MIELE, Maria Luisa
MIELE, Maria Luisa
DIPARTIMENTO DI MEDICINA INTERNA (attivo dal 14/09/1994 al 31/12/2013)
Clinical and genetic study of a Japanese family with complicated hereditary spastic paraplegia and Alzheimer's disease
2017 Montecchiani, C; D’Onofrio, L; Mearini, M; Gaudiello, F; Miele, M; Caltagirone, C; Kawarai, T; Orlacchio, A.
Expression and processing of cathepsin D in fibroblasts of patients with Alzheimer’s disease
2004 Orlacchio, A; Urbanelli, L; Emiliani, C; Miele, M; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Orlacchio, A
Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia
2016 Mearini, M; Pedace, L; Casella, A; Montecchiani, C; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, R; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, A
miR128 up-regulation correlates with impaired Amyloid-β42 degradation in monocytes of patients with sporadic Alzheimer’s disease
2013 Tiribuzi, R; Crispoltoni, L; Porcellati, S; Mearini, M; Di Lullo, M; Florenzano, F; Pirro, M; Bagaglia, F; Palmerini, Ca; Miele, M; Kawarai, T; Zampolini, M; Orlacchio, A; Orlacchio, A
Search for new genes causing dementia: targets for novel diagnostics and therapeutics
2003 Orlacchio, A; Kawarai, T; Totaro, A; Merlo, S; Gallozzi, M; Polidoro, M; Ling, S; Urbanelli, L; Miele, M; Orlacchio, A; Bernardi, G
Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability
2017 Orlacchio, A; Montecchiani, C; Miyamoto, R; D’Onofrio, L; Rumore, R; Miele, M; Gaudiello, F; Izumi, Y; Caltagirone, C; Kaji, R; Kawarai, T.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical and genetic study of a Japanese family with complicated hereditary spastic paraplegia and Alzheimer's disease | 2017 | Montecchiani, C; D’Onofrio, L; Mearini, M; Gaudiello, F; Miele, M; Caltagirone, C; Kawarai, T; Orlacchio, A. | |
| Expression and processing of cathepsin D in fibroblasts of patients with Alzheimer’s disease | 2004 | Orlacchio, A; Urbanelli, L; Emiliani, C; Miele, M; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Orlacchio, A | |
| Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia | 2016 | Mearini, M; Pedace, L; Casella, A; Montecchiani, C; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, R; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, A | |
| miR128 up-regulation correlates with impaired Amyloid-β42 degradation in monocytes of patients with sporadic Alzheimer’s disease | 2013 | Tiribuzi, R; Crispoltoni, L; Porcellati, S; Mearini, M; Di Lullo, M; Florenzano, F; Pirro, M; Bagaglia, F; Palmerini, Ca; Miele, M; Kawarai, T; Zampolini, M; Orlacchio, A; Orlacchio, A | |
| Search for new genes causing dementia: targets for novel diagnostics and therapeutics | 2003 | Orlacchio, A; Kawarai, T; Totaro, A; Merlo, S; Gallozzi, M; Polidoro, M; Ling, S; Urbanelli, L; Miele, M; Orlacchio, A; Bernardi, G | |
| Spastic paraplegia type 4: a novel SPAST splice site donor mutation and expansion of the phenotype variability | 2017 | Orlacchio, A; Montecchiani, C; Miyamoto, R; D’Onofrio, L; Rumore, R; Miele, M; Gaudiello, F; Izumi, Y; Caltagirone, C; Kaji, R; Kawarai, T. |