Sickle cell disease (SCD) is a group of inherited autosomal recessive disorders, including
sickle cell anemia, sickle beta-thalassemia, and other hemoglobinopathies, which are …

This review examines the evidence for some of the common psychological complications
found across the life span of patients with sickle cell disease (SCD), which are likely to be …

Objective. Brain magnetic resonance imaging (MRI) and neuropsychological evaluations
were conducted to determine whether neuroradiographic evidence of infarct in children with …

Objectives: To compare the results of serial neuropsychologic testing in children with sickle
cell disease with the results of serial magnetic resonance imaging (MRI) examinations …

abstract Sickle cell disease (SCD) is the most common genetic disorder of the blood. The
disease produces significantly abnormal hemoglobin (Hgb) molecules in red blood cells …

Health‐related quality of life (HRQL) is an outcome that may be used to measure the impact
of sickle cell disease on the child and their family but has not been routinely assessed in this …

Neurocognitive impairment is common in sickle cell disease (SCD) and is associated with
significant functional limitations. In a cross‐sectional analysis, we examined the association …

Background Sickle cell disease comprises a group of genetic blood disorders. It occurs
when the sickle haemoglobin gene is inherited from both parents. The effects of the …

We report outcomes after myeloablative haematopoietic cell transplantation (HCT) from
human leucocyte antigen (HLA)‐matched sibling donors in 67 patients with sickle cell …

Objective: To examine neurocognitive functioning in children classified with overt cerebral
vascular accidents (CVAs), silent infarcts, or without central nervous system (CNS) …