Searches / Nihon Ishinkin Gakkai Zasshi = Japanese Journal Of Medical Mycology[JOURNAL]

Nihon Ishinkin Gakkai Zasshi = Japanese Journal Of Medical Mycology[JOURNAL]

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Treatment of onychomycosis caused by dermatophytes--an opinion proposed by Committee for Standardization of the Japanese Society for Medical Mycology 2007.

Mohri S, Watanabe S, Toshio K … +8 more , Shibuya K, Nishiyama Y, Abe M, Uno J, Oguri T, Maeasaki S, Ikeda R, Abe S

Nihon Ishinkin Gakkai Zasshi · 2008 · PMID 18277046 · Publisher ↗

After the rapid progress in therapeutic pharmaceutics against onychomycosis caused by dermatophytes in the 1990s, an optimal therapeutic strategy for individual patients with the onychomycosis has become possible for cli... After the rapid progress in therapeutic pharmaceutics against onychomycosis caused by dermatophytes in the 1990s, an optimal therapeutic strategy for individual patients with the onychomycosis has become possible for clinical dermatologists. In this review, we discuss on clinical problems concerning this disease and propose recommendable treatments for each patient with topical and/or systemic use of antifungal agents. Finally, with consideration of already published therapeutic guidelines, we stress the necessity of "order-made" therapy for each patient with his/her medical status and wishes taking into account.

[The 50th Anniversary Educational Symposium of the Japanese Society for Medical Mycology: sporotrichosis and chromomycosis].

Naka W

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 18161224

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[The 50th Anniversary Educational Symposium of the Japanese Society for Medical Mycology: Nocardiosis and actinomycosis].

Mikami Y

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 18161223

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[The 50th Anniversary Educational Symposium of the Japanese Society for Medical Mycology: Pathological study on mycoses].

Shibuya K

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 18161222

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[The 50th Anniversary Educational Symposium of the Japanese Society for Medical Mycology: Visceral mycoses].

Maesaki S

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 18161221

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[The 50th Anniversary Educational Symposium of the Japanese Society for Medical Mycology: Mycological study on Malassezia].

Sugita T

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 18161220

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[Abstracts of the 51st Annual Meeting of the Japanese Society for Medical Mycology, November 9-10, 2007, Gifu, Japan].

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 18046851

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[The 50th Anniversary Educational Symposium of the Japanese Society for Medical Mycology: Dermatomycoses caused by Malassezia].

Sei Y

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17975534 · Publisher ↗

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Identification of Nocardia farcinica by a PCR primer amplifying a specific DNA band for the bacterium.

Hasegawa T, Gonoi T, Ito J … +3 more , Kogure T, Yazawa K, Mikami Y

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17975533 · Publisher ↗

A PCR primer specific to Nocardia farcinica was prepared based on sequence information of random amplified polymorphic DNA (RAPD) analysis. The PCR primer amplifies N. farcinica species only; no amplification was observe... A PCR primer specific to Nocardia farcinica was prepared based on sequence information of random amplified polymorphic DNA (RAPD) analysis. The PCR primer amplifies N. farcinica species only; no amplification was observed in 25 other Nocardia strains that we tested. Specificity of the primer for N. farcinica was also confirmed using other fungal and bacterial strains that are frequently isolated from clinical samples such as sputa and broncho alveolar lavage (VAL).

Detection of pathogenic yeasts from processed fresh edible sea urchins sold in a fish market.

Kajikazawa T, Sugita T, Takashima M … +1 more , Nishikawa A

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17975532 · Publisher ↗

Yeasts of 17 processed fresh edible (raw) sea urchins obtained from seven countries were analyzed. In total, 45 to 7 x 10(4) colony-forming units (CFU)/g of sea urchins were recovered, and 23 yeast species were identifie... Yeasts of 17 processed fresh edible (raw) sea urchins obtained from seven countries were analyzed. In total, 45 to 7 x 10(4) colony-forming units (CFU)/g of sea urchins were recovered, and 23 yeast species were identified. Of these species, six pathogenic yeasts (Candida albicans, C. sake, Debaryomyces hansenii, Pichia anomala, Rhodotorula mucilaginosa, and Trichosporon mucoides) were detected from 11 sea urchins (65%). As these yeasts are opportunistic pathogens, infections in healthy individuals normally will not occur, but it should be understood that processed fresh edible sea urchin includes such opportunistic yeast pathogens.

Transcriptional changes in Candida albicans Genes by both farnesol and high cell density at an early stage of morphogenesis in N-acetyl-D-glucosamine medium.

Cho T, Aoyama T, Toyoda M … +3 more , Nakayama H, Chibana H, Kaminishi H

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17975531 · Publisher ↗

Quorum sensing through farnesol, a quorum sensing molecule, regulates virulence and morphogenesis in Candida albicans. Farnesol and high cell density of C. albicans repress hyphal formation in a minimal medium containing... Quorum sensing through farnesol, a quorum sensing molecule, regulates virulence and morphogenesis in Candida albicans. Farnesol and high cell density of C. albicans repress hyphal formation in a minimal medium containing N-acetyl-D-glucosamine. Global transcription profiling at an early stage of quorum sensing by C. albicans in the N-acetyl-D-glucosamine medium was analyzed. Twenty-two of a total of 53 genes responded to both farnesol and high cell density. From in silico analysis and previous published data, nine of these genes including those encoding amino acid biosynthesis were controlled by the Gcn4p regulator. Nine other genes which included genes encoding central carbon metabolism were controlled by negative regulators including Nrg1p, Tup1p, Ssn6p, and/or Mig1p. Other genes not controlled by these regulators included genes related to oxidative stress, glucose metabolism, and agglutination. Expression of genes related to amino acid biosynthesis and central carbon metabolism in this study is similar to a previous report of transcription profiling in C. albicans following its internalization by phagocyte cells and adaptation to host challenges.

[Clinical evaluation of terbinafine on onychomycosis with a 2 year follow-up].

Shibaki H

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17975530 · Publisher ↗

Over the 2 year period from October, 1997 to September, 2005, the clinical efficacy of 125 mg/day of terbinafine was evaluated in 356 patients with onychomycosis. Of these, 253 patients were followed up for 6 months afte... Over the 2 year period from October, 1997 to September, 2005, the clinical efficacy of 125 mg/day of terbinafine was evaluated in 356 patients with onychomycosis. Of these, 253 patients were followed up for 6 months after oral treatment of terbinafine, 120 for 1 year, and 56 for 2 years. The improvement ratio increased depending on follow-up period: 30.4% in 6 months, 65.0% in 1 year, and 67.9% in 2 years. However, in 25 patients who showed regression from onychomycosis at the 1 year period, 8 patients (32.0%) relapsed. The muddy rate of the first toenail was decreased from pre-treatment with terbinafine in 92.1% at 6 months, 91.7% at 1 year and 87.5% at 2 years. It is considered that efficacy of this medication is maintained within 1 year after the treatment, but the number of patients who experience a relapse is likely to increase from 1 year to 2 years.

Cytological study of cell cycle of the pathogenic yeast Cryptococcus neoformans.

Yamaguchi M, Ohkusu M, Biswas SK … +1 more , Kawamoto S

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17975529 · Publisher ↗

Cryptococcus neoformans is an opportunistic human pathogen belonging to basidiomycetous fungi and has unique properties in cell cycle progression. The purpose of this study was to measure the duration of the cell cycle i... Cryptococcus neoformans is an opportunistic human pathogen belonging to basidiomycetous fungi and has unique properties in cell cycle progression. The purpose of this study was to measure the duration of the cell cycle in this yeast. Under standard liquid culture conditions (1% yeast extract, 1% polypeptone, and 1% glucose; 24 degrees C; and 150 rpm), the doubling time of exponentially growing C. neoformans was 132 +/- 16 min (mean +/- standard deviation), and the durations of the G1, S, G2, and M phases were about 71, 18, 25, and 18 min, respectively. DNA synthesis started before bud emergence, and finished by the time the size of the bud became 1/4 that of the mother cell. The doubling time of the daughter cells was about twice that of the mother cells. The spindle pole body was located on the outer nuclear envelope and showed a duplicated form from the G1 phase to the G2 phase. These data form a basis for further cell cycle study of C. neoformans.

[Simple mycological methods].

Fujihiro M

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17853538

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[Molecular biological methods for dermatomycosis].

Mochizuki T

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17853537

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[Mycological study of Candida].

Nishikawa A

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17853536

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[Clinical aspect of dermal candidiasis].

Kato T

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17853534

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[Clinical aspect and mycology of dermatophytosis--the first step in identifying dermatophytes].

Nishimoto K

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17853533

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[Clinical aspect of dermatophytosis (ringworm)].

Hiruma S

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17667895

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Antifungal potential of disulfiram.

Khan S, Singhal S, Mathur T … +2 more , Upadhyay DJ, Rattan A

Nihon Ishinkin Gakkai Zasshi · 2007 · PMID 17667894 · Publisher ↗

Disulfiram, an alcohol antagonistic drug has been on the market since 1949 with 80% bioavailability and an established safety profile. Recently it has been reported as a P-glycoprotein efflux pump modulator. Herein we re... Disulfiram, an alcohol antagonistic drug has been on the market since 1949 with 80% bioavailability and an established safety profile. Recently it has been reported as a P-glycoprotein efflux pump modulator. Herein we report its antifungal potential. The MIC50 and MIC90 of disulfiram for yeast isolates is 4 and 8 microg/ml, respectively, and the MIC range is 1-16 micro g/ml for both fluconazole sensitive and resistant strains. Interestingly, disulfiram also showed fungicidal activity on Aspergillus spp. with MIC50 and MIC90 of 2 and 8 microg/ml, respectively.
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