102 Denitrification by cystic fibrosis pathogens
نویسندگان
چکیده
منابع مشابه
THE BACTERIAL CYTOSKELETONdA NEW ANTIMICROBIAL TARGET IN CYSTIC FIBROSIS PATHOGENS?
S20 Figure 1 . Conclusion In vitro MreB is an attractive new target for novel antimicrobials. Further analysis of current observations and additional phenotypic analysis will be required to dissect the nature of Q22induced changes. Work supported by Newcastle-Upon-Tyne Hospitals Special Trustees and Italian CF Research Foundation (FFC). S21 IDENTIFICATION OF PSEUDOMONAS AERUGINOSA INFECTION VIA...
متن کاملEmerging cystic fibrosis pathogens: incidence and antimicrobial resistance.
We examined the frequency of isolation and the antimicrobial resistance of Burkholderia cepacia complex, Stenotrophomonas maltophilia and Achromobacter xylosoxidans in cystic fibrosis patients from 2000 to 2004. Strains susceptibility to tobramycin, piperacillin/tazobactam, imipenem, gentamicin, ciprofloxacin and ceftazidime was determined by disc diffusion assay. B. cepacia complex showed a ve...
متن کاملAnaerobic bacteria in cystic fibrosis: pathogens or harmless commensals?
2004;27:453e8. 9. Hillman DR, Murphy AS, Pezzullo L. The Economic Cost of Sleep Disorders. Sleep 2006;29:299e305. 10. Mar J, Rueda JR, Durán-Cantolla J, et al. The costeffectiveness of nCPAP treatment in patients with moderate-to-severe obstructive sleep apnoea. Eur Respir J 2003;21:515e22. 11. Tan MC, Ayas NT, Mulgrew A, et al. Costeffectiveness of continuous positive airway pressure therapy i...
متن کاملPrevalence of pathogens in cystic fibrosis patients in Bahia, Brazil.
INTRODUCTION Recurrent respiratory infections account for most of the morbidity and mortality of cystic fibrosis patients. MATERIALS AND METHODS The objective was to determine the prevalence of pathogens isolated from lower respiratory tract secretions in cystic fibrosis patients. In this descriptive observational study, data from 69 patients was collected from medical records. RESULTS The ...
متن کاملMaintaining Respiratory Health in Cystic Fibrosis Patients
Cystic fibrosis (CF) is an inherited disease that primarily affects the lungs and the digestive system, however, it also affects a number of other organs and systems. More than 90% of mortality of CF patients is due to lung complications. Healthy lungs are important for a long life for people with CF, We will discuss two important topics for maintaining respiratory health. Chronic use of drug...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Cystic Fibrosis
سال: 2013
ISSN: 1569-1993
DOI: 10.1016/s1569-1993(13)60244-1