Evaluation of agreement between hemoglobin A1c, fasting glucose, and fructosamine in Senegalese individuals with and without sickle-cell trait

Significantly elevated foetal haemoglobin levels in individuals with glucose 6-phosphate dehydrogenase disease and/or sickle cell trait: a cross-sectional study in Cape Coast, Ghana

Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia

Abstract Fetal hemoglobin (HbF, α2γ2) is a major contributor to the remarkable phenotypic heterogen

Comparative Abilities of Fasting Plasma Glucose and Haemoglobin A1c in Predicting Metabolic Syndrome among Apparently Healthy Normoglycemic Ghanaian Adults

There are arguments as to whether haemoglobin A1c (HbA1c) better predicts Metabolic syndrome (MetS)

Mitochondrial DNA Variation in Individuals with Sickle Cell Disease

Background: Sickle cell disease (SCD) is a complex multi-system disorder that predominantly affects

Experiences and Management Practices of Individuals Living with Sickle Cell Anemia in Nigeria

Background: Sickle cell anemia (SCA) remains a major public health concern in Nigeria, where it sign

Men with sickle cell disease experience greater sexual dysfunction when compared with men without sickle cell disease

Abstract Recurrent ischemic priapism is a common complication of sickle cell diseas