In Vitro Susceptibilities of Malassezia Species to a New Triazole, Albaconazole (UR-9825), and Other Antifungal Compounds
Author:
Affiliation:
1. Department of Microbiology, Hospital Universitario 12 de Octubre, Madrid
2. Department of Dermatology, Complejo Hospitalario Universitario, Faculty of Medicine, Santiago de Compostela, Spain
Abstract
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Link
https://journals.asm.org/doi/pdf/10.1128/AAC.47.7.2342-2344.2003
Reference30 articles.
1. Ahn, K. J., and H. R. Ashbee. 1996. Determination of minimum inhibitory concentrations of several azole antifungals for Malassezia furfur. Ann. Dermatol.8:187-194.
2. Bartrolí, J., E. Turmo, M. Algueró, E. Boncompte, M. L. Vericat, L. Conte, J. Ramis, M. Merlos, J. García-Rafanell, and J. Forn. 1998. New azole antifungals. 3. Synthesis and antifungal activity of 3-substituted 4 (3H)-quinazolinones. J. Med. Chem.41:1869-1882.
3. Monitoring spread of Malassezia infections in a neonatal intensive care unit by PCR-mediated genetic typing
4. In Vitro Antifungal Activities of the New Triazole UR-9825 against Clinically Important Filamentous Fungi
5. In Vitro Activities of Four Novel Triazoles against Scedosporium spp
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