Conclusion Children's primary nephrotic syndrome should be treated for 8 weeks by routine hormone induction therapy, if no remission, impulsion therapy could be used.
结论小儿原发性肾病综合征首用常规激素诱导治疗8周，不缓解者可考虑用大剂量地塞米松冲击治疗。
The efficiency of induction therapy was related significantly to the amount of the detectable residual leukemic cells in the early remission phase and to clinical relapse.
诱导缓解期的杀伤效应与缓解早期的残留白血病细胞数量显著相关，并与临床复发相关。
APL patients were treated with ATRA for induction remission.
A TRA诱导缓解治疗急性早幼粒细胞白血病202例。
Results : The patients subjected to remission-induction chemotherapy had mild to severe bleeding trends , the platelet transfusion rate was 31.5% ;
结果：接受诱导缓解化疗的急性白血病患者，出血倾向轻重不一，输注血小板的比例为31.5%；
Results : The patients subjected to remission-induction chemotherapy had mild to severe bleeding trends , the platelet transfusion rate was 31.5% ;
结果：接受诱导缓解化疗的急性白血病患者，出血倾向轻重不一，输注血小板的比例为31.5%；
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