Published in Br Med J on June 10, 1978
Causes of death in sickle-cell disease in Jamaica. Br Med J (Clin Res Ed) (1983) 2.17
Current sickle cell screening program for newborns in New York City, 1979-1980. Am J Public Health (1983) 2.12
Sickle-cell disease in a British urban community. Br Med J (Clin Res Ed) (1981) 1.88
Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study. Br Med J (Clin Res Ed) (1986) 1.54
Sickle cell haemoglobinopathies in England. Arch Dis Child (1981) 1.52
Admissions to hospital of children with sickle-cell anaemia: a study in south London. Br Med J (Clin Res Ed) (1981) 1.50
Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. Arch Dis Child (1981) 1.48
Newborn diagnosis of abnormal hemoglobins from a large municipal hospital in Los Angeles. Am J Public Health (1981) 1.42
Sickle cell disease in Africa: burden and research priorities. Ann Trop Med Parasitol (2007) 1.41
Screening cord blood for sickle haemoglobinopathies in Brent. Br Med J (Clin Res Ed) (1984) 1.40
Neonatal screening for sickle haemoglobinopathies in Birmingham. Br Med J (Clin Res Ed) (1982) 1.37
Prediction and diagnosis of sickling disorders in neonates. Arch Dis Child (1989) 1.33
Patterns of mortality in sickle cell disease in the United Kingdom. J Clin Pathol (1991) 1.17
Management of sickle cell disease. Postgrad Med J (1987) 1.17
Newborn screening for hemoglobinopathies in California. Pediatr Blood Cancer (2009) 1.15
Bone marrow transplantation in sickle cell anaemia. Arch Dis Child (1991) 1.14
Hepatic sequestration in sickle cell anaemia. Br Med J (Clin Res Ed) (1985) 1.14
Early rise in the "pitted" red cell count as a guide to susceptibility to infection in childhood sickle cell anaemia. Arch Dis Child (1982) 1.01
Defective yeast opsonisation and functional deficiency of complement in sickle cell disease. Arch Dis Child (1982) 0.92
Evidence review of hydroxyurea for the prevention of sickle cell complications in low-income countries. Arch Dis Child (2013) 0.91
New classification of peripheral retinal vascular changes in sickle cell disease. Br J Ophthalmol (1994) 0.88
Current management of sickle cell anemia. Cold Spring Harb Perspect Med (2013) 0.87
Newborn screening for sickle cell disease: A 1988-2003 Quebec experience. Paediatr Child Health (2006) 0.82
Partial splenectomy in sickle cell syndromes. Arch Dis Child (1991) 0.81
Splenectomy and acute splenic sequestration crises in sickle cell disease. Pediatr Surg Int (2013) 0.80
Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008. Public Health Rep (2016) 0.79
How to reach rapid diagnosis in sickle cell disease? Iran J Pediatr (2010) 0.79
Incidence of sickle cell disease and other hemoglobin variants in 10,095 Lebanese neonates. PLoS One (2014) 0.76
Evolving locally appropriate models of care for indian sickle cell disease. Indian J Med Res (2016) 0.75
Hematologic and oncologic complications in the critically ill child. Yale J Biol Med (1984) 0.75
Sickle cell disease in Saudi Arabs in early childhood. Arch Dis Child (1981) 0.75
Acute splenic sequestration crisis in a young woman with homozygous sickle cell anaemia. Postgrad Med J (1989) 0.75
Perioperative management in children with sickle cell disease undergoing laparoscopic surgery. JSLS (2002) 0.75
A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerations. J Inherit Metab Dis (1989) 0.75
Turf wars: exploring splenomegaly in sickle cell disease in malaria-endemic regions. Br J Haematol (2017) 0.75
Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples. Br J Cancer (1977) 53.23
Natural history of sickle cell disease--the first ten years. Semin Hematol (1975) 3.53
Screening cord bloods for detection of sickle cell disease in Jamaica. Clin Chem (1974) 3.44
Acute splenic sequestration crises (ASSC) in young children with sickle cell anemia. Clinical observations in 20 episodes in 14 children. Clin Pediatr (Phila) (1972) 2.22
AAPM's TG-51 protocol for clinical reference dosimetry of high-energy photon and electron beams. Med Phys (1999) 7.75
Outbreak of aplastic crises in sickle cell anaemia associated with parvovirus-like agent. Lancet (1981) 4.62
Screening cord bloods for detection of sickle cell disease in Jamaica. Clin Chem (1974) 3.44
Effect of season and temperature on mortality in amphibians due to chytridiomycosis. Aust Vet J (2004) 3.16
Ocular findings in hemoglobin SC disease in Jamaica. Am J Ophthalmol (1972) 2.97
The rhythm of the normal human heart. Lancet (1976) 2.94
Relatively benign sickle-cell anaemia in 60 patients aged over 30 in the West Indies. Br Med J (1968) 2.87
The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med (1982) 2.52
Ocular findings in homozygous sickle cell anemia in Jamaica. Am J Ophthalmol (1972) 2.44
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
Causes of death in sickle-cell disease in Jamaica. Br Med J (Clin Res Ed) (1983) 2.17
The development and use of an antibody capture radioimmunoassay for specific IgM to a human parvovirus-like agent. J Hyg (Lond) (1982) 2.09
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
Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. Proc Natl Acad Sci U S A (1984) 2.00
Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns. Br J Haematol (1986) 2.00
Improved survival in homozygous sickle cell disease: lessons from a cohort study. BMJ (1995) 1.99
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
Case of pyomyositis occurring in London. Br Med J (1973) 1.81
Spatio-temporal stages in face and word processing. I. Depth-recorded potentials in the human occipital, temporal and parietal lobes [corrected]. J Physiol Paris (1994) 1.81
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
Blood contamination of anaesthetic and related staff. Anaesthesia (1990) 1.72
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
Intracerebral potentials to rare target and distractor auditory and visual stimuli. I. Superior temporal plane and parietal lobe. Electroencephalogr Clin Neurophysiol (1995) 1.67
The clinical features of sickle-cell- thalassaemia in Jamaica. Br J Haematol (1973) 1.58
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
The irreversibly sickled cell; a determinant of haemolysis in sickle cell anaemia. Br J Haematol (1969) 1.52
Spatio-temporal stages in face and word processing. 2. Depth-recorded potentials in the human frontal and Rolandic cortices. J Physiol Paris (1994) 1.50
Intracerebral potentials to rare target and distractor auditory and visual stimuli. III. Frontal cortex. Electroencephalogr Clin Neurophysiol (1995) 1.50
Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. Arch Dis Child (1981) 1.48
Increased renal reflectivity in sickle cell disease: prevalence and characteristics. Clin Radiol (1995) 1.46
Haemodynamic changes after angiocardiography. Br Heart J (1969) 1.46
Cell surface polypeptide CshA mediates binding of Streptococcus gordonii to other oral bacteria and to immobilized fibronectin. Infect Immun (1996) 1.45
R50 as a beam quality specifier for selecting stopping-power ratios and reference depths for electron dosimetry. Med Phys (1996) 1.45
Biliary sludge in sickle cell disease. J Pediatr (1996) 1.45
Medroxyprogesterone acetate and homozygous sickle-cell disease. Lancet (1982) 1.43
Intracerebral potentials to rare target and distractor auditory and visual stimuli. II. Medial, lateral and posterior temporal lobe. Electroencephalogr Clin Neurophysiol (1995) 1.42
Bacteraemia in homozygous sickle cell disease in Africa: is pneumococcal prophylaxis justified? Arch Dis Child (2006) 1.40
Open access carotid duplex scanning: throughput and resultant surgical workload. Ann R Coll Surg Engl (2000) 1.39
An assessment of lung volumes and gas transfer in sickle-cell anaemia. Thorax (1971) 1.38
Fetal haemoglobin in homozygous sickle cell disease. Clin Haematol (1975) 1.35
Observations on the epidemiology of sickle cell disease. Trans R Soc Trop Med Hyg (1981) 1.33
Macular vasculature, visual acuity, and irreversibly sickled cells in homozygous sickle cell disease. Br J Ophthalmol (1982) 1.31
Advanced neuroblastoma: improved response rate using a multiagent regimen (OPEC) including sequential cisplatin and VM-26. J Clin Oncol (1984) 1.30
Renal function in patients over 40 with homozygous sickle-cell disease. Br Med J (Clin Res Ed) (1981) 1.30
A method for comparing endotracheal cuffs. A controlled study of tracheal trauma in dogs. Br J Anaesth (1978) 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
The sickle-cell and altitude. Br Med J (1971) 1.25
Sickle cell retinopathy in Jamaican children: further observations from a cohort study. Br J Ophthalmol (1988) 1.25
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
Generation of photon energy deposition kernels using the EGS Monte Carlo code. Phys Med Biol (1988) 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
Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. J Pediatr (1981) 1.21
Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease. Br J Haematol (1982) 1.21
Monte Carlo simulation of a typical 60Co therapy source. Med Phys (1999) 1.20
Presentation of thyroid carcinoma as a thrombosed external jugular vein, with intraluminal tumour thrombus in the great veins. Eur J Surg Oncol (2000) 1.20
Selection and breeding of plant cultivars to minimize cadmium accumulation. Sci Total Environ (2007) 1.18
Leg ulceration in sickle cell anemia. Arch Intern Med (1974) 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
Spectra and air-kerma strength for encapsulated 192Ir sources. Med Phys (1999) 1.14
Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease. Br J Haematol (1979) 1.14
Assessment of myocardial function before aortic surgery by radionuclide angiocardiography. Br J Surg (1985) 1.12
Photocoagulation and diathermy in the treatment of proliferative sickle retinopathy. Br J Ophthalmol (1974) 1.10
Climate and painful crisis of sickle-cell disease in Jamaica. Br Med J (1976) 1.10
Heights, weights, and skeletal age of Jamaican adolescents with sickle cell anaemia. Arch Dis Child (1972) 1.10
Sickle cell retinopathy in Jamaican children: a search for prognostic factors. Br J Ophthalmol (1983) 1.10
Photocoagulation in proliferative sickle retinopathy: results of a 5-year study. Br J Ophthalmol (1980) 1.10
Early splenomegaly in homozygous sickle-cell disease: An indicator of susceptibility to infection. Lancet (1978) 1.10
Identification of QTL and association of a phytoene synthase gene with endosperm colour in durum wheat. Theor Appl Genet (2006) 1.09
Fetal haemoglobin and early manifestations of homozygous sickle cell disease. Arch Dis Child (1992) 1.09
Determinants of nocturnal enuresis in homozygous sickle cell disease. Arch Dis Child (1990) 1.09
Body habirus of Jamaican adults with sickle cell anemia. South Med J (1972) 1.09
Prepubertal growth and skeletal maturation in children with sickle cell disease. Pediatrics (1986) 1.09
A comparison of erythrocyte characteristics in sickle cell syndromes in Jamaica. Br J Haematol (1972) 1.09
Intestinal function and intestinal blood supply: a 20 year surgical study. Gut (1985) 1.08
The haematology of steady state homozygous sickle cell disease: frequency distributions, variation with age and sex, longitudinal observations. Br J Haematol (1985) 1.08
The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. Blood (1988) 1.08
Cerebrovascular complications and parvovirus infection in homozygous sickle cell disease. J Pediatr (2001) 1.08