{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,30]],"date-time":"2026-03-30T12:08:24Z","timestamp":1774872504971,"version":"3.50.1"},"reference-count":5,"publisher":"Oxford University Press (OUP)","issue":"5","license":[{"start":{"date-parts":[[2019,3,6]],"date-time":"2019-03-06T00:00:00Z","timestamp":1551830400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2019,11,6]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Neuroschistosomiasis is a rare but severe manifestation of Schistosoma infection. Diagnosis is challenging and surgical biopsy is often required to confirm diagnosis and exclude malignancy. We present a pediatric case of presumed pseudotumoral cerebral schistosomiasis secondary to Schistosoma mansoni with an excellent therapeutic response to empirical praziquantel and corticosteroid treatment.<\/jats:p>","DOI":"10.1093\/jpids\/piz009","type":"journal-article","created":{"date-parts":[[2019,1,29]],"date-time":"2019-01-29T10:19:00Z","timestamp":1548757140000},"page":"489-491","source":"Crossref","is-referenced-by-count":12,"title":["Pediatric Neuroschistosomiasis: A Case Report and Review of the Literature"],"prefix":"10.1093","volume":"8","author":[{"given":"Sophie C H","family":"Wen","sequence":"first","affiliation":[{"name":"Infection Management Prevention Service, Queensland Children\u2019s Hospital, Brisbane, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rebecca","family":"Anderson","sequence":"additional","affiliation":[{"name":"Infectious Diseases Unit, Department of General Medicine, Victoria, 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