Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients

Por Melillo, Paolo, Pecchia, Leandro, Testa, Francesco, Rossi, Settimio, Bennett, Jean, Simonelli, Francesca
Publicado em 2012

Ocriplasmin use in a selected case with preserved visual acuity

Por Rossi, Settimio, Orrico, Ada, Melillo, Paolo, Testa, Francesco, Simonelli, Francesca, Della Corte, Michele
Publicado no BMC Ophthalmol (2015)

Functional improvement assessed by multifocal electroretinogram after Ocriplasmin treatment for vitreomacular traction

Por Rossi, Settimio, Testa, Francesco, Melillo, Paolo, Orrico, Ada, Della Corte, Michele, Simonelli, Francesca
Publicado no BMC Ophthalmol (2016)

Identifying fallers among ophthalmic patients using classification tree methodology

Por Melillo, Paolo, Orrico, Ada, Chirico, Franco, Pecchia, Leandro, Rossi, Settimio, Testa, Francesco, Simonelli, Francesca
Publicado no PLoS One (2017)

Clinical and genetic features in Italian Bietti crystalline dystrophy patients

Por Rossi, Settimio, Testa, Francesco, Li, Anren, Yaylacioğlu, Fulya, Gesualdo, Carlo, Hejtmancik, J Fielding, Simonelli, Francesca
Publicado em 2013

Macular function and morphological features in juvenile Stargardt disease: Longitudinal study

Por Testa, Francesco, Melillo, Paolo, Iorio, Valentina Di, Orrico, Ada, Attanasio, Marcella, Rossi, Settimio, Simonelli, Francesca
Publicado no Ophthalmology (2014)

En Face Spectral-Domain Optical Coherence Tomography for the Monitoring of Lesion Area Progression in Stargardt Disease

Por Melillo, Paolo, Testa, Francesco, Rossi, Settimio, Di Iorio, Valentina, Orrico, Ada, Auricchio, Alberto, Simonelli, Francesca
Publicado no Invest Ophthalmol Vis Sci (2016)

Subretinal Fibrosis in Stargardt's Disease with Fundus Flavimaculatus and ABCA4 Gene Mutation

Por Rossi, Settimio, Testa, Francesco, Attanasio, Marcella, Orrico, Ada, de Benedictis, Antonella, Corte, Michele Della, Simonelli, Francesca
Publicado em 2012

Macular abnormalities in Italian patients with retinitis pigmentosa

Por Testa, Francesco, Rossi, Settimio, Colucci, Raffaella, Gallo, Beatrice, Di Iorio, Valentina, della Corte, Michele, Azzolini, Claudio, Melillo, Paolo, Simonelli, Francesca
Publicado em 2014

Vitreous Substitutes: The Present and the Future

Por Donati, Simone, Caprani, Simona Maria, Airaghi, Giulia, Vinciguerra, Riccardo, Bartalena, Luigi, Testa, Francesco, Mariotti, Cesare, Porta, Giovanni, Simonelli, Francesca, Azzolini, Claudio
Publicado em 2014

The Role of Optical Coherence Tomography in an Atypical Case of Oculocutaneous Albinism: A Case Report

Por Rossi, Settimio, Testa, Francesco, Gargiulo, Annagiusi, Di Iorio, Valentina, Pierri, Raffaella Brunetti, D'Alterio, Francesco Maria, Corte, Michele Della, Surace, Enrico, Simonelli, Francesca
Publicado em 2012

An Atypical Form of Bietti Crystalline Dystrophy

Por Rossi, Settimio, Testa, Francesco, Li, Anren, Di Iorio, Valentina, Zhang, Jun, Gesualdo, Carlo, Corte, Michele Della, Chan, Chi-Chao, Hejtmancik, J. Fielding, Simonelli, Francesca
Publicado em 2011

Melanocortin receptor agonists MCR (1‐5) protect photoreceptors from high‐glucose damage and restore antioxidant enzymes in primary retinal cell culture

Por Maisto, Rosa, Gesualdo, Carlo, Trotta, Maria Consiglia, Grieco, Paolo, Testa, Francesco, Simonelli, Francesca, Barcia, Jorge Miquel, D'Amico, Michele, Di Filippo, Clara, Rossi, Settimio
Publicado no J Cell Mol Med (2016)

Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy

Por Testa, Francesco, Rossi, Settimio, Sodi, Andrea, Passerini, Ilaria, Di Iorio, Valentina, Corte, Michele Della, Banfi, Sandro, Surace, Enrico Maria, Menchini, Ugo, Auricchio, Alberto, Simonelli, Francesca
Publicado no Invest Ophthalmol Vis Sci (2012)

High Levels of Serum Ubiquitin and Proteasome in a Case of HLA-B27 Uveitis

Por Rossi, Settimio, Gesualdo, Carlo, Maisto, Rosa, Trotta, Maria Consiglia, Di Carluccio, Nadia, Brigida, Annalisa, Di Iorio, Valentina, Testa, Francesco, Simonelli, Francesca, D’Amico, Michele, Di Filippo, Clara
Publicado no Int J Mol Sci (2017)

Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy

Por Testa, Francesco, Filippelli, Mariaelena, Brunetti-Pierri, Raffaella, Di Fruscio, Giuseppina, Di Iorio, Valentina, Pizzo, Mariateresa, Torella, Annalaura, Barillari, Maria Rosaria, Nigro, Vincenzo, Brunetti-Pierri, Nicola, Simonelli, Francesca, Banfi, Sandro
Publicado no Eur J Hum Genet (2017)

Molecular epidemiology of Usher syndrome in Italy

Por Vozzi, Diego, Aaspõllu, Anu, Athanasakis, Emmanouil, Berto, Anna, Fabretto, Antonella, Licastro, Danilo, Külm, Maigi, Testa, Francesco, Trevisi, Patrizia, Vahter, Marju, Ziviello, Carmela, Martini, Alessandro, Simonelli, Francesca, Banfi, Sandro, Gasparini, Paolo
Publicado em 2011

The <it>ADAMTS18 </it>gene is responsible for autosomal recessive early onset severe retinal dystrophy

Por Peluso Ivana, Conte Ivan, Testa Francesco, Dharmalingam Gopuraja, Pizzo Mariateresa, Collin Rob WJ, Meola Nicola, Barbato Sara, Mutarelli Margherita, Ziviello Carmela, Barbarulo Anna Maria, Nigro Vincenzo, Melone Mariarosa AB, Simonelli Francesca, Banfi Sandro
Publicado em 2013-01-01

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

Por Peluso, Ivana, Conte, Ivan, Testa, Francesco, Dharmalingam, Gopuraja, Pizzo, Mariateresa, Collin, Rob WJ, Meola, Nicola, Barbato, Sara, Mutarelli, Margherita, Ziviello, Carmela, Barbarulo, Anna Maria, Nigro, Vincenzo, Melone, Mariarosa AB, Simonelli, Francesca, Banfi, Sandro
Publicado em 2013

Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic s...

Por Esposito, Gabriella, Testa, Francesco, Zacchia, Miriam, Crispo, Anna Alessia, Di Iorio, Valentina, Capolongo, Giovanna, Rinaldi, Luca, D’Antonio, Marcella, Fioretti, Tiziana, Iadicicco, Pasquale, Rossi, Settimio, Franzè, Annamaria, Marciano, Elio, Capasso, Giovanbattista, Simonelli, Francesca, Salvatore, Francesco
Publicado no BMC Med Genet (2017)