Regulation of iron homeostasis through the erythroferrone‐hepcidin axis in sickle cell disease

Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease

(2016) Sherif M. Badawy et al.   BRITISH JOURNAL OF HAEMATOLOGY

Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques

(2016) Emma Drasar et al.   BRITISH JOURNAL OF HAEMATOLOGY

Guidelines on red cell transfusion in sickle cell disease Part II: indications for transfusion

(2016) Bernard A. Davis et al.   BRITISH JOURNAL OF HAEMATOLOGY

Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia—TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial

(2016) Russell E Ware et al.   LANCET

Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of  -thalassemia

(2015) L. Kautz et al.   BLOOD

Prevalence and distribution of iron overload in patients with transfusion-dependent anemias differs across geographic regions: results from the CORDELIA study

(2015) Yesim Aydinok et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Controlled Trial of Transfusions for Silent Cerebral Infarcts in Sickle Cell Anemia

(2014) Michael R. DeBaun et al.   NEW ENGLAND JOURNAL OF MEDICINE

Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten years

(2011) Emma Drasar et al.   BRITISH JOURNAL OF HAEMATOLOGY

Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury

(2009) T. V. Adamkiewicz et al.   BLOOD

Pathophysiology of Transfusional Iron Overload: Contrasting Patterns in Thalassemia Major and Sickle Cell Disease

(2009) John B. Porter   HEMOGLOBIN