Zemanick ET - Search Results

1

Inflammation and airway microbiota during cystic fibrosis pulmonary exacerbations.

Zemanick ET, Harris JK, Wagner BD, Robertson CE, Sagel SD, Stevens MJ, Accurso FJ, Laguna TA. Zemanick ET, et al. PLoS One. 2013 Apr 30;8(4):e62917. doi: 10.1371/journal.pone.0062917. Print 2013. PLoS One. 2013. PMID: 23646159 Free PMC article.

2

Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis.

Harris JK, De Groote MA, Sagel SD, Zemanick ET, Kapsner R, Penvari C, Kaess H, Deterding RR, Accurso FJ, Pace NR. Harris JK, et al. Among authors: zemanick et. Proc Natl Acad Sci U S A. 2007 Dec 18;104(51):20529-33. doi: 10.1073/pnas.0709804104. Epub 2007 Dec 11. Proc Natl Acad Sci U S A. 2007. PMID: 18077362 Free PMC article.

3

Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapy.

Zemanick ET, Harris JK, Conway S, Konstan MW, Marshall B, Quittner AL, Retsch-Bogart G, Saiman L, Accurso FJ. Zemanick ET, et al. J Cyst Fibros. 2010 Jan;9(1):1-16. doi: 10.1016/j.jcf.2009.09.003. Epub 2009 Oct 14. J Cyst Fibros. 2010. PMID: 19833563 Free PMC article. Review.

4

Pulmonary exacerbations in cystic fibrosis with negative bacterial cultures.

Zemanick ET, Wagner BD, Harris JK, Wagener JS, Accurso FJ, Sagel SD. Zemanick ET, et al. Pediatr Pulmonol. 2010 Jun;45(6):569-77. doi: 10.1002/ppul.21221. Pediatr Pulmonol. 2010. PMID: 20503282 Free PMC article.

5

Reliability of quantitative real-time PCR for bacterial detection in cystic fibrosis airway specimens.

Zemanick ET, Wagner BD, Sagel SD, Stevens MJ, Accurso FJ, Harris JK. Zemanick ET, et al. PLoS One. 2010 Nov 30;5(11):e15101. doi: 10.1371/journal.pone.0015101. PLoS One. 2010. PMID: 21152087 Free PMC article.

6

The airway microbiome in cystic fibrosis and implications for treatment.

Zemanick ET, Sagel SD, Harris JK. Zemanick ET, et al. Curr Opin Pediatr. 2011 Jun;23(3):319-24. doi: 10.1097/MOP.0b013e32834604f2. Curr Opin Pediatr. 2011. PMID: 21494150 Review.

7

Sputum biomarkers of inflammation and lung function decline in children with cystic fibrosis.

Sagel SD, Wagner BD, Anthony MM, Emmett P, Zemanick ET. Sagel SD, et al. Among authors: zemanick et. Am J Respir Crit Care Med. 2012 Nov 1;186(9):857-65. doi: 10.1164/rccm.201203-0507OC. Epub 2012 Aug 16. Am J Respir Crit Care Med. 2012. PMID: 22904182 Free PMC article.

8

Microbes in bronchiectasis: the forest or the trees?

Harris JK, Zemanick ET. Harris JK, et al. Among authors: zemanick et. Am J Respir Crit Care Med. 2013 May 15;187(10):1044-5. doi: 10.1164/rccm.201302-0240ED. Am J Respir Crit Care Med. 2013. PMID: 23675713 No abstract available.

9

Clinical outcomes after initial pseudomonas acquisition in cystic fibrosis.

Zemanick ET, Emerson J, Thompson V, McNamara S, Morgan W, Gibson RL, Rosenfeld M; EPIC Study Group. Zemanick ET, et al. Pediatr Pulmonol. 2015 Jan;50(1):42-8. doi: 10.1002/ppul.23036. Epub 2014 Mar 18. Pediatr Pulmonol. 2015. PMID: 24644274

10

Cystic fibrosis transmembrane conductance regulator and pseudomonas.

Zemanick ET, Accurso FJ. Zemanick ET, et al. Am J Respir Crit Care Med. 2014 Apr 1;189(7):763-5. doi: 10.1164/rccm.201402-0209ED. Am J Respir Crit Care Med. 2014. PMID: 24684355 Free PMC article. No abstract available.

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