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Guidelines for pediatric management of severe chronic neutropenia

dc.contributor.authorDale, David C.en_US
dc.contributor.authorBoxer, Laurence A.en_US
dc.date.accessioned2012-03-16T16:02:01Z
dc.date.available2013-04-01T14:17:26Zen_US
dc.date.issued2012-02en_US
dc.identifier.citationDale, David C.; Boxer, Laurence A. (2012). "Guidelines for pediatric management of severe chronic neutropenia ." American Journal of Hematology 87(2): 133-133. <http://hdl.handle.net/2027.42/90415>en_US
dc.identifier.issn0361-8609en_US
dc.identifier.issn1096-8652en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/90415
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.titleGuidelines for pediatric management of severe chronic neutropeniaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumPediatric Hematology/Oncology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDeptartment of Medicine, University of Washington, Seattle, Washingtonen_US
dc.contributor.affiliationotherUniversity of Washington, Box 356422, 1959 NE Pacific St., Rm AA522, Seattle, WA 98195en_US
dc.identifier.pmid22237723en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/90415/1/23107_ftp.pdf
dc.identifier.doi10.1002/ajh.23107en_US
dc.identifier.sourceAmerican Journal of Hematologyen_US
dc.identifier.citedreferenceZeidler C, Germeshausen M, Klein C, Welte K. Clinical implications of ELA2‐, HAX1‐, and GCSF‐receptor (CSF3R) mutations in severe congenital neutropenia. Br J Haematol 2009; 144: 459 – 467.en_US
dc.identifier.citedreferenceDale DC, Bonilla MA, Davis MW, et al. A randomized controlled phase III trial of recombinant human granulocyte colony‐stimulating factor (filgrastim) for treatment of severe chronic neutropenia. Blood 1993; 81: 2496 – 2502.en_US
dc.identifier.citedreferenceRosenberg PS, Zeidler C, Bolyard AA, et al. Stable long‐term risk of leukaemia in patients with severe congenital neutropenia maintained on G‐CSF therapy. Br J Haematol 2010; 150: 196 – 199.en_US
dc.identifier.citedreferenceRosenberg PS, Alter BP, Bolyard AA, et al. The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long‐term G‐CSF therapy. Blood 2006; 107: 4628 – 4635.en_US
dc.identifier.citedreferenceDale DC, Bolyard AA, Schwinzer BG, et al. The Severe Chronic Neutropenia International Registry: 10‐year follow‐up report. Support Cancer Ther 2006; 3: 220 – 231.en_US
dc.identifier.citedreferenceDale DC, Cottle TE, Fier CJ, et al. Severe chronic neutropenia: Treatment and follow‐up of patients in the Severe Chronic Neutropenia International Registry. Am J Hematol 2003; 72: 82 – 93.en_US
dc.identifier.citedreferenceFioredda F, Calvillo M, Bonanomi S, et al. Congenital and acquired neutropenias: Consensus guidelines on therapy and follow‐up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato‐Oncologia Pediatrica). Am J Hematol 2011 [Epub ahead of print].en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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