RE-BVS – Piemonte Repository

Sfoglia per AUTORE
CAO M
Collezione ASL Vercelli

Items : 8

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...

Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 33-35 kb D4Z4 reduced alleles: Experience of the Italian National Registry for FSHD in Acta Myologica

2017
ASL Vercelli

Ruggiero L; Mele F; Ricci G; Vercelli L; Govi M; Nikolic A; Louise M; Sera F; Berardinelli A; Angelini C; Antonini G; Bucci E; Filosto M; Cao M; Giardina E; Pegoraro E; Di Muzio A; Telese R; Maggi L; Portaro S; Rodolico C; Villa L; Mongini T; Siciliano G; Tomelleri G; D'Angelo G; Maioli MA; Moggio M; Santoro L; et alii...

A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes in Journal of Neurology

2016
ASL Vercelli

Ricci G; Ruggiero L; Vercelli L; Sera F; Nikolic A; Govi M; Mele F; Daolio J; Angelini C; Antonini G; Berardinelli A; Bucci E; Cao M; D’Amico MC; D’Angelo G; Di Muzio A; Filosto M; Maggi L; Moggio M; Mongini T; Morandi L; Pegoraro E; Rodolico C; Santoro L; Siciliano G; Tomelleri G; Villa L; Tupler R;

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;

Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: Experience of the FSHD Italian National Registry in BMJ Open

2016
ASL Vercelli

Nikolic A; Ricci G; Sera F; Bucci E; Govi M; Mele F; Rossi M; Ruggiero L; Vercelli L; Ravaglia S; Brisca G; Fiorillo C; Villa L; Maggi L; Cao M; D'Amico MC; Siciliano G; Antonini G; Santoro L; Mongini T; Moggio M; Morandi L; Pegoraro E; Angelini C; Di Muzio A; Rodolico C; Tomelleri G; D'Angelo MG; Bruno C; et alii...

From the experience of the Italian national registry a novel tool to dissect the phenotypic complexity of facioscapulohumeral muscular dystrophy: The comprehensive clinical evaluation form in European Journal of Neurology

2015
ASL Vercelli

Mongini T; Ricci G; Vercelli L; Ruggiero L; Sera F; Nikolic A; Govi M; Mele F; Villa L; Maggi L; Cao M; D'Amico MC; Siciliano G; Antonini G; Berardinelli A; Santoro L; Moggio M; Morandi L; Pegoraro E; Angelini C; Di Muzio A; Ricci E; Rodolico C; Tomelleri G; Tupler R;

Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy in Brain

2013
ASL Vercelli

Ricci G; Scionti I; Sera F; Govi M; D'Amico R; Frambolli I; Mele F; Filosto M; Vercelli L; Ruggiero L; Berardinelli A; Angelini C; Antonini G; Bucci E; Cao M; Daolio J; Di Muzio A; Di Leo R; Galluzzi G; Iannaccone E; Maggi L; Maruotti V; Moggio M; Mongini T; Morandi L; Nikolic A; Pastorello E; Ricci E; Rodolico C; et alii...

Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy in American Journal of Human Genetics

2012
ASL Vercelli

Scionti I; Greco F; Ricci G; Govi M; Arashiro P; Vercelli L; Berardinelli A; Angelini C; Antonini G; Cao M; Di Muzio A; Moggio M; Morandi L; Ricci E; Rodolico C; Ruggiero L; Santoro L; Siciliano G; Tomelleri G; Trevisan CP; Galluzzi G; Wright W; Zatz M; Tupler R;