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Frentizole Therapy of Active Systemic lupus Erythematosus

dc.contributor.authorKay, Donald R.en_US
dc.contributor.authorValentine, Thomas V.en_US
dc.contributor.authorWalker, Sara Ellenen_US
dc.contributor.authorValentine, Merilee H.en_US
dc.contributor.authorBole, Giles G.en_US
dc.date.accessioned2006-04-28T16:22:18Z
dc.date.available2006-04-28T16:22:18Z
dc.date.issued1980-12en_US
dc.identifier.citationKay, Donald R.; Valentine, Thomas V.; Walker, Sara E.; Valentine, Merilee H.; Bole, Giles G. (1980)."Frentizole Therapy of Active Systemic lupus Erythematosus." Arthritis & Rheumatism 23(12): 1381-1387. <http://hdl.handle.net/2027.42/37743>en_US
dc.identifier.issn0004-3591en_US
dc.identifier.issn1529-0131en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/37743
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7006613&dopt=citationen_US
dc.description.abstractFrentizole is a benzimidazoleurea that has immunosuppressive properties in mice. Eleven steroid-treated patients with active systemic lupus erythematosus received frentizole (150-350 mg/day) in combination with stable or decreasing doses of prednisone in an open label trial. Nine patients completed at least one 21-to 75-day course of therapy with this drug. Clinical parameters of disease improved in 8 of these 9 patients. Mean DNA binding decreased by 28%, mean CH50 increased by 20%, and mean absolute lymphocyte and T cell counts decreased by 25-26%. Granulocytopenia was not observed. Three patients developed reversible hepatic toxicity. Clinical and serologic improvement was noted in 3 patients who accepted a second 90-day course of frentizole therapy.en_US
dc.format.extent584298 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherRheumatologyen_US
dc.titleFrentizole Therapy of Active Systemic lupus Erythematosusen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeriatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumProfessor of Internal Medicine; University of Michigan Medical School ; Department of Medicine, Division of Immunology and Rheumatology, N403 University of Missouri Medical Center, Columbia, Missouri 65212en_US
dc.contributor.affiliationumProfessor of Internal Medicine; University of Michigan Medical Schoolen_US
dc.contributor.affiliationumProfessor of Internal Medicine; University of Michigan Medical Schoolen_US
dc.contributor.affiliationumProfessor of Internal Medicine; University of Michigan Medical Schoolen_US
dc.contributor.affiliationumProfessor of Internal Medicine; University of Michigan Medical Schoolen_US
dc.identifier.pmid7006613en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/37743/1/1780231209_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/art.1780231209en_US
dc.identifier.sourceArthritis & Rheumatismen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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