BOSCHI, SILVIA
BOSCHI, SILVIA
NEUROSCIENZE "RITA LEVI MONTALCINI"
A mathematical model for the evaluation of iron transport across the blood-cerebrospinal fluid barrier in neurodegenerative diseases
2020-01-01 Ficiara, E; D'Agata, F; Ansari, S; Boschi, S; Rainero, I; Priano, L; Cattaldo, S; Abollino, O; Cavalli, R; Guiot, C
A peculiar case of LGMD with rimmed vacuoles
2016-01-01 Ponzalino V., Vercelli L., Chiadò-Piat L., Vittonatto E., Boschi S., Bortolani S., Xu L., Lek M., Johnson K., Topf A., MacArthur D., Straub V., Mongini T.
Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy.
2017-01-01 E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero;
Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine
2012-01-01 Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G
Clinicopathological features and disease course in three patients with focal myositis
2015-01-01 Bortolani, S.; Vercelli, L.; Ponzalino, V.; Boschi, S.; Vittonatto, E.; Chiadò-Piat, L.; Mongini, T.
Identification of new genetic variants of KCNK18 in migraine with aura and migraine without aura
2013-01-01 I. Rainero; E. Rubino; P. Fenoglio; S. Gallone; P. Zavarise; D. Carli; S. Boschi; A. Gai; L. Pinessi; G. Dalla Volta
Increased p62 levels in cerebrospinal fluid of patients with Alzheimer’s disease and Frontotemporal dementia.
2018-01-01 E. Rubino, S. Boschi, M. Vigliani, C. Borghese, A. Vacca, M. Giordana, I. Rainero,
Investigating involvement of Von Economo neurons in behavioral variant frontotemporal dementia
2017-01-01 Rainero, Innocenzo; Rubino, Elisa; Boschi, Silvia; Vacca, Alessandro; Gai, Annalisa; Govone, Flora; Gallone, Salvatore; Fenoglio, Pierpaola; Rocca, Paola; Vercelli, Alessandro; Giordana, Maria Teresa
Investigating the role of CHCHD2 and CHCHD10 genes in Italian patients with mitochondrial myopathy.
2017-01-01 Boschi, S.; Rubino, E.; Zhang, M.; Mongini, T.; Rogaeva, E.; Giordana, M.; Rainero, I.
Investigation of KCNK18 (TRESK) Genetic Variants in Migraine with and without Aura
2013-01-01 Innocenzo Rainero; Elisa Rubino; Pierpaola Fenoglio; Salvatore Gallone; Paola Zavarise; Daniela Carli; Silvia Boschi; Annalisa Gai; Lorenzo Pinessi; Giorgio Dalla Volta
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.
MC ARDLE DISEASE (GLYCOGENOSIS TYPE 5): LONG TERM FOLLOW UP IN A SMALL COHORT OF ITALIAN PATIENTS
2014-01-01 Bortolani, S.; Vercelli, L.; Ponzalino, V.; Boschi, S.; Vittonatto, E.; Chiadò-Piat, L.; Pinessi, L.; Mongini, T.
Multifactorial analysis of muscle involvement in twenty cases of laminopathies with different phenotypes
2014-01-01 Bortolani, S; Vercelli, L; Ponzalino, V; Boschi, S; Vittonatto, E; Chiadò-Piat, L; Pinessi, L; Mongini, T
Muscle biopsy study in ten cases of lamin a/c mutation with different phenotypes.
2014-01-01 Mongini, T.; Vercelli L.; Ponzalino V.; Bortolani S.; Boschi S.; Vittonatto E.; Chiadò-Piat L.
Mutation Screening of Neuromedin B (NMB) gene in behavioral variant Frontotemporal Dementia
2017-01-01 Rainero, I.; Rubino, E.; Fenoglio, P.; Boschi, S.; Gallone, S.; Rocca, P.; Vercelli, A.; Giordana, M. .
Necrotizing myopathies: the experience of the center for neuromuscular disease in Turin.
2017-01-01 V. Ponzalino, L. Vercelli, S. Bortolani, E. Rolle, S. Boschi, L. Chiadò Piat, E. Vittonatto, T. Mongini, M. Giordana
O057. Altered plasma adipokines concentrations in chronic migraine
2015-01-01 Elisa Rubino, Flora Govone, Alessandro Vacca, Annalisa Gai, Silvia Boschi, Milena Zucca, Lorenzo Pinessi, Innocenzo Rainero
Role of autophagy in an asymptomatic young woman with late-onset glycogen storage disease type 2 (GSD2).
2014-01-01 L. Vercelli; V. Ponzalino; S. Bortolani; E. Vittonatto; S. Boschi; L. Chiadò-Piat; T Mongini.
Unusual symptoms and pathology in a woman with myofibrillar myopathy.
2018-01-01 Bortolani S., Vercelli L., Chiadò-Piat L., Boschi S., Mongini T.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A mathematical model for the evaluation of iron transport across the blood-cerebrospinal fluid barrier in neurodegenerative diseases | 2020 | Ficiara, E; D'Agata, F; Ansari, S; Boschi, S; Rainero, I; Priano, L; Cattaldo, S; Abollino, O; Cavalli, R; Guiot, C | |
| A peculiar case of LGMD with rimmed vacuoles | 2016 | Ponzalino V., Vercelli L., Chiadò-Piat L., Vittonatto E., Boschi S., Bortolani S., Xu L., Lek M., Johnson K., Topf A., MacArthur D., Straub V., Mongini T. | |
| Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy. | 2017 | E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero; | |
| Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine | 2012 | Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G | |
| Clinicopathological features and disease course in three patients with focal myositis | 2015 | Bortolani, S.; Vercelli, L.; Ponzalino, V.; Boschi, S.; Vittonatto, E.; Chiadò-Piat, L.; Mongini, T. | |
| Identification of new genetic variants of KCNK18 in migraine with aura and migraine without aura | 2013 | I. Rainero; E. Rubino; P. Fenoglio; S. Gallone; P. Zavarise; D. Carli; S. Boschi; A. Gai; L. Pinessi; G. Dalla Volta | |
| Increased p62 levels in cerebrospinal fluid of patients with Alzheimer’s disease and Frontotemporal dementia. | 2018 | E. Rubino, S. Boschi, M. Vigliani, C. Borghese, A. Vacca, M. Giordana, I. Rainero, | |
| Investigating involvement of Von Economo neurons in behavioral variant frontotemporal dementia | 2017 | Rainero, Innocenzo; Rubino, Elisa; Boschi, Silvia; Vacca, Alessandro; Gai, Annalisa; Govone, Flora; Gallone, Salvatore; Fenoglio, Pierpaola; Rocca, Paola; Vercelli, Alessandro; Giordana, Maria Teresa | |
| Investigating the role of CHCHD2 and CHCHD10 genes in Italian patients with mitochondrial myopathy. | 2017 | Boschi, S.; Rubino, E.; Zhang, M.; Mongini, T.; Rogaeva, E.; Giordana, M.; Rainero, I. | |
| Investigation of KCNK18 (TRESK) Genetic Variants in Migraine with and without Aura | 2013 | Innocenzo Rainero; Elisa Rubino; Pierpaola Fenoglio; Salvatore Gallone; Paola Zavarise; Daniela Carli; Silvia Boschi; Annalisa Gai; Lorenzo Pinessi; Giorgio Dalla Volta | |
| 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. | |
| MC ARDLE DISEASE (GLYCOGENOSIS TYPE 5): LONG TERM FOLLOW UP IN A SMALL COHORT OF ITALIAN PATIENTS | 2014 | Bortolani, S.; Vercelli, L.; Ponzalino, V.; Boschi, S.; Vittonatto, E.; Chiadò-Piat, L.; Pinessi, L.; Mongini, T. | |
| Multifactorial analysis of muscle involvement in twenty cases of laminopathies with different phenotypes | 2014 | Bortolani, S; Vercelli, L; Ponzalino, V; Boschi, S; Vittonatto, E; Chiadò-Piat, L; Pinessi, L; Mongini, T | |
| Muscle biopsy study in ten cases of lamin a/c mutation with different phenotypes. | 2014 | Mongini, T.; Vercelli L.; Ponzalino V.; Bortolani S.; Boschi S.; Vittonatto E.; Chiadò-Piat L. | |
| Mutation Screening of Neuromedin B (NMB) gene in behavioral variant Frontotemporal Dementia | 2017 | Rainero, I.; Rubino, E.; Fenoglio, P.; Boschi, S.; Gallone, S.; Rocca, P.; Vercelli, A.; Giordana, M. . | |
| Necrotizing myopathies: the experience of the center for neuromuscular disease in Turin. | 2017 | V. Ponzalino, L. Vercelli, S. Bortolani, E. Rolle, S. Boschi, L. Chiadò Piat, E. Vittonatto, T. Mongini, M. Giordana | |
| O057. Altered plasma adipokines concentrations in chronic migraine | 2015 | Elisa Rubino, Flora Govone, Alessandro Vacca, Annalisa Gai, Silvia Boschi, Milena Zucca, Lorenzo Pinessi, Innocenzo Rainero | |
| Role of autophagy in an asymptomatic young woman with late-onset glycogen storage disease type 2 (GSD2). | 2014 | L. Vercelli; V. Ponzalino; S. Bortolani; E. Vittonatto; S. Boschi; L. Chiadò-Piat; T Mongini. | |
| Unusual symptoms and pathology in a woman with myofibrillar myopathy. | 2018 | Bortolani S., Vercelli L., Chiadò-Piat L., Boschi S., Mongini T. |