Sfoglia per Autore
Congenital muscular dystrophies with cognitive impairment. A population study.
2010-01-01 Messina, S; Bruno, C; Moroni, I; Pegoraro, E; D'Amico, A; Biancheri, R; Berardinelli, A; Boffi, P; Cassandrini, D; Farina, L; Minetti, C; Moggio, M; Mongini, T; Mottarelli, E; Pane, M; Pantaleoni, C; Pichiecchio, A; Pini, A; Ricci, E; Saredi, S; Sframeli, Maria; Tortorella, G; Toscano, A; Trevisan, Cp; Uggetti, C; Vasco, G; Comi, Gp; Santorelli, Fm; Bertini, E; Mercuri, E.
Congenital muscular dystrophies with cognitive impairment. A population study.
2010-01-01 Messina, S.; Bruno, C.; Moroni, I.; Pegoraro, E.; D'Amico, A.; Biancheri, R.; Berardinelli, A.; Boffi, P.; Cassandrini, D.; Farina, L.; Minetti, C.; Moggio, M.; Mongini, T.; Mottarelli ,E.; Pane, M.; Pantaleoni, C.; Pichiecchio, A.; Pini, A.; Ricci, E.; Saredi, S.; Sframeli, M.; Tortorella, G.; Toscano, A.; Trevisan, C.P.; Uggetti, C.; Vasco, G.; Comi, G.P.; Santorelli, F.M.; Bertini, E.; Mercuri, E.
Activation of NF-kappaB pathway in Duchenne muscular dystrophy: relation to age
2011-01-01 Messina, Sonia; Vita, Gianluca; Aguennouz, M'Hammed; Sframeli, Maria; Romeo, S; Rodolico, Carmelo; Vita, Giuseppe
Congenital myastenic syndromes due a novel GFPT1 mutation: a new Italian case
2012-01-01 Sframeli, Maria; Messina, Sonia; S., Portaro; M., Dusl; H., Lochmuller; Toscano, Antonio; Rodolico, Carmelo
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy.
2012-01-01 Bello, L.; Piva, L.; Barp, A.; Taglia, A.; Picillo, E.; Vasco, G.; Pane, M.; Previtali, S. C.; Torrente, Y.; Gazzerro, E.; Motta, M. C.; Grieco, G. S.; Napolitano, S.; Magri, F.; D'Amico, A.; Astrea, G.; Messina, Sonia; Sframeli, Maria; Vita, Gianluca; Boffi, P.; Mongini, T.; Ferlini, A.; Gualandi, F.; Soraru', G.; Ermani, M.; Vita, Giuseppe; Battini, R.; Bertini, E.; Comi, G. P.; Berardinelli, A.; Minetti, C.; Bruno, C.; Mercuri, E.; Politano, L.; Angelini, C.; Hoffman, E. P.; Pegoraro, E.
Pilot study of flavocoxid in ambulant DMD patients.
2012-01-01 Licata, Norma; Messina, Sonia; Vita, Gianluca; Sframeli, Maria; Cama, A.; Lo Giudice, C.; Romeo, SARA GIOVANNA; Ciranni, Annamaria; De Pasquale, M. G.; Aguennouz, M'Hammed; Vita, G.
Pilot study of flavocoxid in ambulant DMD patients.
2012-01-01 Messina, Sonia; Vita, Gianluca; Sframeli, Maria; Licata, Norma; Cama, L; Ciranni, Annamaria; Romeo, SARA GIOVANNA; Aguennouz, M'Hammed; Vita, Giuseppe
Pilot study of flavocoxid in ambulant DMD patients.
2013-01-01 Vita, Gianluca; Messina, Sonia; Licata, Norma; Sframeli, Maria; Cama, A; Lo Giudice, C.; Barcellona, C; Distefano, Mg; LA ROSA, Matteo; Romeo S., Ciranni A; De Pasquale, Mg; Aguennouz, M'Hammed; Vita, Giuseppe
The families of children with muscular dystrophies: burden, social network and professional support.
2013-01-01 Politano, L; Scutifero, M; Zaccaro, A; Balottin, U; Berardinelli, A; Camia, M; Motta, Mc; Vita, Gianluca; Messina, Sonia; Sframeli, Maria; Vita, Giuseppe; Pane, M; Lombardo, Me; Scalise, R; D’Amico, A; Catteruccia, M; Colia, G; Angelici, C; Giani, A; Semplicioni, C; Battini, R; Astrea, G; Ricci, G; D’Angelo, Mg; Brighino, E; Civati, F; Catalano, M; Sagliocchi, A; Magliano, L.
Impaired rotational mechanics and strain revealing subclinical left ventricular dysfunction in children with neuromuscolar disorders: a speckle tracking study
2013-01-01 Oreto, Lilia; Zito, Concetta; Cusmà Piccione, M.; Calabrò, M. P.; Todaro, Mariachiara; Vita, G. L.; Messina, Sonia; Vita, Giuseppe; Sframeli, Maria; Carerj, Scipione
Telomere shortening and telomere associated proteins in exercised wild type and mdx mice.
2013-01-01 LA ROSA, Matteo; Romeo, SARA GIOVANNA; Vita, Gianluca; Sframeli, Maria; Licata, Norma; Ciranni, Annamaria; Aguennouz, M'Hammed; Messina, Sonia; Vita, Giuseppe
Outcome measures in Duchenne muscular dystrophy: validation of the Pediatric Quality of Life Inventory TM neuromuscular Module in the Italian population and correlation with other functional assessments.
2013-01-01 Sframeli, Maria; Bertini, E; Vita, Giuseppe; Berardinelli, A; Minetti, C; Politano, L; Mongini, T; Pegoraro, E; Morandi, L; Baranello, G; Vita, Gianluca; D’Angelo, Mg; Mercuri, E; Messina, Sonia
The first report of a patient carrying an out-of-frame exon2 deletion in the dystrophin gene and showing a very unusual phenotype.
2013-01-01 Messina, Sonia; Falzarano, Ms; Szigyarto, C; Uhlen, M; Vattemi, G; Perrone, D; Vita, Gianluca; Sframeli, Maria; Rodolico, Carmelo; Gualandi, F; Flanigan, K; Vita, Giuseppe; Ferlini, A.
study of flavocoxid in ambulant DMD patients.
2013-01-01 Vita, Gianluca; Licata, Norma; Sframeli, Maria; Cama, A; Lo Giudice, C.; Barcellona, C; Distefano, Mg; LA ROSA, Matteo; Romeo S., Ciranni A; De Pasquale, Mg; Aguennouz, M'Hammed; Messina, Sonia; Vita, Giuseppe
The first report of a patient carrying an out-of-frame exon2 deletion in the dystrophin gene and showing a very unusual phenotype.
2013-01-01 Messina, Sonia; Falzarano, Ms; Szigyarto, C; Uhlen, M; Vattemi, G; Perrone, D; Vita, Gianluca; Sframeli, Maria; Rodolico, Carmelo; Gualandi, F; Flanigan, K; Vita, Giuseppe; Ferlini, A.
Neuropsychiatric comorbidities in Duchenne Muscular Dystrophy.
2014-01-01 Messina, Sonia; Ricotti, V; Scoto, M; Mandy, Wpl; Entwistle, K; Pane, M; Deconinck, N; LA FORESTA, Stefania; Sframeli, Maria; Vita, Gianluca; Skuse, Dh; Vita, Giuseppe; Mercuri, E; Muntoni, F.
Modulation of neural nitric oxide synthase by the isoflavone genistein promotes muscle regeneration in mdx mice
2014-01-01 LA ROSA, Matteo; Vita, Gianluca; Licata, Norma; Bitto, Alessandra; Sframeli, Maria; Barcellona, Costanza; Distefano, MARIA GRAZIA; Romeo, SARA GIOVANNA; Ciranni, Annamaria; Aguennouz, M'Hammed; Squadrito, Francesco; Messina, Sonia; Vita, Giuseppe
Outcome measures in Duchenne muscular dystrophy: validation of the Pediatric Quality of Life InventoryTM Neuromuscular Module in the Italian population and correlation with other functional assessments.
2014-01-01 Vita, Gianluca; Bertini, E; Vita, Giuseppe; Sframeli, Maria; LA ROSA, Matteo; Barcellona, Costanza; Berardinelli, A; Minetti, C; Politano, L; Mongini, T; Pegoraro, E; Morandi, L; D’Angelo, M; Mercuri, E; Messina, Sonia
Pilot study of serial casting in muscular dystrophy patients.
2014-01-01 Distefano, MARIA GRAZIA; Cavallaro, Filippo; Vita, Gianluca; Sframeli, Maria; Barcellona, Costanza; LA ROSA, Matteo; Donato, C; Consulo, C; Di Bella, V; Pavone, F; Vita, Giuseppe; Messina, Sonia
Clinical and genetic spectrum in a large cohort of patients with a genetic diagnosis of Congenital Muscular Dystrophies: Analysis of the UK diagnostic service 2001-2013.
2014-01-01 Sframeli, Maria; Sarkozy, A.; Astrea, G.; Scoto, M.; Feng, L.; Mein, R.; Yau, M.; Phadke, R.; Sewry, C.; Messina, Sonia; Robb, S.; Muntoni, F. .
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Congenital muscular dystrophies with cognitive impairment. A population study. | 1-gen-2010 | Messina, S; Bruno, C; Moroni, I; Pegoraro, E; D'Amico, A; Biancheri, R; Berardinelli, A; Boffi, P; Cassandrini, D; Farina, L; Minetti, C; Moggio, M; Mongini, T; Mottarelli, E; Pane, M; Pantaleoni, C; Pichiecchio, A; Pini, A; Ricci, E; Saredi, S; Sframeli, Maria; Tortorella, G; Toscano, A; Trevisan, Cp; Uggetti, C; Vasco, G; Comi, Gp; Santorelli, Fm; Bertini, E; Mercuri, E. | |
| Congenital muscular dystrophies with cognitive impairment. A population study. | 1-gen-2010 | Messina, S.; Bruno, C.; Moroni, I.; Pegoraro, E.; D'Amico, A.; Biancheri, R.; Berardinelli, A.; Boffi, P.; Cassandrini, D.; Farina, L.; Minetti, C.; Moggio, M.; Mongini, T.; Mottarelli ,E.; Pane, M.; Pantaleoni, C.; Pichiecchio, A.; Pini, A.; Ricci, E.; Saredi, S.; Sframeli, M.; Tortorella, G.; Toscano, A.; Trevisan, C.P.; Uggetti, C.; Vasco, G.; Comi, G.P.; Santorelli, F.M.; Bertini, E.; Mercuri, E. | |
| Activation of NF-kappaB pathway in Duchenne muscular dystrophy: relation to age | 1-gen-2011 | Messina, Sonia; Vita, Gianluca; Aguennouz, M'Hammed; Sframeli, Maria; Romeo, S; Rodolico, Carmelo; Vita, Giuseppe | |
| Congenital myastenic syndromes due a novel GFPT1 mutation: a new Italian case | 1-gen-2012 | Sframeli, Maria; Messina, Sonia; S., Portaro; M., Dusl; H., Lochmuller; Toscano, Antonio; Rodolico, Carmelo | |
| Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. | 1-gen-2012 | Bello, L.; Piva, L.; Barp, A.; Taglia, A.; Picillo, E.; Vasco, G.; Pane, M.; Previtali, S. C.; Torrente, Y.; Gazzerro, E.; Motta, M. C.; Grieco, G. S.; Napolitano, S.; Magri, F.; D'Amico, A.; Astrea, G.; Messina, Sonia; Sframeli, Maria; Vita, Gianluca; Boffi, P.; Mongini, T.; Ferlini, A.; Gualandi, F.; Soraru', G.; Ermani, M.; Vita, Giuseppe; Battini, R.; Bertini, E.; Comi, G. P.; Berardinelli, A.; Minetti, C.; Bruno, C.; Mercuri, E.; Politano, L.; Angelini, C.; Hoffman, E. P.; Pegoraro, E. | |
| Pilot study of flavocoxid in ambulant DMD patients. | 1-gen-2012 | Licata, Norma; Messina, Sonia; Vita, Gianluca; Sframeli, Maria; Cama, A.; Lo Giudice, C.; Romeo, SARA GIOVANNA; Ciranni, Annamaria; De Pasquale, M. G.; Aguennouz, M'Hammed; Vita, G. | |
| Pilot study of flavocoxid in ambulant DMD patients. | 1-gen-2012 | Messina, Sonia; Vita, Gianluca; Sframeli, Maria; Licata, Norma; Cama, L; Ciranni, Annamaria; Romeo, SARA GIOVANNA; Aguennouz, M'Hammed; Vita, Giuseppe | |
| Pilot study of flavocoxid in ambulant DMD patients. | 1-gen-2013 | Vita, Gianluca; Messina, Sonia; Licata, Norma; Sframeli, Maria; Cama, A; Lo Giudice, C.; Barcellona, C; Distefano, Mg; LA ROSA, Matteo; Romeo S., Ciranni A; De Pasquale, Mg; Aguennouz, M'Hammed; Vita, Giuseppe | |
| The families of children with muscular dystrophies: burden, social network and professional support. | 1-gen-2013 | Politano, L; Scutifero, M; Zaccaro, A; Balottin, U; Berardinelli, A; Camia, M; Motta, Mc; Vita, Gianluca; Messina, Sonia; Sframeli, Maria; Vita, Giuseppe; Pane, M; Lombardo, Me; Scalise, R; D’Amico, A; Catteruccia, M; Colia, G; Angelici, C; Giani, A; Semplicioni, C; Battini, R; Astrea, G; Ricci, G; D’Angelo, Mg; Brighino, E; Civati, F; Catalano, M; Sagliocchi, A; Magliano, L. | |
| Impaired rotational mechanics and strain revealing subclinical left ventricular dysfunction in children with neuromuscolar disorders: a speckle tracking study | 1-gen-2013 | Oreto, Lilia; Zito, Concetta; Cusmà Piccione, M.; Calabrò, M. P.; Todaro, Mariachiara; Vita, G. L.; Messina, Sonia; Vita, Giuseppe; Sframeli, Maria; Carerj, Scipione | |
| Telomere shortening and telomere associated proteins in exercised wild type and mdx mice. | 1-gen-2013 | LA ROSA, Matteo; Romeo, SARA GIOVANNA; Vita, Gianluca; Sframeli, Maria; Licata, Norma; Ciranni, Annamaria; Aguennouz, M'Hammed; Messina, Sonia; Vita, Giuseppe | |
| Outcome measures in Duchenne muscular dystrophy: validation of the Pediatric Quality of Life Inventory TM neuromuscular Module in the Italian population and correlation with other functional assessments. | 1-gen-2013 | Sframeli, Maria; Bertini, E; Vita, Giuseppe; Berardinelli, A; Minetti, C; Politano, L; Mongini, T; Pegoraro, E; Morandi, L; Baranello, G; Vita, Gianluca; D’Angelo, Mg; Mercuri, E; Messina, Sonia | |
| The first report of a patient carrying an out-of-frame exon2 deletion in the dystrophin gene and showing a very unusual phenotype. | 1-gen-2013 | Messina, Sonia; Falzarano, Ms; Szigyarto, C; Uhlen, M; Vattemi, G; Perrone, D; Vita, Gianluca; Sframeli, Maria; Rodolico, Carmelo; Gualandi, F; Flanigan, K; Vita, Giuseppe; Ferlini, A. | |
| study of flavocoxid in ambulant DMD patients. | 1-gen-2013 | Vita, Gianluca; Licata, Norma; Sframeli, Maria; Cama, A; Lo Giudice, C.; Barcellona, C; Distefano, Mg; LA ROSA, Matteo; Romeo S., Ciranni A; De Pasquale, Mg; Aguennouz, M'Hammed; Messina, Sonia; Vita, Giuseppe | |
| The first report of a patient carrying an out-of-frame exon2 deletion in the dystrophin gene and showing a very unusual phenotype. | 1-gen-2013 | Messina, Sonia; Falzarano, Ms; Szigyarto, C; Uhlen, M; Vattemi, G; Perrone, D; Vita, Gianluca; Sframeli, Maria; Rodolico, Carmelo; Gualandi, F; Flanigan, K; Vita, Giuseppe; Ferlini, A. | |
| Neuropsychiatric comorbidities in Duchenne Muscular Dystrophy. | 1-gen-2014 | Messina, Sonia; Ricotti, V; Scoto, M; Mandy, Wpl; Entwistle, K; Pane, M; Deconinck, N; LA FORESTA, Stefania; Sframeli, Maria; Vita, Gianluca; Skuse, Dh; Vita, Giuseppe; Mercuri, E; Muntoni, F. | |
| Modulation of neural nitric oxide synthase by the isoflavone genistein promotes muscle regeneration in mdx mice | 1-gen-2014 | LA ROSA, Matteo; Vita, Gianluca; Licata, Norma; Bitto, Alessandra; Sframeli, Maria; Barcellona, Costanza; Distefano, MARIA GRAZIA; Romeo, SARA GIOVANNA; Ciranni, Annamaria; Aguennouz, M'Hammed; Squadrito, Francesco; Messina, Sonia; Vita, Giuseppe | |
| Outcome measures in Duchenne muscular dystrophy: validation of the Pediatric Quality of Life InventoryTM Neuromuscular Module in the Italian population and correlation with other functional assessments. | 1-gen-2014 | Vita, Gianluca; Bertini, E; Vita, Giuseppe; Sframeli, Maria; LA ROSA, Matteo; Barcellona, Costanza; Berardinelli, A; Minetti, C; Politano, L; Mongini, T; Pegoraro, E; Morandi, L; D’Angelo, M; Mercuri, E; Messina, Sonia | |
| Pilot study of serial casting in muscular dystrophy patients. | 1-gen-2014 | Distefano, MARIA GRAZIA; Cavallaro, Filippo; Vita, Gianluca; Sframeli, Maria; Barcellona, Costanza; LA ROSA, Matteo; Donato, C; Consulo, C; Di Bella, V; Pavone, F; Vita, Giuseppe; Messina, Sonia | |
| Clinical and genetic spectrum in a large cohort of patients with a genetic diagnosis of Congenital Muscular Dystrophies: Analysis of the UK diagnostic service 2001-2013. | 1-gen-2014 | Sframeli, Maria; Sarkozy, A.; Astrea, G.; Scoto, M.; Feng, L.; Mein, R.; Yau, M.; Phadke, R.; Sewry, C.; Messina, Sonia; Robb, S.; Muntoni, F. . |
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