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dc.contributor.authorDogan, S
dc.contributor.authorKebudi, R
dc.contributor.authorYalciner, A
dc.contributor.authorAyan, I
dc.contributor.authorGorgun, O
dc.contributor.authorTokuc, G
dc.date.accessioned2021-03-06T19:52:45Z
dc.date.available2021-03-06T19:52:45Z
dc.date.issued1997
dc.identifier.citationTokuc G., Yalciner A., Kebudi R., Dogan S., Gorgun O., Ayan I., "Renal dysfunctions secondary to ifosfamide treatment in children", JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, cilt.16, ss.227-230, 1997
dc.identifier.issn0392-9078
dc.identifier.othervv_1032021
dc.identifier.otherav_f85a7696-b723-4412-9da7-c26ae6918cee
dc.identifier.urihttp://hdl.handle.net/20.500.12627/162688
dc.description.abstractWith the increasing use of ifosfamide in pediatric tumors, nephrotoxicity became the point of interest since it may cause chronic morbidity. In this study, the renal glomerular and tubular functions of 25 cases with solid tumors aged between 2-17 years (median 9) who were treated with ifosfamide, were investigated. For this purpose, routine blood urea, creatinine, calcium, phosphorus, electrolytes, urinary creatinine, phosphorus, glucose, protein and urinary retinol binding protein as well as microglobulin were evaluated, Except for two patients who had hyopophosphatemia, phosphaturia, and proteinuria, all the cases had normal blood biochemistry, creatinine clearance, tubular phosphate reabsorption; and none had proteinuria, hematuria, or glycosuria. In spite of these findings, urine beta 2 microglobulin and retinol binding protein were found to be high in 11 patients and this elevation persisted during the following one year in 8 cases whose treatments were stopped and their levels increased in three patients who continued to receive fosfamide therapy.
dc.language.isoeng
dc.subjectOnkoloji
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titleRenal dysfunctions secondary to ifosfamide treatment in children
dc.typeMakale
dc.relation.journalJOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
dc.contributor.department, ,
dc.identifier.volume16
dc.identifier.issue2
dc.identifier.startpage227
dc.identifier.endpage230
dc.contributor.firstauthorID16318


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