Gidaro, Teresa

Gidaro, Teresa  

Mostra records
Risultati 1 - 13 di 13 (tempo di esecuzione: 0.008 secondi).
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