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NOTA: è possibile cercare una corrispondenza esatta usando i doppi apici, ad es: "evoluzione della specie". Qualora si cerchi un identificativo, è consigliabile cercarlo in due modi differenti: tra apici con caratteri speciali es: "978-94-6366-274" oppure senza caratteri speciali solo come sequenza numerica: es 978946366274.
SQSTM1 gene mutations in the Frontotemporal Lobar Degeneration/ Amyotrophic Lateral Sclerosis spectrum
2012-01-01 Rubino E; Gallone S; Rogaeva E; Galimberti D; Fenoglio P; Calvo A; De Martino P; Govone F; Vacca A; Bruni AC; St. George-Hyslop PH; Scarpini E; Pinessi L; Chiò A; Rainero I
SQSTM1 Gene Sequencing in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
2012-01-01 Rainero I; Rubino E; Chio A; Rogaeva E; Galimberti D; Fenoglio P; Grinberg Y; Calvo A; Bruni AC; St George-Hyslop P; Scarpini E; Gallone S; Pinessi L
SQSTM1/p62 gene sequencing in Frontotemporal Lobar Degeneration
2010-01-01 Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Venturelli E; Vacca A; Scarpini E; Pinessi L
The common origin of FAD in the Calabria region
1990-01-01 BRUNI AC; MONTESI MP; GEI G; ERMIO C; RAINERO I; FONCIN JF
The diagnosis of FTD-ALS: a longitudinal study in a specialized dementia unit
2008-01-01 M Magistrello; E Rota; M Caglio; L Rizzi; P Ferrero; I Rainero; P Ghiglione; A Calvo; G Castellano; M T Giordana; L Pinessi
The hemochromatosis (HFE) gene influences the clinical features of migraine
2006-01-01 Rubino E; Rainero I; Rivoiro C; Valfrè W; Binello E; Zampella E; De Martino P; Gentile S; Fenoglio P; Savi L; Gallone S; Pinessi L
The hypothalamo-hypophyso-adrenal axis in epileptic patients treated with sodium valproate
1987-01-01 GENTILE S; CARETTO M; MANENTI M; FRAIRIA R; RAINERO I; PINESSI L
TMEM106B genetic variability in patients with Alzheimer's Disease
2012-01-01 Serpente M; Fenoglio C; Villa C; Bonsi R; Cantoni C; Ridolfi E; Clerici F; Ghidoni R; Binussi L; Marcone A; Cerami C; Franceschi M; Gallone S; Cappa S; Binetti G; Rainero I; Bresolin N; Mariani C; Scarpini E; Galimberti D
Voxel-based Morphometry Reveals Gray Matter Loss in Patients with Paget's Disease of the Bone Carrying SQSTM1 Gene Mutations
2014-01-01 Innocenzo Rainero; Elisa Rubino; Federico D'Agata; Silvia Rossetti; Laura Gastaldi; Mauro Bergui; Laura Orsi; Lorenzo Pinessi; Giancarlo Isaia; Marco Di Stefano
Voxel-based morphometry reveals gray matter loss in patients with Paget's disease of the bone carrying SQSTM1 gene mutations
2014-01-01 Rainero I; Rubino E; D'Agata F; Rossetti S; Gastaldi L; Bergui M; Orsi L; Pinessi L; Isaia GC; Di Stefano M
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| SQSTM1 gene mutations in the Frontotemporal Lobar Degeneration/ Amyotrophic Lateral Sclerosis spectrum | 2012 | Rubino E; Gallone S; Rogaeva E; Galimberti D; Fenoglio P; Calvo A; De Martino P; Govone F; Vacca A; Bruni AC; St. George-Hyslop PH; Scarpini E; Pinessi L; Chiò A; Rainero I | |
| SQSTM1 Gene Sequencing in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis | 2012 | Rainero I; Rubino E; Chio A; Rogaeva E; Galimberti D; Fenoglio P; Grinberg Y; Calvo A; Bruni AC; St George-Hyslop P; Scarpini E; Gallone S; Pinessi L | |
| SQSTM1/p62 gene sequencing in Frontotemporal Lobar Degeneration | 2010 | Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Venturelli E; Vacca A; Scarpini E; Pinessi L | |
| The common origin of FAD in the Calabria region | 1990 | BRUNI AC; MONTESI MP; GEI G; ERMIO C; RAINERO I; FONCIN JF | |
| The diagnosis of FTD-ALS: a longitudinal study in a specialized dementia unit | 2008 | M Magistrello; E Rota; M Caglio; L Rizzi; P Ferrero; I Rainero; P Ghiglione; A Calvo; G Castellano; M T Giordana; L Pinessi | |
| The hemochromatosis (HFE) gene influences the clinical features of migraine | 2006 | Rubino E; Rainero I; Rivoiro C; Valfrè W; Binello E; Zampella E; De Martino P; Gentile S; Fenoglio P; Savi L; Gallone S; Pinessi L | |
| The hypothalamo-hypophyso-adrenal axis in epileptic patients treated with sodium valproate | 1987 | GENTILE S; CARETTO M; MANENTI M; FRAIRIA R; RAINERO I; PINESSI L | |
| TMEM106B genetic variability in patients with Alzheimer's Disease | 2012 | Serpente M; Fenoglio C; Villa C; Bonsi R; Cantoni C; Ridolfi E; Clerici F; Ghidoni R; Binussi L; Marcone A; Cerami C; Franceschi M; Gallone S; Cappa S; Binetti G; Rainero I; Bresolin N; Mariani C; Scarpini E; Galimberti D | |
| Voxel-based Morphometry Reveals Gray Matter Loss in Patients with Paget's Disease of the Bone Carrying SQSTM1 Gene Mutations | 2014 | Innocenzo Rainero; Elisa Rubino; Federico D'Agata; Silvia Rossetti; Laura Gastaldi; Mauro Bergui; Laura Orsi; Lorenzo Pinessi; Giancarlo Isaia; Marco Di Stefano | |
| Voxel-based morphometry reveals gray matter loss in patients with Paget's disease of the bone carrying SQSTM1 gene mutations | 2014 | Rainero I; Rubino E; D'Agata F; Rossetti S; Gastaldi L; Bergui M; Orsi L; Pinessi L; Isaia GC; Di Stefano M |
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Opzioni
Scopri
Tipologia
- 04-CONTRIBUTO IN ATTI DI CONVEGNO 151
- 04-CONTRIBUTO IN ATTI DI CONVEGNO... 151
Data di pubblicazione
- 2010 - 2017 75
- 2000 - 2009 55
- 1990 - 1999 15
- 1986 - 1989 6
Rivista
- NEUROLOGICAL SCIENCES 47
- THE JOURNAL OF HEADACHE AND PAIN 26
- NEUROLOGY 24
- JOURNAL OF ALZHEIMER'S DISEASE 11
- CLINICAL NEUROPATHOLOGY 6
- CEPHALALGIA 5
- NEUROBIOLOGY OF AGING 5
- DEMENTIA AND GERIATRIC COGNITIVE ... 4
- ELECTROENCEPHALOGRAPHY AND CLINIC... 4
- GIORNALE DELLE CEFALEE 4
Keyword
- migraine 19
- Alzheimer's Disease 11
- Frontotemporal Lobar Degeneration 9
- Migraine 9
- genetics 8
- FTLD 7
- cluster headache 6
- Alzheimer's disease 5
- frontotemporal lobar degeneration 5
- medication-overuse headache 5
Lingua
- eng 143
- ita 8
Accesso al fulltext
- no fulltext 117
- reserved 25
- open 9