Selicorni A - Search Results

1

Williams-Beuren Syndrome and celiac disease: A real association?

Pangallo E, Parma B, Mariani M, Cianci P, De Paoli A, Maitz S, Fossati C, Panceri R, Agosti M, Selicorni A. Pangallo E, et al. Among authors: selicorni a. Eur J Med Genet. 2020 Sep;63(9):103999. doi: 10.1016/j.ejmg.2020.103999. Epub 2020 Jul 2. Eur J Med Genet. 2020. PMID: 32622956

2

Thyroid anomalies in Williams syndrome: investigation of 95 patients.

Selicorni A, Fratoni A, Pavesi MA, Bottigelli M, Arnaboldi E, Milani D. Selicorni A, et al. Am J Med Genet A. 2006 May 15;140(10):1098-101. doi: 10.1002/ajmg.a.31210. Am J Med Genet A. 2006. PMID: 16596673

3

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

4

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

5

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

6

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.

7

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

8

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.

9

The association of neural axis and craniovertebral junction anomalies with scoliosis in Rubinstein-Taybi syndrome.

Giussani C, Selicorni A, Fossati C, Ingelmo P, Canonico F, Landi A, Trezza A, Riva M, Sganzerla EP. Giussani C, et al. Among authors: selicorni a. Childs Nerv Syst. 2012 Dec;28(12):2163-8. doi: 10.1007/s00381-012-1893-7. Epub 2012 Aug 23. Childs Nerv Syst. 2012. PMID: 22914921

10

Omphalocele in a patient with Noonan syndrome.

Longoni L, D'Apolito V, Cianci P, Selicorni A. Longoni L, et al. Among authors: selicorni a. Clin Dysmorphol. 2012 Oct;21(4):215-217. doi: 10.1097/MCD.0b013e3283590a5a. Clin Dysmorphol. 2012. PMID: 22932443 No abstract available.

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