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- W2224500828 endingPage "89" @default.
- W2224500828 startingPage "71" @default.
- W2224500828 abstract "In Canada and the United States, more than 30,000 people suffer from cystic fibrosis (CF); it is therefore the most common potentially fatal inherited disease among Caucasians in those North American countries. Infection of the lung is the leading cause of death in patients with CF, and Pseudomonas aeruginosa is the predominant infectious agent. Whereas CF patients may become infected with other organisms (such as Staphylococcus aureus, Haemophilus influenzae, Burkholderia cepacia, and atypical mycobacteria),P. aeruginosa is the predominant pathogen, ultimately infecting approximately 80% of patients. Once infected with P. aeruginosa, patients usually retain the organism for the duration of their lives. This host-microbe interaction is unique and raises many important questions about mode of acquisition, microbial virulence, host susceptibility and strategies for control of infection. This brief chapter will review the latest information on the host-microbial détente in the CF lung, focusing on new observations from a North American perspective. Chapter 6 will reflect on observations from Europe." @default.
- W2224500828 created "2016-06-24" @default.
- W2224500828 creator A5010363328 @default.
- W2224500828 creator A5031624178 @default.
- W2224500828 creator A5057425693 @default.
- W2224500828 date "2003-01-01" @default.
- W2224500828 modified "2023-09-26" @default.
- W2224500828 title "Pseudomonas Aeruginosa Infections in Individuals with Cystic Fibrosis" @default.
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- W2224500828 doi "https://doi.org/10.1007/978-1-4615-0433-7_5" @default.
- W2224500828 hasPublicationYear "2003" @default.