Marino B - Search Results

1

Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot.

Marino B, Digilio MC, Grazioli S, Formigari R, Mingarelli R, Giannotti A, Dallapiccola B. Marino B, et al. Am J Cardiol. 1996 Mar 1;77(7):505-8. doi: 10.1016/s0002-9149(97)89345-9. Am J Cardiol. 1996. PMID: 8629592

2

Genetic syndromes and outcome after surgical correction of tetralogy of Fallot.

Michielon G, Marino B, Formigari R, Gargiulo G, Picchio F, Digilio MC, Anaclerio S, Oricchio G, Sanders SP, Di Donato RM. Michielon G, et al. Among authors: marino b. Ann Thorac Surg. 2006 Mar;81(3):968-75. doi: 10.1016/j.athoracsur.2005.09.033. Ann Thorac Surg. 2006. PMID: 16488703

3

Echocardiographically guided repair of tetralogy of Fallot.

Santoro G, Marino B, Di Carlo D, Formigari R, de Zorzi A, Mazzera E, Rinelli G, Marcelletti C, De Simone G, Pasquini L. Santoro G, et al. Among authors: marino b. Am J Cardiol. 1994 Apr 15;73(11):808-11. doi: 10.1016/0002-9149(94)90885-0. Am J Cardiol. 1994. PMID: 8160620

4

Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia.

Digilio MC, Marino B, Grazioli S, Agostino D, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Cardiol. 1996 Jun 15;77(15):1375-6. doi: 10.1016/s0002-9149(96)00212-3. Am J Cardiol. 1996. PMID: 8677886

5

Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canal.

Digilio MC, Marino B, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. J Med Genet. 1996 May;33(5):416-8. doi: 10.1136/jmg.33.5.416. J Med Genet. 1996. PMID: 8733055 Free PMC article.

6

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: marino b. 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.

7

Tricuspid atresia and 22q11 deletion.

Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B. Marino B, et al. Am J Med Genet. 1997 Oct 3;72(1):40-2. doi: 10.1002/(sici)1096-8628(19971003)72:1<40::aid-ajmg8>3.0.co;2-z. Am J Med Genet. 1997. PMID: 9295072

8

Cardiac malformations in patients with oral-facial-skeletal syndromes: clinical similarities with heterotaxia.

Digilio MC, Marino B, Ammirati A, Borzaga U, Giannotti A, Dallapiccola B. Digilio MC, et al. Among authors: marino b. Am J Med Genet. 1999 Jun 4;84(4):350-6. doi: 10.1002/(sici)1096-8628(19990604)84:4<350::aid-ajmg8>3.0.co;2-e. Am J Med Genet. 1999. PMID: 10340650

9

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. 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

10

Anatomic patterns of conotruncal defects associated with deletion 22q11.

Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B. Marino B, et al. Genet Med. 2001 Jan-Feb;3(1):45-8. doi: 10.1097/00125817-200101000-00010. Genet Med. 2001. PMID: 11339377 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

952 results

Search Page

Filters