Results 191 to 200 of about 7,424 (208)

Studies on Haemagglutinins of Microsporum gypseum

Mycoses, 1985
Summary: 36 isolates of Microsporum gypseum recovered from Egyptian soil were found to be capable of agglutinating red blood cells of cow, buffalo, camel, sheep, chicken, duck, pigeon, Guinea pig and mouse. Also microconidial variants obtained dnring repeated subculturing had the same property.
F. El‐Far, Mohamed Refai, R. Soliman, S. Attia   +3 more
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Atypical strains of Microsporum canis

Mycopathologia, 1978
Four atypical isolates of Microsporum canis, three from humans and one from a cat, were obtained from North-West London. These and a further human isolate were compared with each other and with a typical isolate of the fungus. Immediately after isolation the atypical isolates were very labile, but were stabilised after a few subcultures from selected ...
W. D. L. Tucker, Mary P. English
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The changing face of Microsporum spp infections

Clinics in Dermatology, 2010
Significant changes in epidemiology, etiology, and the clinical pattern of mycotic infections caused by Microsporum spp have been observed in recent years. Fungal infections caused by M canis, followed by M gypseum and M hominis, involving skin and its appendages, represent one of the most common diseases worldwide and a recalcitrant problem in ...
Mihael Skerlev, Paola Miklić
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Partial characterization of proteolytic enzymes of Microsporum canis and Microsporum cookei

Mycoses, 1996
Summary. Characterization by proteinase inhibitors of the enzymes produced by Microsporum spp. revealed that Microsporum canis and Microsporum cookei produce serine proteinase(s), but only M. canis expresses aspartic and cysteine proteinases and probably a metalloproteinase. Both M. canis and M. cookei expressed metalloelastinolytic proteinases.
M. Baxter, M. F. Simpanya
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FUSEAUX FORMATION OF THE GENUS MICROSPORUM

Archives of Dermatology, 1950
IN 1947, three strains of Microsporum were isolated from the scalp of an adolescent girl with tinea capitis. The infection was noteworthy for its resistance to therapy and for the joint occurrence of Microsporum audouini and Microsporum canis. 1 The strains were named A, B and C.
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Epidemic Due to Microsporum Canis

Archives of Dermatology, 1958
Although tinea capitis and tinea circinata caused by Microsporum canis are fairly common diseases, they most often cause sporadic infections. 1,2 In the summer of 1957, a sudden small epidemic involving at least 12 persons occurred in a small town, and all cases could be traced to one kitten.
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The Macroconidium Appendage in Microsporum Gypseum

Mycologia, 1969
The macroconidial appendages in Microsporum gypseum are borne by a group of macroconidia whose frequency in one strain varies with age and growth conditions of the culture. Most frequently the appendages are borne singly on the apical cell; infrequently they are borne singly on the basal cell, in pairs on the apical cell, or one at each end of the ...
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Protoplasts of Microsporum Gypseum Conidia:* Protoplasten der Konidien von Microsporum gypseum

Mycoses, 1979
Summary: The technique of cell wall enzymatic lysis was used to prepare protoplasts from the microconidia of Microsporum gypseum. Cell wall elimination was immunologically verified. Protoplasts isolated from microconidia were found to be of the following two types: large with a vacuole and small without one. The small protoplasts regenerated on plates
E. Weigl, M. Hejtmänek
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Perfect Stage of Microsporum gypseum

Nature, 1960
IN 1927, Nannizzi1 reported the discovery of the perfect stage of Microsporum gypseum (Bodin) Guiart and Grigoraki and named it Gymnoascus gypseum Nannizzi. This work was criticized on a number of grounds, and, as there has been no record of its successful repetition, it has been generally disregarded.
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MICROSPORUM CANIS DERMATOMYCOSIS

Medical Journal of Australia, 1965
A. Rao, D. J. Hodges
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