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François Caméléna

Researcher at University of Paris

Publications -  22
Citations -  322

François Caméléna is an academic researcher from University of Paris. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 7, co-authored 12 publications receiving 187 citations. Previous affiliations of François Caméléna include Paris Diderot University.

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Multidrug-resistant Neisseria gonorrhoeae failing treatment with ceftriaxone and doxycycline in France, November 2017

TL;DR: In this article, a multidrug-resistant Neisseria gonorrhoeae urogenital and pharyngeal infection with ceftriaxone resistance and intermediate resistance to azithromycin in a heterosexual woman in her 20s in France was reported.
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Bacterial Pneumonia in COVID-19 critically ill patients: a case series.

TL;DR: Bacterial pneumonia in critically ill patients with COVID-19 diagnosed by bacterial cultures of blind bronchoalveolar lavage (BBAL) is reported, with significant rate of bacterial pneumonia, mostly late-onset VAP, in critically critically ill Patients with CO VID-19 in the authors' unit.
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Prospective evaluation of the Alere i Influenza A&B nucleic acid amplification versus Xpert Flu/RSV

TL;DR: The results indicate that the Alere i Influenza A&B assay has a good overall analytical performance and a high degree of concordance with the PCR-based Xpert Flu/RSV assay.
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Performance of a multiplex polymerase chain reaction panel for identifying bacterial pathogens causing pneumonia in critically ill patients with COVID-19.

TL;DR: The FA-PP results from BBAL in critically ill patients with COVID-19 were consistent with bacterial culture findings for bacteria present in theFA-PP panel; showing sensitivity, specificity, positive and negative predictive value of 95%, 99%, 82% and 100%, respectively.
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Rapid and Simple Universal Escherichia coli Genotyping Method Based on Multiple-Locus Variable-Number Tandem-Repeat Analysis Using Single-Tube Multiplex PCR and Standard Gel Electrophoresis.

TL;DR: A multiplex PCR method based on multiple-locus variable-number tandem-repeat (VNTR) analysis (MLVA) that was designed for the rapid typing of Escherichia coli and Shigella isolates and has a discriminatory power superior to that of MLST and DiversiLab REP-PCR but slightly lower than that of PFGE.