FREZZA, ERICA
FREZZA, ERICA
Dipartimento di Medicina dei sistemi
A Clinical and Epidemiological Prevalence Study on Friedreich’s Ataxia in Latium, Italy
2022-01-01 Romano, S; Bacigalupo, I; Marcotulli, C; Cioffi, E; Silvio Bertini, E; Vasco, G; Perna, A; Petrucci, A; Massa, R; Frezza, E; Romano, C; Salvetti, M; Ristori, G; Silvestri, G; Vanacore, N; Casali, C
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
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
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
Cardiovascular reflex tests detect autonomic dysfunction in symptomatic and pre-symptomatic subjects with hereditary transthyretin amyloidosis
2023-01-01 Guaraldi, P; Rocchi, C; Cani, I; Gagliardi, C; Longhi, S; Baschieri, F; Rinaldi, R; Frezza, E; D?angelo, R; Barletta, G; Calandra-Buonaura, G; Gali(\`e), N; Massa, R; Cortelli, P
Changes in body composition revealed by bioelectrical impedance analysis reflect strength and motor performance in myotonic dystrophy type 2
2024-12-01 Frezza, E; Merra, G; Greco, G; Goglia, M; Seraceno, S; Boffa, L; Mercuri, Nb; DE LORENZO, A; Massa, R
Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1)
2021-01-01 Frezza, E; Fuccillo, E; Petrucci, A; Greco, G; Nucera, G; Bruno, E; Giardina, E; Tupler, R; Di Mauro, R; DI GIROLAMO, S; Massa, R
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
2024-10-22 Strafella, C; Megalizzi, D; Trastulli, G; Proietti Piorgo, E; Colantoni, L; Tasca, G; Monforte, M; Zampatti, S; Primiano, G; Sancricca, C; Bortolani, S; Torchia, E; Ravera, B; Torri, F; Gadaleta, G; Risi, B; Caria, F; Gerardi, F; Carraro, E; Gioiosa, V; Garibaldi, M; Tufano, L; Frezza, E; Massa, R; Caltagirone, C; Pennisi, E; Petrucci, A; Pane, M; Frongia, A; Gragnani, F; Scutifero, M; Mandich, P; Grandis, M; Maioli, M; Casali, C; Manfroi, E; Politano, L; Passamano, L; Petillo, R; Rodolico, C; Pugliese, A; Previtali, S; Sansone, V; Vercelli, L; Mongini, T; Ricci, G; Siciliano, G; Filosto, M; Ricci, E; Cascella, R; Giardina, E; FSHD Italian Clinical, G
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
2024-10-22 Strafella, C; Megalizzi, D; Trastulli, G; Proietti Piorgo, E; Colantoni, L; Tasca, G; Monforte, M; Zampatti, S; Primiano, G; Sancricca, C; Bortolani, S; Torchia, E; Ravera, B; Torri, F; Gadaleta, G; Risi, B; Caria, F; Gerardi, F; Carraro, E; Gioiosa, V; Garibaldi, M; Tufano, L; Frezza, E; Massa, R; Caltagirone, C; Pennisi, Em; Petrucci, A; Pane, M; Frongia, A; Gragnani, F; Scutifero, M; Mandich, P; Grandis, M; Maioli, Ma; Casali, C; Manfroi, E; Politano, L; Passamano, L; Petillo, R; Rodolico, C; Pugliese, A; Previtali, Sc; Sansone, V; Vercelli, L; Mongini, Te; Ricci, G; Siciliano, G; Filosto, M; Ricci, E; Cascella, R; Giardina, E; Null, N
Late-onset Pompe disease with nemaline bodies
2018-01-01 Frezza, E; Terracciano, C; Giacanelli, M; Rastelli, E; Greco, G; Massa, R
NEFL-Related Charcot-Marie Tooth Disease due to P440L Mutation in Two Italian Families: Expanding the Phenotype and Defining Modulating Factors
2023-01-01 Petrucci, A; Lispi, L; Garibaldi, M; Frezza, E; Moro, F; Massa, R; Maria Santorelli, F
Objective assessment of walking impairments in myotonic dystrophy by means of a wearable technology and a novel severity index
2021-01-01 Saggio, G; Manoni, A; Errico, V; Frezza, E; Mazzetta, I; Rota, R; Massa, R; Irrera, F
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy
2024-01-01 Bettio, C; Banchelli, F; Salsi, V; Vicini, R; Crisafulli, O; Ruggiero, L; Ricci, G; Bucci, E; Angelini, C; Berardinelli, A; Bonanno, S; D'Angelo, Mg; Di Muzio, A; Filosto, M; Frezza, E; Maggi, L; Mongini, T; Pegoraro, E; Rodolico, C; Scarlato, M; Vattemi, G; Velardo, D; Tomelleri, G; D'Amico, R; D'Antona, G; Tupler, R
Response to letter to the editor "Auditory dysfunction in facioscapulohumeral muscular dystrophy type 1: beyond the inner ear involvement" by Gheller et al.
2022-03-01 Fuccillo, E; Frezza, E; Massa, R; Di Girolamo, S
The actigraphic documentation of circadian sleep-wake rhythm dysregulation in myotonic dystrophy type 1
2021-01-01 Liguori, C; Spanetta, M; Fernandes, M; Placidi, F; Massa, R; Romigi, A; Izzi, F; Mauro, L; Greco, G; Frezza, E; Cattaneo, F; Rubino, A; Agostoni, Ec; Nobili, L; Mercuri, Nb; Sansone, Va; Proserpio, P
Thymomatous myasthenia gravis: novel association with HLA DQB1*05:01 and strengthened evidence of high clinical and serological severity
2019-01-01 Massa, R; Greco, G; Testi, M; Rastelli, E; Terracciano, C; Frezza, E; Garibaldi, M; Marfia, Ga; Locatelli, F; Mercuri, Nb; Pompeo, E; Antonini, G; Andreani, M
Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1
2018-01-01 Cutelle, C; Rastelli, E; Gibellini, M; Greco, G; Frezza, E; Botta, A; Terracciano, C; Massa, R
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2022 | A Clinical and Epidemiological Prevalence Study on Friedreich’s Ataxia in Latium, Italy | Romano, S; Bacigalupo, I; Marcotulli, C; Cioffi, E; Silvio Bertini, E; Vasco, G; Perna, A; Petrucci, A; Massa, R; Frezza, E; Romano, C; Salvetti, M; Ristori, G; Silvestri, G; Vanacore, N; Casali, C | 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-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-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 | |
| 1-gen-2023 | Cardiovascular reflex tests detect autonomic dysfunction in symptomatic and pre-symptomatic subjects with hereditary transthyretin amyloidosis | Guaraldi, P; Rocchi, C; Cani, I; Gagliardi, C; Longhi, S; Baschieri, F; Rinaldi, R; Frezza, E; D?angelo, R; Barletta, G; Calandra-Buonaura, G; Gali(\`e), N; Massa, R; Cortelli, P | Articolo su rivista | |
| 1-dic-2024 | Changes in body composition revealed by bioelectrical impedance analysis reflect strength and motor performance in myotonic dystrophy type 2 | Frezza, E; Merra, G; Greco, G; Goglia, M; Seraceno, S; Boffa, L; Mercuri, Nb; DE LORENZO, A; Massa, R | Articolo su rivista | |
| 1-gen-2021 | Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1) | Frezza, E; Fuccillo, E; Petrucci, A; Greco, G; Nucera, G; Bruno, E; Giardina, E; Tupler, R; Di Mauro, R; DI GIROLAMO, S; Massa, R | Articolo su rivista | |
| 22-ott-2024 | Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients | Strafella, C; Megalizzi, D; Trastulli, G; Proietti Piorgo, E; Colantoni, L; Tasca, G; Monforte, M; Zampatti, S; Primiano, G; Sancricca, C; Bortolani, S; Torchia, E; Ravera, B; Torri, F; Gadaleta, G; Risi, B; Caria, F; Gerardi, F; Carraro, E; Gioiosa, V; Garibaldi, M; Tufano, L; Frezza, E; Massa, R; Caltagirone, C; Pennisi, E; Petrucci, A; Pane, M; Frongia, A; Gragnani, F; Scutifero, M; Mandich, P; Grandis, M; Maioli, M; Casali, C; Manfroi, E; Politano, L; Passamano, L; Petillo, R; Rodolico, C; Pugliese, A; Previtali, S; Sansone, V; Vercelli, L; Mongini, T; Ricci, G; Siciliano, G; Filosto, M; Ricci, E; Cascella, R; Giardina, E; FSHD Italian Clinical, G | Articolo su rivista | |
| 22-ott-2024 | Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients | Strafella, C; Megalizzi, D; Trastulli, G; Proietti Piorgo, E; Colantoni, L; Tasca, G; Monforte, M; Zampatti, S; Primiano, G; Sancricca, C; Bortolani, S; Torchia, E; Ravera, B; Torri, F; Gadaleta, G; Risi, B; Caria, F; Gerardi, F; Carraro, E; Gioiosa, V; Garibaldi, M; Tufano, L; Frezza, E; Massa, R; Caltagirone, C; Pennisi, Em; Petrucci, A; Pane, M; Frongia, A; Gragnani, F; Scutifero, M; Mandich, P; Grandis, M; Maioli, Ma; Casali, C; Manfroi, E; Politano, L; Passamano, L; Petillo, R; Rodolico, C; Pugliese, A; Previtali, Sc; Sansone, V; Vercelli, L; Mongini, Te; Ricci, G; Siciliano, G; Filosto, M; Ricci, E; Cascella, R; Giardina, E; Null, N | Articolo su rivista | |
| 1-gen-2018 | Late-onset Pompe disease with nemaline bodies | Frezza, E; Terracciano, C; Giacanelli, M; Rastelli, E; Greco, G; Massa, R | Articolo su rivista | |
| 1-gen-2023 | NEFL-Related Charcot-Marie Tooth Disease due to P440L Mutation in Two Italian Families: Expanding the Phenotype and Defining Modulating Factors | Petrucci, A; Lispi, L; Garibaldi, M; Frezza, E; Moro, F; Massa, R; Maria Santorelli, F | Articolo su rivista | |
| 1-gen-2021 | Objective assessment of walking impairments in myotonic dystrophy by means of a wearable technology and a novel severity index | Saggio, G; Manoni, A; Errico, V; Frezza, E; Mazzetta, I; Rota, R; Massa, R; Irrera, F | Articolo su rivista | |
| 1-gen-2024 | Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy | Bettio, C; Banchelli, F; Salsi, V; Vicini, R; Crisafulli, O; Ruggiero, L; Ricci, G; Bucci, E; Angelini, C; Berardinelli, A; Bonanno, S; D'Angelo, Mg; Di Muzio, A; Filosto, M; Frezza, E; Maggi, L; Mongini, T; Pegoraro, E; Rodolico, C; Scarlato, M; Vattemi, G; Velardo, D; Tomelleri, G; D'Amico, R; D'Antona, G; Tupler, R | Articolo su rivista | |
| 1-mar-2022 | Response to letter to the editor "Auditory dysfunction in facioscapulohumeral muscular dystrophy type 1: beyond the inner ear involvement" by Gheller et al. | Fuccillo, E; Frezza, E; Massa, R; Di Girolamo, S | Articolo su rivista | |
| 1-gen-2021 | The actigraphic documentation of circadian sleep-wake rhythm dysregulation in myotonic dystrophy type 1 | Liguori, C; Spanetta, M; Fernandes, M; Placidi, F; Massa, R; Romigi, A; Izzi, F; Mauro, L; Greco, G; Frezza, E; Cattaneo, F; Rubino, A; Agostoni, Ec; Nobili, L; Mercuri, Nb; Sansone, Va; Proserpio, P | Articolo su rivista | |
| 1-gen-2019 | Thymomatous myasthenia gravis: novel association with HLA DQB1*05:01 and strengthened evidence of high clinical and serological severity | Massa, R; Greco, G; Testi, M; Rastelli, E; Terracciano, C; Frezza, E; Garibaldi, M; Marfia, Ga; Locatelli, F; Mercuri, Nb; Pompeo, E; Antonini, G; Andreani, M | Articolo su rivista | |
| 1-gen-2018 | Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1 | Cutelle, C; Rastelli, E; Gibellini, M; Greco, G; Frezza, E; Botta, A; Terracciano, C; Massa, R | Articolo su rivista |