Selicorni A - Search Results

1

Modeling Cornelia de Lange syndrome in vitro and in vivo reveals a role for cohesin complex in neuronal survival and differentiation.

Bottai D, Spreafico M, Pistocchi A, Fazio G, Adami R, Grazioli P, Canu A, Bragato C, Rigamonti S, Parodi C, Cazzaniga G, Biondi A, Cotelli F, Selicorni A, Massa V. Bottai D, et al. Among authors: selicorni a. Hum Mol Genet. 2019 Jan 1;28(1):64-73. doi: 10.1093/hmg/ddy329. Hum Mol Genet. 2019. PMID: 30239720 Free article.

2

Variability of the Brachmann-de Lange syndrome.

Selicorni A, Lalatta F, Livini E, Briscioli V, Piguzzi T, Bagozzi DC, Mastroiacovo P, Zampino G, Gaeta G, Pugliese A, et al. Selicorni A, et al. Am J Med Genet. 1993 Nov 15;47(7):977-82. doi: 10.1002/ajmg.1320470708. Am J Med Genet. 1993. PMID: 8291540

3

Gastroesophageal reflux and Cornelia de Lange syndrome: typical and atypical symptoms.

Luzzani S, Macchini F, Valadè A, Milani D, Selicorni A. Luzzani S, et al. Among authors: selicorni a. Am J Med Genet A. 2003 Jun 15;119A(3):283-7. doi: 10.1002/ajmg.a.20191. Am J Med Genet A. 2003. PMID: 12784293

4

X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations.

Musio A, Selicorni A, Focarelli ML, Gervasini C, Milani D, Russo S, Vezzoni P, Larizza L. Musio A, et al. Among authors: selicorni a. Nat Genet. 2006 May;38(5):528-30. doi: 10.1038/ng1779. Epub 2006 Apr 9. Nat Genet. 2006. PMID: 16604071

5

Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation.

Selicorni A, Russo S, Gervasini C, Castronovo P, Milani D, Cavalleri F, Bentivegna A, Masciadri M, Domi A, Divizia MT, Sforzini C, Tarantino E, Memo L, Scarano G, Larizza L. Selicorni A, et al. Clin Genet. 2007 Aug;72(2):98-108. doi: 10.1111/j.1399-0004.2007.00832.x. Clin Genet. 2007. PMID: 17661813

6

Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes.

Gervasini C, Pfundt R, Castronovo P, Russo S, Roversi G, Masciadri M, Milani D, Zampino G, Selicorni A, Schoenmakers EF, Larizza L. Gervasini C, et al. Among authors: selicorni a. Clin Genet. 2008 Dec;74(6):531-8. doi: 10.1111/j.1399-0004.2008.01086.x. Epub 2008 Sep 16. Clin Genet. 2008. PMID: 18798846

7

Somatic mosaicism in Cornelia de Lange syndrome: a further contributor to the wide clinical expressivity?

Castronovo P, Delahaye-Duriez A, Gervasini C, Azzollini J, Minier F, Russo S, Masciadri M, Selicorni A, Verloes A, Larizza L. Castronovo P, et al. Among authors: selicorni a. Clin Genet. 2010 Dec;78(6):560-4. doi: 10.1111/j.1399-0004.2010.01408.x. Clin Genet. 2010. PMID: 20331678

8

Immunogenicity, safety and tolerability of monovalent 2009 pandemic influenza A/H1N1 MF59-adjuvanted vaccine in children and adolescents with Williams or Cornelia De Lange syndrome.

Esposito S, Selicorni A, Daleno C, Valzano A, Cerutti M, Galeone C, Consolo S, Menni F, Principi N. Esposito S, et al. Among authors: selicorni a. Hum Vaccin. 2011 Jun;7(6):613-7. doi: 10.4161/hv.7.6.15133. Epub 2011 Jun 1. Hum Vaccin. 2011. PMID: 21508673

9

Intragenic and large NIPBL rearrangements revealed by MLPA in Cornelia de Lange patients.

Russo S, Masciadri M, Gervasini C, Azzollini J, Cereda A, Zampino G, Haas O, Scarano G, Di Rocco M, Finelli P, Tenconi R, Selicorni A, Larizza L. Russo S, et al. Among authors: selicorni a. Eur J Hum Genet. 2012 Jul;20(7):734-41. doi: 10.1038/ejhg.2012.7. Epub 2012 Feb 22. Eur J Hum Genet. 2012. PMID: 22353942 Free PMC article.

10

A new report of Cornelia de Lange syndrome associated with split hand and feet.

Barboni C, Cereda A, Mariani M, Gervasini C, Ajmone P, Biondi A, Selicorni A. Barboni C, et al. Among authors: selicorni a. Am J Med Genet A. 2012 Nov;158A(11):2953-5. doi: 10.1002/ajmg.a.35623. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991273

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