| Literature DB >> 24391197 |
Laura Häfner1, Georg Peters, Barbara C Kahl.
Abstract
Respiratory specimens from cystic fibrosis (CF) patients challenge microbiological laboratories with their complexity of pathogens and atypical variants. We evaluated the diagnostic procedures in German laboratories by use of a questionnaire. Although most laboratories followed guidelines, some of them served only a small number of patients, while others did not use the recommended selective agars to culture the particular CF-relevant species.Entities:
Mesh:
Year: 2014 PMID: 24391197 PMCID: PMC3957798 DOI: 10.1128/JCM.02866-13
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948