Dallapiccola B - Search Results

1

Manco M, Dallapiccola B. Manco M, et al. Among authors: dallapiccola b. Pediatrics. 2012 Jul;130(1):123-33. doi: 10.1542/peds.2011-2717. Epub 2012 Jun 4. Pediatrics. 2012. PMID: 22665408 Review.

2

Early-life gut microbiota under physiological and pathological conditions: the central role of combined meta-omics-based approaches.

Del Chierico F, Vernocchi P, Bonizzi L, Carsetti R, Castellazzi AM, Dallapiccola B, de Vos W, Guerzoni ME, Manco M, Marseglia GL, Muraca M, Roncada P, Salvatori G, Signore F, Urbani A, Putignani L. Del Chierico F, et al. Among authors: dallapiccola b. J Proteomics. 2012 Aug 3;75(15):4580-7. doi: 10.1016/j.jprot.2012.02.018. Epub 2012 Feb 23. J Proteomics. 2012. PMID: 22387117 Review.

3

Reference ranges of HOMA-IR in normal-weight and obese young Caucasians.

Shashaj B, Luciano R, Contoli B, Morino GS, Spreghini MR, Rustico C, Sforza RW, Dallapiccola B, Manco M. Shashaj B, et al. Among authors: dallapiccola b. Acta Diabetol. 2016 Apr;53(2):251-60. doi: 10.1007/s00592-015-0782-4. Epub 2015 Jun 13. Acta Diabetol. 2016. PMID: 26070771

4

Percentiles of serum uric acid and cardiometabolic abnormalities in obese Italian children and adolescents.

Luciano R, Shashaj B, Spreghini M, Del Fattore A, Rustico C, Wietrzykowska Sforza R, Morino GS, Dallapiccola B, Manco M. Luciano R, et al. Among authors: dallapiccola b. Ital J Pediatr. 2017 Jan 3;43(1):3. doi: 10.1186/s13052-016-0321-0. Ital J Pediatr. 2017. PMID: 28049502 Free PMC article.

5

Association of Bright Liver With the PNPLA3 I148M Gene Variant in 1-Year-Old Toddlers.

Bedogni G, De Matteis G, Fabrizi M, Alisi A, Crudele A, Pizzolante F, Signore F, Dallapiccola B, Nobili V, Manco M. Bedogni G, et al. Among authors: dallapiccola b. J Clin Endocrinol Metab. 2019 Jun 1;104(6):2163-2170. doi: 10.1210/jc.2018-01998. J Clin Endocrinol Metab. 2019. PMID: 30649436

6

Relationship between glucose homeostasis and obesity in early life-a study of Italian children and adolescents.

Balkhiyarova Z, Luciano R, Kaakinen M, Ulrich A, Shmeliov A, Bianchi M, Chioma L, Dallapiccola B, Prokopenko I, Manco M. Balkhiyarova Z, et al. Among authors: dallapiccola b. Hum Mol Genet. 2022 Mar 3;31(5):816-826. doi: 10.1093/hmg/ddab287. Hum Mol Genet. 2022. PMID: 34590674 Free PMC article.

7

Noonan syndrome: structural abnormalities of the mitral valve causing subaortic obstruction.

Marino B, Gagliardi MG, Digilio MC, Polletta B, Grazioli S, Agostino D, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: dallapiccola b. Eur J Pediatr. 1995 Dec;154(12):949-52. doi: 10.1007/BF01958636. Eur J Pediatr. 1995. PMID: 8801101

8

Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal.

Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: dallapiccola b. J Pediatr. 1999 Dec;135(6):703-6. doi: 10.1016/s0022-3476(99)70088-0. J Pediatr. 1999. PMID: 10586172

9

PTPN11 gene mutations: linking the Gln510Glu mutation to the "LEOPARD syndrome phenotype".

Digilio MC, Sarkozy A, Pacileo G, Limongelli G, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: dallapiccola b. Eur J Pediatr. 2006 Nov;165(11):803-5. doi: 10.1007/s00431-006-0163-7. Epub 2006 May 30. Eur J Pediatr. 2006. PMID: 16733669

10

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. Among authors: dallapiccola b. 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.

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