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NIKOLIC A
Collezione ASL Vercelli

  

Items : 7

Interpretation of the epigenetic signature of facioscapulohumeral muscular dystrophy in light of genotype-phenotype studies in International Journal of Molecular Sciences

2020
ASL Vercelli

Nikolic A; Jones TI; Govi M; Mele F; Maranda L; Sera F; Ricci G; Ruggiero L; Vercelli L; Portaro S; Villa L; Fiorillo C; Maggi L; Santoro L; Antonini G; Filosto M; Moggio M; Angelini C; Pegoraro E; Berardinelli A; Maioli MA; D’Angelo G; Di Muzio A; Siciliano G; Tomelleri G; D’Esposito M; Ragione FD; Brancaccio A; Piras 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...