<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Martinez-Peinado N</submitter><funding>Ministerio de Ciencia e Innovación</funding><funding>Departament de Salut, Generalitat de Catalunya</funding><funding>&amp;apos;la Caixa&amp;apos; Foundation</funding><pagination>e0012166</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11326570</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(8)</volume><pubmed_abstract>Chagas disease, caused by the parasite Trypanosoma cruzi, affects over 6 million people, mainly in Latin America. Two different clinical phases, acute and chronic, are recognised. Currently, 2 anti-parasitic drugs are available to treat the disease (nifurtimox and benznidazole), but diagnostic methods require of a relatively complex infrastructure and trained personnel, limiting its widespread use in endemic areas, and the access of patients to treatment. New diagnostic methods, such as rapid tests (RDTs) to diagnose chronic Chagas disease, or loop-mediated isothermal amplification (LAMP), to detect acute infections, represent valuable alternatives, but the parasite's remarkable genetic diversity might make its implementation difficult. Furthermore, determining the efficacy of Chagas disea</pubmed_abstract><journal>PLoS neglected tropical diseases</journal><pubmed_title>A guide for the generation of repositories of clinical samples for research on Chagas disease.</pubmed_title><pmcid>PMC11326570</pmcid><funding_grant_id>CERCA Program</funding_grant_id><funding_grant_id>PID2019-109090RB-100/AEI/10.13039/501100011033</funding_grant_id><funding_grant_id>CEX2018-000806-S</funding_grant_id><funding_grant_id>LCF/BQ/DI21/11860037</funding_grant_id><pubmed_authors>Aguero F</pubmed_authors><pubmed_authors>Carmen Thomas M</pubmed_authors><pubmed_authors>Lopez MC</pubmed_authors><pubmed_authors>Pinazo MJ</pubmed_authors><pubmed_authors>Gascon J</pubmed_authors><pubmed_authors>Scandale I</pubmed_authors><pubmed_authors>Alonso-Padilla J</pubmed_authors><pubmed_authors>Alarcon de Noya B</pubmed_authors><pubmed_authors>Gomez A</pubmed_authors><pubmed_authors>NHEPACHA Network (New Tools for the Diagnosis and Evaluation of Chagas Disease)</pubmed_authors><pubmed_authors>Hasslocher-Moreno AM</pubmed_authors><pubmed_authors>Losada Galvan I</pubmed_authors><pubmed_authors>Schijman AG</pubmed_authors><pubmed_authors>Rodrigues Ferreira R</pubmed_authors><pubmed_authors>Torrico F</pubmed_authors><pubmed_authors>Gabaldon-Figueira JC</pubmed_authors><pubmed_authors>Cremonini Araujo-Jorge T</pubmed_authors><pubmed_authors>Martinez-Peinado N</pubmed_authors><pubmed_authors>Noya-Gonzalez O</pubmed_authors><pubmed_authors>Mariano Ruiz A</pubmed_authors><pubmed_authors>Rojas G</pubmed_authors><pubmed_authors>Gonzalez Martinez A</pubmed_authors><pubmed_authors>Beron S</pubmed_authors><pubmed_authors>Magalhaes Saraiva R</pubmed_authors><pubmed_authors>Ramsey J</pubmed_authors><pubmed_authors>Maldonado RA</pubmed_authors><pubmed_authors>Pinto J</pubmed_authors></additional><is_claimable>false</is_claimable><name>A guide for the generation of repositories of clinical samples for research on Chagas disease.</name><description>Chagas disease, caused by the parasite Trypanosoma cruzi, affects over 6 million people, mainly in Latin America. Two different clinical phases, acute and chronic, are recognised. Currently, 2 anti-parasitic drugs are available to treat the disease (nifurtimox and benznidazole), but diagnostic methods require of a relatively complex infrastructure and trained personnel, limiting its widespread use in endemic areas, and the access of patients to treatment. New diagnostic methods, such as rapid tests (RDTs) to diagnose chronic Chagas disease, or loop-mediated isothermal amplification (LAMP), to detect acute infections, represent valuable alternatives, but the parasite's remarkable genetic diversity might make its implementation difficult. Furthermore, determining the efficacy of Chagas disea</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2025-04-21T22:06:54.203Z</modification><creation>2025-04-05T18:37:03.717Z</creation></dates><accession>S-EPMC11326570</accession><cross_references><pubmed>39146233</pubmed><doi>10.1371/journal.pntd.0012166</doi></cross_references></HashMap>