MONGINI, Tiziana Enrica
MONGINI, Tiziana Enrica
NEUROSCIENZE "RITA LEVI MONTALCINI"
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.
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors
2011-01-01 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.
2017-01-01 E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero;
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.
Complete recovery in a severe case of anti-ssa positive necrotizing myopathy after rituximab therapy
2012-01-01 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.
2017-01-01 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
2012-01-01 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
2014-01-01 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
2014-01-01 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.
2014-01-01 Mongini, T.; Vercelli L.; Ponzalino V.; Bortolani S.; Boschi S.; Vittonatto E.; Chiadò-Piat L.
Muscular involvement in Whipple's disease with gastrointestinal sparing
2010-01-01 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.
2017-01-01 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
1980-01-01 Palmucci L; Bertolotto A; Doriguzzi C; Mongini T; Verzé L.
Progressive muscular dystrophy in childhood: differential diagnosis and prevention strategy
1983-01-01 Schiffer D; Doriguzzi C; Mongini T
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.
Unusual symptoms and pathology in a woman with myofibrillar myopathy.
2018-01-01 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.
2003-01-01 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.
| 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. |