Castaldo G - Search Results

1

Clinical expression of cystic fibrosis in a large cohort of Italian siblings.

Terlizzi V, Lucarelli M, Salvatore D, Angioni A, Bisogno A, Braggion C, Buzzetti R, Carnovale V, Casciaro R, Castaldo G, Cirilli N, Collura M, Colombo C, Di Lullo AM, Elce A, Lucidi V, Madarena E, Padoan R, Quattrucci S, Raia V, Seia M, Termini L, Zarrilli F. Terlizzi V, et al. Among authors: castaldo g. BMC Pulm Med. 2018 Dec 22;18(1):196. doi: 10.1186/s12890-018-0766-6. BMC Pulm Med. 2018. PMID: 30577776 Free PMC article.

2

Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.

Salvatore F, Scudiero O, Castaldo G. Salvatore F, et al. Among authors: castaldo g. Am J Med Genet. 2002 Jul 22;111(1):88-95. doi: 10.1002/ajmg.10461. Am J Med Genet. 2002. PMID: 12124743 Review.

3

Molecular diagnosis of cystic fibrosis: comparison of four analytical procedures.

Tomaiuolo R, Spina M, Castaldo G. Tomaiuolo R, et al. Among authors: castaldo g. Clin Chem Lab Med. 2003 Jan;41(1):26-32. doi: 10.1515/CCLM.2003.006. Clin Chem Lab Med. 2003. PMID: 12636046

4

Cystic fibrosis presenting as metabolic alkalosis in a boy with the rare D579G mutation.

Salvatore D, Tomaiuolo R, Abate R, Vanacore B, Manieri S, Mirauda MP, Scavone A, Schiavo MV, Castaldo G, Salvatore F. Salvatore D, et al. Among authors: castaldo g. J Cyst Fibros. 2004 Jun;3(2):135-6. doi: 10.1016/j.jcf.2004.01.007. J Cyst Fibros. 2004. PMID: 15463898 Free article.

5

Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation.

Polizzi A, Francavilla R, Castaldo G, Santostasi T, Tomaiuolo R, Manca A, De Robertis F, Mappa L, Oliverio FP, Salvatore F, Rigillo N. Polizzi A, et al. Among authors: castaldo g. Am J Med Genet A. 2005 Feb 1;132A(4):434-40. doi: 10.1002/ajmg.a.30493. Am J Med Genet A. 2005. PMID: 15633186

6

Isolated elevated sweat chloride concentrations in the presence of the rare mutation S1455X: an extremely mild form of CFTR dysfunction.

Salvatore D, Tomaiuolo R, Vanacore B, Elce A, Castaldo G, Salvatore F. Salvatore D, et al. Among authors: castaldo g. Am J Med Genet A. 2005 Mar 1;133A(2):207-8. doi: 10.1002/ajmg.a.30518. Am J Med Genet A. 2005. PMID: 15666307

7

Phenotypic discordance in three siblings affected by atypical cystic fibrosis with the F508del/D614G genotype.

Castaldo G, Tomaiuolo R, Vanacore B, Ferrara P, DEL Vecchio S, Carnovale V, Abete P, Rengo F, Salvatore F. Castaldo G, et al. J Cyst Fibros. 2006 Aug;5(3):193-5. doi: 10.1016/j.jcf.2005.12.001. Epub 2006 Feb 14. J Cyst Fibros. 2006. PMID: 16478680 Free article.

8

Haemophilia A: molecular insights.

Castaldo G, D'Argenio V, Nardiello P, Zarrilli F, Sanna V, Rocino A, Coppola A, Di Minno G, Salvatore F. Castaldo G, et al. Clin Chem Lab Med. 2007;45(4):450-61. doi: 10.1515/CCLM.2007.093. Clin Chem Lab Med. 2007. PMID: 17439320 Review.

9

Three novel CFTR polymorphic repeats improve segregation analysis for cystic fibrosis.

Elce A, Boccia A, Cardillo G, Giordano S, Tomaiuolo R, Paolella G, Castaldo G. Elce A, et al. Among authors: castaldo g. Clin Chem. 2009 Jul;55(7):1372-9. doi: 10.1373/clinchem.2008.119545. Epub 2009 May 14. Clin Chem. 2009. PMID: 19443567 Free article.

10

Genetic modifiers of liver disease in cystic fibrosis.

Bartlett JR, Friedman KJ, Ling SC, Pace RG, Bell SC, Bourke B, Castaldo G, Castellani C, Cipolli M, Colombo C, Colombo JL, Debray D, Fernandez A, Lacaille F, Macek M Jr, Rowland M, Salvatore F, Taylor CJ, Wainwright C, Wilschanski M, Zemková D, Hannah WB, Phillips MJ, Corey M, Zielenski J, Dorfman R, Wang Y, Zou F, Silverman LM, Drumm ML, Wright FA, Lange EM, Durie PR, Knowles MR; Gene Modifier Study Group. Bartlett JR, et al. Among authors: castaldo g. JAMA. 2009 Sep 9;302(10):1076-83. doi: 10.1001/jama.2009.1295. JAMA. 2009. PMID: 19738092 Free PMC article.

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