RE-BVS – Piemonte Repository

Sfoglia per AUTORE
CERRUTI MAINARDI P
Collezione ASL Vercelli

Items : 18

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...

[The Cri du Chat syndrome: a study on the quality of care]. in Minerva pediatrica / Minerva Pediatr. 2012 Aug;64(4):395-400.

2012
ASL Vercelli

Cerruti Mainardi P; Spunton M; Arcuri V; Pastore G; Pedrinazzi M; Nardi S; Castronovo C; Alessi D; Guala A;

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...

Cri du Chat syndrome. in Orphanet journal of rare diseases / Orphanet J Rare Dis. 2006 Sep 5;1:33. doi: 10.1186/1750-1172-1-33.

2006
ASL Vercelli

Cerruti Mainardi P;

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;

Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity. in Journal of medical genetics / J Med Genet. 2004 Feb;41(2):e16. doi: 10.1136/jmg.2003.009548.

2004
ASL Vercelli

Cerruti Mainardi P; Pastore G; Zweier C; Rauch A;

[Malformations of the midline. A case-control study]. in La Pediatria medica e chirurgica : Medical and surgical pediatrics / Pediatr Med Chir. 1997 Mar-Apr;19(2):117-9.

1997
ASL Vercelli

Guala A; Pastore G; Cerruti Mainardi P; Liverani E; Ghini T; Tagliabue A; Capo A; Quazza G; Cigolotti AC; Zaffaroni M; Foracchia P; Garassino L; Uasone R;

[Implementation of the pediatric services in the region of Piedmont. A Piedmont pediatric team]. in Minerva pediatrica / Minerva Pediatr. 1996 Sep;48(9):373-8.

1996
ASL Vercelli

Cerruti Mainardi P; Repinto A; Guala A; Pastore G;

Severe sideropenic anemia in a young middle-distance runner in Minerva pediatrica

1992
ASL Vercelli

Guala A; Giorcelli V; Gallo G; Pastore G; Rossi M; Cerruti Mainardi P;

[Hypophosphatasia: a family study]. in La Pediatria medica e chirurgica : Medical and surgical pediatrics / Pediatr Med Chir. 1991 Mar-Apr;13(2):179-86.

1991
ASL Vercelli

Guala A; Tomà P; Liverani ME; Fresia A; Biroli E; Cerruti Mainardi P;

Resumption of breast feeding in low-birth-weight newborn infants in La Pediatria medica e chirurgica : Medical and surgical pediatrics

1986
ASL Vercelli

Cerruti Mainardi P; Caliman L; Gallo G; Guola A; Liverani ME; Pastore G;

Survey into the frequency of three congenital malformations among newborns in the Province of Vercelli in 1975-1979 in Minerva Pediatrica

1985
ASL Vercelli

Cerruti Mainardi P; Ziliotto A; Liverani ME;

Mannosidosis. Study of two families and prenatal diagnosis in Pediatria Medica e Chirurgica

1982
ASL Vercelli

Cerruti Mainardi P; Gatti R; Javarone A;

A case of intermediate thalassemia of Piedmontese origin. A genetic, clinical, hematological and biosynthetic study in Minerva Pediatrica