VITTONATTO, ELISA
Dettaglio
VITTONATTO, ELISA
Pubblicazioni
Risultati 1 - 16 di 16 (tempo di esecuzione: 0.001 secondi).
Titolo | Data di pubblicazione | Autore(i) | |
---|---|---|---|
1 | A case of to treatment with piridostigmine bromide: a new phenotype? | 2011 | L. Vercelli; S. Benedetti; E. Vittonatto ; L. Chiadò-Piat; E. Pilati; T. Mongini. |
2 | 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. |
3 | A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors | 2011 | Vercelli, L; Benedetti, S; Vittonatto, E; Chiado'-Piat, L; Pilati, E; Pinessi, L; Mongini, T |
4 | 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. |
5 | Complete recovery in a severe case of anti-ssa positive necrotizing myopathy after rituximab therapy | 2012 | Giobbe, Ml; Vercelli, L; Vittonatto, E; Chiadò-Piat, L; Roccatello, D; Pinessi, L; Mongini, T |
6 | Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry | 2017 | Vittonatto, Elisa; Boschi, Silvia; CHIADò-Piat, Loredana; Ponzalino, Valentina; Bortolani, Sara; Brusa, Chiara; Rainero, Innocenzo; Ricci, Federica; Vercelli, Liliana; Mongini, Tiziana |
7 | Glycogen storage disease type II diagnosed in a 74-year-old woman | 2004 | BOSONE I; VERCELLI L; MONGINI T; CHIADÓ-PIAT L; VITTONATTO E; PALMUCCI L; SERVIDEI S; SILVESTRI G |
8 | Late-onset glycogen storage disease type II: therapeutical indications in a subset of paucisymptomatic patients with a single mutation | 2012 | Vercelli, L; Vittonatto, E; Grifoni, S; Chiadò-Piat, L; Rolle, E; Spada, M; Danesino, C; Comi, G; Pinessi, L; Mongini, T |
9 | 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. |
10 | 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 |
11 | 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. |
12 | Muscular involvement in Whipple's disease with gastrointestinal sparing | 2010 | Vercelli, L.; Palmucci, L.; Vittonatto, E.; Chiadò-Piat, L.; Fenollar, F.; Mongini, T. |
13 | 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 |
14 | 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. |
15 | Symptomatic heterozygous patients in late-onset glycogen storage disease type 2. | 2012 | L. Vercelli; E. Vittonatto ; S. Grifoni; L. Chiado-Piat; M. Spada; C. Danesino; G. Comi; T. Mongini. |
16 | Young girl with relapsing- remitting hyperCKemia and limb·girdle weakness in the last ten years. | 2011 | T. Mongini; L. Vercelli; L. Chiadò-Piat; E. Vittonatto |