Reticulocyte parameters and hemoglobin F production in sickle cell disease patients undergoing hydroxyurea therapy-Reference-Cited by-同舟云学术

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Reticulocyte parameters and hemoglobin F production in sickle cell disease patients undergoing hydroxyurea therapy

Published:2003 Issue:2 Volume:17 Page:66-72
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J. Clin. Lab. Anal.

Author:

Borba R.,Lima C.S.P.,Grotto H.Z.W.

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry, medical,Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference37 articles.

1. Participation of hemoglobins A and F in polymerization of sickle hemoglobin.

2. Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia [see comments]

3. Minimal doses of hydroxyurea for sickle cell disease

4. Fetal hemoglobin in acute and chronic states of erythroid expansion

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Therapeutics for sickle cell disease intravascular hemolysis;Frontiers in Physiology;2024-09-13

2. Characterization of a cohort of Angolan children with sickle cell anemia treated with hydroxyurea;Blood Cells, Molecules, and Diseases;2024-03

3. Sickle cell disease in the new era: advances in drug treatment;Transfusion and Apheresis Science;2022-10

4. Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea;Haematologica;2021-10-28

5. Nitric Oxide Synthase Dependency in Hydroxyurea Inhibition of Erythroid Progenitor Growth;Genes;2021-07-27

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