## Abstract ## Background Due to severe side effects in virtually all children treated with a standard dose of 45 mg/m^2^/day allβ__trans__βretinoic acid (ATRA) for acute promyelocytic leukemia (APL) the AMLβBFM study group reduced the dosage to 25 mg/m^2^/day. For the lack of data on the use of A
β¦ LIBER β¦
171. Clinical and pharmacologic aspects of all-trans retinoic acid treatment in acute promyelocytic leukemia
β Scribed by Warrell, RP; Frankel, S; Miller, WH; Muindi, J; Young, C; Dmitrovsky, E
- Book ID
- 122431560
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 138 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0753-3322
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