{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T04:25:27Z","timestamp":1790915127942,"version":"4.1.0"},"reference-count":17,"publisher":"American Society for Microbiology","issue":"5","license":[{"start":{"date-parts":[[2010,5,1]],"date-time":"2010-05-01T00:00:00Z","timestamp":1272672000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Clin Vaccine Immunol"],"published-print":{"date-parts":[[2010,5]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            The plasmatic levels of 1,3-\u03b2-\n            <jats:sc>d<\/jats:sc>\n            -glucan (BDG) were &gt;523 pg\/ml in 4 children, 2 low-birth-weight neonates and 2 stem cell transplant recipients, with the following invasive fungal diseases (IFD) proven apart from this BDG test: 3 cases of\n            <jats:italic>Candida parapsilosis<\/jats:italic>\n            candidemias and 1 case of disseminated aspergillosis. The BDG test may be useful for identification of IFD in pediatrics.\n          <\/jats:p>","DOI":"10.1128\/cvi.00038-10","type":"journal-article","created":{"date-parts":[[2010,3,25]],"date-time":"2010-03-25T03:29:05Z","timestamp":1269487745000},"page":"882-883","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":46,"title":["High Levels of \u03b2-\n            <scp>d<\/scp>\n            -Glucan in Immunocompromised Children with Proven Invasive Fungal Disease"],"prefix":"10.1128","volume":"17","author":[{"given":"Alessandra","family":"Mularoni","sequence":"first","affiliation":[{"name":"Infectious Diseases Unit"},{"name":"Hemopoietic Stem Cell Transplant Unit"},{"name":"Pediatric Intensive Care Unit"},{"name":"Neonatal Intensive Care Unit"},{"name":"Laboratory of Clinical Microbiology, G. 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