MASSA, ROBERTO
MASSA, ROBERTO
Dipartimento di Medicina dei sistemi
A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles
2021-06-01 Botta, A; Visconti, Vv; Fontana, L; Bisceglia, P; Bengala, M; Massa, R; Bagni, I; Cardani, R; Sangiuolo, F; Meola, G; Antonini, G; Petrucci, A; Pegoraro, E; D'Apice, Mr; Novelli, G
A case of fulminant subacute sclerosing panencephalitis presenting with acute myoclonic-astatic epilepsy
2017-01-01 Magurano, F; Marella, Gl; Marchi, A; Filia, A; Marsella, Lt; Potenza, S; Massa, R; Bucci, P; Baggieri, M; Nicoletti, L
A clinical and kinematic evaluation of foot drop in myotonic dystrophy type I: A pilot study
2021-01-01 Frezza, E; Manoni, A; Errico, V; Rota, R; Greco, G; Goglia, M; Irrera, F; Saggio, G; Massa, R
A mobile app for patients with Pompe disease and its possible clinical applications
2018-01-01 Ricci, G; Baldanzi, S; Seidita, F; Proietti, C; Carlini, F; Peviani, S; Antonini, G; Vianello, A; Siciliano, G; Musumeci, O; Toscano, A; Ravaglia, S; Moggio, M; Comi, G; Pegoraro, E; Filosto, M; Marrosu, G; Maggi, L; Liguori, R; Massa, R; Di Iorio, G; Servidei, S; Angelini, C; Mongini, T
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease
2014-08-01 Ciotti, P; Luigetti, M; Geroldi, A; Capponi, S; Pezzini, I; Gulli, R; Pazzaglia, C; Padua, L; Massa, R; Mandich, P; Bellone, E
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues
2012-01-01 Rinaldi, F; Terracciano, C; Pisani, V; Massa, R; Loro, E; Vergani, L; DI GIROLAMO, S; Angelini, C; Gourdon, G; Novelli, G; Botta, A
Active muscle length reduction progressively damages soleus in hindlimb-suspended rabbits
1992-09-01 Sancesario, G; Massa, R; Anzil, A; Bernardi, G
Acute demyelinating sensorimotor polyneuropathy in B-cell lymphoma with IGM autoantibodies against glycolipid GD1B
2004-04-22 Marfia, Ga; Pachatz, C; Terracciano, C; Leone, G; Massa, R
Adrenomyeloneuropathy partially responsive to steroid pulse therapy
2002-01-01 Panico, Mb; Rizzo, C; Desiato, M; Calabresi, P; Floris, R; Massa, R
Adult polyglucosan body disease: Proton magnetic resonance spectroscopy of the brain and novel mutation in the GBE1 gene
2008-01-01 Massa, R; Bruno, C; Martorana, A; De Stefano, N; Van Diggelen, O; Federico, A
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease
2016-01-01 Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, J; Terracciano, C; Caltagirone, C; Massa, R; Phst, S; Barsottini, O; Kawarai, T; Orlacchio, A
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease
2016-01-01 Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, Jl; Terracciano, C; Caltagirone, C; Massa, R; S, Tgphs; Barsottini, Ogp; Kawarai, T; Orlacchio, A
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy
2016-02-01 Vanacore, N; Rastelli, E; Antonini, G; Bianchi, M; Botta, A; Bucci, E; Casali, C; Costanzi Porrini, S; Giacanelli, M; Gibellini, M; Modoni, A; Novelli, G; Pennisi, E; Petrucci, A; Piantadosi, C; Silvestri, G; Terracciano, C; Massa, R
Aquaporin 4 expression in human skeletal muscle fiber types.
2018-05-01 Vizzaccaro, E; Terracciano, C; Rastelli, E; Massa, R
Assessment of self-reported and objective daytime sleepiness in adult-onset myotonic dystrophy type 1
2021-01-01 Sansone, Va; Proserpio, P; Mauro, L; Biostat, Al; Frezza, E; Lanza, A; Rogliani, P; Pezzuto, G; Falcier, E; Aggradi, Cf; Pirola, A; Rao, F; Roma, E; Galluzzi, C; Spanetta, M; Cattaneo, F; Rubino, A; Agostoni, Ec; Amico, F; Zanolini, A; Izzi, F; Greco, G; Romigi, A; Liguori, C; Nobili, L; Placidi, F; Massa, R
Association of HLA-DQB1*05:02 with Myasthenia gravis in Italian patients
2011-01-01 Testi, M; Andreani, M; Terracciano, C; Battarra, M; Troiano, M; Guagnano, A; Galluccio, T; Massa, R
Association of HLA-DQB1∗05:02 and DRB1∗16 Alleles with Late-Onset, Nonthymomatous, AChR-Ab-Positive Myasthenia Gravis
2012-01-01 Testi, M; Terracciano, C; Guagnano, A; Testa, G; Marfia, Ga; Pompeo, E; Andreani, M; Massa, R
Association of HLA-DQB1∗05:02 and DRB1∗16 Alleles with Late-Onset,Nonthymomatous, AChR-Ab-Positive Myasthenia Gravis
2012-01-01 Testi, M; Terracciano, C; Guagnano, A; Testa, G; Marfia, Ga; Pompeo, E; Andreani, M; Massa, R
Attrv in lazio-italy: A high-prevalence region in a non-endemic country
2021-01-01 Luigetti, M; Guglielmino, V; Antonini, G; Casali, C; Ceccanti, M; Chiappini, Mg; De Giglio, L; Di Lazzaro, V; Di Muzio, A; Goglia, M; Inghilleri, M; Leonardi, L; Massa, R; Pennisi, Em; Petrucci, A; Proietti, E; Rispoli, M; Sabatelli, M; Di Girolamo, M
Automatic Detection of Myotonia using a Sensory Glove with Resistive Flex Sensors and Machine Learning Techniques
2023-01-01 Cesarini, V; Costantini, G; Amato, F; Errico, V; Pietrosanti, L; Calado, Al; Massa, R; Frezza, E; Irrera, F; Manoni, A; Saggio, G
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-giu-2021 | A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles | Botta, A; Visconti, Vv; Fontana, L; Bisceglia, P; Bengala, M; Massa, R; Bagni, I; Cardani, R; Sangiuolo, F; Meola, G; Antonini, G; Petrucci, A; Pegoraro, E; D'Apice, Mr; Novelli, G | Articolo su rivista | |
| 1-gen-2017 | A case of fulminant subacute sclerosing panencephalitis presenting with acute myoclonic-astatic epilepsy | Magurano, F; Marella, Gl; Marchi, A; Filia, A; Marsella, Lt; Potenza, S; Massa, R; Bucci, P; Baggieri, M; Nicoletti, L | Articolo su rivista | |
| 1-gen-2021 | A clinical and kinematic evaluation of foot drop in myotonic dystrophy type I: A pilot study | Frezza, E; Manoni, A; Errico, V; Rota, R; Greco, G; Goglia, M; Irrera, F; Saggio, G; Massa, R | Articolo su rivista | |
| 1-gen-2018 | A mobile app for patients with Pompe disease and its possible clinical applications | Ricci, G; Baldanzi, S; Seidita, F; Proietti, C; Carlini, F; Peviani, S; Antonini, G; Vianello, A; Siciliano, G; Musumeci, O; Toscano, A; Ravaglia, S; Moggio, M; Comi, G; Pegoraro, E; Filosto, M; Marrosu, G; Maggi, L; Liguori, R; Massa, R; Di Iorio, G; Servidei, S; Angelini, C; Mongini, T | Articolo su rivista | |
| 1-ago-2014 | A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease | Ciotti, P; Luigetti, M; Geroldi, A; Capponi, S; Pezzini, I; Gulli, R; Pazzaglia, C; Padua, L; Massa, R; Mandich, P; Bellone, E | Articolo su rivista | |
| 1-gen-2012 | Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues | Rinaldi, F; Terracciano, C; Pisani, V; Massa, R; Loro, E; Vergani, L; DI GIROLAMO, S; Angelini, C; Gourdon, G; Novelli, G; Botta, A | Articolo su rivista | |
| 1-set-1992 | Active muscle length reduction progressively damages soleus in hindlimb-suspended rabbits | Sancesario, G; Massa, R; Anzil, A; Bernardi, G | Articolo su rivista | |
| 22-apr-2004 | Acute demyelinating sensorimotor polyneuropathy in B-cell lymphoma with IGM autoantibodies against glycolipid GD1B | Marfia, Ga; Pachatz, C; Terracciano, C; Leone, G; Massa, R | Articolo su rivista | |
| 1-gen-2002 | Adrenomyeloneuropathy partially responsive to steroid pulse therapy | Panico, Mb; Rizzo, C; Desiato, M; Calabresi, P; Floris, R; Massa, R | Articolo su rivista | |
| 1-gen-2008 | Adult polyglucosan body disease: Proton magnetic resonance spectroscopy of the brain and novel mutation in the GBE1 gene | Massa, R; Bruno, C; Martorana, A; De Stefano, N; Van Diggelen, O; Federico, A | Articolo su rivista | |
| 1-gen-2016 | ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease | Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, J; Terracciano, C; Caltagirone, C; Massa, R; Phst, S; Barsottini, O; Kawarai, T; Orlacchio, A | Articolo su rivista | |
| 1-gen-2016 | ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease | Montecchiani, C; Pedace, L; Lo Giudice, T; Casella, A; Mearini, M; Gaudiello, F; Pedroso, Jl; Terracciano, C; Caltagirone, C; Massa, R; S, Tgphs; Barsottini, Ogp; Kawarai, T; Orlacchio, A | Articolo su rivista | |
| 1-feb-2016 | An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy | Vanacore, N; Rastelli, E; Antonini, G; Bianchi, M; Botta, A; Bucci, E; Casali, C; Costanzi Porrini, S; Giacanelli, M; Gibellini, M; Modoni, A; Novelli, G; Pennisi, E; Petrucci, A; Piantadosi, C; Silvestri, G; Terracciano, C; Massa, R | Articolo su rivista | |
| 1-mag-2018 | Aquaporin 4 expression in human skeletal muscle fiber types. | Vizzaccaro, E; Terracciano, C; Rastelli, E; Massa, R | Articolo su rivista | |
| 1-gen-2021 | Assessment of self-reported and objective daytime sleepiness in adult-onset myotonic dystrophy type 1 | Sansone, Va; Proserpio, P; Mauro, L; Biostat, Al; Frezza, E; Lanza, A; Rogliani, P; Pezzuto, G; Falcier, E; Aggradi, Cf; Pirola, A; Rao, F; Roma, E; Galluzzi, C; Spanetta, M; Cattaneo, F; Rubino, A; Agostoni, Ec; Amico, F; Zanolini, A; Izzi, F; Greco, G; Romigi, A; Liguori, C; Nobili, L; Placidi, F; Massa, R | Articolo su rivista | |
| 1-gen-2011 | Association of HLA-DQB1*05:02 with Myasthenia gravis in Italian patients | Testi, M; Andreani, M; Terracciano, C; Battarra, M; Troiano, M; Guagnano, A; Galluccio, T; Massa, R | Intervento a convegno | |
| 1-gen-2012 | Association of HLA-DQB1∗05:02 and DRB1∗16 Alleles with Late-Onset, Nonthymomatous, AChR-Ab-Positive Myasthenia Gravis | Testi, M; Terracciano, C; Guagnano, A; Testa, G; Marfia, Ga; Pompeo, E; Andreani, M; Massa, R | Articolo su rivista | |
| 1-gen-2012 | Association of HLA-DQB1∗05:02 and DRB1∗16 Alleles with Late-Onset,Nonthymomatous, AChR-Ab-Positive Myasthenia Gravis | Testi, M; Terracciano, C; Guagnano, A; Testa, G; Marfia, Ga; Pompeo, E; Andreani, M; Massa, R | Articolo su rivista | |
| 1-gen-2021 | Attrv in lazio-italy: A high-prevalence region in a non-endemic country | Luigetti, M; Guglielmino, V; Antonini, G; Casali, C; Ceccanti, M; Chiappini, Mg; De Giglio, L; Di Lazzaro, V; Di Muzio, A; Goglia, M; Inghilleri, M; Leonardi, L; Massa, R; Pennisi, Em; Petrucci, A; Proietti, E; Rispoli, M; Sabatelli, M; Di Girolamo, M | Articolo su rivista | |
| 1-gen-2023 | Automatic Detection of Myotonia using a Sensory Glove with Resistive Flex Sensors and Machine Learning Techniques | Cesarini, V; Costantini, G; Amato, F; Errico, V; Pietrosanti, L; Calado, Al; Massa, R; Frezza, E; Irrera, F; Manoni, A; Saggio, G | Intervento a convegno |