Nasr SZ - Search Results

1

Magnetic resonance imaging of cystic fibrosis: Multi-organ imaging in the age of CFTR modulator therapies.

McBennett K, MacAskill CJ, Keshock E, Mahani MG, Mata J, Towbin AJ, Sankararaman S, Drumm ML, Yu X, Ren CL, Nasr SZ, Kutney K, Flask CA. McBennett K, et al. Among authors: nasr sz. J Cyst Fibros. 2022 Mar;21(2):e148-e157. doi: 10.1016/j.jcf.2021.11.006. Epub 2021 Dec 5. J Cyst Fibros. 2022. PMID: 34879996 Free article. Review. No abstract available.

2

Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Strong TV, Smit LS, Nasr S, Wood DL, Cole JL, Iannuzzi MC, Stern RC, Collins FS. Strong TV, et al. Hum Mutat. 1992;1(5):380-7. doi: 10.1002/humu.1380010506. Hum Mutat. 1992. PMID: 1284540 Free article.

3

Identification of a CFTR frameshift mutation (1013 delAA) in trans to delta F508 in a pancreatic sufficient cystic fibrosis patient.

Nasr SZ, Strong TV, Collins FS. Nasr SZ, et al. Hum Mol Genet. 1994 Nov;3(11):2063-4. Hum Mol Genet. 1994. PMID: 7533026 No abstract available.

4

An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levels.

Smit LS, Nasr SZ, Iannuzzi MC, Collins FS. Smit LS, et al. Among authors: nasr sz. Hum Mutat. 1993;2(2):148-51. doi: 10.1002/humu.1380020217. Hum Mutat. 1993. PMID: 7686423 Free article. No abstract available.

5

Cystic fibrosis in adolescents and young adults.

Nasr SZ. Nasr SZ. Adolesc Med. 2000 Oct;11(3):589-603. Adolesc Med. 2000. PMID: 11060556 Review.

6

Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis.

Naguib ML, Schrijver I, Gardner P, Pique LM, Doss SS, Abu Zekry MA, Aziz M, Nasr SZ. Naguib ML, et al. Among authors: nasr sz. J Cyst Fibros. 2007 Apr;6(2):111-6. doi: 10.1016/j.jcf.2006.04.004. Epub 2006 Jul 11. J Cyst Fibros. 2007. PMID: 16837250 Free article.

7

High resolution computerized tomography of the chest and pulmonary function testing in evaluating the effect of tobramycin solution for inhalation in cystic fibrosis patients.

Nasr SZ, Gordon D, Sakmar E, Yu X, Christodoulou E, Eckhardt BP, Strouse PJ. Nasr SZ, et al. Pediatr Pulmonol. 2006 Dec;41(12):1129-37. doi: 10.1002/ppul.20447. Pediatr Pulmonol. 2006. PMID: 17068818 Free article. Clinical Trial.

8

EUR-1008 pancreatic enzyme replacement is safe and effective in patients with cystic fibrosis and pancreatic insufficiency.

Wooldridge JL, Heubi JE, Amaro-Galvez R, Boas SR, Blake KV, Nasr SZ, Chatfield B, McColley SA, Woo MS, Hardy KA, Kravitz RM, Straforini C, Anelli M, Lee C. Wooldridge JL, et al. Among authors: nasr sz. J Cyst Fibros. 2009 Dec;8(6):405-17. doi: 10.1016/j.jcf.2009.07.006. Epub 2009 Aug 15. J Cyst Fibros. 2009. PMID: 19683970 Free article. Clinical Trial.

9

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

10

Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort.

Rosenfeld M, Emerson J, McNamara S, Joubran K, Retsch-Bogart G, Graff GR, Gutierrez HH, Kanga JF, Lahiri T, Noyes B, Ramsey B, Ren CL, Schechter M, Morgan W, Gibson RL; EPIC Study Group Participating Clinical Sites. Rosenfeld M, et al. Pediatr Pulmonol. 2010 Sep;45(9):934-44. doi: 10.1002/ppul.21279. Pediatr Pulmonol. 2010. PMID: 20597081

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