Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia-Reference-Cited by-同舟云学术

Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia

Published:2018-08-20 Issue:2 Volume:33 Page:e22656
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Olatunya Oladele S.¹²^ORCID,Albuquerque Dulcineia M.¹,Adekile Adekunle³,Costa Fernando F.¹

Affiliation:

1. Hematology and Hemotherapy Center; University of Campinas; Campinas São Paulo State Brazil

2. Department of Paediatrics; College of Medicine; Ekiti State University; Ado Ekiti Ekiti State Nigeria

3. Department of Pediatrics; Faculty of Medicine; Kuwait University; Kuwait Kuwait

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcla.22656/fullpdf

Reference40 articles.

1. Global epidemiology of sickle hemoglobin in neonates: a contemporary geostatistical model-based map and population estimates;Piel;Lancet,2013

2. Blood transfusion services for patients with sickle cell disease in Nigeria;Diaku-Akinwumi;Int Health,2016

3. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes;Kato;Blood Rev,2007

4. Comment on molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia;Goncalves;Rev Bras Hematol Hemoter,2014

5. Influence of α thalassemia trait on spleen function in sickle cell anemia patients with high HbF;Adekile;Am J Hematol,1996

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