Erythrocytapheresis Can Reduce Iron Overload and Prevent the Need for Chelation Therapy in Chronically Transfused Pediatric Patients-Reference-Cited by-同舟云学术

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Erythrocytapheresis Can Reduce Iron Overload and Prevent the Need for Chelation Therapy in Chronically Transfused Pediatric Patients

Published:1996-02 Issue:1 Volume:18 Page:46-50
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:Journal of Pediatric Hematology/Oncology

Author:

Adams Denise M.,Schultz William H.,Ware Russell E.,Kinney Thomas R.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. The natural history of stroke in sickle cell disease

2. Transfusion management of sickle cell disease

3. High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease

4. A modified transfusion program for prevention of stroke in sickle cell disease

Cited by 63 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. Logistics, risks, and benefits of automated red blood cell exchange for patients with sickle cell disease;Hematology;2023-12-08

2. Erythrocytapheresis in Children and Young Adults with Hemoglobinopathies and Iron Overload in Need of Iron Chelation Therapy;Journal of Clinical Medicine;2023-09-29

3. 5567917 COST COMPARISON OF TRANSFUSION CHOICES IN OMAN FOR PATIENTS SUFFERING FROM SICKLE CELL DISEASE;HemaSphere;2023-04

4. Implementation of national blood conservation recommendations at an adult sickle cell center;Transfusion;2022-07-15

5. Comparative evaluation of efficacy and safety of automated versus manual red cell exchange in sickle cell disease: A systematic review and meta‐analysis;Vox Sanguinis;2022-05-30

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