Sickle Cell-Hemoglobin D Iran: A Benign Sickle Cell Syndrome

Gelijkaardige items

• Elderly survivors with homozygous sickle cell disease.
  door: Serjeant, G, et al.
  Gepubliceerd in: (2007)
• The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
  door: Vyas, P, et al.
  Gepubliceerd in: (1988)
• Are there clinical phenotypes of homozygous sickle cell disease?
  door: Alexander, N, et al.
  Gepubliceerd in: (2004)
• The red cell distribution width in sickle cell disease--is it of clinical value?
  door: Thame, M, et al.
  Gepubliceerd in: (1991)
• The changing face of homozygous sickle cell disease: 102 patients over 60 years.
  door: Serjeant, G, et al.
  Gepubliceerd in: (2009)