A case‐control analysis of hyperhemolysis syndrome in adults and laboratory correlates of complement involvement

Author:

Merrill Samuel A.1ORCID,Brodsky Robert A.1,Lanzkron Sophie M.1,Naik Rakhi1ORCID

Affiliation:

1. Division of Hematology, Department of MedicineJohns Hopkins School of Medicine Baltimore Maryland

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Reference54 articles.

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2. Acute splenic sequestration in homozygous sickle cell disease: Natural history and management

3. The mechanism of red cell aging. I. Relationship between cell age and specific gravity evaluated by ultracentrifugation in a discontinuous density gradient;Piomelli S;J Lab Clin Med,1967

4. Transfusion therapy for cerebrovascular abnormalities in sickle cell disease

5. Scheduled outpatient red blood cell exchange program reduces admission and complications in sickle cell disease;Bumma N;Blood,2017

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