Calcagni G - Search Results

1

Familial recurrence of congenital heart disease: an overview and review of the literature.

Calcagni G, Digilio MC, Sarkozy A, Dallapiccola B, Marino B. Calcagni G, et al. Eur J Pediatr. 2007 Feb;166(2):111-6. doi: 10.1007/s00431-006-0295-9. Epub 2006 Nov 8. Eur J Pediatr. 2007. PMID: 17091259 Review.

2

Influence of heart rate on left ventricular isovolumic relaxation time: a Doppler study in healthy newborns.

De Merulis A, Calcagni G, Versacci P, Lucchini R, Ventriglia F, Marino B. De Merulis A, et al. Among authors: calcagni g. J Am Soc Echocardiogr. 2004 Apr;17(4):330-1. doi: 10.1016/j.echo.2003.12.014. J Am Soc Echocardiogr. 2004. PMID: 15044865 No abstract available.

3

[Cardiac defects in Mexican children with down syndrome].

Marino B, Calcagni G, Digilio C. Marino B, et al. Among authors: calcagni g. Rev Esp Cardiol. 2004 May;57(5):482; author reply 482. Rev Esp Cardiol. 2004. PMID: 15151784 Free article. Spanish. No abstract available.

4

Outcome in Down syndrome fetuses with cardiac anomalies.

Marino B, Diociaiuti L, Calcagni G, Mastroiacovo P. Marino B, et al. Among authors: calcagni g. Am J Med Genet A. 2004 Jul 1;128A(1):101-2; author reply 103. doi: 10.1002/ajmg.a.20690. Am J Med Genet A. 2004. PMID: 15211668 No abstract available.

5

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. Clin Dysmorphol. 2006 Oct;15(4):203-206. doi: 10.1097/01.mcd.0000228417.36295.4d. Clin Dysmorphol. 2006. PMID: 16957472

6

Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature review.

Calcagni G, Baban A, De Luca E, Leonardi B, Pongiglione G, Digilio MC. Calcagni G, et al. Am J Med Genet A. 2016 Mar;170(3):665-9. doi: 10.1002/ajmg.a.37505. Epub 2015 Dec 21. Am J Med Genet A. 2016. PMID: 26686981

7

Congenital heart defects in Noonan syndrome and RIT1 mutation.

Calcagni G, Baban A, Lepri FR, Marino B, Tartaglia M, Digilio MC. Calcagni G, et al. Genet Med. 2016 Dec;18(12):1320. doi: 10.1038/gim.2016.137. Epub 2016 Sep 29. Genet Med. 2016. PMID: 27684039 Free article. No abstract available.

8

Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.

Calcagni G, Unolt M, Digilio MC, Baban A, Versacci P, Tartaglia M, Baldini A, Marino B. Calcagni G, et al. Expert Rev Mol Diagn. 2017 Sep;17(9):861-870. doi: 10.1080/14737159.2017.1360766. Epub 2017 Aug 3. Expert Rev Mol Diagn. 2017. PMID: 28745539 Review.

9

Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results.

Calcagni G, Limongelli G, D'Ambrosio A, Gesualdo F, Digilio MC, Baban A, Albanese SB, Versacci P, De Luca E, Ferrero GB, Baldassarre G, Agnoletti G, Banaudi E, Marek J, Kaski JP, Tuo G, Russo MG, Pacileo G, Milanesi O, Messina D, Marasini M, Cairello F, Formigari R, Brighenti M, Dallapiccola B, Tartaglia M, Marino B. Calcagni G, et al. Int J Cardiol. 2017 Oct 15;245:92-98. doi: 10.1016/j.ijcard.2017.07.068. Epub 2017 Jul 21. Int J Cardiol. 2017. PMID: 28768581

10

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies.

Calcagni G, Adorisio R, Martinelli S, Grutter G, Baban A, Versacci P, Digilio MC, Drago F, Gelb BD, Tartaglia M, Marino B. Calcagni G, et al. Heart Fail Clin. 2018 Apr;14(2):225-235. doi: 10.1016/j.hfc.2017.12.005. Heart Fail Clin. 2018. PMID: 29525650 Review.

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