MONGINI, Tiziana Enrica

MONGINI, Tiziana Enrica  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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Risultati 1 - 17 di 17 (tempo di esecuzione: 0.018 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.
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
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;
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
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 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
Osteomalacic myopaty: observation on a case 1980 Palmucci L; Bertolotto A; Doriguzzi C; Mongini T; Verzé L.
Progressive muscular dystrophy in childhood: differential diagnosis and prevention strategy 1983 Schiffer D; Doriguzzi C; Mongini T
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.
X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families. 2003 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.