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1 anidulafungin, caspofungin, micafungin, and terbinafine.
2 ytotoxic effect of Transfersome(R)-delivered terbinafine.
3 ars to potentiate the antifungal activity of terbinafine.
4 nazole and less active than itraconazole and terbinafine.
5 fluconazole, griseofulvin, itraconazole, and terbinafine.
6 avoid harm when treating patients with oral terbinafine.
7 y overall for the azoles, echinocandins, and terbinafine.
9 ween both methods were as follows: 100% with terbinafine, 97.8% with ciclopirox, and 89.1% with voric
11 ts had comparable effects on the activity of terbinafine, an inhibitor of squalene epoxidase within t
12 ubrum strains known to have elevated MICs to terbinafine and five Trichophyton mentagrophytes strains
14 gainst the Ochroconis isolates revealed that terbinafine and micafungin were the most active drugs.
17 ith those of the Transfersome vehicle, naked terbinafine, and commercially available terbinafine (1%)
18 the mean MICs of fluconazole, itraconazole, terbinafine, and griseofulvin were 2.07 +/- 0.29, 0.13 +
21 ally relevant liver toxic effects related to terbinafine at a prevalence of 75% was between $18.2 mil
23 ifungal susceptibilities of dermatophytes to terbinafine, ciclopirox, and voriconazole in comparison
24 o 0.25 mug/ml, and 0.008 to 0.025 mug/ml for terbinafine, ciclopirox, and voriconazole, respectively.
26 e results show that empirical treatment with terbinafine for patients with suspected onychomycosis is
27 d cure outcome, butenafine hydrochloride and terbinafine hydrochloride were significantly more effica
28 ed dosage form (liquid spray) of 15 mg/ml of terbinafine in Transfersome that has been developed to d
29 t TDT 067 (a topical formulation of 15 mg/ml terbinafine in Transfersome(R) vesicles) has a much more
30 or the treatment of tinea capitis, including terbinafine, itraconazole, and fluconazole in this era o
31 of dermatophytes were compared with those of terbinafine, itraconazole, ketoconazole, griseofulvin, a
35 vi) Treatment of S. cerevisiae with azole or terbinafine resulted in transcriptional upregulation of
38 ection using the sterol synthesis inhibitors terbinafine (TBF, targeting squalene epoxidase) and itra
39 f 75%, per-patient cost savings of empirical terbinafine therapy without confirmatory testing was $47
40 ansfersomes deliver the lipophilic fungicide Terbinafine to the fungal cell wall, (b) the membrane so
43 n vitro activity of amphotericin B (AMB) and terbinafine (TRB) and of the echinocandins against Penic
44 as used to study the in vitro interaction of terbinafine (TRB) with fluconazole (FLU), itraconazole (
45 mic reticulum, which was more efficient when terbinafine was delivered in Transfersome(R) vesicles (T
48 t activity were caspofungin, micafungin, and terbinafine, while amphotericin B showed the least activ
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