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Items: 1 to 50 of 58

1.

Prevalence, Type, and Molecular Spectrum of NF1 Mutations in Patients with Neurofibromatosis Type 1 and Congenital Heart Disease.

Pinna V, Daniele P, Calcagni G, Mariniello L, Criscione R, Giardina C, Lepri FR, Hozhabri H, Alberico A, Cavone S, Morella AT, Mandile R, Annunziata F, Di Giosaffatte N, D'Asdia MC, Versacci P, Capolino R, Strisciuglio P, Giustini S, Melis D, Digilio MC, Tartaglia M, Marino B, De Luca A.

Genes (Basel). 2019 Sep 4;10(9). pii: E675. doi: 10.3390/genes10090675.

2.

Echocardiographic long-term follow-up of adult survivors of pediatric cancer treated with Dexrazoxane-Anthracyclines association.

Filomena D, Versacci P, Cimino S, Mattiucci C, Maestrini V, Cantisani D, Petronilli V, Agati L, Schiavetti A.

Int J Cardiol. 2020 Jan 15;299:271-275. doi: 10.1016/j.ijcard.2019.07.096. Epub 2019 Aug 5.

PMID:
31422879
3.

Lifestyle and awareness of cholesterol blood levels among 29159 community school children in Italy.

Martino F, Martino E, Versacci P, Niglio T, Zanoni C, Puddu PE.

Nutr Metab Cardiovasc Dis. 2019 Aug;29(8):802-807. doi: 10.1016/j.numecd.2019.05.060. Epub 2019 May 22.

PMID:
31248716
4.

Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy.

Motta M, Giancotti A, Mastromoro G, Chandramouli B, Pinna V, Pantaleoni F, Di Giosaffatte N, Petrini S, Mazza T, D'Ambrosio V, Versacci P, Ventriglia F, Chillemi G, Pizzuti A, Tartaglia M, De Luca A.

Hum Mutat. 2019 Aug;40(8):1046-1056. doi: 10.1002/humu.23767. Epub 2019 May 6.

PMID:
31059601
5.

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.

Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C, Unolt M, Pelliccione E, Anaclerio S, Caprio C, Cioffi S, Bilio M, Baban A, Drago F, Digilio MC, Marino B, Baldini A.

PLoS One. 2019 Apr 1;14(4):e0211170. doi: 10.1371/journal.pone.0211170. eCollection 2019.

6.

Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients.

Maioli M, Gnoli M, Boarini M, Tremosini M, Zambrano A, Pedrini E, Mordenti M, Corsini S, D'Eufemia P, Versacci P, Celli M, Sangiorgi L.

Eur J Hum Genet. 2019 Jul;27(7):1090-1100. doi: 10.1038/s41431-019-0373-x. Epub 2019 Mar 18.

7.

Association of OPG-RANKL ratio with left ventricular hypertrophy and geometric remodeling in male overweight/obese youths.

Zampetti S, Lucantoni F, Pacifico L, Campagna G, Versacci P, Pierimarchi P, Buzzetti R.

J Endocrinol Invest. 2019 Apr;42(4):427-434. doi: 10.1007/s40618-018-0932-y. Epub 2018 Aug 21.

PMID:
30132289
8.

Congenital superior caval vein aneurysm in a newborn with cystic lymphangioma: a rare case report.

Attene J, Casorelli E, Versacci P.

Cardiol Young. 2018 Aug;28(8):1067-1069. doi: 10.1017/S1047951118000823.

PMID:
30043721
9.

Cardiovascular disease in Down syndrome.

Versacci P, Di Carlo D, Digilio MC, Marino B.

Curr Opin Pediatr. 2018 Oct;30(5):616-622. doi: 10.1097/MOP.0000000000000661. Review.

PMID:
30015688
10.

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect.

Ferese R, Bonetti M, Consoli F, Guida V, Sarkozy A, Lepri FR, Versacci P, Gambardella S, Calcagni G, Margiotti K, Piceci Sparascio F, Hozhabri H, Mazza T, Digilio MC, Dallapiccola B, Tartaglia M, Marino B, Hertog JD, De Luca A.

Hum Mutat. 2018 Oct;39(10):1428-1441. doi: 10.1002/humu.23593. Epub 2018 Jul 30.

PMID:
30007050
11.

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

Versacci P, Pugnaloni F, Digilio MC, Putotto C, Unolt M, Calcagni G, Baban A, Marino B.

J Cardiovasc Dev Dis. 2018 May 2;5(2). pii: E24. doi: 10.3390/jcdd5020024. Review.

12.

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Digilio MC, Pugnaloni F, De Luca A, Calcagni G, Baban A, Dentici ML, Versacci P, Dallapiccola B, Tartaglia M, Marino B.

Clin Genet. 2019 Feb;95(2):268-276. doi: 10.1111/cge.13375. Epub 2018 May 23. Review.

PMID:
29722020
13.

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Unolt M, Versacci P, Anaclerio S, Lambiase C, Calcagni G, Trezzi M, Carotti A, Crowley TB, Zackai EH, Goldmuntz E, Gaynor JW, Digilio MC, McDonald-McGinn DM, Marino B.

Am J Med Genet A. 2018 Oct;176(10):2087-2098. doi: 10.1002/ajmg.a.38662. Epub 2018 Apr 16. Review.

14.

Data on 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.

Data Brief. 2017 Dec 2;16:649-654. doi: 10.1016/j.dib.2017.11.085. eCollection 2018 Feb.

15.

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.

Heart Fail Clin. 2018 Apr;14(2):225-235. doi: 10.1016/j.hfc.2017.12.005. Review.

PMID:
29525650
16.

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.

Int J Cardiol. 2017 Oct 15;245:92-98. doi: 10.1016/j.ijcard.2017.07.068. Epub 2017 Jul 21.

PMID:
28768581
17.

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.

Expert Rev Mol Diagn. 2017 Sep;17(9):861-870. doi: 10.1080/14737159.2017.1360766. Epub 2017 Aug 3. Review.

PMID:
28745539
18.

Difficult diagnosis of atypical kawasaki disease in an infant younger than six months: a case report.

Petrarca L, Nenna R, Versacci P, Frassanito A, Cangiano G, Nicolai A, Scalercio F, Russo LL, Papoff P, Moretti C, Midulla F.

Ital J Pediatr. 2017 Mar 8;43(1):30. doi: 10.1186/s13052-017-0345-0.

19.

Association of Nonalcoholic Fatty Liver Disease with Subclinical Cardiovascular Changes: A Systematic Review and Meta-Analysis.

Bonci E, Chiesa C, Versacci P, Anania C, Silvestri L, Pacifico L.

Biomed Res Int. 2015;2015:213737. doi: 10.1155/2015/213737. Epub 2015 Jul 26. Review.

20.

Reply to: Comment on Long-Term Renal Function in Unilateral Non-Syndromic Renal Tumor Survivors Treated According to International Society of Pediatric Oncology Protocols.

Schiavetti A, Altavista P, De Luca L, Andreoli G, Megaro G, Versacci P.

Pediatr Blood Cancer. 2015 Dec;62(12):2250. doi: 10.1002/pbc.25666. Epub 2015 Jul 14. No abstract available.

PMID:
26175106
21.

Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndrome.

Digilio MC, Versacci P, Bernardini L, Novelli A, Marino B, Dallapiccola B.

Eur J Med Genet. 2015 Aug;58(8):406-8. doi: 10.1016/j.ejmg.2015.05.005. Epub 2015 Jul 2. Review. No abstract available.

PMID:
26141236
22.

A double-blind, placebo-controlled randomized trial to evaluate the efficacy of docosahexaenoic acid supplementation on hepatic fat and associated cardiovascular risk factors in overweight children with nonalcoholic fatty liver disease.

Pacifico L, Bonci E, Di Martino M, Versacci P, Andreoli G, Silvestri LM, Chiesa C.

Nutr Metab Cardiovasc Dis. 2015 Aug;25(8):734-41. doi: 10.1016/j.numecd.2015.04.003. Epub 2015 Apr 25.

PMID:
26026214
23.

Long-term renal function in unilateral non-syndromic renal tumor survivors treated according to International Society of Pediatric Oncology protocols.

Schiavetti A, Altavista P, De Luca L, Andreoli G, Megaro G, Versacci P.

Pediatr Blood Cancer. 2015 Sep;62(9):1637-44. doi: 10.1002/pbc.25558. Epub 2015 Apr 20.

PMID:
25893525
24.

Surgical outcomes for patients with Turner syndrome.

Versacci P, Silvestri LM, Maiolo S, Marino B.

Pediatr Cardiol. 2014 Aug;35(6):1080-1. doi: 10.1007/s00246-014-0913-7. Epub 2014 May 7. No abstract available.

PMID:
24801675
25.

Transposition of great arteries: new insights into the pathogenesis.

Unolt M, Putotto C, Silvestri LM, Marino D, Scarabotti A, Valerio Massaccesi, Caiaro A, Versacci P, Marino B.

Front Pediatr. 2013 Jun 6;1:11. doi: 10.3389/fped.2013.00011. Review.

26.

Syndromic non-compaction of the left ventricle: associated chromosomal anomalies.

Digilio MC, Bernardini L, Gagliardi MG, Versacci P, Baban A, Capolino R, Dentici ML, Roberti MC, Angioni A, Novelli A, Marino B, Dallapiccola B.

Clin Genet. 2013 Oct;84(4):362-7. doi: 10.1111/cge.12069. Epub 2012 Dec 28.

PMID:
23210894
27.

Beneficial effects of levosimendan in infants with sepsis-associated cardiac dysfunction: report of 2 cases.

Papoff P, Caresta E, Versacci P, Pinto R, Moretti C, Midulla F.

Pediatr Emerg Care. 2012 Oct;28(10):1062-5. doi: 10.1097/PEC.0b013e31826cebe6.

PMID:
23034494
28.

Atrioventricular canal defect in patients with RASopathies.

Digilio MC, Romana Lepri F, Dentici ML, Henderson A, Baban A, Roberti MC, Capolino R, Versacci P, Surace C, Angioni A, Tartaglia M, Marino B, Dallapiccola B.

Eur J Hum Genet. 2013 Feb;21(2):200-4. doi: 10.1038/ejhg.2012.145. Epub 2012 Jul 11.

29.

Ebstein's anomaly in a child with osteogenesis imperfecta type I.

D'Eufemia P, Celli M, Versacci P, Zambrano A, Lodato V, Persiani P, Sangiorgi L.

Clin Cases Miner Bone Metab. 2011 May;8(2):50-1.

30.

Respiratory complications in patients with heterotaxy syndrome.

Martucci V, Marino D, Versacci P.

J Thorac Cardiovasc Surg. 2012 Mar;143(3):759; author reply 759-60. doi: 10.1016/j.jtcvs.2011.10.086. No abstract available.

31.

Spiral shapes in heart and shells: when form and function do matter.

Amodeo A, Oliverio M, Versacci P, Marino B.

Eur J Cardiothorac Surg. 2012 Mar;41(3):473-5. doi: 10.1093/ejcts/ezr149. Epub 2012 Jan 16. No abstract available.

PMID:
22253372
32.

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.

Mol Syndromol. 2011 Sep;1(6):282-289. Epub 2011 Sep 14.

33.

Right-dominant unbalanced atrioventricular canal and genetic syndromes.

Martucci V, Marino D, Versacci P.

Am J Cardiol. 2011 Nov 15;108(10):1521. doi: 10.1016/j.amjcard.2011.08.001. No abstract available.

PMID:
22040721
34.

Influence of physical activity on cardiorespiratory fitness in children after renal transplantation.

Lubrano R, Tancredi G, Bellelli E, Gentile I, Scateni S, Masciangelo R, De Castro G, Versacci P, Elli M.

Nephrol Dial Transplant. 2012 Apr;27(4):1677-81. doi: 10.1093/ndt/gfr434. Epub 2011 Aug 8.

PMID:
21825306
35.

Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1.

Digilio MC, Bernardini L, Lepri F, Giuffrida MG, Guida V, Baban A, Versacci P, Capolino R, Torres B, De Luca A, Novelli A, Marino B, Dallapiccola B.

Am J Med Genet A. 2011 Sep;155A(9):2196-202. doi: 10.1002/ajmg.a.34131. Epub 2011 Aug 3.

PMID:
21815254
36.

The heart and shell. Anatomical and genetic similarities.

Versacci P, Digilio MC, Oliverio M, Dallapiccola B, Marino B.

Am Heart J. 2011 Apr;161(4):647-9. doi: 10.1016/j.ahj.2010.12.023. No abstract available.

PMID:
21473961
37.

Cardiopulmonary response to exercise and cardiac assessment in patients with turner syndrome.

Tancredi G, Versacci P, Pasquino AM, Vittucci AC, Pucarelli I, Cappa M, Di Mambro C, Marino B.

Am J Cardiol. 2011 Apr 1;107(7):1076-82. doi: 10.1016/j.amjcard.2010.11.035.

PMID:
21419888
38.

Surgical results in patients with cardiac defects and del 22q11.2 syndrome.

Versacci P, Michielon G, Carotti A, Marino B.

Am J Cardiol. 2011 Jan 15;107(2):337-8. doi: 10.1016/j.amjcard.2010.10.034. No abstract available.

PMID:
21211615
39.

Truncus arteriosus with unilateral absence of the left proximal pulmonary artery and DiGeorge syndrome.

Casinelli E, Boccuzzi E, Versacci P, Marino B.

J Card Surg. 2011 Sep;26(5):559. doi: 10.1111/j.1540-8191.2010.01124.x. Epub 2010 Sep 29. No abstract available.

PMID:
20880083
40.

Isolated cleft of the mitral valve: its pathogenic relationship with endocardial cushion defects.

Boccuzzi E, Casinelli E, Versacci P, Marino B.

Tex Heart Inst J. 2010;37(4):503; author reply 503. No abstract available.

41.

Shells and heart: are human laterality and chirality of snails controlled by the same maternal genes?

Oliverio M, Digilio MC, Versacci P, Dallapiccola B, Marino B.

Am J Med Genet A. 2010 Oct;152A(10):2419-25. doi: 10.1002/ajmg.a.33655. Review.

PMID:
20830800
42.

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.

De Luca A, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici ML, Vergara P, De Zorzi A, Versacci P, Digilio MC, Marino B, Dallapiccola B.

Clin Genet. 2011 Aug;80(2):184-90. doi: 10.1111/j.1399-0004.2010.01523.x. Epub 2010 Aug 2.

PMID:
20807224
43.

Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart disease.

Guida V, Lepri F, Vijzelaar R, De Zorzi A, Versacci P, Digilio MC, Marino B, De Luca A, Dallapiccola B.

Dis Markers. 2010;28(5):287-92. doi: 10.3233/DMA-2010-0703.

44.

The heart of Santa Rosa.

D'Anastasio R, Di Silvestro G, Versacci P, Capasso L, Marino B.

Lancet. 2010 Jun 19;375(9732):2168. doi: 10.1016/S0140-6736(09)60729-7. Epub 2010 Jun 11. No abstract available.

PMID:
20541795
45.

Might there be an association between polycystic kidney disease and noncompaction of the ventricular myocardium?

Lubrano R, Versacci P, Guido G, Bellelli E, Andreoli G, Elli M.

Nephrol Dial Transplant. 2009 Dec;24(12):3884-6. doi: 10.1093/ndt/gfp499. Epub 2009 Sep 17.

PMID:
19762607
46.

The role of terlipressin in the management of severe pulmonary hypertension in congenital diaphragmatic hernia.

Papoff P, Caresta E, Versacci P, Grossi R, Midulla F, Moretti C.

Paediatr Anaesth. 2009 Aug;19(8):805-6. doi: 10.1111/j.1460-9592.2009.03078.x. No abstract available.

PMID:
19624374
47.

3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs.

Digilio MC, Bernardini L, Mingarelli R, Capolino R, Capalbo A, Giuffrida MG, Versacci P, Novelli A, Dallapiccola B.

Am J Med Genet A. 2009 Aug;149A(8):1777-81. doi: 10.1002/ajmg.a.32965.

PMID:
19610115
48.

Paroxysmal reciprocating supraventricular tachycardia in infants: electrophysiologically guided medical treatment and long-term evolution of the re-entry circuit.

Drago F, Silvetti MS, De Santis A, Marcora S, Fazio G, Anaclerio S, Versacci P, Iodice F, Di Ciommo V.

Europace. 2008 May;10(5):629-35. doi: 10.1093/europace/eun069. Epub 2008 Apr 2.

PMID:
18385122
49.

Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.

Limongelli G, Pacileo G, Marino B, Digilio MC, Sarkozy A, Elliott P, Versacci P, Calabro P, De Zorzi A, Di Salvo G, Syrris P, Patton M, McKenna WJ, Dallapiccola B, Calabro R.

Am J Cardiol. 2007 Aug 15;100(4):736-41. Epub 2007 Jun 27.

PMID:
17697839
50.

Renal and cardiovascular effects of angiotensin-converting enzyme inhibitor plus angiotensin II receptor antagonist therapy in children with proteinuria.

Lubrano R, Soscia F, Elli M, Ventriglia F, Raggi C, Travasso E, Scateni S, Di Maio V, Versacci P, Masciangelo R, Romero S.

Pediatrics. 2006 Sep;118(3):e833-8. Epub 2006 Aug 21.

PMID:
16923922

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