Nasr S - Search Results

1

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. Among authors: nasr s. Hum Mutat. 1992;1(5):380-7. doi: 10.1002/humu.1380010506. Hum Mutat. 1992. PMID: 1284540 Free article.

2

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.

3

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.

4

Novel missense mutation (G314R) in a cystic fibrosis patient with hepatic failure.

Nasr SZ, Strong TV, Mansoura MK, Dawson DC, Collins FS. Nasr SZ, et al. Hum Mutat. 1996;7(2):151-4. doi: 10.1002/(SICI)1098-1004(1996)7:2<151::AID-HUMU10>3.0.CO;2-1. Hum Mutat. 1996. PMID: 8829633 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

Refining the continuum of CFTR-associated disorders in the era of newborn screening.

Levy H, Nugent M, Schneck K, Stachiw-Hietpas D, Laxova A, Lakser O, Rock M, Dahmer MK, Biller J, Nasr SZ, Baker M, McColley SA, Simpson P, Farrell PM. Levy H, et al. Among authors: nasr sz. Clin Genet. 2016 May;89(5):539-49. doi: 10.1111/cge.12711. Epub 2016 Jan 20. Clin Genet. 2016. PMID: 26671754 Free PMC article.

7

The future of cystic fibrosis care: a global perspective.

Bell SC, Mall MA, Gutierrez H, Macek M, Madge S, Davies JC, Burgel PR, Tullis E, Castaños C, Castellani C, Byrnes CA, Cathcart F, Chotirmall SH, Cosgriff R, Eichler I, Fajac I, Goss CH, Drevinek P, Farrell PM, Gravelle AM, Havermans T, Mayer-Hamblett N, Kashirskaya N, Kerem E, Mathew JL, McKone EF, Naehrlich L, Nasr SZ, Oates GR, O'Neill C, Pypops U, Raraigh KS, Rowe SM, Southern KW, Sivam S, Stephenson AL, Zampoli M, Ratjen F. Bell SC, et al. Among authors: nasr sz. Lancet Respir Med. 2020 Jan;8(1):65-124. doi: 10.1016/S2213-2600(19)30337-6. Epub 2019 Sep 27. Lancet Respir Med. 2020. PMID: 31570318 Free PMC article. Review.

8

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.

9

Transition program from pediatric to adult care for cystic fibrosis patients.

Nasr SZ, Campbell C, Howatt W. Nasr SZ, et al. J Adolesc Health. 1992 Dec;13(8):682-5. doi: 10.1016/1054-139x(92)90063-h. J Adolesc Health. 1992. PMID: 1290768

10

Symptomatic increase in intracranial pressure following pancreatic enzyme replacement therapy for cystic fibrosis.

Nasr SZ, Schaffert D. Nasr SZ, et al. Pediatr Pulmonol. 1995 Jun;19(6):396-7. doi: 10.1002/ppul.1950190615. Pediatr Pulmonol. 1995. PMID: 7567222 Free article.

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