Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia

Haematologica. 2015 May;100(5):e169-71. doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16.
No abstract available

Keywords: erythropoiesis-hepcidin-iron store axis; hemoglobin H disease; β-thalassemia intermedia.

Publication types

  • Letter

MeSH terms

  • Erythropoiesis*
  • Growth Differentiation Factor 15 / blood
  • Growth Differentiation Factor 15 / metabolism
  • Hemolysis
  • Hepcidins / blood
  • Hepcidins / metabolism*
  • Humans
  • Iron / metabolism*
  • Iron Overload / metabolism
  • alpha-Thalassemia / blood
  • alpha-Thalassemia / diagnosis
  • alpha-Thalassemia / metabolism*
  • beta-Thalassemia / blood
  • beta-Thalassemia / diagnosis
  • beta-Thalassemia / metabolism*

Substances

  • Growth Differentiation Factor 15
  • Hepcidins
  • Iron