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

Abdominal Ultrasound With Scintigraphic and Clinical Correlates in Infants With Sickle Cell Anemia: Baseline Data From the BABY HUG Trial

(2011) M. Beth McCarville et al.   AMERICAN JOURNAL OF ROENTGENOLOGY

Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia

(2011) R. E. Ware et al.   BLOOD

Genetic predictors for stroke in children with sickle cell anemia

(2011) J. M. Flanagan et al.   BLOOD

Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acids

(2011) Nisha Vasavda et al.   BRITISH JOURNAL OF HAEMATOLOGY

Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG)

(2011) Winfred C Wang et al.   LANCET

β-Globin Gene Cluster Haplotypes in a Cohort of 221 Children with Sickle Cell Anemia or Sβ⁰-Thalassemia and Their Association with Clinical and Hematological Features

(2010) André Rolim Belisário et al.   ACTA HAEMATOLOGICA

G6PD deficiency and stroke in the CSSCD

(2010) Scott T. Miller et al.   AMERICAN JOURNAL OF HEMATOLOGY

Coinheritance of α-Thalassemia Decreases the Risk of Cerebrovascular Disease in a Cohort of Children with Sickle Cell Anemia

(2010) André Rolim Belisário et al.   HEMOGLOBIN

Glucose 6 phosphate dehydrogenase deficiency is not associated with cerebrovascular disease in children with sickle cell anemia

(2009) D. C. Rees et al.   BLOOD

Renal Function in Infants with Sickle Cell Anemia: Baseline Data from the BABY HUG Trial

(2009) Russell E. Ware et al.   JOURNAL OF PEDIATRICS

G6PD deficiency, absence of  -thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia

(2008) F. Bernaudin et al.   BLOOD

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of  -thalassemia

(2008) M. Uda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A

(2008) Vijay G. Sankaran et al.   SCIENCE