Author: Ana Requena-Méndez; Joaquin Salas-Coronas; Fernando Salvador; Joan Gomez-Junyent; Judith Villar-Garcia; Miguel Santin; Carme Muñoz; Ana Gonzalez-Cordon; Maria Teresa Cabezas Fernández; Elena Sulleiro; Maria del Mar Arenas; Dolors Somoza; Jose Vazquez-Villegas; Begoña Treviño; Esperanza Rodríguez; Maria Eugenia Valls; Carme Subirá; Jose Muñoz
Title: High Prevalence of Strongyloidiasis in Spain: A Hospital-Based Study Document date: 2019_11_22
ID: 5dqhhzff_19
Snippet: . CC-BY 4.0 International license author/funder. It is made available under a The copyright holder for this preprint (which was not peer-reviewed) is the . https://doi.org/10.1101/852558 doi: bioRxiv preprint Serum samples were tested for specific antibodies using a commercial Enzyme Linked Immunosorbent assay (ELISA) assays according to the manufacturer's instructions. A single ELISA test was used (Strongyloidiasis ELISA Kit based on IVD Strongy.....
Document: . CC-BY 4.0 International license author/funder. It is made available under a The copyright holder for this preprint (which was not peer-reviewed) is the . https://doi.org/10.1101/852558 doi: bioRxiv preprint Serum samples were tested for specific antibodies using a commercial Enzyme Linked Immunosorbent assay (ELISA) assays according to the manufacturer's instructions. A single ELISA test was used (Strongyloidiasis ELISA Kit based on IVD Strongyloides stercoralis crude antigen). To reduce the inter-laboratory variability, an internal workshop was carried out before starting the study to standardized the serological techniques and also the interpretation of the results. Positive samples are defined by absorbance greater than 0.2 OD units. The absorbance of study sample/0.2>=1 (calculated value) was used as the cut-off.
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