Can N-acetylcysteine reduce red blood cell transfusion burden in patients with transfusion-dependent β-thalassemia?-Reference-Cited by-同舟云学术

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Can N-acetylcysteine reduce red blood cell transfusion burden in patients with transfusion-dependent β-thalassemia?

Published:2023-12-13 Issue: Volume: Page:1-9
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Bahoush Gholamreza¹,Rahab Mahdi²,Ahmadvand Parnian³

Affiliation:

1. Pediatric Hematology and Oncology Department, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

2. Department of Anesthesiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

3. Fellowship of Pediatric Hematology and Oncology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/08880018.2023.2292556

Reference23 articles.

1. Cappellini M-D Cohen A Eleftheriou A Piga A Porter J Taher A. Guidelines for the clinical management of thalassaemia. 2013.

2. Thalassemias and related disorders: Quantitative disorders of hemoglobin synthesis;Borgna-Pignatti C;Wintrobe’s Clin Hematol,2004

3. Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major

4. Pathogenesis and management of iron toxicity in thalassemia

5. Increased Ascorbate Radical Formation and Ascorbate Depletion in Plasma from Women With Preeclampsia: Implications for Oxidative Stress

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