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Yunsop Chong

Researcher at Yonsei University

Publications -  50
Citations -  1921

Yunsop Chong is an academic researcher from Yonsei University. The author has contributed to research in topics: Acinetobacter & Imipenem. The author has an hindex of 24, co-authored 50 publications receiving 1777 citations.

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Identification of Toxin A-Negative, Toxin B-Positive Clostridium difficile by PCR

TL;DR: The PCR assay for the detection of the repeating sequences combined with PCR amplification of the nonrepeating sequences of either the toxin A or the toxin B gene is indicated to be useful for differentiating toxin A−, toxin B+ strains from toxin A+.
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Multidrug-Resistant Acinetobacter spp.: Increasingly Problematic Nosocomial Pathogens

TL;DR: Efforts to control resistant bacteria in Korea by hospitals, relevant scientific societies and government agencies have only partially been successful and concerted multidisciplinary efforts are needed to preserve the efficacy of currently available antimicrobial agents, by following the principles of antimicrobial stewardship.
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Dissemination of 16S rRNA methylase-mediated highly amikacin-resistant isolates of Klebsiella pneumoniae and Acinetobacter baumannii in Korea

TL;DR: 16S rRNA methylase-producing isolates of Gram-negative bacilli isolated in 2003 and 2005 were highly resistant to arbekacin and amikacin, and were mostly coresistant to levofloxacin.
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Various penA mutations together with mtrR, porB and ponA mutations in Neisseria gonorrhoeae isolates with reduced susceptibility to cefixime or ceftriaxone

TL;DR: In this article, the existence of only one strain having the mosaic penA sequence indicated that ceftriaxone and cefixime resistance in Korea was mostly not associated with a mosaic-penA sequence.
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Increasing Prevalence of Toxin A-Negative, Toxin B-Positive Isolates of Clostridium difficile in Korea: Impact on Laboratory Diagnosis

TL;DR: Of 462 Korean Clostridium difficile isolates, 77.5% were toxin B positive but 21.4% were toxins A negative (A− B+), suggesting that toxin A detection alone may underdiagnose C. difficiles.