Sfoglia per Autore
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
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
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
Genetic variants in the NOTCH4 gene influence the clinical features of migraine
2013-01-01 Rubino E; Fenoglio P; Gallone S; Govone F; Vacca A; De Martino P; Giobbe ML; Boschi S; Pinessi L; Gentile S; Rainero I
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.
KCNK18 (TRESK) genetic variants in Italian patients with migraine
2014-01-01 Rainero I; Rubino E; Gallone S; Zavarise P; Carli D; Boschi S; Fenoglio P; Savi L; Gentile S; Benna P; Pinessi L; Dalla Volta G.
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.
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
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.
Is HCRTR2 a Genetic Risk Factor for Alzheimer's Disease?
2014-01-01 Gallone S;Boschi S;Rubino E;De Martino P;Scarpini E;Galimberti D;Fenoglio C;Acutis PL;Maniaci MG;Pinessi L;Rainero I
Lack of association between APOE gene polymorphisms and amyotrophic lateral sclerosis: A comprehensive meta-analysis.
2014-01-01 Govone F;Vacca A;Rubino E;Gai A;Boschi S;Gentile S;Orsi L;Pinessi L;Rainero I
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
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.
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.
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.
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
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;
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 adipokines in chronic migraine
2017-01-01 Rubino, Elisa; Vacca, Alessandro; Govone, Flora; Gai, Annalisa; Boschi, Silvia; Zucca, Milena; De Martino, Paola; Gentile, Salvatore; Pinessi, Lorenzo; Rainero, Innocenzo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| 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 | |
| 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 | |
| Genetic variants in the NOTCH4 gene influence the clinical features of migraine | 2013 | Rubino E; Fenoglio P; Gallone S; Govone F; Vacca A; De Martino P; Giobbe ML; Boschi S; Pinessi L; Gentile S; Rainero I | |
| 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. | |
| KCNK18 (TRESK) genetic variants in Italian patients with migraine | 2014 | Rainero I; Rubino E; Gallone S; Zavarise P; Carli D; Boschi S; Fenoglio P; Savi L; Gentile S; Benna P; Pinessi L; Dalla Volta G. | |
| 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. | |
| 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 | |
| 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. | |
| Is HCRTR2 a Genetic Risk Factor for Alzheimer's Disease? | 2014 | Gallone S;Boschi S;Rubino E;De Martino P;Scarpini E;Galimberti D;Fenoglio C;Acutis PL;Maniaci MG;Pinessi L;Rainero I | |
| Lack of association between APOE gene polymorphisms and amyotrophic lateral sclerosis: A comprehensive meta-analysis. | 2014 | Govone F;Vacca A;Rubino E;Gai A;Boschi S;Gentile S;Orsi L;Pinessi L;Rainero I | |
| 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 | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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; | |
| 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 adipokines in chronic migraine | 2017 | Rubino, Elisa; Vacca, Alessandro; Govone, Flora; Gai, Annalisa; Boschi, Silvia; Zucca, Milena; De Martino, Paola; Gentile, Salvatore; Pinessi, Lorenzo; Rainero, Innocenzo |
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