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Page 1
Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions.
Paracchini V, Seia M, Coviello D, Porcaro L, Costantino L, Capasso P, Degiorgio D, Padoan R, Corbetta C, Claut L, Costantini D, Colombo C. Paracchini V, et al. Among authors: costantini d. Clin Genet. 2008 Apr;73(4):346-52. doi: 10.1111/j.1399-0004.2007.00957.x. Epub 2008 Feb 13. Clin Genet. 2008. PMID: 18279436
Benefits of breastfeeding in cystic fibrosis: a single-centre follow-up survey.
Colombo C, Costantini D, Zazzeron L, Faelli N, Russo MC, Ghisleni D, Gatelli I, Giovannini M, Riva E, Zetterström R, Agostoni C. Colombo C, et al. Among authors: costantini d. Acta Paediatr. 2007 Aug;96(8):1228-32. doi: 10.1111/j.1651-2227.2007.00397.x. Epub 2007 Jun 21. Acta Paediatr. 2007. PMID: 17590186
Spontaneous hypoglycemia in patients with cystic fibrosis.
Battezzati A, Battezzati PM, Costantini D, Seia M, Zazzeron L, Russo MC, Daccò V, Bertoli S, Crosignani A, Colombo C. Battezzati A, et al. Among authors: costantini d. Eur J Endocrinol. 2007 Mar;156(3):369-76. doi: 10.1530/eje.1.02344. Eur J Endocrinol. 2007. PMID: 17322497
A novel missense mutation (Y89C) in exon 3 of the CFTR (ABCC7) gene in a young male.
Padoan R, Costantini D, Russo MC, Ambrosioni A, Fiori S, Prandoni S, Cantù-Rajnoldi A, Seia M, Giunta A. Padoan R, et al. Among authors: costantini d. Hum Mutat. 2000 May;15(5):486. doi: 10.1002/(SICI)1098-1004(200005)15:5<486::AID-HUMU25>3.0.CO;2-S. Hum Mutat. 2000. PMID: 10790225 No abstract available.
Paranasal mucoceles in children with cystic fibrosis.
Di Cicco M, Costantini D, Padoan R, Colombo C. Di Cicco M, et al. Among authors: costantini d. Int J Pediatr Otorhinolaryngol. 2005 Oct;69(10):1407-13. doi: 10.1016/j.ijporl.2005.03.037. Int J Pediatr Otorhinolaryngol. 2005. PMID: 15939485
238 results