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British Journal of Haematology|May 31, 2001
Red cell antibodies in patients with homozygous sickle cell disease: a comparison of patients in Jamaica and the United KingdomA Olujohungbe, I Hambleton, L Stephens, et al.BMJ (Clinical Research Ed.)|December 16, 1995
Improved survival in homozygous sickle cell disease: lessons from a cohort studyA Lee, P Thomas, L Cupidore, et al.The West Indian Medical Journal|March 25, 2015
Iron Deficiency among Jamaican AdolescentsK Mason, F Gibson, I Hambleton, et al.Clinical and Laboratory Haematology|January 24, 2004
Newborn screening for sickle cell disease in Brazil: the Campinas experienceS Brandelise, V Pinheiro, C S Gabetta, et al.Annals of Saudi Medicine|January 1, 1995
Avascular necrosis of the femoral head in Saudi Arabians with homozygous sickle cell disease - risk factorsA Padmos, G Roberts, S Lindahl, et al.British Journal of Haematology|June 1, 1993
The clinical significance of serum transferrin receptor levels in sickle cell diseaseA Singhal, J D Cook, B S Skikne, et al.Clinical and Laboratory Haematology|January 1, 1991
The red cell distribution width in sickle cell disease--is it of clinical value?M Thame, Y Grandison, K Mason, et al.British Journal of Haematology|January 1, 1996
Determinants of haemoglobin level in steady-state homozygous sickle cell diseaseG Serjeant, B Serjeant, A Stephens, et al.British Journal of Haematology|March 1, 1991
The haematology of homozygous sickle cell disease after the age of 40 yearsJ Morris, D Dunn, M Beckford, et al.The West Indian Medical Journal|October 2, 2015
Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural HistoryG Serjeant, I HambletonPageof 4