Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease-Reference-Cited by-同舟云学术

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Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease

Published:2018-05-24 Issue:10 Volume:103 Page:e483-e485
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Chonat Satheesh,Quarmyne Maa-Ohui,Bennett Caroline M.,Dean Christina L.,Joiner Clinton H.,Fasano Ross M.,Stowell Sean R.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 59 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. Eculizumab for management of hyperhemolysis syndrome in pediatric patients with sickle cell disease: A single‐center case series;Pediatric Blood & Cancer;2024-06-05

2. Comparison of post-decompressive haematuria in rapid versus gradual bladder decompression in patients with chronic urinary retention;Journal of West African College of Surgeons;2024-05-24

3. What is the role of complement in bystander hemolysis? Old concept, new insights;Expert Review of Hematology;2024-05-03

4. La drépanocytose : une transfusion à risque;Bulletin de l'Académie Nationale de Médecine;2024-05

5. Alloimmunization and hyperhemolysis in sickle cell disease;Hematology;2023-12-08

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