Toscano A - Search Results

1

New findings concerning cardiovascular manifestations emerging from long-term follow-up of 150 patients with the Williams-Beuren-Beuren syndrome.

Del Pasqua A, Rinelli G, Toscano A, Iacobelli R, Digilio C, Marino B, Saffirio C, Mondillo S, Pasquini L, Sanders SP, de Zorzi A. Del Pasqua A, et al. Among authors: toscano a. Cardiol Young. 2009 Dec;19(6):563-7. doi: 10.1017/S1047951109990837. Cardiol Young. 2009. PMID: 19941695

2

Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.

Digilio MC, Marino B, Giannotti A, Toscano A, Dallapiccola B. Digilio MC, et al. Among authors: toscano a. J Med Genet. 1997 Mar;34(3):188-90. doi: 10.1136/jmg.34.3.188. J Med Genet. 1997. PMID: 9132487 Free PMC article.

3

Noonan syndrome and aortic coarctation.

Digilio MC, Marino B, Picchio F, Prandstraller D, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: toscano a. Am J Med Genet. 1998 Nov 2;80(2):160-2. Am J Med Genet. 1998. PMID: 9805134

4

Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.

Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: toscano a. Genet Couns. 1999;10(1):25-33. Genet Couns. 1999. PMID: 10191426 Review.

5

Atrioventricular canal defect without Down syndrome: a heterogeneous malformation.

Digilio MC, Marino B, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: toscano a. Am J Med Genet. 1999 Jul 16;85(2):140-6. Am J Med Genet. 1999. PMID: 10406667 Review.

6

Deletion 22q11 in patients with interrupted aortic arch.

Marino B, Digilio MC, Persiani M, Di Donato R, Toscano A, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: toscano a. Am J Cardiol. 1999 Aug 1;84(3):360-1, A9. doi: 10.1016/s0002-9149(99)00297-0. Am J Cardiol. 1999. PMID: 10496456

7

Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal.

Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: toscano a. J Pediatr. 1999 Dec;135(6):703-6. doi: 10.1016/s0022-3476(99)70088-0. J Pediatr. 1999. PMID: 10586172

8

Deficiency of the infundibular septum in patients with interrupted aortic arch and del 22q11.

Marino B, Digilio MC, Toscano A, Dallapiccola B. Marino B, et al. Among authors: toscano a. Cardiol Young. 2000 Oct;10(4):428-9. doi: 10.1017/s104795110000980x. Cardiol Young. 2000. PMID: 10950346 No abstract available.

9

Congenital heart defects in Kabuki syndrome.

Digilio MC, Marino B, Toscano A, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: toscano a. Am J Med Genet. 2001 May 15;100(4):269-74. doi: 10.1002/ajmg.1265. Am J Med Genet. 2001. PMID: 11343317 Review.

10

Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns.

Anaclerio S, Marino B, Carotti A, Digilio MC, Toscano A, Gitto P, Giannotti A, Di Donato R, Dallapiccola B. Anaclerio S, et al. Among authors: toscano a. Ital Heart J. 2001 May;2(5):384-7. Ital Heart J. 2001. PMID: 11392644

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