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Distribution of sickle cell disease
Nomenclature and genetics of sickle
34 other sections not shown
AA controls abnormal acid acute chest syndrome adults African aplastic crisis Arch artery associated autopsy avascular necrosis blood bone marrow cardiac cent cerebral Chapter Charache children with sickle chronic Clin common complications crises deficiency diagnosis Diggs effect erythrocytes erythropoiesis exchange transfusion femoral head fetal haemoglobin folate frequency function gallstones gene genetic genotype globin Goldberg Haematol haematological haemoglobin haemoglobin levels haplotype HbA2 HbF levels hemoglobinopathies hepatic homozygous homozygous sickle cell increased infarction infection Jamaican Cohort Study leg ulceration lesions Nigeria normal observations occlusion occur Ophthalmol osteomyelitis painful crisis pathology patients with sickle patients with SS Pediatr plasma platelet pneumococcal population pregnancy prevalence priapism pulmonary red cell renal reported reticulocyte retinal retinopathy salmonella Saudi Serjeant serum sickle cell anemia sickle cell disease sickle cell trait sickle-cell anemia sickle-cell disease spleen splenectomy splenomegaly SS disease SS patients steady-state thalassaemia therapy vascular vaso-occlusive vessels Vichinsky