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Page 1
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.
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, Licata F, Tarani L, Terazzi E, Mazzanti L, Cerruti Mainardi P, Boni A, Faravelli F, Grasso M, Bianchi P, Zollino M, Franzoni E. Cordelli DM, et al. Among authors: cerruti mainardi p. Am J Med Genet A. 2013 Feb;161A(2):273-84. doi: 10.1002/ajmg.a.35717. Epub 2013 Jan 15. Am J Med Genet A. 2013. PMID: 23322667
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.
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. Garavelli L, et al. Among authors: cerruti mainardi p. Horm Res. 2005;63(4):187-92. doi: 10.1159/000085894. Epub 2005 May 20. Horm Res. 2005. PMID: 15908750
[The Cri du Chat syndrome: a study on the quality of care].
Cerruti Mainardi P, Spunton M, Arcuri V, Pastore G, Pedrinazzi M, Nardi S, Castronovo C, Alessi D, Guala A. Cerruti Mainardi P, et al. Minerva Pediatr. 2012 Aug;64(4):395-400. Minerva Pediatr. 2012. PMID: 22728611 Italian.
[Malformations of the midline. A case-control study].
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. Guala A, et al. Among authors: cerruti mainardi p. Pediatr Med Chir. 1997 Mar-Apr;19(2):117-9. Pediatr Med Chir. 1997. PMID: 9312746 Italian.
Psychomotor development in Cri du Chat Syndrome.
Cerruti Mainardi P, Guala A, Pastore G, Pozzo G, Dagna Bricarelli F, Pierluigi M. Cerruti Mainardi P, et al. Clin Genet. 2000 Jun;57(6):459-61. doi: 10.1034/j.1399-0004.2000.570612.x. Clin Genet. 2000. PMID: 10905669 No abstract available.
Infantile cortical hyperostosis and COL1A1 mutation in four generations.
Cerruti-Mainardi P, Venturi G, Spunton M, Favaron E, Zignani M, Provera S, Dallapiccola B. Cerruti-Mainardi P, et al. Eur J Pediatr. 2011 Nov;170(11):1385-90. doi: 10.1007/s00431-011-1463-0. Epub 2011 May 13. Eur J Pediatr. 2011. PMID: 21567126 Free PMC article.
39 results