Performance evaluation of the FDA-approved Determine™ HIV-1/2 Ag/Ab Combo assay using plasma and whole blood specimens

Author:

Masciotra Silvina,Luo Wei,Westheimer Emily,Cohen Stephanie E.,Gay Cynthia L.,Hall Laura,Pan Yi,Peters Philip J.,Owen S. Michele

Publisher

Elsevier BV

Subject

Infectious Diseases,Virology

Reference30 articles.

1. Establishing the diagnosis of HIV infection: new tests and a new algorithm for the United States;Branson;J. Clin. Virol.,2011

2. Laboratory Testing for the Diagnosis of HIV Infection: Updated Recommendations;Centers for Disease Control and Prevention and Association of Public Health Laboratories,2014

3. Detection of acute HIV infection in two evaluations of a new HIV diagnostic testing algorithm-United States, 2011–2013;Geren;MMWR,2013

4. Evaluation of an alternative HIV diagnostic algorithm using specimens from seroconversion panels and persons with established HIV infections;Masciotra;J. Clin. Virol.,2011

5. Performance evaluation of the Bio-Rad Laboratories GS HIV Combo Ag/Ab EIA, a 4th generation HIV assay for the simultaneous detection of HIV p24 antigen and antibodies to HIV-1 (groups M and O) and HIV-2 in human serum or plasma;Bentsen;J. Clin. Virol.,2011

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