Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Erica Frezza"'
Autor:
Cinzia Bettio, Federico Banchelli, Valentina Salsi, Roberto Vicini, Oscar Crisafulli, Lucia Ruggiero, Giulia Ricci, Elisabetta Bucci, Corrado Angelini, Angela Berardinelli, Silvia Bonanno, Maria Grazia D’Angelo, Antonio Di Muzio, Massimiliano Filosto, Erica Frezza, Lorenzo Maggi, Tiziana Mongini, Elena Pegoraro, Carmelo Rodolico, Marina Scarlato, Gaetano Vattemi, Daniele Velardo, Giuliano Tomelleri, Roberto D’Amico, Giuseppe D’Antona, Rossella Tupler
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background In facioscapulohumeral muscular dystrophy (FSHD), it is not known whether physical activity (PA) practiced at young age is associated with the clinical presentation of disease. To assess this issue, we performed a retrospective co
Externí odkaz:
https://doaj.org/article/61de057bf13d4fb78dcd7f9489634400
Autor:
Luca Mauro, A. Zanolini, Elisa Falcier, Fabio Placidi, Annalisa Rubino, Elisabetta Roma, Federica Amico, Claudio Liguori, Andrea Romigi, Elio Agostoni, Carola Ferrari Aggradi, Paola Rogliani, Francesca Izzi, Federica Cattaneo, Valeria A. Sansone, Matteo Spanetta, Fabrizio Rao, Paola Proserpio, Andrea Lizio Biost, Erica Frezza, Lino Nobili, Roberto Massa, Andrea Lanza, Claudia Galluzzi, Gabriella Pezzuto, Giulia Greco, Alice Pirola
Publikováno v:
J Clin Sleep Med
Web of Science
Web of Science
STUDY OBJECTIVES: Excessive daytime sleepiness (EDS) in myotonic dystrophy type 1 is mostly of central origin but it may coexist with sleep-related breathing disorders. However, there is no consensus on the sleep protocols to be used, assessments var
Autor:
Silvia Romano, Ilaria Bacigalupo, Christian Marcotulli, Ettore Cioffi, Enrico Silvio Bertini, Gessica Vasco, Alessia Perna, Antonio Petrucci, Roberto Massa, Erica Frezza, Carmela Romano, Marco Salvetti, Giovanni Ristori, Gabriella Silvestri, Nicola Vanacore, Carlo Casali
Objective: The aim of this study was to estimate the Friedreich’s ataxia (FRDA) prevalence in a highly populated region of Italy (previous studies in small geographic areas gave a largely variable prevalence) and to define the patients’ molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47d3564412bb59e6722042633ff7cc83
https://hdl.handle.net/10807/213804
https://hdl.handle.net/10807/213804
Autor:
Ivan Mazzetta, Fernanda Irrera, Roberto Massa, Vito Errico, Rosario Rota, Giovanni Saggio, Erica Frezza, Alessandro Manoni
Publikováno v:
Electronics, Vol 10, Iss 708, p 708 (2021)
Electronics
Volume 10
Issue 6
Electronics
Volume 10
Issue 6
Myotonic dystrophy type 1 (DM1) is a genetic inherited autosomal dominant disease characterized by multisystem involvement, including muscle, heart, brain, eye, and endocrine system. Although several methods are available to evaluate muscle strength,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad9495dd19d4a798f6cb23e7b86545ec
http://hdl.handle.net/2108/276675
http://hdl.handle.net/2108/276675
Autor:
Matteo Spanetta, Annalisa Rubino, Lino Nobili, Giulia Greco, Valeria A. Sansone, Federica Cattaneo, Roberto Massa, Luca Mauro, Paola Proserpio, Erica Frezza, Nicola Biagio Mercuri, Mariana Fernandes, Andrea Romigi, Fabio Placidi, Claudio Liguori, Francesca Izzi, Elio Agostoni
Study objectives The present study aimed at identifying the sleep-wake rhythm in patients with myotonic dystrophy type 1 (DM1) compared to healthy controls. Methods Patients with genetic diagnosis of DM1 and healthy controls underwent a 7-day actigra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfbef0f0fc9b34574653c42c5c28c3fb
http://hdl.handle.net/2108/285987
http://hdl.handle.net/2108/285987
Autor:
Gabriele Nucera, Stefano Di Girolamo, Roberta Di Mauro, Ernesto Bruno, Giulia Greco, Rossella Tupler, Antonio Petrucci, Roberto Massa, Emanuela Fuccillo, Erica Frezza, Emiliano Giardina
Introduction: Facioscapulohumeral muscular dystrophy type 1 (FSHD) represents one of the most common forms of muscular hereditary diseases and it is characterized by a great clinical variability with the typical muscular symptoms and other clinical f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803e013145136c2721a03c952084705f
https://hdl.handle.net/11380/1224835
https://hdl.handle.net/11380/1224835
Publikováno v:
Journal of the Neurological Sciences. 429:119771
Autor:
Roberto Massa, Vito Errico, Giulia Greco, Erica Frezza, Giovanni Saggio, Mariangela Goglia, Rosario Rota, Fernanda Irrera, Alessandro Manoni
Publikováno v:
Journal of the Neurological Sciences. 429:119766
Autor:
Girolama Alessandra Marfia, Giovanni Antonini, Roberto Massa, Chiara Terracciano, Marco Andreani, Manuela Testi, Franco Locatelli, Nicola Biagio Mercuri, Matteo Garibaldi, Erica Frezza, Emanuele Rastelli, Giulia Greco, Eugenio Pompeo
The relative prevalence of myasthenia gravis (MG) subtypes is changing, and their differential features and association with HLA class II alleles are not completely understood.Age at onset, presence/absence of autoantibodies (Ab) and thymoma were ret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e55d13d40310fb3671c8683c75f4a163
https://hdl.handle.net/2108/212459
https://hdl.handle.net/2108/212459