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

Slični predmeti

• Liver iron concentrations and urinary hepcidin in β-thalassemia
  od: Raffaella Origa, i dr.
  Izdano: (2007-05-01)
• No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia
  od: Raffaella Origa, i dr.
  Izdano: (2008-07-01)
• Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.
  od: Jones, E, i dr.
  Izdano: (2014)
• Beta-thalassemia
  od: Origa Raffaella, i dr.
  Izdano: (2010-05-01)
• Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia
  od: Maria Carla Sollaino, i dr.
  Izdano: (2009-10-01)