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Evaluation of a cystic fibrosis transition program from pediatric to adult care.
Chaudhry SR, Keaton M, Nasr SZ. Chaudhry SR, et al. Among authors: nasr sz. Pediatr Pulmonol. 2013 Jul;48(7):658-65. doi: 10.1002/ppul.22647. Epub 2012 Aug 8. Pediatr Pulmonol. 2013. PMID: 22888094
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
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
Predicted values for lung diffusing capacity in healthy children.
Nasr SZ, Amato P, Wilmott RW. Nasr SZ, et al. Pediatr Pulmonol. 1991;10(4):267-72. doi: 10.1002/ppul.1950100408. Pediatr Pulmonol. 1991. PMID: 1896235
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.
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
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 No abstract available.
Colonic strictures in children with cystic fibrosis.
Zerin JM, Kuhn-Fulton J, White SJ, Chong SK, Stevens JC, West KW, Teitelbaum DH, Nasr SZ. Zerin JM, et al. Among authors: nasr sz. Radiology. 1995 Jan;194(1):223-6. doi: 10.1148/radiology.194.1.7997557. Radiology. 1995. PMID: 7997557
Correction of vitamin E deficiency with fat-soluble versus water-miscible preparations of vitamin E in patients with cystic fibrosis.
Nasr SZ, O'Leary MH, Hillermeier C. Nasr SZ, et al. J Pediatr. 1993 May;122(5 Pt 1):810-2. doi: 10.1016/s0022-3476(06)80034-x. J Pediatr. 1993. PMID: 8496768 Clinical Trial.
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 No abstract available.
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