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Treatment of Wilson's disease with zinc. I. Oral zinc therapy regimens

dc.contributor.authorHill, Gretchen M.en_US
dc.contributor.authorBrewer, George J.en_US
dc.contributor.authorPrasad, Ananda S.en_US
dc.contributor.authorHydrick, Connie R.en_US
dc.contributor.authorHartmann, Deborah E.en_US
dc.date.accessioned2006-04-28T16:52:57Z
dc.date.available2006-04-28T16:52:57Z
dc.date.issued1987-05en_US
dc.identifier.citationHill, Gretchen M.; Brewer, George J.; Prasad, Ananda S.; Hydrick, Connie R.; Hartmann, Deborah E. (1987)."Treatment of Wilson's disease with zinc. I. Oral zinc therapy regimens." Hepatology 7(3): 522-528. <http://hdl.handle.net/2027.42/38334>en_US
dc.identifier.issn0270-9139en_US
dc.identifier.issn1527-3350en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38334
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3570163&dopt=citationen_US
dc.description.abstractThe standard therapy for preventing copper accumulation in Wilson's disease, D-penicillamine, has been a life-saving drug, but it has many side effects and some patients are completely intolerant. We have been using oral zinc as another approach to the therapy for Wilson's disease, with copper balance studies as the key initial assessment of the adequacy of a given dose or regimen of zinc therapy. We earlier reported that an intensive regimen of zinc (zinc taken every 4 hr) was effective in controlling copper balance. We have now shown with balance studies that a simplified zinc therapy regimen of 50 mg zinc taken 3 times per day is effective in controlling copper balance. Preliminary work presented here with other simplified regimens also indicate their effectiveness. These studies increase the data base, in terms of copper balance, for zinc therapy of Wilson's disease, and expand the dose range and regimens of zinc which have been shown to control copper balance.en_US
dc.format.extent718846 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherW.B. Saundersen_US
dc.publisherWiley Periodiocals, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherHepatologyen_US
dc.titleTreatment of Wilson's disease with zinc. I. Oral zinc therapy regimensen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Clinical Research Center, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Internal Medicine, Wayne State University and Wayne State University School of Medicine, Detroit, Michigan 48201 ; Veterans Administration Hospital, Allen Park, Michigan 48101 ; University of Missouri-Columbia, College of Home Economics, Department of Human Nutrition Foods and Foods Systems Management, Columbia, Missouri 65211en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Clinical Research Center, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Internal Medicine, Wayne State University and Wayne State University School of Medicine, Detroit, Michigan 48201 ; Veterans Administration Hospital, Allen Park, Michigan 48101 ; University of Missouri-Columbia, College of Home Economics, Department of Human Nutrition Foods and Foods Systems Management, Columbia, Missouri 65211 ; Professor of Human Genetics and Internal Medicine, University of Michigan Medical School, Department of Human Genetics, 4708 Med Sci II, Box 0618. Ann Arbor, Michigan 48109–0618en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Clinical Research Center, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Internal Medicine, Wayne State University and Wayne State University School of Medicine, Detroit, Michigan 48201 ; Veterans Administration Hospital, Allen Park, Michigan 48101 ; University of Missouri-Columbia, College of Home Economics, Department of Human Nutrition Foods and Foods Systems Management, Columbia, Missouri 65211en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Clinical Research Center, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Internal Medicine, Wayne State University and Wayne State University School of Medicine, Detroit, Michigan 48201 ; Veterans Administration Hospital, Allen Park, Michigan 48101 ; University of Missouri-Columbia, College of Home Economics, Department of Human Nutrition Foods and Foods Systems Management, Columbia, Missouri 65211en_US
dc.contributor.affiliationumDepartments of Human Genetics and Internal Medicine and the Clinical Research Center, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Internal Medicine, Wayne State University and Wayne State University School of Medicine, Detroit, Michigan 48201 ; Veterans Administration Hospital, Allen Park, Michigan 48101 ; University of Missouri-Columbia, College of Home Economics, Department of Human Nutrition Foods and Foods Systems Management, Columbia, Missouri 65211en_US
dc.identifier.pmid3570163en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38334/1/1840070318_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/hep.1840070318en_US
dc.identifier.sourceHepatologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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