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Cited by 527

The DOI matches its Crossref record; 91 of the 91 references it cites were found in a registry or an index.

Vancomycin resistant Staphylococcus aureus infections: A review of case updating and clinical features

Open access
Cong, Yanguang, Yang, Sijin, Rao, Xiancai·2020·Journal of Advanced Research

Abstract

The infection caused by methicillin-resistant Staphylococcus aureus (MRSA) is a global threat to public health. Vancomycin remains one of the first-line drugs for the treatment of MRSA infections. However, S. aureus isolates with complete resistance to vancomycin have emerged in recent years. Vancomycin-resistant S. aureus (VRSA) is mediated by a vanA gene cluster, which is transferred from vancomycin-resistant enterococcus. Since the first VRSA isolate was recovered from Michigan, USA in 2002, 52 VRSA strains have been isolated worldwide. In this paper, we review the latest progresses in VRSA, highlighting its resistance mechanism, characteristics of VRSA infections, as well as clinical treatments.

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Metadata

Authors
Cong, Y., Yang, S., & Rao, X.
Venue
Journal of Advanced Research
Publisher
Elsevier BV
Published
2020-01
Volume
21
Pages
169-176
ISSN
  • 2090-1224 (ISSN-L)
  • 2090-1232
OpenAlex
W2979805180
Cited by
527
References
91
FWCI
28.83
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Vancomycin resistant Staphylococcus aureus infections: A review of case updating and clinical features. https://app.cochat.ai/papers/10.1016/j.jare.2019.10.005
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Cong, Y., Yang, S., & Rao, X. (2020). Vancomycin resistant Staphylococcus aureus infections: A review of case updating and clinical features. Journal of Advanced Research. https://doi.org/10.1016/j.jare.2019.10.005

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.