Capolino R - Search Results

1

RASopathies: Clinical Diagnosis in the First Year of Life.

Digilio MC, Lepri F, Baban A, Dentici ML, Versacci P, Capolino R, Ferese R, De Luca A, Tartaglia M, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: capolino r. Mol Syndromol. 2011 Sep;1(6):282-289. doi: 10.1159/000331266. Epub 2011 Sep 14. Mol Syndromol. 2011. PMID: 22190897 Free PMC article.

2

Transposition of the great arteries in asplenia and polysplenia phenotypes.

Marino B, Capolino R, Digilio MC, Di Donato R. Marino B, et al. Among authors: capolino r. Am J Med Genet. 2002 Jul 1;110(3):292-4. doi: 10.1002/ajmg.10376. Am J Med Genet. 2002. PMID: 12116241 No abstract available.

3

Hepatic fibrosis in Kabuki syndrome.

Nobili V, Marcellini M, Devito R, Capolino R, Viola L, Digilio MC. Nobili V, et al. Among authors: capolino r. Am J Med Genet A. 2004 Jan 15;124A(2):209-12. doi: 10.1002/ajmg.a.20387. Am J Med Genet A. 2004. PMID: 14699623

4

Polyvalvular heart disease associated with short stature, facial anomalies, and mental retardation: an additional familial report.

Digilio MC, Capolino R, Versacci P, Marino B. Digilio MC, et al. Among authors: capolino r. Am J Med Genet A. 2004 May 15;127A(1):101-103. doi: 10.1002/ajmg.a.20653. Am J Med Genet A. 2004. PMID: 15103728 No abstract available.

5

Congenital intrahepatic portosystemic venous shunt: an unusual feature in LEOPARD syndrome and in neurofibromatosis type 1.

Digilio MC, Capolino R, Marino B, Sarkozy A, Dallapiccola B. Digilio MC, et al. Among authors: capolino r. Am J Med Genet A. 2005 May 1;134(4):457-8. doi: 10.1002/ajmg.a.30582. Am J Med Genet A. 2005. PMID: 15669093 No abstract available.

6

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2.

Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B. Digilio MC, et al. Among authors: capolino r. Am J Med Genet A. 2005 Apr 15;134A(2):158-64. doi: 10.1002/ajmg.a.30587. Am J Med Genet A. 2005. PMID: 15669097

7

Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries.

Piacentini G, Digilio MC, Capolino R, Zorzi AD, Toscano A, Sarkozy A, D'Agostino R, Marasini M, Russo MG, Dallapiccola B, Marino B. Piacentini G, et al. Among authors: capolino r. Am J Med Genet A. 2005 Aug 30;137(2):176-80. doi: 10.1002/ajmg.a.30859. Am J Med Genet A. 2005. PMID: 16059940

8

Concordant familial segregation of atrial septal defect and Axenfeld-Rieger anomaly in father and son.

Calcagni G, Digilio MC, Capolino R, Dallapiccola B, Marino B. Calcagni G, et al. Among authors: capolino r. Clin Dysmorphol. 2006 Oct;15(4):203-206. doi: 10.1097/01.mcd.0000228417.36295.4d. Clin Dysmorphol. 2006. PMID: 16957472

9

Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndrome.

Cambiaso P, Orazi C, Digilio MC, Loche S, Capolino R, Tozzi A, Faedda A, Cappa M. Cambiaso P, et al. Among authors: capolino r. J Pediatr. 2007 Jan;150(1):62-5. doi: 10.1016/j.jpeds.2006.10.060. J Pediatr. 2007. PMID: 17188616

10

Costello syndrome: clinical diagnosis in the first year of life.

Digilio MC, Sarkozy A, Capolino R, Chiarini Testa MB, Esposito G, de Zorzi A, Cutrera R, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: capolino r. Eur J Pediatr. 2008 Jun;167(6):621-8. doi: 10.1007/s00431-007-0558-0. Epub 2007 Aug 29. Eur J Pediatr. 2008. PMID: 17726614

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