BOSCHI, SILVIA

BOSCHI, SILVIA  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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Risultati 1 - 19 di 19 (tempo di esecuzione: 0.044 secondi).
Titolo Data di pubblicazione Autore(i) File
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.
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
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.