Castellani C - Search Results

1

Modulator Therapy in Cystic Fibrosis Patients with cis Variants in F508del Complex Allele: A Short-Term Observational Case Series.

Terlizzi V, Centrone C, Ferrari B, Castellani C, Gunawardena TNA, Taccetti G, Laselva O. Terlizzi V, et al. Among authors: castellani c. J Pers Med. 2022 Aug 31;12(9):1421. doi: 10.3390/jpm12091421. J Pers Med. 2022. PMID: 36143206 Free PMC article.

2

Ex vivo model predicted in vivo efficacy of CFTR modulator therapy in a child with rare genotype.

Terlizzi V, Amato F, Castellani C, Ferrari B, Galietta LJV, Castaldo G, Taccetti G. Terlizzi V, et al. Among authors: castellani c. Mol Genet Genomic Med. 2021 Apr;9(4):e1656. doi: 10.1002/mgg3.1656. Epub 2021 Mar 13. Mol Genet Genomic Med. 2021. PMID: 33713579 Free PMC article.

3

Dornase alfa in Cystic Fibrosis: indications, comparative studies and effects on lung clearance index.

Terlizzi V, Castellani C, Taccetti G, Ferrari B. Terlizzi V, et al. Among authors: castellani c. Ital J Pediatr. 2022 Aug 4;48(1):141. doi: 10.1186/s13052-022-01331-5. Ital J Pediatr. 2022. PMID: 35927765 Free PMC article. Review.

4

The cystic fibrosis transmembrane regulator gene and male infertility.

Quinzii C, Castellani C. Quinzii C, et al. Among authors: castellani c. J Endocrinol Invest. 2000 Nov;23(10):684-9. doi: 10.1007/BF03343794. J Endocrinol Invest. 2000. PMID: 11097434 Review.

5

Neonatal screening for cystic fibrosis: long-term clinical balance.

Mastella G, Zanolla L, Castellani C, Altieri S, Furnari M, Giglio L, Lombardo M, Miano A, Sciuto C, Pardo F, Magazzù G. Mastella G, et al. Among authors: castellani c. Pancreatology. 2001;1(5):531-7. doi: 10.1159/000055856. Pancreatology. 2001. PMID: 12120233

6

Evidence of mild respiratory disease in men with congenital absence of the vas deferens.

Castellani C, Bonizzato A, Pradal U, Filicori M, Foresta C, La Sala GB, Mastella G. Castellani C, et al. Respir Med. 1999 Dec;93(12):869-75. doi: 10.1016/s0954-6111(99)90052-5. Respir Med. 1999. PMID: 10653048 Free article.

7

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: castellani c. JAMA. 2009 Sep 9;302(10):1076-83. doi: 10.1001/jama.2009.1295. JAMA. 2009. PMID: 19738092 Free PMC article.

8

Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis.

Castellani C, Tamanini A, Mastella G. Castellani C, et al. Arch Dis Child. 2000 Jun;82(6):481-2. doi: 10.1136/adc.82.6.481. Arch Dis Child. 2000. PMID: 10833182 Free PMC article.

9

Nasal potential difference in congenital bilateral absence of the vas deferens.

Pradal U, Castellani C, Delmarco A, Mastella G. Pradal U, et al. Among authors: castellani c. Am J Respir Crit Care Med. 1998 Sep;158(3):896-901. doi: 10.1164/ajrccm.158.3.9711029. Am J Respir Crit Care Med. 1998. PMID: 9731023

10

Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis.

Castellani C, Gomez Lira M, Frulloni L, Delmarco A, Marzari M, Bonizzato A, Cavallini G, Pignatti P, Mastella G. Castellani C, et al. Hum Mutat. 2001 Aug;18(2):166. doi: 10.1002/humu.1172. Hum Mutat. 2001. PMID: 11462247

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