Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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Fungal Pathogens in CF Airways: Leave or Treat?[Chronic Pseudomonas aeruginosa airway colonization in cystic fibrosis patients : Prevention concepts].Targeting the quinolone signal quorum sensing system for the discovery of novel anti-infective pathoblockers

P2860

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P2860

Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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http://www.wikidata.org/entity/Q36215326

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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P1476

Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time

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P2093

Ellen Caldwell

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Kathleen J Ramos

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Mathew R Crull

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Moira L Aitken

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Nicole Mayer-Hamblett

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P2860

Longevity of Patients With Cystic Fibrosis in 2000 to 2010 and Beyond: Survival Analysis of the Cystic Fibrosis Foundation Patient Registry

Bacterial biofilms: a common cause of persistent infections

Cystic fibrosis

Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis.

Initial Pseudomonas aeruginosa treatment failure is associated with exacerbations in cystic fibrosis

Statistical analysis of correlated data using generalized estimating equations: an orientation.

Classic respiratory disease but atypical diagnostic testing distinguishes adult presentation of cystic fibrosis.

The changing microbial epidemiology in cystic fibrosis.

Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype.

Conditions associated with the cystic fibrosis defect promote chronic Pseudomonas aeruginosa infection

P2888

s12890-016-0333-y

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scholarly article

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10.1186/S12890-016-0333-Y

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Christopher H Goss

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2016-12-07T00:00:00Z

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1022030003

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cystic fibrosis

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5142409

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Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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P2860

P2860

Change in Pseudomonas aeruginosa prevalence in cystic fibrosis adults over time.

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