Challenges in preventing and treating hemolytic complications associated with red blood cell transfusion-Reference-Cited by-同舟云学术

Challenges in preventing and treating hemolytic complications associated with red blood cell transfusion

Published:2019-05 Issue:2 Volume:26 Page:130-134
ISSN:1246-7820
Container-title:Transfusion Clinique et Biologique
language:en
Short-container-title:Transfusion Clinique et Biologique

Author:

Chonat Satheesh,Arthur Connie M.,Zerra Patricia E.,Maier Cheryl L.,Jajosky Ryan P.,Yee Marianne E.M.,Miller Maureen J.,Josephson Cassandra D.,Roback John D.,Fasano Ross,Stowell Sean R.

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology

Reference85 articles.

1. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography;Adams;N Engl J Med,1998

2. Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia;DeBaun;N Engl J Med,2014

4. Challenges of alloimmunization in patients with haemoglobinopathies;Chou;Br J Haematol,2012

5. Red blood cell alloimmunization in sickle cell disease: pathophysiology, risk factors, and transfusion management;Yazdanbakhsh;Blood,2012

Cited by 18 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. Harnessing the potential of red blood cells in immunotherapy;Human Immunology;2024-11

2. Prevention of potential delayed hemolytic transfusion reaction in two sickle cell patients using intravenous immunoglobulins and steroids before and after red blood cell exchange with antigen positive units and review literature;Transfusion and Apheresis Science;2024-06

3. Characterising the challenges of managing difficult red blood cell alloantibodies in liver transplant recipients;Journal of Clinical Pathology;2024-05-15

4. The ongoing challenge of RBC alloimmunization in the management of patients with sickle cell disease;La Presse Médicale;2023-12

5. “Don’t Add Fuel to the Fire”– Hyperhemolysis Syndrome in a Pregnant Woman with Compound Sickle Cell Disease/β0-Thalassemia: Case Report and Review of the Literature;Acta Haematologica;2023-10-13