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Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease
Haematologica
.
2018 Oct;103(10):e483-e485.
doi: 10.3324/haematol.2018.194670.
Epub 2018 May 24.
Authors
Satheesh Chonat
1
2
,
Maa-Ohui Quarmyne
3
2
,
Caroline M Bennett
3
2
,
Christina L Dean
4
,
Clinton H Joiner
3
2
,
Ross M Fasano
2
4
,
Sean R Stowell
4
Affiliations
1
Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA schonat@emory.edu.
2
Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA, USA.
3
Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
4
Center for Transfusion and Cellular Therapy, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.
PMID:
29794144
PMCID:
PMC6165824
DOI:
10.3324/haematol.2018.194670
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adolescent
Anemia, Sickle Cell / blood*
Anemia, Sickle Cell / therapy*
Complement Pathway, Alternative*
Erythrocyte Transfusion / adverse effects*
Female
Hemolysis*
Humans
Transfusion Reaction / blood*
Grants and funding
R01 HL135575/HL/NHLBI NIH HHS/United States