FERRERO, Patrizia
FERRERO, Patrizia
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation
2013-01-01 Galimberti D; Fenoglio C; Serpente M; Villa C; Bonsi R; Arighi A; Fumagalli GG; Del Bo R; Bruni AC; Anfossi M; Clodomiro A; Cupidi C; Nacmias B; Sorbi S; Piaceri I; Bagnoli S; Bessi V; Marcone A; Cerami C; Cappa SF; Filippi M; Agosta F; Magnani G; Comi G; Franceschi M; Rainero I; Giordana M; Rubino E; Ferrero P; Rogaeva E; Xi Z; Confaloni A; Piscopo P; Bruno G; Talarico G; Cagnin A; Clerici F; Dell'osso B; Comi GP; Altamura AC; Mariani C; Scarpini E
Epilepsie: crise, pseudo-crise et psychothérapie.
1995-01-01 G. Angelini; P. Bergantin; P. Benna; E. Montalenti; M. Bonzanino; L. Tarenzi; P. Ferrero.
Frequency of the Chromosome 9 C9ORF72 Hexanucleotide Repeats in Italian Patients with Frontotemporal Lobar Degeneration
2012-01-01 Galimberti D; Fenoglio C; Serpente M; Nacmias B; Sorbi S; Marcone A; Cappa S; Magnani G; Agosta F; Filippi M; Comi G; Franceschi M; Rainero I; Pinessi L; Ferrero P; Gonfaloni A; Piscopo P; Bruno G; Bruni A; Maletta R; Cagnin A; Clerici F; Mariani C; Bresolin N; Scarpini E
Late onset bipolar disorder and frontotemporal dementia with mutation in progranulin gene: a case report
2017-01-01 Rubino, Elisa; Vacca, Alessandro; Gallone, Salvatore; Govone, Flora; Zucca, Milena; Gai, Annalisa; Ferrero, Patrizia; Fenoglio, Pierpaola; Giordana, Maria Teresa; Rainero, Innocenzo
Late onset bipolar disorder preceding frontotemporal dementia with mutation in progranulin gene: a case report
2017-01-01 Rubino, E.; Vacca, A.; Gallone, S.; Govone, F.; Zucca, M.; Gai, A.; Ferrero, P.; Fenoglio, P.; Boschi, S.; Giordana, M.; Rainero, I.
O056. Migraine as presenting symptom of SLC20A2gene mutations
2015-01-01 Rubino, Elisa; Giorgio, Elisa; Rainero, Innocenzo; Ferrero, Patrizia; Gallone, Salvatore; Govone, Flora; Pinessi, Lorenzo; Orsi, Laura; Duca, Sergio; Brusco, Alfredo
Polymorphisms of the IL-1α, IL-1β and IL-6 genes and frontotemporal dementia: an association study
2004-01-01 Rainero I; Rota E; Gallone S; Cappa G; Valfrè W; Rivoiro C; Gentile S; Ferrero P; Molaschi M; Pinessi L
Prediction of Alzheimer's disease in patients with mild cognitive impairment using CSF biomarkers
2013-01-01 Rubino E; Vacca A; Rossetti S; Vigliani M; Imperiale D; Gastaldi L; Pastorelli S; Ferrero P; Pinessi L; Rainero I
Three novel missense mutations in SLC20A2 associated with idiopathic basal ganglia calcification
2017-01-01 Rubino, E; Giorgio, E; Godani, M; Grosso, E; Zibetti, M; Lopiano, L; Ferrero, P; Duca, S; Moretti, L; Gallone, S; Rainero, I; Brusco, A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation | 2013 | Galimberti D; Fenoglio C; Serpente M; Villa C; Bonsi R; Arighi A; Fumagalli GG; Del Bo R; Bruni AC; Anfossi M; Clodomiro A; Cupidi C; Nacmias B; Sorbi S; Piaceri I; Bagnoli S; Bessi V; Marcone A; Cerami C; Cappa SF; Filippi M; Agosta F; Magnani G; Comi G; Franceschi M; Rainero I; Giordana M; Rubino E; Ferrero P; Rogaeva E; Xi Z; Confaloni A; Piscopo P; Bruno G; Talarico G; Cagnin A; Clerici F; Dell'osso B; Comi GP; Altamura AC; Mariani C; Scarpini E | |
| Epilepsie: crise, pseudo-crise et psychothérapie. | 1995 | G. Angelini; P. Bergantin; P. Benna; E. Montalenti; M. Bonzanino; L. Tarenzi; P. Ferrero. | |
| Frequency of the Chromosome 9 C9ORF72 Hexanucleotide Repeats in Italian Patients with Frontotemporal Lobar Degeneration | 2012 | Galimberti D; Fenoglio C; Serpente M; Nacmias B; Sorbi S; Marcone A; Cappa S; Magnani G; Agosta F; Filippi M; Comi G; Franceschi M; Rainero I; Pinessi L; Ferrero P; Gonfaloni A; Piscopo P; Bruno G; Bruni A; Maletta R; Cagnin A; Clerici F; Mariani C; Bresolin N; Scarpini E | |
| Late onset bipolar disorder and frontotemporal dementia with mutation in progranulin gene: a case report | 2017 | Rubino, Elisa; Vacca, Alessandro; Gallone, Salvatore; Govone, Flora; Zucca, Milena; Gai, Annalisa; Ferrero, Patrizia; Fenoglio, Pierpaola; Giordana, Maria Teresa; Rainero, Innocenzo | |
| Late onset bipolar disorder preceding frontotemporal dementia with mutation in progranulin gene: a case report | 2017 | Rubino, E.; Vacca, A.; Gallone, S.; Govone, F.; Zucca, M.; Gai, A.; Ferrero, P.; Fenoglio, P.; Boschi, S.; Giordana, M.; Rainero, I. | |
| O056. Migraine as presenting symptom of SLC20A2gene mutations | 2015 | Rubino, Elisa; Giorgio, Elisa; Rainero, Innocenzo; Ferrero, Patrizia; Gallone, Salvatore; Govone, Flora; Pinessi, Lorenzo; Orsi, Laura; Duca, Sergio; Brusco, Alfredo | |
| Polymorphisms of the IL-1α, IL-1β and IL-6 genes and frontotemporal dementia: an association study | 2004 | Rainero I; Rota E; Gallone S; Cappa G; Valfrè W; Rivoiro C; Gentile S; Ferrero P; Molaschi M; Pinessi L | |
| Prediction of Alzheimer's disease in patients with mild cognitive impairment using CSF biomarkers | 2013 | Rubino E; Vacca A; Rossetti S; Vigliani M; Imperiale D; Gastaldi L; Pastorelli S; Ferrero P; Pinessi L; Rainero I | |
| Three novel missense mutations in SLC20A2 associated with idiopathic basal ganglia calcification | 2017 | Rubino, E; Giorgio, E; Godani, M; Grosso, E; Zibetti, M; Lopiano, L; Ferrero, P; Duca, S; Moretti, L; Gallone, S; Rainero, I; Brusco, A. |