VITTONATTO, ELISA

VITTONATTO, ELISA  

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Titolo Data di pubblicazione Autore(i) File
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.
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.
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
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.
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
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
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
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
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.
Muscular involvement in Whipple's disease with gastrointestinal sparing 2010 Vercelli, L.; Palmucci, L.; Vittonatto, E.; Chiadò-Piat, L.; Fenollar, F.; Mongini, T.
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
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.
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.
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