Mayer-Hamblett N - Search Results

1

Standard care versus protocol based therapy for new onset Pseudomonas aeruginosa in cystic fibrosis.

Mayer-Hamblett N, Rosenfeld M, Treggiari MM, Konstan MW, Retsch-Bogart G, Morgan W, Wagener J, Gibson RL, Khan U, Emerson J, Thompson V, Elkin EP, Ramsey BW; EPIC; ESCF Investigators. Mayer-Hamblett N, et al. Pediatr Pulmonol. 2013 Oct;48(10):943-53. doi: 10.1002/ppul.22693. Epub 2013 Jul 2. Pediatr Pulmonol. 2013. PMID: 23818295 Free PMC article. Clinical Trial.

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

Azithromycin in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa: a randomized controlled trial.

Saiman L, Marshall BC, Mayer-Hamblett N, Burns JL, Quittner AL, Cibene DA, Coquillette S, Fieberg AY, Accurso FJ, Campbell PW 3rd; Macrolide Study Group. Saiman L, et al. JAMA. 2003 Oct 1;290(13):1749-56. doi: 10.1001/jama.290.13.1749. JAMA. 2003. PMID: 14519709 Clinical Trial.

7

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.

8

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.

9

Use of phage display to identify potential Pseudomonas aeruginosa gene products relevant to early cystic fibrosis airway infections.

Beckmann C, Brittnacher M, Ernst R, Mayer-Hamblett N, Miller SI, Burns JL. Beckmann C, et al. Infect Immun. 2005 Jan;73(1):444-52. doi: 10.1128/IAI.73.1.444-452.2005. Infect Immun. 2005. PMID: 15618183 Free PMC article.

10

Improving the estimation of change from baseline in a continuous outcome measure in the clinical trial setting.

Mayer-Hamblett N, Kronmal RA. Mayer-Hamblett N, et al. Contemp Clin Trials. 2005 Feb;26(1):2-16. doi: 10.1016/j.cct.2004.08.008. Epub 2005 Jan 27. Contemp Clin Trials. 2005. PMID: 15837448

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