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Items: 42

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.

SOS1 mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature review.

Baban A, Olivini N, Lepri FR, Calì F, Mucciolo M, Digilio MC, Calcagni G, di Mambro C, Dallapiccola B, Adorisio R, Novelli A, Drago F.

Am J Med Genet A. 2019 Oct;179(10):2083-2090. doi: 10.1002/ajmg.a.61312. Epub 2019 Aug 1.

PMID:
31368652
3.

Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations.

Calcagni G, Digilio MC, Marino B, Tartaglia M.

Orphanet J Rare Dis. 2019 Jul 5;14(1):163. doi: 10.1186/s13023-019-1151-0.

4.

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.

5.

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience.

Baban A, Cantarutti N, Adorisio R, Lombardi R, Calcagni G, Piano Mortari E, Dallapiccola B, Marino B, Iorio FS, Carsetti R, Digilio MC, Giannico S, Drago F, Carotti A.

Int J Cardiol. 2018 Oct 1;268:100-105. doi: 10.1016/j.ijcard.2018.02.050.

PMID:
30041775
6.

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
7.

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.

8.

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
9.

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.

10.

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.

11.

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
12.

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
13.

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
14.

Black holes in multi-fractional and Lorentz-violating models.

Calcagni G, Rodríguez Fernández D, Ronco M.

Eur Phys J C Part Fields. 2017;77(5):335. doi: 10.1140/epjc/s10052-017-4879-5. Epub 2017 May 20.

15.

Paroxysmal atrioventricular block after heart transplantation in children: an early sign of rejection?

Grutter G, Alfieri S, Calcagni G, Castelluzzo MA, Silvetti MS, Parisi F, Drago F.

Pediatr Transplant. 2016 Dec;20(8):1164-1167. doi: 10.1111/petr.12832. Epub 2016 Oct 14.

PMID:
27743416
16.

Congenital heart defects in Noonan syndrome and RIT1 mutation.

Calcagni G, Baban A, Lepri FR, Marino B, Tartaglia M, Digilio MC.

Genet Med. 2016 Dec;18(12):1320. doi: 10.1038/gim.2016.137. Epub 2016 Sep 29. No abstract available.

PMID:
27684039
17.

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.

Am J Med Genet A. 2016 Mar;170(3):665-9. doi: 10.1002/ajmg.a.37505. Epub 2015 Dec 21.

PMID:
26686981
18.

Multifaceted approach to plastic bronchitis.

Calcagni G, Di Carlo D, Grutter G.

Ann Thorac Surg. 2015 Mar;99(3):1110-1. doi: 10.1016/j.athoracsur.2014.09.055. No abstract available.

PMID:
25742853
19.

[Informed consent in pediatric cardiology and cardiac surgery].

Albanese SB, Sellaroni V, Montis S, Calcagni G, Baban A, Santoro F, Pongiglione G, Calabrò MP; nome del Consent Committee.

G Ital Cardiol (Rome). 2013 Sep;14(9):613-21. doi: 10.1714/1311.14486. Italian.

PMID:
23903280
20.

Diffusion in multiscale spacetimes.

Calcagni G.

Phys Rev E Stat Nonlin Soft Matter Phys. 2013 Jan;87(1):012123. Epub 2013 Jan 18.

PMID:
23410299
21.

Observational constraints on loop quantum cosmology.

Bojowald M, Calcagni G, Tsujikawa S.

Phys Rev Lett. 2011 Nov 18;107(21):211302. Epub 2011 Nov 15.

PMID:
22181869
22.

Fractal universe and quantum gravity.

Calcagni G.

Phys Rev Lett. 2010 Jun 25;104(25):251301. Epub 2010 Jun 24.

PMID:
20867360
23.

Cardiac tamponade and bilateral pleural effusion in a very low birth weight infant.

Haass C, Sorrentino E, Tempera A, Consigli C, De Paola D, Calcagni G, Piastra M, Finocchi M.

J Matern Fetal Neonatal Med. 2009 Feb;22(2):137-9. doi: 10.1080/14767050802509561.

PMID:
19253161
24.

Coronary myocardial bridging in Noonan syndrome: definitive diagnosis with high-resolution CT.

Leye M, Calcagni G, Brunelle F, Bonnet D, Sidi D, Ou P.

Br J Radiol. 2009 Jan;82(973):e8-10. doi: 10.1259/bjr/35749180.

PMID:
19095812
25.

Right superior vena cava draining into the left atrium.

Calcagni G, Batisse A, Vouhé P, Sidi D, Bonnet D, Ou P.

Pediatr Radiol. 2008 Aug;38(8):912-4. doi: 10.1007/s00247-008-0897-7. Epub 2008 Jun 21.

PMID:
18568344
26.

Arterial aneurysms and tuberous sclerosis: a classic but little known association.

Calcagni G, Gesualdo F, Tamisier D, Brunelle F, Sidi D, Ou P.

Pediatr Radiol. 2008 Jul;38(7):795-7. doi: 10.1007/s00247-008-0813-1. Epub 2008 Apr 18.

PMID:
18421453
27.

CT demonstration of "chicken trachea" resulting from complete cartilaginous rings of the trachea in ring-sling complex.

Calcagni G, Brunelle F, Vouhe P, Bonnet D, Sidi D, Ou P.

Pediatr Radiol. 2008 Jul;38(7):798-800. doi: 10.1007/s00247-008-0814-0. Epub 2008 Apr 17.

PMID:
18418589
28.

An unusual case of left aberrant innominate artery with right aortic arch: evaluation with high-resolution CT.

Calcagni G, Gesualdo F, Brunelle F, Ou P.

Pediatr Radiol. 2008 Jan;38(1):115-7. Epub 2007 Oct 2.

PMID:
17909783
29.

Pediatric coronary artery bypass after arterial switch operation: noninvasive evaluation with ECG-gated 64-slice CT in routine practice.

Jemmali M, Marini D, Calcagni G, Brunelle F, Sidi D, Bonnet D, Ou P.

Ann Thorac Surg. 2007 Oct;84(4):1398-9.

PMID:
17889015
30.

Percutaneous treatment of aorto-pulmonary window in a one year old child.

Marini D, Calcagni G, Ou P, Bonnet D, Agnoletti G.

Int J Cardiol. 2008 Oct 13;129(3):e91-3. Epub 2007 Sep 14. No abstract available.

PMID:
17869356
31.

Unusual systemic venous return with absence of superior caval veins.

Ou P, Calcagni G, Marini D, Le Bidois J, Gallo P, Brunelle F, Bonnet D.

J Thorac Cardiovasc Surg. 2007 May;133(5):1368-9. No abstract available.

32.

Atresia of the coronary sinus ostium: surgical implications.

Calcagni G, Ou P, Marini D, Bonnet D, Agnoletti G.

Int J Cardiol. 2007 Apr 4;116(3):e92-4. Epub 2006 Nov 14.

PMID:
17107725
33.

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

Calcagni G, Digilio MC, Sarkozy A, Dallapiccola B, Marino B.

Eur J Pediatr. 2007 Feb;166(2):111-6. Epub 2006 Nov 8. Review.

PMID:
17091259
34.

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.

Clin Dysmorphol. 2006 Oct;15(4):203-6.

PMID:
16957472
35.

Three-dimensional CT scanning: a new diagnostic modality in congenital heart disease.

Ou P, Celermajer DS, Calcagni G, Brunelle F, Bonnet D, Sidi D.

Heart. 2007 Aug;93(8):908-13. Epub 2006 Sep 4. Review.

36.

Outcome in Down syndrome fetuses with cardiac anomalies.

Marino B, Diociaiuti L, Calcagni G, Mastroiacovo P.

Am J Med Genet A. 2004 Jul 1;128A(1):101-2; author reply 103. No abstract available.

PMID:
15211668
37.

[Cardiac defects in Mexican children with down syndrome].

Marino B, Calcagni G, Digilio C.

Rev Esp Cardiol. 2004 May;57(5):482; author reply 482. Spanish. No abstract available.

38.

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.

J Am Soc Echocardiogr. 2004 Apr;17(4):330-1. No abstract available.

PMID:
15044865
39.

[ACTION OF HIGH ENERGY BETA PARTICLES (3 MEV-9 MEV) ON THE MOTOR FUNCTION OF MICROBIAL CELLS OF VARIOUS SPECIES].

FIGURA V, CALCAGNI G.

Nuovi Ann Ig Microbiol. 1964 Mar-Apr;15:144-9. Italian. No abstract available.

PMID:
14200874
40.

[Action of x-rays (45kV-lmA) on the motor function of microbial cells of various species].

FIGURA V, CALCAGNI G.

Nuovi Ann Ig Microbiol. 1961 Nov-Dec;12:499-507. Italian. No abstract available.

PMID:
13945124
41.

[Action of x-rays (45kV-lmA) on the reproductive function of microbial cells of various species].

FIGURA V, CALCAGNI G.

Nuovi Ann Ig Microbiol. 1961 Nov-Dec;12:508-16. Italian. No abstract available.

PMID:
13945123
42.

[Hygienic and bacteriologic control of ice cream].

MAIDA S, ADORNO L, CALCAGNI G.

Nuovi Ann Ig Microbiol. 1953 Nov-Dec;4(6):467-73. Undetermined Language. No abstract available.

PMID:
13145116

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