Haptoglobin genotype predicts severe acute vaso‐occlusive pain episodes in children with sickle cell anemia-Reference-Cited by-同舟云学术

Haptoglobin genotype predicts severe acute vaso‐occlusive pain episodes in children with sickle cell anemia

Published:2020-01-30 Issue:4 Volume:95 Page:
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Willen Shaina M.¹^ORCID,McNeil Joel Brennan²^ORCID,Rodeghier Mark³,Kerchberger Vern Eric²,Shaver Ciara M.²,Bastarache Julie A.²⁴⁵,Steinberg Martin H.⁶^ORCID,DeBaun Michael R.⁷^ORCID,Ware Lorraine B.²⁴

Affiliation:

1. Division of Pulmonary Medicine, Department of Pediatrics UCSF Benioff Children's Hospital San Francisco San Francisco California

2. Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine Vanderbilt University School of Medicine Nashville Tennessee

3. Rodeghier Consultants Chicago Illinois

4. Department of Pathology, Microbiology and Immunology Vanderbilt University School of Medicine Nashville Tennessee

5. Department of Cell and Developmental Biology Vanderbilt University School of Medicine Nashville Tennessee

6. Division of Hematology, Department of Medicine Boston University School of Medicine Boston Massachusetts

7. Division of Hematology/Oncology, Department of Pediatrics, Vanderbilt‐Meharry Center for Excellence in Sickle Cell Disease Vanderbilt University Medical Center Nashville Tennessee

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.25728

Reference30 articles.

1. Intravascular hemolysis and the pathophysiology of sickle cell disease

2. Exposure of endothelial cells to free heme potentiates damage mediated by granulocytes and toxic oxygen species;Balla G;Lab Invest,1991

3. Free heme toxicity and its detoxification systems in human