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dc.contributor.authorHazeldine, S.
dc.contributor.authorTrinder, D.
dc.contributor.authorOlynyk, John
dc.date.accessioned2017-01-30T14:22:41Z
dc.date.available2017-01-30T14:22:41Z
dc.date.created2014-01-20T20:01:12Z
dc.date.issued2013
dc.identifier.citationHazeldine, Simon and Trinder, Debbie and Olynyk, John K. 2013. Non-Hfe iron overload: Is phlebotomy the answer? Current Hepatitis Reports. 12 (1): pp. 20-27.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/38540
dc.identifier.doi10.1007/s11901-012-0153-3
dc.description.abstract

Non-Hfe Iron Overload: Is Phlebotomy the Answer?Iron is an essential factor for life, however a physiologically optimal balance is critical. In this article we explore the role of iron as a co-factor in a range of chronic liver diseases and how it may contribute to the development of liver injury, fibrosis, cirrhosis and ultimately hepatocellular carcinoma. Whilst iron depletion therapy through phlebotomy is the most effective method of reducing iron stores, it is unclear whether this offers utility in the therapy of liver diseases in which iron is not the primary insult resulting in tissue injury. Here we examine the emerging evidence in the field of non-HFE hereditary haemochromatosis conditions associated with iron overload – is phlebotomy the answer?

dc.publisherCurrent Science, Inc
dc.titleNon-Hfe iron overload: Is phlebotomy the answer?
dc.typeJournal Article
dcterms.source.volume12
dcterms.source.startPage20
dcterms.source.endPage27
dcterms.source.issn1540-3416
dcterms.source.titleCurrent Hepatitis Reports
curtin.note

The final publication is available at link.springer.com

curtin.note

NOTICE: This is the author’s version of a work in which changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication.

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curtin.accessStatusOpen access


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