SIMONELLI, Francesca
SIMONELLI, Francesca
Dipartimento Multidisciplinare di Specialità Medico-Chirurgiche e Odontoiatriche
'Target Sign' - A near infrared feature and multimodal imaging in a pluri-ethnic cohort with RDH5-related fundus albipunctatus
In corso di stampa 1, Hadas Newman; Perlman, Ido; Pras, Eran; Rozenberg, Assaf; Ben-Yosef, Tamar; Iovino, Claudio; Simonelli, Francesca; DI IORIO, Valentina; Rotenstreich, Ygal; Katzburg, Etti; Ehrenberg, Miriam; Iglicki, Matias; Zur, Dinah
A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot
2018 Alagia, Marianna; Cappuccio, Gerarda; Pinelli, Michele; Torella, Annalaura; Brunetti-Pierri, Raffaella; Simonelli, Francesca; Limongelli, Giuseppe; Oppido, Guido; Nigro, Vincenzo; Brunetti-Pierri, Nicola; Brunetti Pierri, Raffaella
A collaborative RESTful cloud-based tool for management of chromatic pupillometry in a clinical trial
2019 Iadanza, E.; Fabbri, R.; Luschi, A.; Melillo, P.; Simonelli, F.
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice
2023 Murro, Vittoria; Banfi, Sandro; Testa, Francesco; Iarossi, Giancarlo; Falsini, Benedetto; Sodi, Andrea; Signorini, Sabrina; Iolascon, Achille; Russo, Roberta; Mucciolo, Dario Pasquale; Caputo, Roberto; Bacci, Giacomo Maria; Bargiacchi, Sara; Turco, Simona; Fortini, Stefania; Simonelli, Francesca
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene
2008 Testa, Francesco; Rossi, Settimio; Passerini, I; Sodi, A; Di Iorio, V; Interlandi, E; Della Corte, M; Menchini, U; Rinaldi, E; Torricelli, F; Simonelli, Francesca
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene
2007 Rossi, Settimio; Testa, Francesco; Passerini, I.; DI IORIO, V.; Interlandi, E.; Rinaldi, Michele; Sodi, A.; Torricelli, F.; Simonelli, Francesca
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2
2014 Mozzillo, Enza; Delvecchio, Maurizio; Carella, Massimo; Grandone, Elvira; Palumbo, Pietro; Salina, Alessandro; Aloi, Concetta; Buono, Pietro; Izzo, Antonella; D'Annunzio, Giuseppe; Vecchione, Gennaro; Orrico, Ada; Genesio, Rita; Simonelli, Francesca; Franzese, Adriana
A novel mutation in the RDS gene in an Italian family with pattern dystrophy
2005 Testa, Francesco; Marini, V; Rossi, Settimio; Interlandi, E; Nesti, A; Rinaldi, Michele; Varano, M; Garré, C; Simonelli, Francesca
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy
2007 Sodi, A; Passerini, I; Simonelli, Francesca; Testa, Francesco; Menchini, U; Torricelli, F.
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients
2015 Melillo, Paolo; Orrico, A.; Attanasio, M.; Rossi, Settimio; Pecchia, L.; Chirico, Franco; Testa, Francesco; Simonelli, Francesca
AAV-mediated photoreceptor transduction of the pig cone-enriched retina
2011 Mussolino, C; Della Corte, M; Rossi, Settimio; Viola, F; Di Vicino, U; Marrocco, E; Neglia, S; Doria, M; Testa, Francesco; Giovannoni, R; Crasta, M; Giunti, M; Villani, E; Lavitrano, M; Bacci, Ml; Ratiglia, R; Simonelli, Francesca; Auricchio, A; Surace, Em
Accuracy of Formulas for Intraocular Lens Power Calculation After Myopic Refractive Surgery
2022 Lanza, Michele; Ruggiero, Adriano; Ha, Jason; Simonelli, Francesca; Kane, Jack X
Accuracy of formulas for intraocular lens power for eyes undergoing descemet stripping automated endothelial keratoplasty and cataract surgery
2024 Boccia, Rosa; Scorcia, Vincenzo; Lanza, Michele; Luciano, Giuseppe; Lucisano, Andrea; Sbordone, Sandro; Melillo, Paolo; Simonelli, Francesca
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy
2016 Rossi, Settimio; Maisto, R.; Gesualdo, C.; Trotta, M. C.; Ferraraccio, Franca; Kaneva, M. K.; Getting, S. J.; Surace, E.; Testa, Francesco; Simonelli, Francesca; Grieco, P.; Merlino, F.; Perretti, M.; D'Amico, Michele; DI FILIPPO, Clara
Acute macular neuroretinopathy following uncomplicated epiretinal membrane removal
2024 Iovino, Claudio; Damiano, Luciana; Simonelli, Francesca; Sarraf, David
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial
2009 Maguire, Am; High, Ka; Auricchio, A; Wright, Jf; Pierce, Ea; Testa, Francesco; Mingozzi, F; Bennicelli, Jl; Ying, Gs; Rossi, Settimio; Fulton, A; Marshall, Ka; Banfi, Sandro; Chung, Dc; Morgan, Ji; Hauck, B; Zelenaia, O; Zhu, X; Raffini, L; Coppieters, F; De Baere, E; Shindler, Ks; Volpe, Nj; Surace, Em; Acerra, C; Lyubarsky, A; Redmond, Tm; Stone, E; Sun, J; Mcdonnell, Jw; Leroy, Bp; Simonelli, Francesca; Bennett, J.
Alterazione dei livelli ematici di Malondialdeide in una famiglia con soggetti affetti da Retinite Pigmentosa
1987 Simonelli, Francesca; Costagliola, C; Giardino, I; Magli, A; Rinaldi, Michele; Rinaldi, E.
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs
2020 Bedoni, Nicola; Quinodoz, Mathieu; Pinelli, Michele; Cappuccio, Gerarda; Torella, Annalaura; Nigro, Vincenzo; Testa, Francesco; Simonelli, Francesca; Corton, Marta; Lualdi, Susanna; Lanza, Federica; Morana, Giovanni; Ayuso, Carmen; Di Rocco, Maja; Filocamo, Mirella; Banfi, Sandro; Brunetti-Pierri, Nicola; Superti-Furga, Andrea; Rivolta, Carlo
An Atypical Form of Bietti Crystalline Dystrophy
2011 Rossi, Settimio; Testa, Francesco; Li, A; DI IORIO, Valentina; Zhang, J; Gesualdo, C; Corte, Md; Chan, Cc; Fielding Hejtmancik, J; Simonelli, Francesca
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
2016 Bonnet, Crystel; Riahi, Zied; Chantot Bastaraud, Sandra; Smagghe, Luce; Letexier, Mélanie; Marcaillou, Charles; Lefèvre, Gaëlle M; Hardelin, Jean Pierre; El Amraoui, Aziz; Singh Estivalet, Amrit; Mohand Saïd, Saddek; Kohl, Susanne; Kurtenbach, Anne; Sliesoraityte, Ieva; Zobor, Ditta; Gherbi, Souad; Testa, Francesco; Simonelli, Francesca; Banfi, Sandro; Fakin, Ana; Glavač, Damjan; Jarc Vidmar, Martina; Zupan, Andrej; Battelino, Saba; Martorell Sampol, Loreto; Claveria, Maria Antonia; Catala Mora, Jaume; Dad, Shzeena; Møller, Lisbeth B; Rodriguez Jorge, Jesus; Hawlina, Marko; Auricchio, Alberto; Sahel, José Alain; Marlin, Sandrine; Zrenner, Eberhart; Audo, Isabelle; Petit, Christine
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
'Target Sign' - A near infrared feature and multimodal imaging in a pluri-ethnic cohort with RDH5-related fundus albipunctatus | In corso di stampa | 1, Hadas Newman; Perlman, Ido; Pras, Eran; Rozenberg, Assaf; Ben-Yosef, Tamar; Iovino, Claudio; Simonelli, Francesca; DI IORIO, Valentina; Rotenstreich, Ygal; Katzburg, Etti; Ehrenberg, Miriam; Iglicki, Matias; Zur, Dinah | |
A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot | 1-gen-2018 | Alagia, Marianna; Cappuccio, Gerarda; Pinelli, Michele; Torella, Annalaura; Brunetti-Pierri, Raffaella; Simonelli, Francesca; Limongelli, Giuseppe; Oppido, Guido; Nigro, Vincenzo; Brunetti-Pierri, Nicola; Brunetti Pierri, Raffaella | |
A collaborative RESTful cloud-based tool for management of chromatic pupillometry in a clinical trial | 1-gen-2019 | Iadanza, E.; Fabbri, R.; Luschi, A.; Melillo, P.; Simonelli, F. | |
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice | 1-gen-2023 | Murro, Vittoria; Banfi, Sandro; Testa, Francesco; Iarossi, Giancarlo; Falsini, Benedetto; Sodi, Andrea; Signorini, Sabrina; Iolascon, Achille; Russo, Roberta; Mucciolo, Dario Pasquale; Caputo, Roberto; Bacci, Giacomo Maria; Bargiacchi, Sara; Turco, Simona; Fortini, Stefania; Simonelli, Francesca | |
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene | 1-gen-2008 | Testa, Francesco; Rossi, Settimio; Passerini, I; Sodi, A; Di Iorio, V; Interlandi, E; Della Corte, M; Menchini, U; Rinaldi, E; Torricelli, F; Simonelli, Francesca | |
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene | 1-gen-2007 | Rossi, Settimio; Testa, Francesco; Passerini, I.; DI IORIO, V.; Interlandi, E.; Rinaldi, Michele; Sodi, A.; Torricelli, F.; Simonelli, Francesca | |
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2 | 1-gen-2014 | Mozzillo, Enza; Delvecchio, Maurizio; Carella, Massimo; Grandone, Elvira; Palumbo, Pietro; Salina, Alessandro; Aloi, Concetta; Buono, Pietro; Izzo, Antonella; D'Annunzio, Giuseppe; Vecchione, Gennaro; Orrico, Ada; Genesio, Rita; Simonelli, Francesca; Franzese, Adriana | |
A novel mutation in the RDS gene in an Italian family with pattern dystrophy | 1-gen-2005 | Testa, Francesco; Marini, V; Rossi, Settimio; Interlandi, E; Nesti, A; Rinaldi, Michele; Varano, M; Garré, C; Simonelli, Francesca | |
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy | 1-gen-2007 | Sodi, A; Passerini, I; Simonelli, Francesca; Testa, Francesco; Menchini, U; Torricelli, F. | |
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients | 1-gen-2015 | Melillo, Paolo; Orrico, A.; Attanasio, M.; Rossi, Settimio; Pecchia, L.; Chirico, Franco; Testa, Francesco; Simonelli, Francesca | |
AAV-mediated photoreceptor transduction of the pig cone-enriched retina | 1-gen-2011 | Mussolino, C; Della Corte, M; Rossi, Settimio; Viola, F; Di Vicino, U; Marrocco, E; Neglia, S; Doria, M; Testa, Francesco; Giovannoni, R; Crasta, M; Giunti, M; Villani, E; Lavitrano, M; Bacci, Ml; Ratiglia, R; Simonelli, Francesca; Auricchio, A; Surace, Em | |
Accuracy of Formulas for Intraocular Lens Power Calculation After Myopic Refractive Surgery | 1-gen-2022 | Lanza, Michele; Ruggiero, Adriano; Ha, Jason; Simonelli, Francesca; Kane, Jack X | |
Accuracy of formulas for intraocular lens power for eyes undergoing descemet stripping automated endothelial keratoplasty and cataract surgery | 1-gen-2024 | Boccia, Rosa; Scorcia, Vincenzo; Lanza, Michele; Luciano, Giuseppe; Lucisano, Andrea; Sbordone, Sandro; Melillo, Paolo; Simonelli, Francesca | |
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy | 1-gen-2016 | Rossi, Settimio; Maisto, R.; Gesualdo, C.; Trotta, M. C.; Ferraraccio, Franca; Kaneva, M. K.; Getting, S. J.; Surace, E.; Testa, Francesco; Simonelli, Francesca; Grieco, P.; Merlino, F.; Perretti, M.; D'Amico, Michele; DI FILIPPO, Clara | |
Acute macular neuroretinopathy following uncomplicated epiretinal membrane removal | 1-gen-2024 | Iovino, Claudio; Damiano, Luciana; Simonelli, Francesca; Sarraf, David | |
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial | 1-gen-2009 | Maguire, Am; High, Ka; Auricchio, A; Wright, Jf; Pierce, Ea; Testa, Francesco; Mingozzi, F; Bennicelli, Jl; Ying, Gs; Rossi, Settimio; Fulton, A; Marshall, Ka; Banfi, Sandro; Chung, Dc; Morgan, Ji; Hauck, B; Zelenaia, O; Zhu, X; Raffini, L; Coppieters, F; De Baere, E; Shindler, Ks; Volpe, Nj; Surace, Em; Acerra, C; Lyubarsky, A; Redmond, Tm; Stone, E; Sun, J; Mcdonnell, Jw; Leroy, Bp; Simonelli, Francesca; Bennett, J. | |
Alterazione dei livelli ematici di Malondialdeide in una famiglia con soggetti affetti da Retinite Pigmentosa | 1-gen-1987 | Simonelli, Francesca; Costagliola, C; Giardino, I; Magli, A; Rinaldi, Michele; Rinaldi, E. | |
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs | 1-gen-2020 | Bedoni, Nicola; Quinodoz, Mathieu; Pinelli, Michele; Cappuccio, Gerarda; Torella, Annalaura; Nigro, Vincenzo; Testa, Francesco; Simonelli, Francesca; Corton, Marta; Lualdi, Susanna; Lanza, Federica; Morana, Giovanni; Ayuso, Carmen; Di Rocco, Maja; Filocamo, Mirella; Banfi, Sandro; Brunetti-Pierri, Nicola; Superti-Furga, Andrea; Rivolta, Carlo | |
An Atypical Form of Bietti Crystalline Dystrophy | 1-gen-2011 | Rossi, Settimio; Testa, Francesco; Li, A; DI IORIO, Valentina; Zhang, J; Gesualdo, C; Corte, Md; Chan, Cc; Fielding Hejtmancik, J; Simonelli, Francesca | |
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients | 1-gen-2016 | Bonnet, Crystel; Riahi, Zied; Chantot Bastaraud, Sandra; Smagghe, Luce; Letexier, Mélanie; Marcaillou, Charles; Lefèvre, Gaëlle M; Hardelin, Jean Pierre; El Amraoui, Aziz; Singh Estivalet, Amrit; Mohand Saïd, Saddek; Kohl, Susanne; Kurtenbach, Anne; Sliesoraityte, Ieva; Zobor, Ditta; Gherbi, Souad; Testa, Francesco; Simonelli, Francesca; Banfi, Sandro; Fakin, Ana; Glavač, Damjan; Jarc Vidmar, Martina; Zupan, Andrej; Battelino, Saba; Martorell Sampol, Loreto; Claveria, Maria Antonia; Catala Mora, Jaume; Dad, Shzeena; Møller, Lisbeth B; Rodriguez Jorge, Jesus; Hawlina, Marko; Auricchio, Alberto; Sahel, José Alain; Marlin, Sandrine; Zrenner, Eberhart; Audo, Isabelle; Petit, Christine |