Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time-Reference-Cited by-同舟云学术

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time

Published:2016-12 Issue:1 Volume:16 Page:
ISSN:1471-2466
Container-title:BMC Pulmonary Medicine
language:en
Short-container-title:BMC Pulm Med

Author:

Crull Mathew R.,Ramos Kathleen J.,Caldwell Ellen,Mayer-Hamblett Nicole,Aitken Moira L.,Goss Christopher H.

Funder

National Heart, Lung, and Blood Institute

Cystic Fibrosis Foundation

U.S. Food and Drug Administration

Publisher

Springer Science and Business Media LLC

Subject

Pulmonary and Respiratory Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12890-016-0333-y.pdf

Reference34 articles.

1. Rogers GB, Hart CA, Mason JR, Hughes M, Walshaw MJ, Bruce KD. Bacterial Diversity in Cases of Lung Infection in Cystic Fibrosis Patients: 16S Ribosomal DNA (rDNA) Length Heterogeneity PCR and 16S rDNA Terminal Restriction Fragment Length Polymorphism Profiling. J Clin Microbiol. 2003;41(8):3548–58.

2. MacKenzie T, Gifford AH, Sabadosa KA, Quinton HB, Knapp EA, Goss CH, et al. Longevity of Patients With Cystic Fibrosis in 2000 to 2010 and Beyond: Survival Analysis of the Cystic Fibrosis Foundation Patient Registry. Ann Intern Med. 2014;161(4):233–41.

3. Cystic Fibrosis Foundation Patient Registry: 2013 Annual Data Report. Bethesda, MD: Cystic Fibrosis Foundation; 2014.

4. Ratjen F, Döring G. Cystic fibrosis. Lancet. 2003;361(9358):681–9.

5. Treggiari MM, Rosenfeld M, Retsch-Bogart G, Gibson R, Ramsey B. Approach to eradication of initial Pseudomonas aeruginosa infection in children with cystic fibrosis. Pediatr Pulmonol. 2007;42(9):751–6.

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