GAUDIELLO, FABRIZIO
GAUDIELLO, FABRIZIO
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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease
2016-01-01 Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, Jl; Terracciano, C; Caltagirone, C; Massa, R; S, Tgphs; Barsottini, Ogp; Kawarai, T; Orlacchio, A
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
2015-06-01 Carosi, L; Lo Giudice, T; Di Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, Ga; Massa, R; Kawarai, T; Orlacchio, A
Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10
2015-01-01 Carosi, L; Giudice, T; Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, G; Massa, R; Kawarai, T; Orlacchio, A
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2016 | ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease | Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, Jl; Terracciano, C; Caltagirone, C; Massa, R; S, Tgphs; Barsottini, Ogp; Kawarai, T; Orlacchio, A | Articolo su rivista | |
| 1-giu-2015 | Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10 | Carosi, L; Lo Giudice, T; Di Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, Ga; Massa, R; Kawarai, T; Orlacchio, A | Articolo su rivista | |
| 1-gen-2015 | Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10 | Carosi, L; Giudice, T; Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, G; Massa, R; Kawarai, T; Orlacchio, A | Articolo su rivista |