, Luigi De Rosa, Giuseppe De Rosa, Francesca Simonelli
Gepubliceerd in 2015Artigo -
7
-
8
-
9
RPE65-associated inherited retinal diseases: consensus recommendations for eligibility to gene therapy door Andrea Sodi, Sandro Banfi, Francesco Testa, Michele Della Corte, Ilaria Passerini, Elisabetta Pelo, Settimio Rossi, Francesca Simonelli
Gepubliceerd in 2021Artigo -
10
Yellow Subthreshold Micropulse Laser in Retinal Diseases: An In-Depth Analysis and Review of the Literature door Claudio Iovino, Clemente Maria Iodice, Danila Pisani, Andrea Rosolia, Francesco Testa, Giuseppe Giannaccare, Jay Chhablani, Francesca Simonelli
Gepubliceerd in 2023Revisão -
11
A Novel Variant in <scp><i>TUBB4B</i></scp> Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss door Margherita Scarpato, Francesco Testa, Anna Nesti, Roberta Zeuli, Rosa Boccia, Gennaro Auletta, Sandro Banfi, Francesca Simonelli, Marianthi Karali
Gepubliceerd in 2025Artigo -
12
-
13
-
14
Triple Vectors Expand AAV Transfer Capacity in the Retina door Andrea Maddalena, Patrizia Tornabene, Paola Tiberi, Renato Minopoli, Anna Manfredi, Margherita Mutarelli, Settimio Rossi, Francesca Simonelli, Jürgen Κ. Naggert, Davide Cacchiarelli, Alberto Auricchio
Gepubliceerd in 2017Artigo -
15
Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors door Pasqualina Colella, Ivana Trapani, Giulia Cesi, Andrea Sommella, Anna Manfredi, Agostina Puppo, Carolina Iodice, Settimio Rossi, Francesca Simonelli, Massimo Giunti, Maria Laura Bacci, Alberto Auricchio
Gepubliceerd in 2014Artigo -
16
Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy door Francesco Testa, Settimio Rossi, Andrea Sodi, Ilaria Passerini, Valentina Di Iorio, Michele Della Corte, Sandro Banfi, Enrico Maria Surace, Ugo Menchini, Alberto Auricchio, Francesca Simonelli
Gepubliceerd in 2012Artigo -
17
Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice door Francesco Testa, Giacomo Maria Bacci, Benedetto Falsini, Giancarlo Iarossi, Paolo Melillo, Dario Pasquale Mucciolo, Vittoria Murro, Anna Paola Salvetti, Andrea Sodi, Giovanni Staurenghi, Francesca Simonelli
Gepubliceerd in 2024Revisão -
18
The human visual cortex responds to gene therapy–mediated recovery of retinal function door Manzar Ashtari, Laura Cyckowski, Justin F. Monroe, Kathleen Marshall, Daniel C. Chung, Alberto Auricchio, Francesca Simonelli, Bart P. Leroy, Albert M. Maguire, Kenneth S. Shindler, Jean Bennett
Gepubliceerd in 2011Artigo -
19
Rhodopsin targeted transcriptional silencing by DNA-binding door Salvatore Botta, Elena Marrocco, Nicola de Prisco, Fabiola Curion, Mario Renda, Martina Sofia, Mariangela Lupo, Annamaria Carissimo, Maria Laura Bacci, Carlo Gesualdo, Settimio Rossi, Francesca Simonelli, Enrico Maria Surace
Gepubliceerd in 2016Artigo -
20
Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease door Albert M. Maguire, Stephen R. Russell, Daniel C. Chung, Zi‐Fan Yu, Amy Tillman, Arlene V. Drack, Francesca Simonelli, Bart P. Leroy, Kathleen Z. Reape, Katherine A. High, Jean Bennett
Gepubliceerd in 2021Artigo
Zoekinstrumenten:
Gerelateerde Onderwerpen
Biology
Medicine
Genetics
Gene
Ophthalmology
Retinal
Internal medicine
Neuroscience
Phenotype
Retinal pigment epithelium
Retinitis pigmentosa
Genetic enhancement
Visual acuity
RPE65
Retina
Cell biology
Mutation
ABCA4
Recombinant DNA
Bioinformatics
Clinical trial
Vector (molecular biology)
Audiology
Biochemistry
Pediatrics
Stargardt disease
Cis-trans-Isomerases
Disease
Exon
Genotype