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Titolo Data di pubblicazione Autore(i) File
CHM/REP1 transcript expression and loss of visual function in patients affected by choroideremia 1-gen-2019 Di Iorio, V.; Esposito, G.; De Falco, F.; Boccia, R.; Fioretti, T.; Colucci, R.; De Rosa, G.; Melillo, P.; Salvatore, F.; Simonelli, F.; Testa, F.
Toward a novel medical device based on chromatic pupillometry for screening and monitoring of inherited ocular disease: A pilot study 1-gen-2019 Melillo, Paolo; de Benedictis, Antonella; Villani, Edoardo; Ferraro, Maria Concetta; Iadanza, Ernesto; Gherardelli, Monica; Testa, Francesco; Banfi, Sandro; Nucci, Paolo; Simonelli, Francesca
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.
Is Shouldice the best NON-MESH inguinal hernia repair technique? A systematic review and network metanalysis of randomized controlled trials comparing Shouldice and Desarda 1-gen-2019 Bracale, U.; Melillo, P.; Piaggio, D.; Pecchia, L.; Cuccurullo, D.; Milone, M.; De Palma, G. D.; Cavallaro, G.; Campanelli, G.; Merola, G.; Stabilini, C.
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 1-gen-2019 Testa, F.; Di Iorio, V.; Gallo, B.; Marchese, M.; Nesti, A.; De Rosa, G.; Melillo, P.; Simonelli, F.
Ultra-short term HRV features as surrogates of short term HRV: A case study on mental stress detection in real life 1-gen-2019 Castaldo, R.; Montesinos, L.; Melillo, P.; James, C.; Pecchia, L.
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 1-gen-2019 Di Iorio, V.; Orrico, A.; Esposito, G.; Melillo, P.; Rossi, S.; Sbordone, S.; Auricchio, A.; Testa, F.; Simonelli, F.
Mild form of Zellweger Spectrum Disorders (ZSD) due to variants in PEX1: Detailed clinical investigation in a 9-years-old female 1-gen-2020 Barillari, Maria Rosaria; Karali, Marianthi; Di Iorio, Valentina; Contaldo, Maria; Piccolo, Vincenzo; Esposito, Maria; Costa, Giuseppe; Argenziano, Giuseppe; Serpico, Rosario; Carotenuto, Marco; Cappuccio, Gerarda; Banfi, Sandro; Melillo, Paolo; Simonelli, Francesca
An automatic system supporting clinical decision for chronic obstructive pulmonary disease 1-gen-2020 Iadanza, E.; Mudura, V.; Melillo, P.; Gherardelli, M.
Biofeedback rehabilitation and visual cortex response in stargardt’s disease: A randomized controlled trial 1-gen-2020 Melillo, P.; Prinster, A.; Di Iorio, V.; Olivo, G.; D'Alterio, F. M.; Cocozza, S.; Quarantelli, M.; Testa, F.; Brunetti, A.; Simonelli, F.
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations 1-gen-2020 Di Iorio, Valentina; Karali, Marianthi; Melillo, Paolo; Testa, Francesco; Brunetti-Pierri, Raffaella; Musacchia, Francesco; Condroyer, Christel; Neidhardt, John; Audo, Isabelle; Zeitz, Christina; Banfi, Sandro; Simonelli, Francesca
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 1-gen-2020 Karali, M.; Testa, F.; Brunetti Pierri, R.; Di Iorio, V; Pizzo, M.; Melillo, P.; Barillari, M. R.; Torella, A.; Musacchia, F.; D'Angelo, L.; Banfi, S.; Simonelli, F.
Automatic Detection of Genetic Diseases in Pediatric Age Using Pupillometry 1-gen-2020 Iadanza, E.; Goretti, F.; Sorelli, M.; Melillo, P.; Pecchia, L.; Simonelli, F.; Gherardelli, M.
ORÁO: Restful cloud-based ophthalmologic medical record for chromatic pupillometry 1-gen-2020 Iadanza, E.; Fabbri, R.; Luschi, A.; Gavazzi, F.; Melillo, P.; Simonelli, F.; Gherardelli, M.
Oct analysis in patients with relapsing-remitting multiple sclerosis during fingolimod therapy: 2-year longitudinal retrospective study 1-gen-2020 Rossi, S.; Gesualdo, C.; Gallo, A.; Melillo, P.; Martines, F.; Colucci, R.; D'Ambrosio, A.; Tedeschi, G.; Simonelli, F.
Baseline characteristics of patients with Usher Syndrome due to MYO7A mutations enrolled in a prospective natural history study 1-gen-2020 Testa, F; Carreno, E; Vermeer, K; Di Lorio, V; Jimenez-Rolando, B; Karali, M; Sandoval, Bg; Romero, Ip; Salvador, Jm; Melillo, P; Banfi, S; Auricchio, A; van den Born, Li; Ayuso, C; Simonelli, F
Pericentral Retinitis Pigmentosa is associated with a high prevalence of USH2A pathogenic variants in an Italian cohort of patients 1-gen-2020 Brunetti-Pierri, R; Melillo, P; Di Lorio, V; Karali, M; Angeli, C; Nesti, A; Barillari, Mr; Banfi, S; Testa, F; Simonelli, F
Clinical and molecular characterization of achromatopsia patients: A longitudinal study 1-gen-2021 Brunetti-Pierri, R.; Karali, M.; Melillo, P.; Di Iorio, V.; De Benedictis, A.; Iaccarino, G.; Testa, F.; Banfi, S.; Simonelli, F.
A Model of Pupillometric Signals for Studying Inherited Retinal Diseases in Childhood Population 1-gen-2021 Ermini, D.; Fabbri, R.; Iadanza, E.; Gherardelli, M.; Melillo, P.; Bocchi, L.
Evaluation of Donor and Recipient Characteristics Involved in Descemet Stripping Automated Endothelial Keratoplasty Outcomes 1-gen-2021 Lanza, M.; Boccia, R.; Ruggiero, A.; Melillo, P.; Bifani Sconocchia, M.; Simonelli, F.; Sbordone, S.
Mostrati risultati da 61 a 80 di 98
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