Epidemiological cut‐off values for itraconazole and ravuconazole for Madurella mycetomatis, the most common causative agent of mycetoma
暂无分享,去创建一个
A. Verbon | A. Fahal | E. Zijlstra | W. V. D. van de Sande | E. Siddig | N. Mhmoud | S. Bakhiet | B. Nyaoke | B. Nyuykonge
[1] S. de Hoog,et al. A Short-Tandem-Repeat Assay (MmySTR) for Studying Genetic Variation in Madurella mycetomatis , 2020, Journal of Clinical Microbiology.
[2] J. Guinea. Updated EUCAST Clinical Breakpoints against Aspergillus, Implications for the Clinical Microbiology Laboratory , 2020, Journal of fungi.
[3] M. A. Mohamed,et al. Madurella mycetomatis causing eumycetoma medical treatment: The challenges and prospects , 2020, PLoS Neglected Tropical Diseases.
[4] P. Hamal,et al. How to: interpret MICs of antifungal compounds according to the revised clinical breakpoints v. 10.0 European committee on antimicrobial susceptibility testing (EUCAST). , 2020, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.
[5] S. Smit,et al. The development of a novel diagnostic PCR for Madurella mycetomatis using a comparative genome approach , 2020, bioRxiv.
[6] G. S. de Hoog,et al. Diagnostic implications of mycetoma derived from Madurella pseudomycetomatis isolates from Mexico , 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.
[7] A. Verbon,et al. Madurella mycetomatis, the main causative agent of eumycetoma, is highly susceptible to olorofim , 2020, The Journal of antimicrobial chemotherapy.
[8] J. Guarro,et al. Azole resistance mechanisms in Aspergillus: update and recent advances , 2020 .
[9] J. Frisvad,et al. cyp51A Mutations, Extrolite Profiles, and Antifungal Susceptibility in Clinical and Environmental Isolates of the Aspergillus viridinutans Species Complex , 2019, Antimicrobial Agents and Chemotherapy.
[10] S. Kelly,et al. Mutations in hmg1, Challenging the Paradigm of Clinical Triazole Resistance in Aspergillus fumigatus , 2019, mBio.
[11] A. Fahal,et al. VNTR confirms the heterogeneity of Madurella mycetomatis and is a promising typing tool for this mycetoma causing agent. , 2018, Medical mycology.
[12] O. Kurzai,et al. Azole-induced cell wall carbohydrate patches kill Aspergillus fumigatus , 2018, Nature Communications.
[13] A. Fahal,et al. Drug therapy for Mycetoma , 2018, Cochrane Database of Systematic Reviews.
[14] Torsten Schwede,et al. SWISS-MODEL: homology modelling of protein structures and complexes , 2018, Nucleic Acids Res..
[15] A. Fahal,et al. Closing the mycetoma knowledge gap. , 2018, Medical mycology.
[16] J. Guarro,et al. Multicenter, International Study of MIC/MEC Distributions for Definition of Epidemiological Cutoff Values for Sporothrix Species Identified by Molecular Methods , 2017, Antimicrobial Agents and Chemotherapy.
[17] E. Berkow,et al. Azole Antifungal Resistance in Candida albicans and Emerging Non-albicans Candida Species , 2017, Frontiers in microbiology.
[18] Ling Lu,et al. Screening and Characterization of a Non-cyp51A Mutation in an Aspergillus fumigatus cox10 Strain Conferring Azole Resistance , 2016, Antimicrobial Agents and Chemotherapy.
[19] G. Goldman,et al. Epidemiological and Genomic Landscape of Azole Resistance Mechanisms in Aspergillus Fungi , 2016, Front. Microbiol..
[20] J. Turnidge,et al. The role of epidemiological cutoff values (ECVs/ECOFFs) in antifungal susceptibility testing and interpretation for uncommon yeasts and moulds. , 2016, Revista iberoamericana de micologia.
[21] M. Goodfellow,et al. Mycetoma: a unique neglected tropical disease. , 2016, The Lancet. Infectious diseases.
[22] J. Turnidge,et al. Multicenter Study of Epidemiological Cutoff Values and Detection of Resistance in Candida spp. to Anidulafungin, Caspofungin, and Micafungin Using the Sensititre YeastOne Colorimetric Method , 2015, Antimicrobial Agents and Chemotherapy.
[23] G. S. de Hoog,et al. Application of Isothermal Amplification Techniques for Identification of Madurella mycetomatis, the Prevalent Agent of Human Mycetoma , 2015, Journal of Clinical Microbiology.
[24] Wendy Kloezen,et al. A Madurella mycetomatis Grain Model in Galleria mellonella Larvae , 2015, PLoS neglected tropical diseases.
[25] L. Cowen,et al. Mechanisms of Antifungal Drug Resistance. , 2015, Cold Spring Harbor perspectives in medicine.
[26] G. S. de Hoog,et al. In Vitro Interaction of Currently Used Azoles with Terbinafine against Madurella mycetomatis , 2014, Antimicrobial Agents and Chemotherapy.
[27] D. Stevens,et al. Revision of agents of black-grain eumycetoma in the order Pleosporales , 2014, Persoonia.
[28] M. Goodfellow,et al. Merits and Pitfalls of Currently Used Diagnostic Tools in Mycetoma , 2014, PLoS neglected tropical diseases.
[29] G. S. de Hoog,et al. Madurella mycetomatis Is Highly Susceptible to Ravuconazole , 2014, PLoS neglected tropical diseases.
[30] M. Bougnoux,et al. Azole resistant Aspergillus fumigatus: an emerging problem. , 2013, Medecine et maladies infectieuses.
[31] J. Pemán,et al. Antifungal Susceptibility Testing of Filamentous Fungi , 2012, Current Fungal Infection Reports.
[32] E. Zijlstra,et al. The safety and efficacy of itraconazole for the treatment of patients with eumycetoma due to Madurella mycetomatis. , 2011, Transactions of the Royal Society of Tropical Medicine and Hygiene.
[33] P. Escribano,et al. Aspergillus fumigatus Strains with Mutations in the cyp51A Gene Do Not Always Show Phenotypic Resistance to Itraconazole, Voriconazole, or Posaconazole , 2011, Antimicrobial Agents and Chemotherapy.
[34] Gert Vriend,et al. Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces , 2010, BMC Bioinformatics.
[35] G Kahlmeter,et al. Statistical characterisation of bacterial wild-type MIC value distributions and the determination of epidemiological cut-off values. , 2006, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.
[36] A. van Belkum,et al. In Vitro Susceptibilities of Madurella mycetomatis to Itraconazole and Amphotericin B Assessed by a Modified NCCLS Method and a Viability-Based 2,3-Bis(2-Methoxy-4-Nitro-5- Sulfophenyl)-5-[(Phenylamino)Carbonyl]-2H- Tetrazolium Hydroxide (XTT) Assay , 2004, Antimicrobial Agents and Chemotherapy.
[37] M. Ghannoum,et al. Antifungal Agents: Mode of Action, Mechanisms of Resistance, and Correlation of These Mechanisms with Bacterial Resistance , 1999, Clinical Microbiology Reviews.