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Impact of Pseudomonas and Staphylococcus infection on inflammation and clinical status in young children with cystic fibrosis.
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Bronchoalveolar lavage or oropharyngeal cultures to identify lower respiratory pathogens in infants with cystic fibrosis.
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Mutations in the Staphylococcus aureus Global Regulator CodY confer tolerance to an interspecies redox-active antimicrobial.
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Mutations in the Global Regulator CodY Confer Tolerance to an Interspecies Redox-Active Antimicrobial.
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Iron Sequestration by Murine Calprotectin Induces Starvation Responses in .
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Citrate cross-feeding by supports mutant fitness.
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Ethnic differences in staphylococcus aureus acquisition in cystic fibrosis.
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Interactions between metabolism and growth can determine the co-existence of and .
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3
A 5 YEAR CLINICAL EVALUATION OF A THERAPEUTIC PROGRAM FOR PATIENTS WITH CYSTIC FIBROSIS.
J Pediatr. 1964 Nov;65:677-93. doi: 10.1016/s0022-3476(64)80152-9.
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Sequential genotyping of Pseudomonas aeruginosa from upper and lower airways of cystic fibrosis patients.
Eur Respir J. 2002 Dec;20(6):1457-63. doi: 10.1183/09031936.02.00268002.
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Significant microbiological effect of inhaled tobramycin in young children with cystic fibrosis.
Am J Respir Crit Care Med. 2003 Mar 15;167(6):841-9. doi: 10.1164/rccm.200208-855OC. Epub 2002 Dec 12.
7
Inflammation, infection, and pulmonary function in infants and young children with cystic fibrosis.
Am J Respir Crit Care Med. 2002 Apr 1;165(7):904-10. doi: 10.1164/ajrccm.165.7.2010139.
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Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis.
Pediatr Pulmonol. 2001 Nov;32(5):356-66. doi: 10.1002/ppul.1144.
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Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis.
J Pediatr. 2001 May;138(5):699-704. doi: 10.1067/mpd.2001.112897.

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