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Reduction of the chromosome 19q minimal candidate region in autosomal dominant pure hereditary spastic paraplegia
2001 Orlacchio, Antonio; Kawarai ì, T; Rogaeva, Ea; Polidoro, M; Paciotti, E; Bernardi, G; St George Hyslop, Ph
Refined SPG12 locus in autosomal dominant pure hereditary spastic paraplegia
2001 Orlacchio, Antonio; Kawarai, T; Rogaeva, Ea; Polidoro, M; Paciotti, E; Bernardi, G; St George Hyslop, Ph
Regulation of lysosomal enzymes expression in fibroblasts from Alzheimer’s disease patients
2004 Orlacchio, A; Urbanelli, L; Mencarelli, S; Orlacchio, A; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Emiliani, C
Restoration of arylsulphatase A activity in murine metachromatic leukodistrophy oligodendrocytes by retroviral vector-mediated gene transfer
2000 Consiglio, A; Martino, Sabata; Dolcetta, D; Troiani, A; Severini, Gm; Benaglia, G; Wrabetz, L; Cusella, G; Orlacchio, Antonio; Orlacchio, A; Marchesini, S; Aebischer, P; Bordignon, C.
Reticulon mutations in Hereditary Spastic Paraplegia
2011 Orlacchio, Antonio; Rebelo, A; Montenegro, G; Connell, J; Allison, R; Huang, J; Babalini, C; Bernardi, G; Pericak Vance, M; Reid, E; Züchner, S.
Secretion of th1 and th2 type cytokines by mononuclear cells of patients with multiple sclerosis undergoing treatment with IFN-b1b
1997 Sarchielli, P; Tognoloni, M; Alberti, A; Vicinanza, F; Orlacchio, Antonio; Saccardi, C; Pelliccioli, Gp; Gallai, V.
Silver syndrome variant of hereditary spastic paraplegia: identification of a novel locus
2007 Orlacchio, A; Patrono, C; Gaudiello, F; Moschella, V; Borreca, A; Orlacchio, A; Floris, R; Bernardi, G; Kawarai, T
Silver syndrome variant of hereditary spastic paraplegia: new locus maps to chromosome 4p16-p15 and allelism with SPG4
2007 Orlacchio, Antonio; Patrono, C; Gaudiello, F; Rocchi, C; Moschella, V; Floris, R; Bernardi, G; Kawarai, T.
Silver syndrome: clinicogenetic analysis of two Italian pedigrees
2006 Orlacchio, Antonio; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Kawarai, T; 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; Mearini, M; D'Onofrio, L; Miele, M; Gaudiello, F; Izumi, Y; Caltagirone, C; Kaji, R; Kawarai, T
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Reduction of the chromosome 19q minimal candidate region in autosomal dominant pure hereditary spastic paraplegia | 2001 | Orlacchio, Antonio; Kawarai ì, T; Rogaeva, Ea; Polidoro, M; Paciotti, E; Bernardi, G; St George Hyslop, Ph | |
| Refined SPG12 locus in autosomal dominant pure hereditary spastic paraplegia | 2001 | Orlacchio, Antonio; Kawarai, T; Rogaeva, Ea; Polidoro, M; Paciotti, E; Bernardi, G; St George Hyslop, Ph | |
| Regulation of lysosomal enzymes expression in fibroblasts from Alzheimer’s disease patients | 2004 | Orlacchio, A; Urbanelli, L; Mencarelli, S; Orlacchio, A; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Emiliani, C | |
| Restoration of arylsulphatase A activity in murine metachromatic leukodistrophy oligodendrocytes by retroviral vector-mediated gene transfer | 2000 | Consiglio, A; Martino, Sabata; Dolcetta, D; Troiani, A; Severini, Gm; Benaglia, G; Wrabetz, L; Cusella, G; Orlacchio, Antonio; Orlacchio, A; Marchesini, S; Aebischer, P; Bordignon, C. | |
| Reticulon mutations in Hereditary Spastic Paraplegia | 2011 | Orlacchio, Antonio; Rebelo, A; Montenegro, G; Connell, J; Allison, R; Huang, J; Babalini, C; Bernardi, G; Pericak Vance, M; Reid, E; Züchner, S. | |
| Secretion of th1 and th2 type cytokines by mononuclear cells of patients with multiple sclerosis undergoing treatment with IFN-b1b | 1997 | Sarchielli, P; Tognoloni, M; Alberti, A; Vicinanza, F; Orlacchio, Antonio; Saccardi, C; Pelliccioli, Gp; Gallai, V. | |
| Silver syndrome variant of hereditary spastic paraplegia: identification of a novel locus | 2007 | Orlacchio, A; Patrono, C; Gaudiello, F; Moschella, V; Borreca, A; Orlacchio, A; Floris, R; Bernardi, G; Kawarai, T | |
| Silver syndrome variant of hereditary spastic paraplegia: new locus maps to chromosome 4p16-p15 and allelism with SPG4 | 2007 | Orlacchio, Antonio; Patrono, C; Gaudiello, F; Rocchi, C; Moschella, V; Floris, R; Bernardi, G; Kawarai, T. | |
| Silver syndrome: clinicogenetic analysis of two Italian pedigrees | 2006 | Orlacchio, Antonio; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Kawarai, T; 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; Mearini, M; D'Onofrio, L; Miele, M; Gaudiello, F; Izumi, Y; Caltagirone, C; Kaji, R; Kawarai, T |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 127
- 1 Contributo su Rivista::1.5 Abst... 127
Data di pubblicazione
- 2020 - 2022 5
- 2010 - 2019 28
- 2000 - 2009 75
- 1995 - 1999 19
Rivista
- JOURNAL OF NEUROLOGY 31
- NEUROLOGICAL SCIENCES 15
- MOVEMENT DISORDERS 12
- NEUROBIOLOGY OF AGING 11
- ALZHEIMER'S & DEMENTIA 10
- JOURNAL OF THE NEUROLOGICAL SCIENCES 6
- ITALIAN JOURNAL OF BIOCHEMISTRY 5
- MOVEMENT DISORDERS 5
- NEUROLOGICAL SCIENCES 5
- ALZHEIMER'S & DEMENTIA 3
Keyword
- amyloid-beta 1
- monocytes 1
- Saffron 1
Lingua
- eng 123
- ita 3
Accesso al fulltext
- no fulltext 127