Selicorni A - Search Results

1

Patients with DeSanto-Shinawi syndrome: Further extension of phenotype from Italy.

Pasquali D, Torella A, Grandone A, Luongo C, Morleo M, Peduto C, di Fraia R, Selvaggio LD, Allosso F, Accardo G, Zanobio MT, Maitz S, Mariani M, Selicorni A, Banfi S, Nigro V; TUDP Study Group. Pasquali D, et al. Among authors: selicorni a. Am J Med Genet A. 2023 Mar;191(3):823-830. doi: 10.1002/ajmg.a.63061. Epub 2022 Nov 24. Am J Med Genet A. 2023. PMID: 36420948

2

Analysis of congenital heart defects in 87 consecutive patients with Brachmann-de Lange syndrome.

Selicorni A, Colli AM, Passarini A, Milani D, Cereda A, Cerutti M, Maitz S, Alloni V, Salvini L, Galli MA, Ghiglia S, Salice P, Danzi GB. Selicorni A, et al. Am J Med Genet A. 2009 Jun;149A(6):1268-72. doi: 10.1002/ajmg.a.32838. Am J Med Genet A. 2009. PMID: 19449412

3

Clinical problems and everyday abilities of a group of Italian adolescent and young adults with Cornelia de Lange syndrome.

Olioso G, Passarini A, Atzeri F, Milani D, Cereda A, Cerutti M, Maitz S, Menni F, Selicorni A. Olioso G, et al. Among authors: selicorni a. Am J Med Genet A. 2009 Nov;149A(11):2532-7. doi: 10.1002/ajmg.a.33075. Am J Med Genet A. 2009. PMID: 19876900

4

A 12.4 Mb duplication of 17q11.2q12 in a patient with psychomotor developmental delay and minor anomalies.

Caselli R, Ballarati L, Selicorni A, Milani D, Maitz S, Valtorta C, Larizza L, Giardino D. Caselli R, et al. Among authors: selicorni a. Eur J Med Genet. 2010 Sep-Oct;53(5):325-8. doi: 10.1016/j.ejmg.2010.05.004. Epub 2010 Jun 2. Eur J Med Genet. 2010. PMID: 20621612

5

Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.

Ballarati L, Cereda A, Caselli R, Selicorni A, Recalcati MP, Maitz S, Finelli P, Larizza L, Giardino D. Ballarati L, et al. Among authors: selicorni a. Eur J Med Genet. 2011 Jan-Feb;54(1):55-9. doi: 10.1016/j.ejmg.2010.10.003. Epub 2010 Oct 20. Eur J Med Genet. 2011. PMID: 20969981 Review.

6

Clinical follow-up of young adults affected by Williams syndrome: experience of 45 Italian patients.

Bedeschi MF, Bianchi V, Colli AM, Natacci F, Cereda A, Milani D, Maitz S, Lalatta F, Selicorni A. Bedeschi MF, et al. Among authors: selicorni a. Am J Med Genet A. 2011 Feb;155A(2):353-9. doi: 10.1002/ajmg.a.33819. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271653

7

Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia.

Ballarati L, Cereda A, Caselli R, Maitz S, Russo S, Selicorni A, Larizza L, Giardino D. Ballarati L, et al. Among authors: selicorni a. Eur J Med Genet. 2012 Feb;55(2):124-7. doi: 10.1016/j.ejmg.2011.12.001. Epub 2011 Dec 17. Eur J Med Genet. 2012. PMID: 22210230 Free article.

8

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

9

Germline mosaicism in Cornelia de Lange syndrome: dilemmas and risk figures.

Mariani M, Bettini LR, Cereda A, Maitz S, Gervasini C, Russo S, Masciadri M, Biondi A, Larizza L, Selicorni A. Mariani M, et al. Among authors: selicorni a. Am J Med Genet A. 2013 Jul;161A(7):1825-6. doi: 10.1002/ajmg.a.35988. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696053 No abstract available.

10

Two cases of hepatic adenomas in patients with Wolf-Hirschhorn syndrome: a new rare complication?

Prunotto G, Cianci P, Cereda A, Scatigno A, Fossati C, Maitz S, Biondi A, Selicorni A. Prunotto G, et al. Among authors: selicorni a. Am J Med Genet A. 2013 Jul;161A(7):1759-62. doi: 10.1002/ajmg.a.35966. Epub 2013 May 21. Am J Med Genet A. 2013. PMID: 23696331

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