Gidaro, Teresa
Gidaro, Teresa
TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis
2012 Morosetti, Roberta; Gliubizzi, Carla; Sancricca, Cristina; Broccolini, Aldobrando; Gidaro, Teresa; Lucchini, Matteo; Mirabella, Massimiliano
Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle
2011 Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta; Sancricca, Cristina; Mirabella, Massimiliano
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior.
2011 Morosetti, Roberta; Gidaro, Teresa; Broccolini, Aldobrando; Gliubizzi, Carla; Sancricca, Cristina; Tonali, Pietro Attilio; Ricci, Enzo; Mirabella, Massimiliano
Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).
2010 Ricci, Enzo; Santoro, Massimo; Masciullo, Marcella; Gidaro, Teresa; Broccolini, Aldobrando; Modoni, Anna; Tonali, Pietro Attilio; Silvestri, Gabriella
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy
2010 Broccolini, Aldobrando; Gidaro, Teresa; Tasca, Giorgio; Rodolico, Carmelo; Morosetti, Roberta; Ricci, Enzo; Mirabella, Massimiliano
Increased aging in primary muscle cultures of sporadic inclusion-body myositis.
2010 Morosetti, Roberta; Broccolini, Aldobrando; Sancricca, Cristina; Gliubizzi, Carla; Gidaro, Teresa; Tonali, Pietro Attilio; Ricci, Enzo; Mirabella, Massimiliano
Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy
2010 Sancricca, Cristina; Mirabella, Massimiliano; Gliubizzi, Carla; Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta
Hereditary inclusion-body myopathy: clues on pathogenesis and possible therapy
2009 Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta; Mirabella, Massimiliano
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene
2008 Gidaro, Teresa; Modoni, Anna; Sabatelli, Mario; Tasca, Giorgio; Broccolini, Aldobrando; Mirabella, Massimiliano
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle
2008 Broccolini, Aldobrando; Gidaro, Teresa; De Cristofaro, Raimondo; Morosetti, Roberta; Gliubizzi, Carla; Ricci, Enzo; Tonali, Pietro Attilio; Mirabella, Massimiliano
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle.
2006 Morosetti, Roberta; Mirabella, Massimiliano; Gliubizzi, Carla; Broccolini, Aldobrando; De Angelis, L; Tagliafico, E; Sampaolesi, M; Gidaro, Teresa; Papacci, Manuela; Roncaglia, E; Rutella, Sergio; Ferrari, S; Tonali, Pietro Attilio; Ricci, Enzo; Cossu, G.
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.
2006 Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta; Gliubizzi, Carla; Servidei, Tiziana; Pescatori, Mario; Tonali, Pietro Attilio; Ricci, Enzo; Mirabella, Massimiliano
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy
2005 Broccolini, Aldobrando; Gliubizzi, Carla; Pavoni, Ernesto; Gidaro, Teresa; Morosetti, Roberta; Sciadra, Francesca; Giardina, Bruno; Tonali, Pietro Attilio; Ricci, Enzo; Brancaccio, Andrea; Mirabella, Massimiliano
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2012 | TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis | Morosetti, Roberta; Gliubizzi, Carla; Sancricca, Cristina; Broccolini, Aldobrando; Gidaro, Teresa; Lucchini, Matteo; Mirabella, Massimiliano | |
| 1-gen-2011 | Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle | Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta; Sancricca, Cristina; Mirabella, Massimiliano | |
| 1-gen-2011 | Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. | Morosetti, Roberta; Gidaro, Teresa; Broccolini, Aldobrando; Gliubizzi, Carla; Sancricca, Cristina; Tonali, Pietro Attilio; Ricci, Enzo; Mirabella, Massimiliano | |
| 1-gen-2010 | Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2). | Ricci, Enzo; Santoro, Massimo; Masciullo, Marcella; Gidaro, Teresa; Broccolini, Aldobrando; Modoni, Anna; Tonali, Pietro Attilio; Silvestri, Gabriella | |
| 1-gen-2010 | Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy | Broccolini, Aldobrando; Gidaro, Teresa; Tasca, Giorgio; Rodolico, Carmelo; Morosetti, Roberta; Ricci, Enzo; Mirabella, Massimiliano | |
| 1-gen-2010 | Increased aging in primary muscle cultures of sporadic inclusion-body myositis. | Morosetti, Roberta; Broccolini, Aldobrando; Sancricca, Cristina; Gliubizzi, Carla; Gidaro, Teresa; Tonali, Pietro Attilio; Ricci, Enzo; Mirabella, Massimiliano | |
| 1-gen-2010 | Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy | Sancricca, Cristina; Mirabella, Massimiliano; Gliubizzi, Carla; Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta | |
| 1-gen-2009 | Hereditary inclusion-body myopathy: clues on pathogenesis and possible therapy | Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta; Mirabella, Massimiliano | |
| 1-gen-2008 | An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene | Gidaro, Teresa; Modoni, Anna; Sabatelli, Mario; Tasca, Giorgio; Broccolini, Aldobrando; Mirabella, Massimiliano | |
| 1-gen-2008 | Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle | Broccolini, Aldobrando; Gidaro, Teresa; De Cristofaro, Raimondo; Morosetti, Roberta; Gliubizzi, Carla; Ricci, Enzo; Tonali, Pietro Attilio; Mirabella, Massimiliano | |
| 1-gen-2006 | MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. | Morosetti, Roberta; Mirabella, Massimiliano; Gliubizzi, Carla; Broccolini, Aldobrando; De Angelis, L; Tagliafico, E; Sampaolesi, M; Gidaro, Teresa; Papacci, Manuela; Roncaglia, E; Rutella, Sergio; Ferrari, S; Tonali, Pietro Attilio; Ricci, Enzo; Cossu, G. | |
| 1-gen-2006 | Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. | Broccolini, Aldobrando; Gidaro, Teresa; Morosetti, Roberta; Gliubizzi, Carla; Servidei, Tiziana; Pescatori, Mario; Tonali, Pietro Attilio; Ricci, Enzo; Mirabella, Massimiliano | |
| 1-gen-2005 | alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy | Broccolini, Aldobrando; Gliubizzi, Carla; Pavoni, Ernesto; Gidaro, Teresa; Morosetti, Roberta; Sciadra, Francesca; Giardina, Bruno; Tonali, Pietro Attilio; Ricci, Enzo; Brancaccio, Andrea; Mirabella, Massimiliano |