Published in Br Med J on July 13, 1968
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Improved rapid methods for the determination of iron content and binding capacity of serum. J Clin Pathol (1962) 1.52
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Further observations on abnormal haemoglobins in Jamaica. West Indian Med J (1958) 0.94
A trial of chemoprophylaxis in sicklecell anaemia. Preliminary communication. East Afr Med J (1962) 0.92
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The management of leg ulcers in sickle cell anaemia. West Indian Med J (1967) 0.88
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Screening cord bloods for detection of sickle cell disease in Jamaica. Clin Chem (1974) 3.44
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Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia. Blood (1992) 3.09
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Direct identification of sickle cell anemia by blot hybridization. Proc Natl Acad Sci U S A (1981) 2.68
The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med (1982) 2.52
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Ifosfamide-induced Fanconi syndrome. Lancet (1989) 2.43
Is there an acute-phase response in steady-state sickle cell disease? Lancet (1993) 2.35
Prevention of pneumococcal infection in children with homozygous sickle cell disease. Br Med J (Clin Res Ed) (1984) 2.34
Haemoglobin Constant Spring--a chain termination mutant? Nature (1971) 2.25
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The development and use of an antibody capture radioimmunoassay for specific IgM to a human parvovirus-like agent. J Hyg (Lond) (1982) 2.09
Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia. J Clin Invest (1968) 2.06
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Stroke in a cohort of patients with homozygous sickle cell disease. J Pediatr (1992) 2.02
Central retinal artery occlusion without retrobulbar hemorrhage after retrobulbar anesthesia. Am J Ophthalmol (1982) 2.02
Acute splenic sequestration in homozygous sickle cell disease: natural history and management. J Pediatr (1985) 2.02
Behaviour of untreated proliferative sickle retinopathy. Br J Ophthalmol (1980) 2.02
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Erythrocyte Hb-S concentration. An important factor in the low oxygen affinity of blood in sickle cell anemia. J Clin Invest (1973) 1.91
Sickle cell disease in Orissa State, India. Lancet (1986) 1.90
Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation. Am J Hum Genet (1986) 1.89
Priapism and impotence in homozygous sickle cell disease. Arch Intern Med (1980) 1.85
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. Proc Natl Acad Sci U S A (1984) 1.84
Resting metabolic rate in homozygous sickle cell disease. Am J Clin Nutr (1993) 1.79
Comparison of homozygous sickle cell disease in northern Greece and Jamaica. Lancet (1990) 1.78
Septicemia caused by Salmonella infection: an overlooked complication of sickle cell disease. J Pediatr (1997) 1.76
Irreversibly sickled cells and splenomegaly in sickle-cell anaemia. Br J Haematol (1970) 1.71
Neural tube defects in hurricane aftermath. Lancet (1991) 1.69
The clinical features of sickle-cell- thalassaemia in Jamaica. Br J Haematol (1973) 1.58
Kinetics of assembly of a parvovirus, minute virus of mice, in synchronized rat brain cells. J Virol (1977) 1.57
Long-term follow-up of Barrett's high-grade dysplasia. Am J Gastroenterol (2000) 1.56
Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain. Lancet (1971) 1.55
Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease. Br J Ophthalmol (1981) 1.55
The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to 6 years. Br J Haematol (1981) 1.54
Ocular findings in sickle cell thalassemia in Jamaica. Am J Ophthalmol (1972) 1.54
The painful crisis of homozygous sickle cell disease. A study of the risk factors. Arch Intern Med (1987) 1.53
Intestinal malabsorption in Strongyloides stercoralis infestation. Gut (1965) 1.52
The irreversibly sickled cell; a determinant of haemolysis in sickle cell anaemia. Br J Haematol (1969) 1.52
Cell cycle-dependent replication of the DNA of minute virus of mice, a parvovirus. Biochim Biophys Acta (1980) 1.49
Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. Arch Dis Child (1981) 1.48
Three-dimensional CT analysis to determine acetabular retroversion and the implications for the management of femoro-acetabular impingement. J Bone Joint Surg Br (2009) 1.47
Increased renal reflectivity in sickle cell disease: prevalence and characteristics. Clin Radiol (1995) 1.46
Biliary sludge in sickle cell disease. J Pediatr (1996) 1.45
Absorption and disposition kinetics of cromolyn sodium and the influence of inhalation technique. J Pharmacol Exp Ther (1987) 1.45
Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia. J Med Genet (1986) 1.44
Medroxyprogesterone acetate and homozygous sickle-cell disease. Lancet (1982) 1.43
The prevention of asbestos-induced hemolysis. Life Sci (1975) 1.42
Bacteraemia in homozygous sickle cell disease in Africa: is pneumococcal prophylaxis justified? Arch Dis Child (2006) 1.40
A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structure. J Mol Med (Berl) (2000) 1.39
Heat exhaustion in The Sun-Herald City to Surf fun run. Med J Aust (1994) 1.38
An assessment of lung volumes and gas transfer in sickle-cell anaemia. Thorax (1971) 1.38
Very low-dose computed tomography for planning and outcome measurement in knee replacement. The imperial knee protocol. J Bone Joint Surg Br (2006) 1.36
Fetal haemoglobin in homozygous sickle cell disease. Clin Haematol (1975) 1.35
Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C. N Engl J Med (1970) 1.35
Observations on the epidemiology of sickle cell disease. Trans R Soc Trop Med Hyg (1981) 1.33
Analysis of cover of the femoral head in normal and dysplastic hips: new CT-based technique. J Bone Joint Surg Br (2008) 1.31
Macular vasculature, visual acuity, and irreversibly sickled cells in homozygous sickle cell disease. Br J Ophthalmol (1982) 1.31
Renal function in patients over 40 with homozygous sickle-cell disease. Br Med J (Clin Res Ed) (1981) 1.30
Thalassaemia trait and pregnancy. J Clin Pathol (1985) 1.30
A comparison between the characteristics of Jamaican adults with normal hemoglobin and those with sickle cell trait. Am J Epidemiol (1969) 1.29
Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parenteral Hb F levels. Br J Haematol (1982) 1.29
The progression of sickle cell eye disease in Jamaica. Doc Ophthalmol (1975) 1.28
alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease. N Engl J Med (1983) 1.28
Characterization of pulmonary surfactant from ox, rabbit, rat and sheep. Biochem J (1975) 1.27
Use of restriction endonucleases for mapping the allele for beta s-globin. Proc Natl Acad Sci U S A (1982) 1.26
Sickle cell retinopathy in Jamaican children: further observations from a cohort study. Br J Ophthalmol (1988) 1.25
The sickle-cell and altitude. Br Med J (1971) 1.25
A phase II study of ifosfamide in children with recurrent solid tumours. Cancer Chemother Pharmacol (1985) 1.24
Sickle cell retinopathy in young children in Jamaica. Br J Ophthalmol (1982) 1.24
Oral zinc sulphate in sickle-cell ulcers. Lancet (1970) 1.24
The clinical features of haemoglobin SC disease in Jamaica. Br J Haematol (1973) 1.23
Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease. Br J Ophthalmol (1981) 1.23
Retinal and choroidal neovascularization in sickle cell disease. Trans Ophthalmol Soc U K (1980) 1.22
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene. Lancet (1979) 1.22
Ingestion of talc particles by cultured lung fibroblasts. Environ Res (1975) 1.22
Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. J Pediatr (1981) 1.21
A prospective study of computer-aided design and manufacture of titanium plate for cranioplasty and its clinical outcome. Br J Neurosurg (1999) 1.21
Coronary arteries of cardiac patients are hyperreactive and contain stores of amines: a mechanism for coronary spasm. Science (1984) 1.21
Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease. Br J Haematol (1982) 1.21
Reducing the hazards in Sydney's the Sun City-to-Surf runs, 1971 to 1979. Med J Aust (1979) 1.20
Leg ulceration in sickle cell anemia. Arch Intern Med (1974) 1.17
Haematological investigations of population samples in Jamaica. Br J Prev Soc Med (1967) 1.17
Two different forms of homozygous sickle cell disease occur in Saudi Arabia. Br J Haematol (1991) 1.15
Gallstones in sickle cell disease: observations from The Jamaican Cohort study. J Pediatr (2000) 1.15
Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease. Br J Haematol (1979) 1.14
Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia. Am J Hematol (1995) 1.13
Operative treatment of palsy of the posterior interosseous nerve of the forearm. J Bone Joint Surg Am (1990) 1.11
Photocoagulation and diathermy in the treatment of proliferative sickle retinopathy. Br J Ophthalmol (1974) 1.10