Mayer-Hamblett N - Search Results

1

Association between Stenotrophomonas maltophilia and lung function in cystic fibrosis.

Goss CH, Mayer-Hamblett N, Aitken ML, Rubenfeld GD, Ramsey BW. Goss CH, et al. Thorax. 2004 Nov;59(11):955-9. doi: 10.1136/thx.2003.017707. Thorax. 2004. PMID: 15516471 Free PMC article.

2

Developing cystic fibrosis lung transplant referral criteria using predictors of 2-year mortality.

Mayer-Hamblett N, Rosenfeld M, Emerson J, Goss CH, Aitken ML. Mayer-Hamblett N, et al. Am J Respir Crit Care Med. 2002 Dec 15;166(12 Pt 1):1550-5. doi: 10.1164/rccm.200202-087OC. Epub 2002 Aug 15. Am J Respir Crit Care Med. 2002. PMID: 12406843

3

The cystic fibrosis therapeutics development network (CF TDN): a paradigm of a clinical trials network for genetic and orphan diseases.

Goss CH, Mayer-Hamblett N, Kronmal RA, Ramsey BW. Goss CH, et al. Adv Drug Deliv Rev. 2002 Dec 5;54(11):1505-28. doi: 10.1016/s0169-409x(02)00163-1. Adv Drug Deliv Rev. 2002. PMID: 12458158 Review.

4

Susceptibility testing of Pseudomonas aeruginosa isolates and clinical response to parenteral antibiotic administration: lack of association in cystic fibrosis.

Smith AL, Fiel SB, Mayer-Hamblett N, Ramsey B, Burns JL. Smith AL, et al. Chest. 2003 May;123(5):1495-502. doi: 10.1378/chest.123.5.1495. Chest. 2003. PMID: 12740266

5

Inflammatory and microbiologic markers in induced sputum after intravenous antibiotics in cystic fibrosis.

Ordoñez CL, Henig NR, Mayer-Hamblett N, Accurso FJ, Burns JL, Chmiel JF, Daines CL, Gibson RL, McNamara S, Retsch-Bogart GZ, Zeitlin PL, Aitken ML. Ordoñez CL, et al. Am J Respir Crit Care Med. 2003 Dec 15;168(12):1471-5. doi: 10.1164/rccm.200306-731OC. Epub 2003 Sep 11. Am J Respir Crit Care Med. 2003. PMID: 12969869 Clinical Trial.

6

Randomized, double-blind, placebo-controlled, dose-escalating study of aerosolized interferon gamma-1b in patients with mild to moderate cystic fibrosis lung disease.

Moss RB, Mayer-Hamblett N, Wagener J, Daines C, Hale K, Ahrens R, Gibson RL, Anderson P, Retsch-Bogart G, Nasr SZ, Noth I, Waltz D, Zeitlin P, Ramsey B, Starko K. Moss RB, et al. Pediatr Pulmonol. 2005 Mar;39(3):209-18. doi: 10.1002/ppul.20152. Pediatr Pulmonol. 2005. PMID: 15573395 Clinical Trial.

7

Laboratory parameter profiles among patients with cystic fibrosis.

Goss CH, Mayer-Hamblett N, Kronmal RA, Williams J, Ramsey BW. Goss CH, et al. J Cyst Fibros. 2007 Apr;6(2):117-23. doi: 10.1016/j.jcf.2006.05.012. Epub 2006 Jul 7. J Cyst Fibros. 2007. PMID: 16829217 Free article.

8

Association between pulmonary function and sputum biomarkers in cystic fibrosis.

Mayer-Hamblett N, Aitken ML, Accurso FJ, Kronmal RA, Konstan MW, Burns JL, Sagel SD, Ramsey BW. Mayer-Hamblett N, et al. Am J Respir Crit Care Med. 2007 Apr 15;175(8):822-8. doi: 10.1164/rccm.200609-1354OC. Epub 2007 Jan 18. Am J Respir Crit Care Med. 2007. PMID: 17234902 Free PMC article.

9

No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations.

Clancy JP, Rowe SM, Bebok Z, Aitken ML, Gibson R, Zeitlin P, Berclaz P, Moss R, Knowles MR, Oster RA, Mayer-Hamblett N, Ramsey B. Clancy JP, et al. Am J Respir Cell Mol Biol. 2007 Jul;37(1):57-66. doi: 10.1165/rcmb.2006-0173OC. Epub 2007 Mar 8. Am J Respir Cell Mol Biol. 2007. PMID: 17347447 Free PMC article. Clinical Trial.

10

Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypes.

Nguyen D, Emond MJ, Mayer-Hamblett N, Saiman L, Marshall BC, Burns JL. Nguyen D, et al. Pediatr Pulmonol. 2007 Jun;42(6):533-41. doi: 10.1002/ppul.20620. Pediatr Pulmonol. 2007. PMID: 17469154 Clinical Trial.

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