β-地中海贫血特征和铁超载患者的病例系列：从多因子hepcidin抑制到小静脉切开术治疗。

IF 7.9 1区医学 Q1 HEMATOLOGY

Haematologica Pub Date : 2025-09-11 DOI:10.3324/haematol.2025.289073

Fabiana Busti,Domenico Girelli

引用次数: 0

摘要

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本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Response to Comment on: a case series of patients with β- thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies.

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来源期刊

Haematologica 医学-血液学

CiteScore

14.10

自引率

2.00%

发文量

349

审稿时长

3-6 weeks

期刊介绍： Haematologica is a journal that publishes articles within the broad field of hematology. It reports on novel findings in basic, clinical, and translational research. Scope: The scope of the journal includes reporting novel research results that: Have a significant impact on understanding normal hematology or the development of hematological diseases. Are likely to bring important changes to the diagnosis or treatment of hematological diseases.