Peca D[au] - Search Results

Year	Number of Results
2008	1
2011	2
2012	1
2013	4
2014	2
2015	3
2016	2
2019	1
2024	0

1

ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system.

Peca D, Cutrera R, Masotti A, Boldrini R, Danhaive O. Peca D, et al. Biochem Soc Trans. 2015 Oct;43(5):913-9. doi: 10.1042/BST20150100. Biochem Soc Trans. 2015. PMID: 26517903 Free article. Review.

2

Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertension.

Galambos C, Mullen MP, Shieh JT, Schwerk N, Kielt MJ, Ullmann N, Boldrini R, Stucin-Gantar I, Haass C, Bansal M, Agrawal PB, Johnson J, Peca D, Surace C, Cutrera R, Pauciulo MW, Nichols WC, Griese M, Ivy D, Abman SH, Austin ED, Danhaive O. Galambos C, et al. Among authors: peca d. Eur Respir J. 2019 Aug 22;54(2):1801965. doi: 10.1183/13993003.01965-2018. Print 2019 Aug. Eur Respir J. 2019. PMID: 31151956 Free article.

3

Impaired surfactant protein B synthesis in infants with congenital diaphragmatic hernia.

Cogo PE, Simonato M, Danhaive O, Verlato G, Cobellis G, Savignoni F, Peca D, Baritussio A, Carnielli VP. Cogo PE, et al. Among authors: peca d. Eur Respir J. 2013 Mar;41(3):677-82. doi: 10.1183/09031936.00032212. Epub 2012 Jun 14. Eur Respir J. 2013. PMID: 22700843 Free article.

4

Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.

Peca D, Boldrini R, Johannson J, Shieh JT, Citti A, Petrini S, Salerno T, Cazzato S, Testa R, Messina F, Onofri A, Cenacchi G, Westermark P, Ullmann N, Cogo P, Cutrera R, Danhaive O. Peca D, et al. Eur J Hum Genet. 2015 Aug;23(8):1033-41. doi: 10.1038/ejhg.2015.45. Epub 2015 Mar 18. Eur J Hum Genet. 2015. PMID: 25782673 Free PMC article.

5

Surfactant Protein C-associated interstitial lung disease; three different phenotypes of the same SFTPC mutation.

Salerno T, Peca D, Menchini L, Schiavino A, Boldrini R, Esposito F, Danhaive O, Cutrera R. Salerno T, et al. Among authors: peca d. Ital J Pediatr. 2016 Feb 29;42:23. doi: 10.1186/s13052-016-0235-x. Ital J Pediatr. 2016. PMID: 26925580 Free PMC article.

6

New ATP-binding cassette A3 mutation causing surfactant metabolism dysfunction pulmonary type 3.

Piersigilli F, Peca D, Campi F, Corsello M, Landolfo F, Boldrini R, Danhaive O, Dotta A. Piersigilli F, et al. Among authors: peca d. Pediatr Int. 2015 Oct;57(5):970-4. doi: 10.1111/ped.12673. Epub 2015 Aug 19. Pediatr Int. 2015. PMID: 26508177

7

Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.

Peca D, Boldrini R, Johannson J, Shieh JT, Citti A, Petrini S, Salerno T, Cazzato S, Testa R, Messina F, Onofri A, Cenacchi G, Westermark P, Ullmann N, Cogo P, Cutrera R, Danhaive O. Peca D, et al. Eur J Hum Genet. 2016 May;24(5):780. doi: 10.1038/ejhg.2016.12. Eur J Hum Genet. 2016. PMID: 27075519 Free PMC article. No abstract available.

8

Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review.

Citti A, Peca D, Petrini S, Cutrera R, Biban P, Haass C, Boldrini R, Danhaive O. Citti A, et al. Among authors: peca d. Ultrastruct Pathol. 2013 Oct;37(5):356-65. doi: 10.3109/01913123.2013.811454. Ultrastruct Pathol. 2013. PMID: 24047351

9

Bronchiectasis and severe respiratory insufficiency associated with a new surfactant protein C mutation.

Salerno T, Peca D, Rossi FP, Menchini L, Danhaive O, Cutrera R. Salerno T, et al. Among authors: peca d. Acta Paediatr. 2013 Jan;102(1):e1-2. doi: 10.1111/apa.12043. Acta Paediatr. 2013. PMID: 23025826 No abstract available.

10

Respiratory insufficiency in a newborn with congenital hypothyroidism due to a new mutation of TTF-1/NKX2.1 gene.

Salerno T, Peca D, Menchini L, Schiavino A, Petreschi F, Occasi F, Cogo P, Danhaive O, Cutrera R. Salerno T, et al. Among authors: peca d. Pediatr Pulmonol. 2014 Mar;49(3):E42-4. doi: 10.1002/ppul.22788. Epub 2013 Sep 2. Pediatr Pulmonol. 2014. PMID: 23997037

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