Lv11
80 积分 2023-07-02 加入
Literature review on genotype–phenotype correlation in patients with hereditary spherocytosis
2小时前
待确认
JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study
3个月前
已完结
Genotype–phenotype correlation in children with hereditary spherocytosis
5个月前
已完结
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis
6个月前
已关闭
Literature review on genotype–phenotype correlation in patients with hereditary spherocytosis
6个月前
已完结
Erythropoiesis defect observed in STAT3 GOF patients with severe anemia
7个月前
已完结
Hematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency
8个月前
已完结
Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years
9个月前
已完结
Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy
9个月前
已关闭
Successful management of transfusion-dependent congenital dyserythropoietic anemia type 1b with interferon alfa-2a
9个月前
已完结
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