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dc.contributor.authorCovitz, Wesley-
dc.contributor.authorFelice, Alex-
dc.contributor.authorMilner, Paul F.-
dc.contributor.authorMcKie, Virgil C.-
dc.contributor.authorMcKie, Kathleen Mood-
dc.contributor.authorStrong, William B.-
dc.contributor.authorDavis, Harry C.-
dc.date.accessioned2018-04-09T10:11:32Z-
dc.date.available2018-04-09T10:11:32Z-
dc.date.issued1987-
dc.identifier.citationCovitz, W., Felice, A. E., Milner, P. F., McKie, V. C., McKie, K. M., Strong, W. B., & Davis, H. C. (1987). Heart disease In thalassemia heterozygotes with sickle cell anemia. Pediatric Research, 21(4), 188A.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/28924-
dc.description.abstractThe purpose of this study was to ascertain whether thalassemia heterozygotes (α thal) who have sickle cell anemia (SCA) suffer fewer cardiac effects of their SCA due to an increased oxygen carrying capacity or decreased sickling. Echocardiograms and graded, maximal exercise tests were performed in 22 subjects withα thal and SCA, and in 22 age and sex matched controls (C) with SCA alone. The patients ranged in age from 8-32 years.en_GB
dc.language.isoenen_GB
dc.publisherNature Publishing Groupen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectHeart -- Diseasesen_GB
dc.subjectThalassemiaen_GB
dc.subjectSickle cell anemiaen_GB
dc.titleHeart disease in thalassemia heterozygotes with sickle cell anemiaen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.publication.titlePediatric Researchen_GB
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