Unolt M - Search Results

1

Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

Óskarsdóttir S, Boot E, Crowley TB, Loo JCY, Arganbright JM, Armando M, Baylis AL, Breetvelt EJ, Castelein RM, Chadehumbe M, Cielo CM, de Reuver S, Eliez S, Fiksinski AM, Forbes BJ, Gallagher E, Hopkins SE, Jackson OA, Levitz-Katz L, Klingberg G, Lambert MP, Marino B, Mascarenhas MR, Moldenhauer J, Moss EM, Nowakowska BA, Orchanian-Cheff A, Putotto C, Repetto GM, Schindewolf E, Schneider M, Solot CB, Sullivan KE, Swillen A, Unolt M, Van Batavia JP, Vingerhoets C, Vorstman J, Bassett AS, McDonald-McGinn DM. Óskarsdóttir S, et al. Among authors: unolt m. Genet Med. 2023 Mar;25(3):100338. doi: 10.1016/j.gim.2022.11.006. Epub 2023 Feb 2. Genet Med. 2023. PMID: 36729053 Free article. Review.

2

Atrioventricular septal defect prognosis for patients with Down syndrome.

Unolt M, Putotto C, Marino D. Unolt M, et al. Pediatr Cardiol. 2012 Dec;33(8):1476. doi: 10.1007/s00246-012-0491-5. Epub 2012 Aug 25. Pediatr Cardiol. 2012. PMID: 22923010 No abstract available.

3

Smith-Lemli-Opitz syndrome, cardiac defects, and spleen anomalies.

Putotto C, Unolt M, Marino D. Putotto C, et al. Among authors: unolt m. Eur J Med Genet. 2013 Feb;56(2):123. doi: 10.1016/j.ejmg.2012.09.008. Epub 2012 Sep 27. Eur J Med Genet. 2013. PMID: 23022980 No abstract available.

4

Congenital heart disease, genetic syndromes, and major noncardiac malformations.

Unolt M, Putotto C, Marino D. Unolt M, et al. Eur J Pediatr. 2012 Dec;171(12):1861; author reply 1863. doi: 10.1007/s00431-012-1838-x. Epub 2012 Oct 2. Eur J Pediatr. 2012. PMID: 23052614 No abstract available.

5

Aortic arch interruption without ductus arteriosus and no ventricular septal defect.

Putotto C, Unolt M, Marino D. Putotto C, et al. Among authors: unolt m. J Thorac Cardiovasc Surg. 2013 Jan;145(1):311. doi: 10.1016/j.jtcvs.2012.08.076. J Thorac Cardiovasc Surg. 2013. PMID: 23244265 Free article. No abstract available.

6

Double outlet right ventricle versus aortic dextroposition: morphologically distinct defects.

Restivo A, Unolt M, Putotto C, Marino B. Restivo A, et al. Among authors: unolt m. Anat Rec (Hoboken). 2013 Apr;296(4):559-63. doi: 10.1002/ar.22657. Epub 2013 Feb 9. Anat Rec (Hoboken). 2013. PMID: 23401466 Free article.

7

Double-orifice left atrioventricular valve in patients with atrioventricular septal defect with and without down syndrome.

Unolt M, Putotto C, Marino D. Unolt M, et al. Ann Thorac Surg. 2013 May;95(5):1843-4. doi: 10.1016/j.athoracsur.2012.11.048. Ann Thorac Surg. 2013. PMID: 23608283 No abstract available.

8

Double-outlet left ventricle with L-malposition of the great arteries and subpulmonary ventricular septal defect.

Putotto C, Unolt M, Marino D. Putotto C, et al. Among authors: unolt m. Pediatr Cardiol. 2013 Aug;34(6):1521. doi: 10.1007/s00246-013-0722-4. Epub 2013 May 21. Pediatr Cardiol. 2013. PMID: 23689608 No abstract available.

9

Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome.

Radio FC, Digilio MC, Capolino R, Dentici ML, Unolt M, Alesi V, Novelli A, Marino B, Dallapiccola B. Radio FC, et al. Among authors: unolt m. Am J Med Genet A. 2016 Mar;170(3):661-4. doi: 10.1002/ajmg.a.37503. Epub 2015 Dec 21. Am J Med Genet A. 2016. PMID: 26686844

10

Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

Unolt M, DiCairano L, Schlechtweg K, Barry J, Howell L, Kasperski S, Nance M, Adzick NS, Zackai EH, McDonald-McGinn DM. Unolt M, et al. Am J Med Genet A. 2017 Jan;173(1):135-142. doi: 10.1002/ajmg.a.37980. Epub 2016 Sep 28. Am J Med Genet A. 2017. PMID: 27682988

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