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Iron overload in thalassemia and sickle cell disease

Show simple item record Taher A.
dc.contributor.editor Apr-2005 2017-10-05T15:38:42Z 2017-10-05T15:38:42Z 2005
dc.identifier 10.1053/j.seminhematol.2005.01.005
dc.identifier.issn 00371963
dc.description.abstract [No abstract available]
dc.language English
dc.publisher PHILADELPHIA
dc.relation.ispartof Publication Name: Seminars in Hematology; Publication Year: 2005; Volume: 42; suppl. 1;
dc.source Scopus
dc.title Iron overload in thalassemia and sickle cell disease
dc.type Conference Paper
dc.contributor.affiliation Taher, A., Hematology and Oncology, American University, Beirut Medical Center, Beirut, Lebanon, Department of Internal Medicine, American University of Beirut, Medical Center, PO Box 11-0236, Beirut 1107 2020, Lebanon
dc.contributor.authorAddress Taher, A.; Department of Internal Medicine, American University of Beirut, Medical Center, PO Box 11-0236, Beirut 1107 2020, Lebanon; email:
dc.contributor.authorCorporate University: American University of Beirut Medical Center; Faculty: Faculty of Medicine; Department: Internal Medicine;
dc.contributor.authorDepartment Internal Medicine
dc.contributor.authorFaculty Faculty of Medicine
dc.contributor.authorInitials Taher, A
dc.contributor.authorReprintAddress Taher, A (reprint author), Amer Univ Beirut, Dept Internal Med, Div Hematol Oncol, Med Ctr, POB 11-0236, Beirut 11072020, Lebanon.
dc.contributor.authorUniversity American University of Beirut Medical Center
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dc.description.citedCount 16
dc.description.citedTotWOSCount 10
dc.description.citedWOSCount 10
dc.format.extentCount 5
dc.identifier.coden SEHEA
dc.identifier.pubmedID 15846583
dc.identifier.scopusID 15744372350
dc.relation.ispartOfISOAbbr Semin. Hematol.
dc.relation.ispartofPubTitle Seminars in Hematology
dc.relation.ispartofPubTitleAbbr Semin. Hematol.
dc.relation.ispartOfSuppl 1
dc.relation.ispartOfVolume 42
dc.source.ID WOS:000228754900003
dc.type.publication Journal
dc.subject.otherChemCAS deferasirox, 201530-41-8
dc.subject.otherChemCAS deferiprone, 30652-11-0
dc.subject.otherChemCAS deferoxamine, 70-51-9
dc.subject.otherChemCAS Iron, 7439-89-6
dc.subject.otherIndex deferasirox
dc.subject.otherIndex deferiprone
dc.subject.otherIndex deferoxamine
dc.subject.otherIndex alpha thalassemia
dc.subject.otherIndex beta globin gene
dc.subject.otherIndex beta thalassemia
dc.subject.otherIndex bone marrow transplantation
dc.subject.otherIndex cell maturation
dc.subject.otherIndex chelation therapy
dc.subject.otherIndex conference paper
dc.subject.otherIndex correlation analysis
dc.subject.otherIndex cytokine production
dc.subject.otherIndex demography
dc.subject.otherIndex drug dose regimen
dc.subject.otherIndex drug tolerance
dc.subject.otherIndex erythrocyte
dc.subject.otherIndex erythropoiesis
dc.subject.otherIndex gene
dc.subject.otherIndex gene mutation
dc.subject.otherIndex gene silencing
dc.subject.otherIndex gene therapy
dc.subject.otherIndex genetic disorder
dc.subject.otherIndex hemoglobin determination
dc.subject.otherIndex human
dc.subject.otherIndex iron chelation
dc.subject.otherIndex iron metabolism
dc.subject.otherIndex iron overload
dc.subject.otherIndex pathophysiology
dc.subject.otherIndex priority journal
dc.subject.otherIndex sickle cell anemia
dc.subject.otherIndex statistical significance
dc.subject.otherIndex Anemia, Sickle Cell
dc.subject.otherIndex Humans
dc.subject.otherIndex Iron
dc.subject.otherIndex Iron Overload
dc.subject.otherIndex Models, Biological
dc.subject.otherIndex Thalassemia
dc.subject.otherKeywordPlus BONE-MARROW-TRANSPLANTATION
dc.subject.otherKeywordPlus BETA-THALASSEMIA
dc.subject.otherKeywordPlus ENDOCRINE FUNCTION
dc.subject.otherKeywordPlus CHELATING THERAPY
dc.subject.otherKeywordPlus FETAL-HEMOGLOBIN
dc.subject.otherKeywordPlus HEART-FAILURE
dc.subject.otherKeywordPlus HYDROXYUREA
dc.subject.otherKeywordPlus MANAGEMENT
dc.subject.otherKeywordPlus INTERMEDIA
dc.subject.otherKeywordPlus SURVIVAL
dc.subject.otherWOS Hematology

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