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dc.contributor.authorLoreto, Érico Silvapt_BR
dc.contributor.authorTondolo, Juliana Simoni Moraespt_BR
dc.contributor.authorJesus, Francielli Pantella Kunz dept_BR
dc.contributor.authorVerdi, Camila Marinapt_BR
dc.contributor.authorWeiblen, Carlapt_BR
dc.contributor.authorAzevedo, Maria Isabel dept_BR
dc.contributor.authorKommers, Glaucia Denisept_BR
dc.contributor.authorSantúrio, Jânio Moraispt_BR
dc.contributor.authorZanette, Regis Adrielpt_BR
dc.contributor.authorAlves, Sydney Hartzpt_BR
dc.date.accessioned2019-02-15T02:33:50Zpt_BR
dc.date.issued2019pt_BR
dc.identifier.issn0066-4804pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/188815pt_BR
dc.description.abstractWe evaluated the efficacy of azithromycin (50 mg/kg, every 12 h [q12h] orally) and miltefosine (25 mg/kg, q24h orally) treatments in an experimental model of vascular/disseminated pythiosis in immunosuppressed mice. Azithromycin was the only treatment able to reduce mortality. The histopathological findings showed acute vascular inflammation, pathogen dissemination, necrotizing myositis, neuritis, and arteritis. The results suggest that azithromycin, but not miltefosine, may have clinical relevance in the treatment of vascular/disseminated pythiosis.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofAntimicrobial agents and chemotherapy. Washington. Vol. 63, no. 1 (Jan. 2019), e01385-18, 7 p.pt_BR
dc.rightsOpen Accessen
dc.subjectAzitromicinapt_BR
dc.subjectPythium insidiosumen
dc.subjectAntifúngicospt_BR
dc.subjectAzithromycinen
dc.subjectMiltefosineen
dc.subjectPitiosept_BR
dc.subjectTreatmenten
dc.titleEfficacy of azithromycin and miltefosine in experimental systemic pythiosis in immunosuppressed micept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001084932pt_BR
dc.type.originEstrangeiropt_BR


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