RE-BVS – Piemonte Repository

Sfoglia per AUTORE
ZOLLINO M
Collezione ASL Vercelli

Items : 4

Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype in American Journal of Medical Genetics, Part A

2013
ASL Vercelli

Cordelli DM; Garavelli L; Savasta S; Guerra A; Pellicciari A; Giordano L; Bonetti S; Cecconi I; Wischmeijer A; Seri M; Rosato S; Gelmini C; Della Giustina E; Ferrari AR; Zanotta N; Epifanio R; Grioni D; Malbora B; Mammi I; Mari F; Buoni S; Mostardini R; Grosso S; Pantaleoni C; Doz M; Poch-Olivé ML; Rivieri F; Sorge G; Simonte G; et alii...

Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature in American Journal of Medical Genetics, Part A

2009
ASL Vercelli

Garavelli L; Zollino M; Cerruti Mainardi P; Gurrieri F; Rivieri F; Soli F; Verri R; Albertini E; Favaron E; Zignani M; Orteschi D; Bianchi P; Faravelli F; Forzano F; Seri M; Wischmeijer A; Turchetti D; Pompilii E; Gnoli M; Cocchi G; Mazzanti L; Bergamaschi R; De Brasi D; Sperandeo MP; Mari F; Uliana V; Mostardini R; Cecconi M; Grasso M; et alii...

Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B): Report of three Italian cases with hypospadias and review in Hormone Research

2005
ASL Vercelli

Garavelli L; Cerruti-Mainardi P; Virdis R; Pedori S; Pastore G; Godi M; Provera S; Rauch A; Zweier C; Zollino M; Banchini G; Longo N; Mowat D; Neri G; Bernasconi S;

Mowat-Wilson syndrome and mutation of the Zinc Finger Homeo Box 1B gene: A new syndrome probably under-diagnosed in Italian Journal of Pediatrics

2005
ASL Vercelli

Cerruti Mainardi P; Garavelli L; Pastore G; Virdis R; Pedori S; Godi M; Provera S; Rauch A; Zweier C; Castronovo C; Zollino M; Banchini G; Bernasconi S; Neri G;