Evaluation of six commercial kits for detection of human immunoglobulin M antibodies to Toxoplasma gondii. The FDA Toxoplasmosis Ad Hoc Working Group.

As a result of reports received by the Food and Drug Administration (FDA) of false-positive results obtained with FDA-cleared in vitro diagnostic kits for the detection of Toxoplasma-specific human immunoglobulin M (IgM) antibodies, an FDA-sponsored evaluation of six kits was performed. A battery of...

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Bibliografske podrobnosti

izdano v:	J Clin Microbiol
Principais autores:	Wilson, M, Remington, J S, Clavet, C, Varney, G, Press, C, Ware, D
Format:	Artigo
Jezik:	Inglês
Izdano:	American Society for Microbiology (ASM) 1997
Teme:	Research Article
Online dostop:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC230132/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9399504/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jcm.35.12.3112-3115.1997
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