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
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
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
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.
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
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.
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
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.
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.
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.
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
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.
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.
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
| 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 | |
| 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 | |
| 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 | |
| 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. | |
| 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 | |
| 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. | |
| 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 | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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. | |
| 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. | |
| 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 |
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