RE-BVS – Piemonte Repository

Sfoglia per AUTORE
SCARLATO M
Collezione ASL Vercelli

Items : 8

A 5-year clinical follow-up study from the Italian National Registry for FSHD in Journal of Neurology

2021
ASL Vercelli

Vercelli L; Mele F; Ruggiero L; Sera F; Tripodi S; Ricci G; Vallarola A; Villa L; Govi M; Maranda L; Di Muzio A; Scarlato M; Bucci E; Maggi L; Rodolico C; Moggio M; Filosto M; Antonini G; Previtali S; Angelini C; Berardinelli A; Pegoraro E; Siciliano G; Tomelleri G; Santoro L; Mongini T; Tupler R;

Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis in Scientific reports

2020
ASL Vercelli

Ricci G; Mele F; Govi M; Ruggiero L; Sera F; Vercelli L; Bettio C; Santoro L; Mongini T; Villa L; Moggio M; Filosto M; Scarlato M; Previtali SC; Tripodi SM; Pegoraro E; Telese R; Di Muzio A; Rodolico C; Bucci E; Antonini G; D'Angelo MG; Berardinelli A; Maggi L; Piras R; Maioli MA; Siciliano G; Tomelleri G; Angelini C; et alii...

Phenotypic Variability among Patients with D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy in JAMA Network Open

2020
ASL Vercelli

Ruggiero L; Mele F; Manganelli F; Bruzzese D; Ricci G; Vercelli L; Govi M; Vallarola A; Tripodi S; Villa L; Di Muzio A; Scarlato M; Bucci E; Antonini G; Maggi L; Rodolico C; Tomelleri G; Filosto M; Previtali S; Angelini C; Berardinelli A; Pegoraro E; Moggio M; Mongini T; Siciliano G; Santoro L; Tupler R;

Large scale genotype phenotype corelation study in 1703 carriers of D4Z4 reduced alleles from the Italian National Register for FSHD in Acta Myologica

2019
ASL Vercelli

Mele F; Ruggiero L; Ricci G; Vercelli L; Bettio C; Tripodi S; Govi M; Bucci E; Di Muzio A; Maggi L; Scarlato M; Villa L; D'Angelo G; Antonini G; Filosto M; Rodolico C; Piras R; Maioli MA; Massa R; Previtali S; Angelini C; Berardinelli A; Pegoraro E; Moggio M; Santoro L; Siciliano G; Mongini T; Tomelleri G; Tupler R; et alii...

Five-year follow-up study and new predictors in disease progression for facioscapolohumeral muscular dystrophy in Acta Myologica

2019
ASL Vercelli

Vercelli L; Mele F; Tripodi S; Ruggiero L; Sera F; Ricci G; Villa L; Govi M; Maranda L; Di Muzio A; Scarlato M; Bucci E; Maggi L; Rodolico C; Tomelleri G; Filosto M; Antonini G; Previtali S; Angelini C; Berardinelli A; Pegoraro E; Moggio M; Santoro L; Siciliano G; Mongini T; Tupler R;

Large scale genotype-phenotype correlation study in 1703 carriers of D4Z4 reduced alleles from the Italian National Register for FSHD in Acta Myologica

2019
ASL Vercelli

Mele F; Ruggiero L; Ricci G; Vercelli L; Bettio C; Tripodi S; Govi M; Bucci E; Di Muzio A; Maggi L; Scarlato M; Villa L; D'Angelo G; Antonini G; Filosto M; Rodolico C; Piras R; Maioli MA; Massa R; Previtali S; Angelini C; Berardinelli A; Pegoraro E; Moggio M; Santoro M; Siciliano G; Mongini T; Tomelleri G; Tupler R; et alii...

Are there different clinical entities with distinct disease course among D4Z4 reduced allele carriers? in Journal of Neuromuscular Diseases

2018
ASL Vercelli

Ricci G; Mele F; Ruggiero L; Bucci E; Maggi L; Govi M; Sera F; Vercelli L; Santoro L; Mongini T; Villa L; Moggio M; Filosto M; Scarlato M; Previtali SC; Cao M; Pegoraro E; Telese R; Di Muzio A; Rodolico C; Antonini G; D'Angelo MG; Berardinelli A; Piras R; Maioli MA; Tomelleri G; Angelini C; Siciliano G; Tupler R; et alii...

Longitudinal study of disease progression in 232 FSHD patients from the Italian registry in Acta Myologica

2016
ASL Vercelli

Vercelli L; Rolle E; Ponzalino V; Ricci G; Ruggiero L; Villa L; Di Muzio A; Cao M; Scarlato M; Bucci E; Rodolico C; Pasanisi MB; Tomelleri G; Filosto M; Mele F; Nikolic A; Govi M; Maggi L; Antonini G; Previtali SC; Angelini C; Pegoraro E; Moggio M; Santoro L; Siciliano G; Tupler R; Mongini T;