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Microsporum gypseum

Kanbe, T. and Tanaka, K. (1982). Ultrastructure of the invasion of human hair in vitro by the keratinophilic fungus Microsporum gypseum. Infect. Immun. 38, 706-715. [Pg.145]

Kunert, J. (1992) Effect of reducing agents on proteolytic and keratinolytic activity of enzymes of Microsporum gypseum. Mycoses 35, 343-348. [Pg.145]

Kunert, J. (1987). Utilization of various concentrations of free cystine by the fungus Microsporum gypseum. J. Basic Microbiol. 27, 207-213. [Pg.145]

Kunert, J. (1989a). Biochemical Mechanism of Keratin Degradation by the actino-mycete Streptomyces fradiae and the fungus Microsporum gypseum a comparison. /. Basic Microbiol. 29, 597-604. [Pg.145]

Kunert, J. and Krajci, D. (1981). An electron microscopy study of keratin degradation by the fungus Microsporum gypseum in vitro. Mykosen 24, 485-496. [Pg.145]

The minimum inhibitory concentrations (MIC) of liriodenine versus the superficial dermatophytes Trichophyton mentagrophytes (ATCC 9972) and Microsporum gypseum (ATCC 14683) in a complex medium were 3.12 pg/ml and 100 pg/ml, respectively. In a defined medium against the same organisms, the values were 0.78 pg/ml and 3.12 pg/ml, respectively [337],... [Pg.153]

Tolnaftate is a thiocarbamate. Tolnaftate is effective in the treatment of most cutaneous mycoses caused by T. rubrum, T. mentagrophytes, T. tonsurans, E. floccosum, M. canis, M. audouinii, Microsporum gypseum, and M. furfur, but it is ineffective against Candida. In tinea pedis, the cure rate is around 80%, compared with about 95% for miconazole. Toxic or allergic reactions to tolnaftate have not been reported. [Pg.697]

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