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dc.contributor.authorWanee Wisuthsarewongen_US
dc.contributor.authorSuchitra Viravanen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:07:14Z-
dc.date.available2018-07-24T03:07:14Z-
dc.date.issued2002-08-01en_US
dc.identifier.citationJournal of the Medical Association of Thailand. Vol.85, No.SUPPL. 2 (2002)en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-0036702888en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036702888&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/20438-
dc.description.abstractTwo patients with severe atopic dermatitis unresponsive to conventional therapy were enrolled in a clinical trial on thymostimulin (TP-1). TP-1 was administered by subcutaneous injection 1 mg/kg/day for 14 days and then 1 mg/kg/day on alternate days for 2 months. Clinical and immunological status were evaluated at baseline and at regular intervals during the treatment. Clinical severity scores included eight skin conditions (erythema, edema, vesicle, crust, excoriation, scaling, lichenification, pigmentation), two subjective components (itchiness and loss of sleep), and extent of area affected. There was a statistically significant improvement in the overall assessment of the severity scores. There were no definite changes in immunological parameters including CD4, CD8 T-cell subpopulations and serum IgE, but eosinophil count showed a mark decrease in one case. No serious side effects were observed.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036702888&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleManagement of severe atopic dermatitis with thymostimulinen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 2001-2005

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