Measurement of post‐transfusion red blood cell survival kinetics in sickle cell disease and β‐Thalassemia: A biotin label approach-Reference-Cited by-同舟云学术

Measurement of post‐transfusion red blood cell survival kinetics in sickle cell disease and β‐Thalassemia: A biotin label approach

Published:2022-08-02 Issue:10 Volume:62 Page:1984-1996
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Gerritsma Jorn J.¹²^ORCID,van der Bolt Nieke¹³,van Bruggen Robin⁴,ten Brinke Anja¹,van Dam John⁵,Guerrero Guillermo³,Vermeulen Christie⁶,de Bruin Sanne⁷,Vlaar Alexander P. J.⁷^ORCID,Biemond Bart J.⁸,Nur Erfan⁸,van der Schoot Ellen³,Fijnvandraat Karin²⁹^ORCID,

Affiliation:

1. Sanquin Research and Landsteiner Laboratory, Immunopathology, Amsterdam UMC University of Amsterdam Amsterdam the Netherlands

2. Amsterdam UMC University of Amsterdam, Emma Children's Hospital, Pediatric Hematology Amsterdam the Netherlands

3. Sanquin Research and Landsteiner Laboratory, Immunohematology, Amsterdam UMC University of Amsterdam Amsterdam the Netherlands

4. Sanquin Research and Landsteiner Laboratory, Blood Cell Research, Amsterdam UMC University of Amsterdam Amsterdam the Netherlands

5. Sanquin Research and Landsteiner Laboratory, Molecular Hematology, Amsterdam UMC University of Amsterdam Amsterdam the Netherlands

6. Sanquin Research and Landsteiner Laboratory, Product and Process Development, Amsterdam UMC University of Amsterdam Amsterdam the Netherlands

7. Amsterdam UMC University of Amsterdam, Intensive Care Medicine Amsterdam the Netherlands

8. Amsterdam UMC University of Amsterdam, Department of Hematology Amsterdam the Netherlands

9. Sanquin Research and Landsteiner Laboratory, Molecular and Cellular Hemostasis, Amsterdam UMC University of Amsterdam, Sanquin Research Amsterdam the Netherlands

Funder

Ministerie van Volksgezondheid, Welzijn en Sport

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.17033

Reference39 articles.

1. Sickle-cell disease

2. Pathophysiology and treatment of patients with beta-thalassemia – an update

3. American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support

4. Benefits and Complications of Regular Blood Transfusion in Patients with Beta-Thalassaemia major

5. Role of Adhesion Molecules and Vascular Endothelium in the Pathogenesis of Sickle Cell Disease

Cited by 4 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. Survival of transfused red blood cells from a donor with alpha‐thalassemia trait in a recipient with sickle cell disease;Transfusion;2024-05

2. Post‐transfusion biotin‐labeled red blood cell survival studies in pediatric sickle cell disease with antibodies of uncertain significance;Transfusion;2024-03-20

3. Novel approaches to measure transfusion effectiveness;Current Opinion in Hematology;2023-08-18

4. Modeling hemoglobin levels of patients chronically transfused with red blood cells;Transfusion;2023-04-02