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   1 redict the susceptibility of Candida spp. to ravuconazole.                                           
     2 fluconazole, voriconazole, posaconazole, and ravuconazole.                                           
     3 redict the susceptibility of Candida spp. to ravuconazole.                                           
     4 ew triazoles voriconazole, posaconazole, and ravuconazole.                                           
     5  of isolates at <or=1 microg/ml, followed by ravuconazole (91%), voriconazole (90%), and itraconazole
  
     7 gin, a new echinocandin, in combination with ravuconazole, a second-generation triazole, against expe
  
  
    10  of cross-resistance between fluconazole and ravuconazole and the use of fluconazole as a surrogate m
  
  
  
  
  
    16  The investigational triazoles posaconazole, ravuconazole, and voriconazole had excellent in vitro ac
    17 ment was good to excellent for itraconazole, ravuconazole, and voriconazole MFCs with RPMI and M3 (93
    18  The investigational triazoles posaconazole, ravuconazole, and voriconazole were all highly active ag
    19 ) MICs of three new triazoles (posaconazole, ravuconazole, and voriconazole) and the echinocandin cas
  
  
    22     Cross-resistance between fluconazole and ravuconazole applies most directly to fluconazole-resist
    23 azoles all have some in vitro activity, with ravuconazole being the most active (MIC(50), 0.25 microg
    24 ecies were inhibited by < or =1 microg/ml of ravuconazole (concentration at which 50% were inhibited 
    25 hagas, and antifungal drugs posaconazole and ravuconazole have entered clinical trials in Spain, Boli
    26 agonism between liposomal amphotericin B and ravuconazole in simultaneous treatment of experimental i
  
    28  of caspofungin, posaconazole, voriconazole, ravuconazole, itraconazole, and amphotericin B against 4
  
  
  
    32 azole MICs of </=32 microg/ml susceptible to ravuconazole, resulting in a categorical agreement rate 
    33 nce of fluconazole as a surrogate marker for ravuconazole susceptibility was improved by designating 
  
    35  laboratories of itraconazole, posaconazole, ravuconazole, voriconazole, and amphotericin B MFCs for 
    36 n B, flucytosine, fluconazole, posaconazole, ravuconazole, voriconazole, and caspofungin of 601 invas
  
    38 rains were inhibited by < or =1 microg/ml of ravuconazole, voriconazole, itraconazole, and amphoteric
  
    40 fluconazole, voriconazole, posaconazole, and ravuconazole were determined by the National Committee f
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