Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54836
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dc.contributor.authorSuwakon Wongjaikamen_US
dc.contributor.authorSirinart Kumfuen_US
dc.contributor.authorSiriporn C. Chattipakornen_US
dc.contributor.authorSuthat Fucharoenen_US
dc.contributor.authorNipon Chattipakornen_US
dc.date.accessioned2018-09-04T10:24:49Z-
dc.date.available2018-09-04T10:24:49Z-
dc.date.issued2015-10-15en_US
dc.identifier.issn18790712en_US
dc.identifier.issn00142999en_US
dc.identifier.other2-s2.0-84940040361en_US
dc.identifier.other10.1016/j.ejphar.2015.08.017en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84940040361&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54836-
dc.description.abstract© 2015 Elsevier B.V. All rights reserved. Iron overload cardiomyopathy is the major cause of death in transfusion-dependent thalassemia (TDT) patients. Growing evidence demonstrates that combined iron chelators, or the combination of an iron chelator with antioxidant(s) are effective in diminishing myocardial iron deposition and attenuating cardiac dysfunction. This review comprehensively summarizes basic and clinical reports on the therapeutic efficacy of combined iron chelators, or the combination of an iron chelator with antioxidant(s) on the heart. Promising benefits of these treatments in preventing cardiac dysfunction due to iron overload could provide extensive insight into future therapeutic strategies for better treatment and prevention of cardiomyopathy in TDT patients.en_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleCurrent and future treatment strategies for iron overload cardiomyopathyen_US
dc.typeJournalen_US
article.title.sourcetitleEuropean Journal of Pharmacologyen_US
article.volume765en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMahidol Universityen_US
Appears in Collections:CMUL: Journal Articles

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