Serum lactate dehydrogenase activity as a biomarker in children with sickle cell disease
DOI 10.1111/j.1365-2141.2007.06894.x
O'Driscoll S, Height SE, Dick MC, Rees DC. Serum lactate dehydrogenase activity as a biomarker in children with sickle cell disease. Br J Haematol. 2008; 140:206-209. (Pubitemid 350265040)
G6PD deficiency, absence of alphathalassaemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia
Bernaudin F, Verlhac S, Chevret S, et al. G6PD deficiency, absence of alphathalassaemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia. Blood. 2008;112:4314-4317.
A simple index using age, hemoglobin, and aspartate transaminase predicts increased intracerebral blood velocity as measured by transcranial Doppler scanning in children with sickle cell anemia
Rees DC, Dick MC, Height SE, et al. A simple index using age, hemoglobin, and aspartate transaminase predicts increased intracerebral blood velocity as measured by transcranial Doppler scanning in children with sickle cell anemia. Pediatrics. 2008;121:e1628-e1632.
α Thalassemia and the hematology of homozygous sickle cell disease in childhood
Stevens MC, Maude GH, Beckford M, et al. Alpha thalassemia and the hematology of homozygous sickle cell disease in childhood. Blood. 1986;67: 411-414. (Pubitemid 16164657)