1. Serum oa-hydroxybuyrate dehydrogenase levels in children with sickle cell disease;Karayalin, G.; Lanzkowsky, P.; Kazi, A.B.;Am J Pediatr Hematol Oncol,1981
2. Serum calcium and protein in haemoglobin-SS patients;Nduka, N.; Ekeke, G.I.;Folia Haematol,1987
3. The antisickling role of uric acid in sickle cell disease;Ekeke, G.I.; Nduka, N.;Trop Geogr Med,1987
4. Plasma uric acid, urea and creatinine in sickle cell disease;El-Hazmi, M.A.F.; Al-Faleh, F.Z.; Warsy, A.S.;Saudi Med Jf,1989
5. Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease;Neely, C.L.; Wajima, T.; Kraus, A.P.; Diggs, L.W.; Barreras, L.;Am J Clin Pathol,1969