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PROVERA S
Collezione ASL Vercelli
Items : 6
Infantile cortical hyperostosis and COL1A1 mutation in four generations. in European journal of pediatrics / Eur J Pediatr. 2011 Nov;170(11):1385-90. doi: 10.1007/s00431-011-1463-0. Epub 2011 May 13.
2011
ASL Vercelli
Cerruti-Mainardi P; Venturi G; Spunton M; Favaron E; Zignani M; Provera S; Dallapiccola B;
[Assessment of breast feeding rates during compulsory vaccination: preliminary outcomes]. in Minerva pediatrica / Minerva Pediatr. 2009 Feb;61(1):9-14.
2009
ASL Vercelli
Candriella M; Uga E; Perino A; Angilella G; Alloni V; Trada M; Grossi L; Tripaldi C; Bagnasco G; Silano V; Olmo LM; Allen M; Provera S;
Heel lance in newborn during breastfeeding: An evaluation of analgesic effect of this procedure in Italian Journal of Pediatrics
2008
ASL Vercelli
Uga E; Candriella M; Perino A; Alloni V; Angilella G; Trada M; Ziliotto AM; Rossi MB; Tozzini D; Tripaldi C; Vaglio M; Grossi L; Allen M; Provera S;
The natural history of Cri du Chat Syndrome. A report from the Italian Register. in European journal of medical genetics / Eur J Med Genet. 2006 Sep-Oct;49(5):363-83. doi: 10.1016/j.ejmg.2005.12.004. Epub 2006 Jan 13.
2006
ASL Vercelli
Mainardi PC; Pastore G; Castronovo C; Godi M; Guala A; Tamiazzo S; Provera S; Pierluigi M; Bricarelli FD;
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;