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Antibacterial activities of a fosfomycin/tobramycin combination: a novel inhaled antibiotic for bronchiectasis.
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- Journal of Antimicrobial Chemotherapy (JAC), 2009, v. 64, n. 4, p. 829, doi. 10.1093/jac/dkp282
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- Article
Use of Pseudomonas biofilm susceptibilities to assign simulated antibiotic regimens for cystic fibrosis airway infection.
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- Journal of Antimicrobial Chemotherapy (JAC), 2005, v. 56, n. 5, p. 879, doi. 10.1093/jac/dki338
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- Article
In Vitro Antibiotic Susceptibility of Initial Pseudomonas aeruginosa Isolates From United States Cystic Fibrosis Patients.
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- Journal of the Pediatric Infectious Diseases Society, 2015, v. 4, n. 2, p. 151, doi. 10.1093/jpids/pit052
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- Article
Azithromycin in Patients With Cystic Fibrosis Chronically Infected With Pseudomonas aeruginosa: A Randomized Controlled Trial.
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- JAMA: Journal of the American Medical Association, 2003, v. 290, n. 13, p. 1749, doi. 10.1001/jama.290.13.1749
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- Article
Anaerobic killing of mucoid Pseudomonas aeruginosa by acidified nitrite derivatives under cystic fibrosis airway conditions.
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- 2006
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- Publication type:
- journal article
Longitudinal Assessment of Pseudomonas aeruginosa in Young Children with Cystic Fibrosis.
- Published in:
- Journal of Infectious Diseases, 2001, v. 183, n. 3, p. 444, doi. 10.1086/318075
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- Publication type:
- Article
Aminoglycoside-Resistance Mechanisms for Cystic Fibrosis Pseudomonas aeruginosa Isolates Are...
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- Journal of Infectious Diseases, 2000, v. 181, n. 3, p. 1180, doi. 10.1086/315312
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- Article
Effect of Chronic Intermittent Administration of Inhaled Tobramycin on Respiratory Microbial Flora in Patients with Cystic Fibrosis.
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- Journal of Infectious Diseases, 1999, v. 179, n. 5, p. 1190, doi. 10.1086/314727
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- Publication type:
- Article
Comparison of Biophysical and Biologic Properties of α-Helical Enantiomeric Antimicrobial Peptides.
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- Chemical Biology & Drug Design, 2006, v. 67, n. 2, p. 162, doi. 10.1111/j.1747-0285.2006.00349.x
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- Article
Open-label, follow-on study of azithromycin in pediatric patients with CF uninfected with Pseudomonas aeruginosa.
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- Pediatric Pulmonology, 2012, v. 47, n. 7, p. 641, doi. 10.1002/ppul.21601
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- Article
Initial Pseudomonas aeruginosa treatment failure is associated with exacerbations in cystic fibrosis.
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- Pediatric Pulmonology, 2012, v. 47, n. 2, p. 125, doi. 10.1002/ppul.21525
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- Article
Randomized trial of biofilm testing to select antibiotics for cystic fibrosis airway infection.
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- Pediatric Pulmonology, 2011, v. 46, n. 2, p. 184, doi. 10.1002/ppul.21350
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- Article
Changes in cystic fibrosis sputum microbiology in the United States between 1995 and 2008.
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- Pediatric Pulmonology, 2010, v. 45, n. 4, p. 363, doi. 10.1002/ppul.21198
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- Publication type:
- Article
A phase 2 study of aztreonam lysine for inhalation to treat patients with cystic fibrosis and Pseudomonas aeruginosa infection.
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- Pediatric Pulmonology, 2008, v. 43, n. 1, p. 47, doi. 10.1002/ppul.20736
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- Article
Duration of treatment effect after tobramycin solution for inhalation in young children with cystic fibrosis.
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- Pediatric Pulmonology, 2007, v. 42, n. 7, p. 610, doi. 10.1002/ppul.20625
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- Article
Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypes.
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- Pediatric Pulmonology, 2007, v. 42, n. 6, p. 533, doi. 10.1002/ppul.20620
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- Article
Microbiology, safety, and pharmacokinetics of aztreonam lysinate for inhalation in patients with cystic fibrosisSome of the results of this study were previously reported at the North American Cystic Fibrosis Conference in October 2004.
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- Pediatric Pulmonology, 2006, v. 41, n. 7, p. 656, doi. 10.1002/ppul.20429
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- Article
Early pulmonary infection, inflammation, and clinical outcomes in infants with cystic fibrosis.
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- Pediatric Pulmonology, 2001, v. 32, n. 5, p. 356, doi. 10.1002/ppul.1144
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- Publication type:
- Article
Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients.
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- Molecular Microbiology, 2007, v. 64, n. 2, p. 512, doi. 10.1111/j.1365-2958.2007.05678.x
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- Article
Neutrophil Extracellular Trap (NET)-Mediated Killing of Pseudomonas aeruginosa: Evidence of Acquired Resistance within the CF Airway, Independent of CFTR.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0023637
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- Article
Unique Lipid A Modifications in Pseudomonas aeruginosa Isolated from the Airways of Patients with Cystic Fibrosis.
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- Journal of Infectious Diseases, 2007, v. 196, n. 7, p. 1088, doi. 10.1086/521367
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- Article
Effect of Azithromycin on Pulmonary Function in Patients With Cystic Fibrosis Uninfected With Pseudomonas aeruginosa.
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- JAMA: Journal of the American Medical Association, 2010, v. 303, n. 17, p. 1707, doi. 10.1001/jama.2010.563
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- Article
Genome mosaicism is conserved but not unique in Pseudomonas aeruginosa isolates from the airways of young children with cystic fibrosis.
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- Environmental Microbiology, 2003, v. 5, n. 12, p. 1341, doi. 10.1111/j.1462-2920.2003.00518.x
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- Article
Pseudomonas aeruginosa in Cystic Fibrosis Patients With G551D-CFTR Treated With Ivacaftor.
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- Clinical Infectious Diseases, 2015, v. 60, n. 5, p. 703, doi. 10.1093/cid/ciu944
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- Article
Pseudomonas aeruginosa Phenotypes Associated With Eradication Failure in Children With Cystic Fibrosis.
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- Clinical Infectious Diseases, 2014, v. 59, n. 5, p. 624, doi. 10.1093/cid/ciu385
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- Article
Staphylococcus aureus Small-Colony Variants Are Independently Associated With Worse Lung Disease in Children With Cystic Fibrosis.
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- Clinical Infectious Diseases, 2013, v. 57, n. 3, p. 384, doi. 10.1093/cid/cit270
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- Article
Pseudomonas aeruginosa in vitro phenotypes distinguish cystic fibrosis infection stages and outcomes.
- Published in:
- 2014
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- Publication type:
- journal article
Pseudomonas aeruginosa In Vitro Phenotypes Distinguish Cystic Fibrosis Infection Stages and Outcomes.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2014, v. 190, n. 3, p. 289, doi. 10.1164/rccm.201404-0681oc
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- Article
Association between Pulmonary Function and Sputum Biomarkers in Cystic Fibrosis.
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- American Journal of Respiratory & Critical Care Medicine, 2007, v. 175, n. 8, p. 822, doi. 10.1164/rccm.200609-1354oc
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- Article
Inflammatory and Microbiologic Markers in Induced Sputum after Intravenous Antibiotics in Cystic Fibrosis.
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- American Journal of Respiratory & Critical Care Medicine, 2003, v. 168, n. 12, p. 1471, doi. 10.1164/rccm.200306-731OC
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- Article
Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis.
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- American Journal of Respiratory & Critical Care Medicine, 2003, v. 168, n. 8, p. 918, doi. 10.1164/rccm.200304-505SO
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- Publication type:
- Article
Significant Microbiological Effect of Inhaled Tobramycin in Young Children with Cystic Fibrosis.
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- American Journal of Respiratory & Critical Care Medicine, 2003, v. 167, n. 6, p. 841, doi. 10.1164/rccm.200208-855OC
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- Article
Nutrient Availability as a Mechanism for Selection of Antibiotic Tolerant Pseudomonas aeruginosa within the CF Airway.
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- PLoS Pathogens, 2010, v. 6, n. 1, p. 1, doi. 10.1371/journal.ppat.1000712
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- Article
Respiratory viruses in children with cystic fibrosis: viral detection and clinical findings.
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- Influenza & Other Respiratory Viruses, 2012, v. 6, n. 3, p. 218, doi. 10.1111/j.1750-2659.2011.00292.x
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- Article
Directly Sampling the Lung of a Young Child with Cystic Fibrosis Reveals Diverse Microbiota.
- Published in:
- 2014
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- Publication type:
- journal article
Clinical utilization of genomics data produced by the international Pseudomonas aeruginosa consortium.
- Published in:
- Frontiers in Microbiology, 2015, p. 1, doi. 10.3389/fmicb.2015.01036
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- Article
Microbiology of Sputum from Patients at Cystic Fibrosis Centers in the United States.
- Published in:
- Clinical Infectious Diseases, 1998, v. 27, n. 1, p. 158, doi. 10.1086/514631
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- Article
No evidence for chromosomal mosaicism in multiple tissues of 10 patients with 45 XO Turner syndrome.
- Published in:
- Clinical Genetics, 1979, v. 15, n. 1, p. 22, doi. 10.1111/j.1399-0004.1979.tb02025.x
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- Article