Silengo MC - Search Results

1

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A. Sparago A, et al. Among authors: silengo mc. Nat Genet. 2004 Sep;36(9):958-60. doi: 10.1038/ng1410. Epub 2004 Aug 15. Nat Genet. 2004. PMID: 15314640

2

Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.

Sparago A, Russo S, Cerrato F, Ferraiuolo S, Castorina P, Selicorni A, Schwienbacher C, Negrini M, Ferrero GB, Silengo MC, Anichini C, Larizza L, Riccio A. Sparago A, et al. Among authors: silengo mc. Hum Mol Genet. 2007 Feb 1;16(3):254-64. doi: 10.1093/hmg/ddl448. Epub 2006 Dec 11. Hum Mol Genet. 2007. PMID: 17158821

3

Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.

Riccio A, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Ferrero GB, Silengo MC, Russo S, Larizza L, Cerrato F. Riccio A, et al. Among authors: silengo mc. Endocr Dev. 2009;14:1-9. doi: 10.1159/000207461. Epub 2009 Feb 27. Endocr Dev. 2009. PMID: 19293570 Review.

4

Prevalence of Beckwith-Wiedemann syndrome in North West of Italy.

Mussa A, Russo S, De Crescenzo A, Chiesa N, Molinatto C, Selicorni A, Richiardi L, Larizza L, Silengo MC, Riccio A, Ferrero GB. Mussa A, et al. Among authors: silengo mc. Am J Med Genet A. 2013 Oct;161A(10):2481-6. doi: 10.1002/ajmg.a.36080. Epub 2013 Aug 5. Am J Med Genet A. 2013. PMID: 23918458

5

Fetal growth patterns in Beckwith-Wiedemann syndrome.

Mussa A, Russo S, de Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Silengo MC, Larizza L, Riccio A, Ferrero GB. Mussa A, et al. Among authors: silengo mc. Clin Genet. 2016 Jul;90(1):21-7. doi: 10.1111/cge.12759. Epub 2016 Mar 15. Clin Genet. 2016. PMID: 26857110

6

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

Murrell A, Ito Y, Verde G, Huddleston J, Woodfine K, Silengo MC, Spreafico F, Perotti D, De Crescenzo A, Sparago A, Cerrato F, Riccio A. Murrell A, et al. Among authors: silengo mc. PLoS One. 2008 Mar 26;3(3):e1849. doi: 10.1371/journal.pone.0001849. PLoS One. 2008. PMID: 18365005 Free PMC article.

7

Pachygyria and cerebellar hypoplasia in a patient with a 2q22-q23 deletion that includes the ZFHX1B gene.

Silengo M, Ferrero GB, Wakamatsu N. Silengo M, et al. Am J Med Genet A. 2004 May 15;127A(1):109. doi: 10.1002/ajmg.a.20607. Am J Med Genet A. 2004. PMID: 15103730 No abstract available.

8

Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome.

Mussa A, Peruzzi L, Chiesa N, De Crescenzo A, Russo S, Melis D, Tarani L, Baldassarre G, Larizza L, Riccio A, Silengo M, Ferrero GB. Mussa A, et al. Pediatr Nephrol. 2012 Mar;27(3):397-406. doi: 10.1007/s00467-011-2009-4. Epub 2011 Oct 21. Pediatr Nephrol. 2012. PMID: 22015620

9

A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome.

Silengo M, Barberis L, Ferrero GB, Sorasio L, Valenzise M. Silengo M, et al. Clin Dysmorphol. 2002 Oct;11(4):293-4. doi: 10.1097/00019605-200210000-00012. Clin Dysmorphol. 2002. PMID: 12401997

10

The overlap between Sotos and Beckwith-Wiedemann syndromes.

Mussa A, Chiesa N, Porta F, Baldassarre G, Silengo MC, Ferrero GB. Mussa A, et al. Among authors: silengo mc. J Pediatr. 2010 Jun;156(6):1035-1036. doi: 10.1016/j.jpeds.2010.02.063. Epub 2010 Apr 14. J Pediatr. 2010. PMID: 20394943 No abstract available.

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