Marlene Allman
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g(HbF): a genetic model of fetal hemoglobin in sickle cell disease Open
Key Points The 3 established HbF genetic loci can be summarized into 1 quantitative variable, g(HbF), in SCD and influence markers of SCD severity. g(HbF) provides a quantitative marker for the genetic component of HbF% variability, potent…
View article: Survival in adults with sickle cell disease in a high-income setting
Survival in adults with sickle cell disease in a high-income setting Open
To the editor: Survival of patients with sickle cell disease (SCD) in high-income countries has improved greatly in the last 60 years. In 1960, it was described as a “disease of childhood”[1][1] whereas 25 years later, the Cooperative Stud…