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Clinical and Vaccine Immunology, June 2007, p. 802-803, Vol. 14, No. 6
1071-412X/07/$08.00+0 doi:10.1128/CVI.00035-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

MiraVista Diagnostics and MiraBella Technologies, Indianapolis, Indiana
Received 16 January 2007/ Returned for modification 8 March 2007/ Accepted 22 March 2007
The sensitivity of detection of antigenuria in patients positive by the MiraVista Diagnostics Histoplasma enzyme immunoassay (MVD EIA) was 44% with the IMMY ALPHA Histoplasma antigen EIA. The specificity was 84% with the IMMY EIA versus 98% with the MVD EIA. The correlation between assays for positive cases was weak (r2 = 0.430).
Published ahead of print on 4 April 2007.
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