What Makes Pseudomonas Aeruginosa Persist in the Lungs of CF Patients?

H. Johansen, Lea Mette Madsen Sommer, Rasmus Lykke Marvig, L. Jensen, M. Skov, T. Pressler, Søren Molin

Research output: Contribution to journalConference abstract in journalResearchpeer-review

Abstract

The most important problem for cystic fibrosis (CF) patients is the airway infections responsible for the gradually decreasing lung function as the infections persist. We have investigated properties that may be involved in persistence of P. aeruginosa (PA) in the lungs of young CF children by combining genomics, “phenomics” (phenotypes and molecular data), and clinical data.
Original languageEnglish
Article number309
JournalPediatric Pulmonology
Volume50
Pages (from-to)308-308
ISSN8755-6863
DOIs
Publication statusPublished - 2015
EventThe 29th Annual North American Cystic Fibrosis Conference - Phoenix, United States
Duration: 8 Oct 201510 Oct 2015
Conference number: 29

Conference

ConferenceThe 29th Annual North American Cystic Fibrosis Conference
Number29
CountryUnited States
CityPhoenix
Period08/10/201510/10/2015

Fingerprint Dive into the research topics of 'What Makes <i>Pseudomonas Aeruginosa </i>Persist in the Lungs of CF Patients?'. Together they form a unique fingerprint.

Cite this