Clinical and Hematological Response to Hydroxyurea in a Patient with Hb Leporbp-Thalassemia-Reference-Cited by-同舟云学术

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Clinical and Hematological Response to Hydroxyurea in a Patient with Hb Leporbp-Thalassemia

Published:1997-01 Issue:3 Volume:21 Page:219-226
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Rigano P.,Manfré L.,Galla R. La,Renda D.,Renda M. C.,Calabrese A.,Calzolari R.,Maggio A.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269708997382

Reference23 articles.

1. 5-Azacytidine stimulates fetal hemoglobin synthesis in anemic baboons.

2. Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.

3. Isobutyramide, an orally bioavailable butyrate analogue, stimulates fetal globin gene expression in vitro and in vivo

4. Augmentation by Erythropoietin of the Fetal-Hemoglobin Response to Hydroxyurea in Sickle Cell Disease

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1. Compresión medular con paraparesia reversible en paciente con ß-talasemia;Neurología;2019-05

2. Reversible paraparesis secondary to spinal cord compression in a patient with ß-thalassaemia;Neurología (English Edition);2019-05

3. Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease andβ-Thalassemia Patients;Hemoglobin;2015-05-27

4. Meta-analysis on effectiveness of hydroxyurea to treat transfusion-dependent beta-thalassemia;Hematology;2014-12-23

5. Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia;Blood;2013-03-21

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