Elevated serum and bronchoalveolar lavage fluid levels of interleukin 8 and granulocyte colony-stimulating factor associated with the acute chest syndrome in patients with sickle cell disease-Reference-Cited by-同舟云学术

Elevated serum and bronchoalveolar lavage fluid levels of interleukin 8 and granulocyte colony-stimulating factor associated with the acute chest syndrome in patients with sickle cell disease

Published:2000-11 Issue:2 Volume:111 Page:482-490
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Abboud Miguel R.,Taylor Ellen C.,Habib David,Dantzler-Johnson Terrie,Jackson Sherron M.,Xu Fushen,Laver Joseph,Ballas Samir K.

Publisher

Wiley

Subject

Hematology

Reference45 articles.

1. Interleukin-8 and Related Chemotactic Cytokines

2. Interleukin-8 and eicosanoid production in the lung during moderate to severe Pneumocystis carinii pneumonia in AIDS: a role of interleukin-8 in the pathogenesis of P. carinii pneumonia

3. Acute chest syndrome in sickle cell disease: CT evidence of microvascular occlusion.

4. Role of interleukin-8 in community-acquired pneumonia: Relation to microbial load and pulmonary function

Cited by 39 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. Burden and outcome of respiratory morbidities among children and adolescents with sickle cell disease—A retrospective review of emergency presentations in some Nigerian tertiary institutions;PLOS ONE;2024-05-16

2. Acute chest syndrome of sickle cell disease: genetics, risk factors, prognosis, and management;Expert Review of Hematology;2022-02-01

3. Granulocyte Colony-Stimulating Factor Is Safe and Well Tolerated following Allogeneic Transplantation in Patients with Sickle Cell Disease;Transplantation and Cellular Therapy;2021-12

4. The Role of Pro-Inflammatory Cytokines in Sickle Cell Disease Saudi Patients;Bioscience Biotechnology Research Communications;2021-09-25

5. Genetic diversity of CD14, CD28, CTLA-4 and ICOS gene promoter polymorphism in African and American sickle cell disease;Human Immunology;2019-11