Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes-Reference-Cited by-同舟云学术

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Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes

Published:2013-05-30 Issue:7 Volume:88 Page:571-576
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Sheehan Vivien A.¹,Luo Zhaoyu²,Flanagan Jonathan M.¹,Howard Thad A.¹,Thompson Bruce W.²,Wang Winfred C.³,Kutlar Abdullah⁴,Ware Russell E.¹,

Affiliation:

1. Department of Pediatrics; Hematology Center, Baylor College of Medicine; Houston Texas

2. Clinical Trials and Surveys Corporation; Owings Mills Maryland

3. Department of Hematology; St. Jude Children's Research Hospital; Memphis Tennessee

4. Division of Hematology/Oncology; Georgia Health Sciences Center; Augusta Georgia

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23457/fullpdf

Reference45 articles.

1. Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease;Gill;Blood,1995

2. Prediction of adverse outcomes in children with sickle cell disease;Miller;N Engl J Med,2000

3. Renal function in infants with sickle cell anemia: Baseline data from the BABY HUG trial;Ware;J Pediatr,2010

4. Sickle cell disease: No longer a single gene disorder;Chui;Curr Opin Pediatr,2001

5. Effect of alpha-globin genotype on the pathophysiology of sickle cell disease;Ballas;Pediatr Pathol Mol Med,2001

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