Early detection of central visual function decline in cone-rod dystrophy by the use of macular focal cone electroretinogram
2013-01-01 Galli-Resta, L; Piccardi, M; Ziccardi, L; Fadda, A; Minnella, A; Marangoni, D; Placidi, G; Resta, G; Falsini, B
USH2A -Related Retinitis Pigmentosa: Staging of Disease Severity and Morpho-Functional Studies.
2021-01-01 Falsini, B; Placidi, G; De Siena, E; Savastano, Mc; Minnella, Am; Maceroni, M; Midena, G; Ziccardi, L; Parisi, V; Bertelli, M; Maltese, Pe; Chiurazzi, P; Rizzo, S.
Visual System Abnormalities in a Case of Nonsyndromic, Complete, Isolated CorpusCallosum Agenesis.
2024-01-01 Barbano, L; Ziccardi, L; Antonelli, G; Tinelli, E; Parisi, V
Morpho-Functional Macular Assessment in a Case of Facioscapulohumeral MuscularDystrophy: Photoreceptor Degeneration as Possible Cause for Reduced Visual Acuityover Three Years of Follow-Up.
2022-01-01 Parravano, M; Costanzo, E; Barbano, L; Viggiano, P; De Geronimo, D; Antonelli, G; Parisi, V; Varano, M; Ziccardi, L
Temporal response properties of the macular cone system: effect of normal aging and age-related maculopathy.
2007-01-01 Falsini, B; Ziccardi, L; Stifano, G; Iarossi, G; Merendino, E; Minnella, Am; Fadda, A; Balestrazzi, E.
Retinal dysfunction characterizes subtypes of dominant optic atrophy
2018-01-01 Cascavilla, Ml; Parisi, V; Triolo, G; Ziccardi, L; Borrelli, E; Di Renzo, A; Balducci, N; Lamperti, C; Bianchi Marzoli, S; Darvizeh, F; Sadun, Aa; Carelli, V; Bandello, F; Barboni, P
Multimodal Study of PRPH2 Gene-Related Retinal Phenotypes.
2022-01-01 Antonelli, G; Parravano, M; Barbano, L; Costanzo, E; Bertelli, M; Medori, Mc; Parisi, V; Ziccardi, L
Morphological Outer Retina Findings in Multiple Sclerosis Patients With or WithoutOptic Neuritis
2020-01-01 Ziccardi, L; Barbano, L; Boffa, L; Albanese, M; Grzybowski, A; Centonze, D; Parisi, V.
Genetic testing for cone rod dystrophies
2017-01-01 Abeshi, A; Zulian, A; Beccari, T; Dundar, M; Ziccardi, L; Bertelli, M
Bilateral Symmetry of Visual Function Loss in Cone-Rod Dystrophies
2016-01-01 Galli-Resta, L; Falsini, B; Rossi, G; Piccardi, M; Ziccardi, L; Fadda, A; Minnella, A; Marangoni, D; Placidi, G; Campagna, F; Abed, E; Bertelli, M; Zuntini, M; Resta, G
Macular function in eyes with open-angle glaucoma evaluated by multifocal electroretinogram
2012-01-01 Parisi, V; Ziccardi, L; Centofanti, M; Tanga, L; Gallinaro, G; Falsini, B; Bucci MG,
Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-up
2019-01-01 Parisi, V; Ziccardi, L; Sadun, F; De Negri, Am; La Morgia, C; Barbano, L; Carelli, V; Barboni, P
Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology
2019-01-01 Frecer, V; Iarossi, G; Salvetti, Ap; Maltese, Pe; Delledonne, G; Oldani, M; Staurenghi, G; Falsini, B; Minnella, Am; Ziccardi, L; Magli, A; Colombo, L; D'Esposito, F; Miertus, J; Viola, F; Attanasio, M; Maggio, E; Bertelli, M
Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis andthe Structure of the Primary Cilium
2022-01-01 Ziccardi, L; Niceta, M; Stellacci, E; Ciolfi, A; Tatti, M; Bruselles, A; Mancini, C; Barbano, L; Cecchetti, S; Costanzo, E; Cappa, M; Parravano, M; Varano, M; Tartaglia, M; Cordeddu, V.
Genetic testing for Bietti crystalline dystrophy
2017-01-01 Abeshi, A; Bruson, A; Beccari, T; Dundar, M; Ziccardi, L; Bertelli, M
Design and Validation of a New MLPA-Based Assay for the Detection of RS1 Gene Deletions and Application in a Large Family with X-Linked Juvenile Retinoschisis
2017-01-01 Nicoletti, A; Ziccardi, L; Maltese, Pe; Benedetti, S; Palumbo, O; Rendina, M; D'Agruma, L; Falsini, B; Wang, X; Bertelli, M
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56.
2021-01-01 Legrand, A; Pujol, C; Durand, Cm; Mesnil, A; Rubera, I; Duranton, C; Zuily, S; Sousa, Ab; Renaud, M; Boucher, Jl; Pietrancosta, N; Adham, S; Orssaud, C; Marelli, C; Casali, C; Ziccardi, L; Villain, N; Ewenczyk, C; Durr, A; Mignot, C; Stevaning, ; Billon, C; Hureaux, M; Jeunemaitre, X; Goizet, C; Albuisson, J.
Intravitreal bevacizumab (Avastin) in proliferative diabetic retinopathy.
2008-01-01 Minnella, Am; Savastano, Cm; Ziccardi, L; Scupola, A; Falsini, B; Balestrazzi, E.
Early and localized retinal dysfunction in patients with type 1 diabetes mellitus studied by multifocal electroretinogram
2018-01-01 Ziccardi, L; Parisi, V; Picconi, F; Di Renzo, A; Lombardo, M; Frontoni, S; Parravano, M
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery
2018-01-01 Cukras, C; Wiley, He; Jeffrey, Bg; Sen, Hn; Turriff, A; Zeng, Y; Vijayasarathy, C; Marangoni, D; Ziccardi, L; Kjellstrom, S; Park, Tk; Hiriyanna, S; Wright, Jf; Colosi, P; Wu, Z; Bush, Ra; Wei, Ll; Sieving, Pa
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Early detection of central visual function decline in cone-rod dystrophy by the use of macular focal cone electroretinogram | 1-gen-2013 | Galli-Resta, L; Piccardi, M; Ziccardi, L; Fadda, A; Minnella, A; Marangoni, D; Placidi, G; Resta, G; Falsini, B | |
| USH2A -Related Retinitis Pigmentosa: Staging of Disease Severity and Morpho-Functional Studies. | 1-gen-2021 | Falsini, B; Placidi, G; De Siena, E; Savastano, Mc; Minnella, Am; Maceroni, M; Midena, G; Ziccardi, L; Parisi, V; Bertelli, M; Maltese, Pe; Chiurazzi, P; Rizzo, S. | |
| Visual System Abnormalities in a Case of Nonsyndromic, Complete, Isolated CorpusCallosum Agenesis. | 1-gen-2024 | Barbano, L; Ziccardi, L; Antonelli, G; Tinelli, E; Parisi, V | |
| Morpho-Functional Macular Assessment in a Case of Facioscapulohumeral MuscularDystrophy: Photoreceptor Degeneration as Possible Cause for Reduced Visual Acuityover Three Years of Follow-Up. | 1-gen-2022 | Parravano, M; Costanzo, E; Barbano, L; Viggiano, P; De Geronimo, D; Antonelli, G; Parisi, V; Varano, M; Ziccardi, L | |
| Temporal response properties of the macular cone system: effect of normal aging and age-related maculopathy. | 1-gen-2007 | Falsini, B; Ziccardi, L; Stifano, G; Iarossi, G; Merendino, E; Minnella, Am; Fadda, A; Balestrazzi, E. | |
| Retinal dysfunction characterizes subtypes of dominant optic atrophy | 1-gen-2018 | Cascavilla, Ml; Parisi, V; Triolo, G; Ziccardi, L; Borrelli, E; Di Renzo, A; Balducci, N; Lamperti, C; Bianchi Marzoli, S; Darvizeh, F; Sadun, Aa; Carelli, V; Bandello, F; Barboni, P | |
| Multimodal Study of PRPH2 Gene-Related Retinal Phenotypes. | 1-gen-2022 | Antonelli, G; Parravano, M; Barbano, L; Costanzo, E; Bertelli, M; Medori, Mc; Parisi, V; Ziccardi, L | |
| Morphological Outer Retina Findings in Multiple Sclerosis Patients With or WithoutOptic Neuritis | 1-gen-2020 | Ziccardi, L; Barbano, L; Boffa, L; Albanese, M; Grzybowski, A; Centonze, D; Parisi, V. | |
| Genetic testing for cone rod dystrophies | 1-gen-2017 | Abeshi, A; Zulian, A; Beccari, T; Dundar, M; Ziccardi, L; Bertelli, M | |
| Bilateral Symmetry of Visual Function Loss in Cone-Rod Dystrophies | 1-gen-2016 | Galli-Resta, L; Falsini, B; Rossi, G; Piccardi, M; Ziccardi, L; Fadda, A; Minnella, A; Marangoni, D; Placidi, G; Campagna, F; Abed, E; Bertelli, M; Zuntini, M; Resta, G | |
| Macular function in eyes with open-angle glaucoma evaluated by multifocal electroretinogram | 1-gen-2012 | Parisi, V; Ziccardi, L; Centofanti, M; Tanga, L; Gallinaro, G; Falsini, B; Bucci MG, | |
| Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-up | 1-gen-2019 | Parisi, V; Ziccardi, L; Sadun, F; De Negri, Am; La Morgia, C; Barbano, L; Carelli, V; Barboni, P | |
| Pathogenicity of new BEST1 variants identified in Italian patients with best vitelliform macular dystrophy assessed by computational structural biology | 1-gen-2019 | Frecer, V; Iarossi, G; Salvetti, Ap; Maltese, Pe; Delledonne, G; Oldani, M; Staurenghi, G; Falsini, B; Minnella, Am; Ziccardi, L; Magli, A; Colombo, L; D'Esposito, F; Miertus, J; Viola, F; Attanasio, M; Maggio, E; Bertelli, M | |
| Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis andthe Structure of the Primary Cilium | 1-gen-2022 | Ziccardi, L; Niceta, M; Stellacci, E; Ciolfi, A; Tatti, M; Bruselles, A; Mancini, C; Barbano, L; Cecchetti, S; Costanzo, E; Cappa, M; Parravano, M; Varano, M; Tartaglia, M; Cordeddu, V. | |
| Genetic testing for Bietti crystalline dystrophy | 1-gen-2017 | Abeshi, A; Bruson, A; Beccari, T; Dundar, M; Ziccardi, L; Bertelli, M | |
| Design and Validation of a New MLPA-Based Assay for the Detection of RS1 Gene Deletions and Application in a Large Family with X-Linked Juvenile Retinoschisis | 1-gen-2017 | Nicoletti, A; Ziccardi, L; Maltese, Pe; Benedetti, S; Palumbo, O; Rendina, M; D'Agruma, L; Falsini, B; Wang, X; Bertelli, M | |
| Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56. | 1-gen-2021 | Legrand, A; Pujol, C; Durand, Cm; Mesnil, A; Rubera, I; Duranton, C; Zuily, S; Sousa, Ab; Renaud, M; Boucher, Jl; Pietrancosta, N; Adham, S; Orssaud, C; Marelli, C; Casali, C; Ziccardi, L; Villain, N; Ewenczyk, C; Durr, A; Mignot, C; Stevaning, ; Billon, C; Hureaux, M; Jeunemaitre, X; Goizet, C; Albuisson, J. | |
| Intravitreal bevacizumab (Avastin) in proliferative diabetic retinopathy. | 1-gen-2008 | Minnella, Am; Savastano, Cm; Ziccardi, L; Scupola, A; Falsini, B; Balestrazzi, E. | |
| Early and localized retinal dysfunction in patients with type 1 diabetes mellitus studied by multifocal electroretinogram | 1-gen-2018 | Ziccardi, L; Parisi, V; Picconi, F; Di Renzo, A; Lombardo, M; Frontoni, S; Parravano, M | |
| Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery | 1-gen-2018 | Cukras, C; Wiley, He; Jeffrey, Bg; Sen, Hn; Turriff, A; Zeng, Y; Vijayasarathy, C; Marangoni, D; Ziccardi, L; Kjellstrom, S; Park, Tk; Hiriyanna, S; Wright, Jf; Colosi, P; Wu, Z; Bush, Ra; Wei, Ll; Sieving, Pa |
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