Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/27102
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dc.contributor.authorRibas, Christian [UNIFESP]
dc.contributor.authorColleoni, Gisele Wally Braga [UNIFESP]
dc.date.accessioned2016-01-24T12:33:40Z-
dc.date.available2016-01-24T12:33:40Z-
dc.date.issued2003-01-01
dc.identifierhttp://dx.doi.org/10.1080/1042819021000035671
dc.identifier.citationLeukemia & Lymphoma. Abingdon: Taylor & Francis Ltd, v. 44, n. 2, p. 291-298, 2003.
dc.identifier.issn1042-8194
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/27102-
dc.description.abstractMultiple myeloma (MM) accounts for 1% of all malignancies and 10% of malignant hematological neoplasms. in spite of high-dose therapy with stem cell rescue, relapse and disease resistance are common events in the course of the disease. Thalidomide (Thal) has been successfully used in such situations and it's use has also been expanded to the up-front therapy and as adjuvant to stem cell transplantation. Here, we review the underlying concepts and current clinical data regarding Thal in the treatment of MM.en
dc.format.extent291-298
dc.language.isoeng
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofLeukemia & Lymphoma
dc.rightsAcesso restrito
dc.subjectmultiple myelomaen
dc.subjectthalidomideen
dc.subjecttreatmenten
dc.subjectreviewen
dc.titleAdvances in the treatment of multiple myeloma: the role of thalidomideen
dc.typeArtigo
dc.rights.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.description.affiliationUniversidade Federal de São Paulo, EPM, Dept Med, Discipline Hematol & Hemotherapy, São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, EPM, Dept Med, Discipline Hematol & Hemotherapy, São Paulo, Brazil
dc.identifier.doi10.1080/1042819021000035671
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000179633700012
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