Hepcidin is suppressed by erythropoiesis in hemoglobin E  -thalassemia and  -thalassemia trait

Identification of erythroferrone as an erythroid regulator of iron metabolism

(2014) Léon Kautz et al.   NATURE GENETICS

Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with  -thalassemia major: a longitudinal study

(2013) S.-R. Pasricha et al.   BLOOD

A systematic analysis of global anemia burden from 1990 to 2010

(2013) N. J. Kassebaum et al.   BLOOD

Hepcidin expression from monocyte of splenectomized and non-splenectomized patients with HbE-β-thalassemia

(2013) Kanita Pratummo et al.   Hematology

Hepcidin is the major predictor of erythrocyte iron incorporation in anemic African children

(2012) A. M. Prentice et al.   BLOOD

Alpha Thalassaemia and extended alpha globin genes in Sri Lanka

(2012) Sasikala Suresh et al.   BLOOD CELLS MOLECULES AND DISEASES

Iron overload in non-transfusion-dependent thalassemia: a clinical perspective

(2012) Khaled M. Musallam et al.   BLOOD REVIEWS

Regulation of hepcidin expression at high altitude

(2011) N. P. Talbot et al.   BLOOD

Adaptation to anemia in hemoglobin E-  thalassemia

(2010) A. Allen et al.   BLOOD

The inherited diseases of hemoglobin are an emerging global health burden

(2010) D. J. Weatherall   BLOOD

Studies in haemoglobin E beta-thalassaemia

(2010) Nancy F. Olivieri et al.   BRITISH JOURNAL OF HAEMATOLOGY

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice

(2010) Sara Gardenghi et al.   JOURNAL OF CLINICAL INVESTIGATION

Global epidemiology of haemoglobin disorders and derived service indicators

(2008) Bernadette Modell   BULLETIN OF THE WORLD HEALTH ORGANIZATION

Anemia in -thalassemia patients targets hepatic hepcidin transcript levels independently of iron metabolism genes controlling hepcidin expression

(2008) E. Camberlein et al.   HAEMATOLOGICA