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

Genetic Etiologies for Phenotypic Diversity in Sickle Cell Anemia

(2011) Martin H. Steinberg   TheScientificWorldJOURNAL

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

ACUTE SPLENIC SEQUESTRATION IN JAMAICAN ADULTS WITH HOMOZYGOUS SICKLE CELL DISEASE: A ROLE OF ALPHA THALASSAEMIA

(2010) K. De Ceulaer et al.   BRITISH JOURNAL OF HAEMATOLOGY

Acute splenic sequestration in a cohort of children with sickle cell anemia

(2009) Paulo V. Rezende et al.   Jornal de Pediatria

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

The natural history of conditional transcranial Doppler flow velocities in children with sickle cell anaemia

(2008) Jane S. Hankins et al.   BRITISH JOURNAL OF HAEMATOLOGY

Genetic Modifiers in Hemoglobinopathies

(2008) Deborah Rund et al.   CURRENT MOLECULAR MEDICINE

Clinical and molecular characteristics of sickle cell anemia in the northeast of Brazil

(2008) Elisângela Vitória Adorno et al.   GENETICS AND MOLECULAR BIOLOGY