Graham Roger Serjeant
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(Suggest an Edit or Addition)Graham Roger Serjeant's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Sickle-cell disease (1984) (662)
- OUTBREAK OF APLASTIC CRISES IN SICKLE CELL ANAEMIA ASSOCIATED WITH PARVOVIRUS-LIKE AGENT (1981) (375)
- Stroke in a cohort of patients with homozygous sickle cell disease. (1992) (373)
- The interaction of alpha-thalassemia and homozygous sickle-cell disease. (1982) (282)
- Causes of death in sickle-cell disease in Jamaica. (1982) (272)
- The natural history of sickle cell disease. (1982) (243)
- Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation. (1986) (235)
- Acute splenic sequestration in homozygous sickle cell disease: natural history and management. (1985) (228)
- Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. (1984) (216)
- Priapism and impotence in homozygous sickle cell disease. (1980) (215)
- Improved survival in homozygous sickle cell disease: lessons from a cohort study (1995) (188)
- Outcome of Pregnancy in Homozygous Sickle Cell Disease (2004) (179)
- The Irreversibly Sickled Cell; a Determinant of Haemolysis in Sickle Cell Anaemia (1969) (176)
- SICKLE CELL DISEASE IN ORISSA STATE, INDIA (1986) (175)
- The painful crisis of homozygous sickle cell disease. A study of the risk factors. (1987) (172)
- Incidence and natural history of proliferative sickle cell retinopathy: observations from a cohort study. (2005) (164)
- The emerging understanding of sickle cell disease (2001) (160)
- The painful crisis of homozygous sickle cell disease: clinical features (1994) (160)
- Prevention of pneumococcal infection in children with homozygous sickle cell disease. (1984) (150)
- Early deaths in Jamaican children with sickle cell disease. (1978) (149)
- Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. (1981) (144)
- Two different forms of homozygous sickle cell disease occur in Saudi Arabia (1991) (138)
- Human parvovirus infection in homozygous sickle cell disease (1993) (136)
- Screening cord bloods for detection of sickle cell disease in Jamaica. (1974) (131)
- Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease. (1987) (122)
- Oral zinc sulphate in sickle-cell ulcers. (1970) (120)
- Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2 (1992) (120)
- An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age. (1995) (118)
- Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns (1986) (117)
- Behaviour of untreated proliferative sickle retinopathy. (1980) (114)
- MEDROXYPROGESTERONE ACETATE AND HOMOZYGOUS SICKLE-CELL DISEASE (1982) (114)
- Ocular findings in homozygous sickle cell anemia in Jamaica. (1972) (112)
- Gallstones in sickle cell disease: observations from The Jamaican Cohort study. (2000) (111)
- Central retinal artery occlusion without retrobulbar hemorrhage after retrobulbar anesthesia. (1982) (111)
- STILBOESTROL AND STUTTERING PRIAPISM IN HOMOZYGOUS SICKLE-CELL DISEASE (1985) (110)
- Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease. (2002) (106)
- Clinical presentation of homozygous sickle cell disease. (1985) (102)
- Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. (1992) (99)
- Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study. (2007) (96)
- G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. (1984) (95)
- Prepubertal growth and skeletal maturation in children with sickle cell disease. (1986) (95)
- Ocular findings in hemoglobin SC disease in Jamaica. (1972) (94)
- Risk factors for proliferative sickle retinopathy. (1990) (91)
- Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. (1981) (90)
- Climate and painful crisis of sickle-cell disease in Jamaica. (1976) (89)
- Leg ulceration in sickle cell anemia. (1974) (89)
- Relatively Benign Sickle-cell Anaemia in 60 Patients Aged Over 30 in the West Indies (1968) (86)
- The Development of Haematological Changes in Homozygous Sickle Cell Disease: a Cohort Study from Birth to 6 Years (1981) (85)
- Fetal haemoglobin and early manifestations of homozygous sickle cell disease. (1992) (84)
- Cerebrovascular complications and parvovirus infection in homozygous sickle cell disease. (2001) (82)
- Mortality from sickle cell disease in Africa (2005) (81)
- Resting metabolic rate in homozygous sickle cell disease. (1993) (81)
- Delayed adolescent growth in homozygous sickle cell disease. (1994) (81)
- alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease. (1983) (79)
- Glomerulonephritis after human parvovirus infection in homozygous sickle-cell disease (1995) (79)
- Management of sickle cell disease; lessons from the Jamaican Cohort Study. (1993) (79)
- Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease. (1981) (78)
- Is there an acute-phase response in steady-state sickle cell disease? (1993) (77)
- Bacteraemia in homozygous sickle cell disease in Africa: is pneumococcal prophylaxis justified? (2006) (76)
- Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease (1982) (75)
- Height and weight reference curves for homozygous sickle cell disease (2000) (73)
- The Clinical Features of Sickle‐Cell/β Thalassaemia in Jamaica (1973) (73)
- Natural history and determinants of clinical severity of sickle cell disease (1995) (72)
- The development and use of an antibody capture radioimmunoassay for specific IgM to a human parvovirus-like agent (1982) (71)
- Coagulation Changes during the Steady State in Homozygous Sickle‐Cell Disease in Jamaica (1975) (71)
- Septicemia caused by Salmonella infection: an overlooked complication of sickle cell disease. (1997) (71)
- Leg ulceration in sickle cell disease: medieval medicine in a modern world. (2005) (69)
- Recurrent infections in homozygous sickle cell disease (1999) (69)
- Haematological response to parvovirus B19 infection in homozygous sickle-cell disease (2001) (69)
- Heights, Weights, and Skeletal Age of Jamaican Adolescents with Sickle Cell Anaemia (1972) (69)
- Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin (1980) (66)
- The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene (1988) (66)
- Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem (2011) (65)
- One hundred years of sickle cell disease (2010) (65)
- The clinical features of sickle cell disease. (1993) (65)
- Irreversibly Sickled Cells and Splenomegaly in Sickle‐Cell Anaemia (1970) (65)
- Pulse oximetry in a cohort study of sickle cell disease. (1997) (64)
- Parvovirus associated aplastic crisis in homozygous sickle cell disease. (1987) (63)
- Protein C and protein S in homozygous sickle cell disease: does hepatic dysfunction contribute to low levels? (1997) (63)
- Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study (2001) (63)
- Comparison of Sickle Cell‐β° Thalassaemia with Homozygous Sickle Cell Disease (1979) (61)
- Patterns of visual loss in untreated sickle cell retinopathy (1988) (60)
- New classification of peripheral retinal vascular changes in sickle cell disease. (1994) (60)
- A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease? (1985) (60)
- Sickle cell retinopathy in Jamaican children: further observations from a cohort study. (1988) (58)
- A trial of folate supplementation in children with homozygous sickle cell disease (1983) (58)
- Benign clinical course in homozygous sickle cell disease: a search for predictors. (1997) (57)
- Geography and the Clinical Picture of Sickle Cell Disease (1989) (57)
- A randomized clinical trial of scatter photocoagulation of proliferative sickle cell retinopathy. (1991) (57)
- Factors associated with lowered intelligence in homozygous sickle cell disease. (1995) (57)
- Observations on the Natural History of Dactylitis in Homozygous Sickle Cell Disease (1981) (56)
- Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease. (1985) (55)
- Energy intake and resting metabolic rate in preschool Jamaican children with homozygous sickle cell disease. (2002) (55)
- Ocular findings of elderly cases of homozygous sickle-cell disease in Jamaica. (1976) (54)
- An assessment of lung volumes and gas transfer in sickle-cell anaemia (1971) (53)
- Postsplenectomy course in homozygous sickle cell disease. (1999) (52)
- Post‐natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parental Hb F levels (1982) (52)
- ROLE OF SPLENECTOMY IN HOMOZYGOUS SICKLE CELL DISEASE IN CHILDHOOD (1984) (51)
- Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease (1983) (50)
- Gall stones in Jamaican children with homozygous sickle cell disease. (1989) (50)
- The conjunctival sign in sickle cell anemia. A relationship with irreversibly sickled cells. (1972) (49)
- Sensori-neural hearing loss in Jamaicans with SS disease. (1973) (49)
- Pregnancy in Jamaican women with homozygous sickle cell disease. Fetal and maternal outcome (1986) (48)
- Is there an energy deficiency in homozygous sickle cell disease? (1995) (48)
- Renal function in patients over 40 with homozygous sickle-cell disease. (1981) (47)
- Dopamine D4 receptor variant in Africans, D4valine194glycine, is insensitive to dopamine and clozapine: report of a homozygous individual. (1996) (47)
- Chronic leg ulceration in homozygous sickle cell disease: the role of venous incompetence (2002) (46)
- Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster. (1984) (46)
- The Clinical Features of Haemoglobin SC Disease in Jamaica (1973) (46)
- Elderly survivors with homozygous sickle cell disease. (2007) (46)
- The New Genetics and Clinical Practice 3rd edn. (1992) (46)
- Phenotype/genotype relationships in sickle cell disease: a pilot twin study. (2005) (45)
- The Mechanisms of Low Birth Weight in Infants of Mothers With Homozygous Sickle Cell Disease (2007) (45)
- Comparison of homozygous sickle cell disease in Northern Greece and Jamaica (1990) (44)
- Comparison of Haematological Features of the β0 and β+ Thalassaemia Traits in Jamaican Negroes (1977) (43)
- Ocular findings in sickle cell thalassemia in Jamaica. (1972) (43)
- Significance of fever in Jamaican patients with homozygous sickle cell disease (2001) (42)
- A randomized clinical trial of feeder vessel photocoagulation of proliferative sickle cell retinopathy. I. Preliminary results. (1983) (42)
- A Comparison of Erythrocyte Characteristics in Sickle Cell Syndromes in Jamaica (1972) (42)
- Current concerns in haematology. 1. Is the painful crisis of sickle cell disease a "steal" syndrome? (1990) (42)
- NEGRO α-THALASSÆMIA IS CAUSED BY DELETION OF A SINGLE α-GLOBIN GENE (1979) (42)
- EARLY SPLENOMEGALY IN HOMOZYGOUS SICKLE-CELL DISEASE: AN INDICATOR OF SUSCEPTIBILITY TO INFECTION (1978) (41)
- Fetal haemoglobin in homozygous sickle cell disease. (1975) (41)
- Early rise in the "pitted" red cell count as a guide to susceptibility to infection in childhood sickle cell anaemia. (1982) (41)
- The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. (1988) (41)
- Sickle cell disease in Uganda: a time for action. (2004) (41)
- Determinants of nocturnal enuresis in homozygous sickle cell disease. (1990) (40)
- Calcification of Bruch's membrane in angioid streaks with homozygous sickle cell disease. (1987) (40)
- Nocturnal enuresis in normal Jamaican children. Implications for therapy. (1991) (40)
- Sickle cell retinopathy in young children in Jamaica. (1982) (39)
- Newborn screening for sickle cell disease in Brazil: the Campinas experience. (2004) (39)
- The Sickle-cell and Altitude (1971) (39)
- BLOOD PRESSURE IN ADULTS WITH HOMOZYGOUS SICKLE CELL DISEASE (1981) (39)
- The haematology of homozygous sickle cell disease after the age of 40 years (1991) (38)
- Haematological indices in normal negro children: a Jamaican cohort from birth to five years. (1980) (37)
- The geography of sickle cell disease: Opportunities for understanding its diversity. (1994) (37)
- Postural vasoconstriction and leg ulceration in homozygous sickle cell disease. (1997) (36)
- Psychosocial aspects of sickle cell disease. (1976) (36)
- Penile prostheses in the management of impotence in sickle cell disease. (1987) (35)
- Factors affecting prepubertal growth in homozygous sickle cell disease. (1996) (35)
- Peripheral vascular response to mild indirect cooling in patients with homozygous sickle cell (SS) disease and the frequency of painful crisis. (1998) (35)
- The Genetics and Molecular Basis of Alpha Thalassaemia in Association with Hb S in Jamaican Negroes (1981) (35)
- Invasive pneumococcal disease in homozygous sickle cell disease: Jamaican experience 1973-1997. (2001) (34)
- Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birth (2018) (34)
- Homozygous sickle cell disease in Jamaica. (1973) (32)
- Screening for sickle-cell disease in Brazil (2000) (32)
- Inhaled nitric oxide for acute chest syndrome in people with sickle cell disease. (2008) (32)
- Endoscopic and gastric acid studies in homozygous sickle cell disease and upper abdominal pain. (1989) (32)
- Sickle cell disease in India: A perspective (2016) (31)
- Bacteriology of sickle cell leg ulcers. (1986) (31)
- Sickle cell‐hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes (1988) (30)
- Biliary sludge in sickle cell disease. (1996) (30)
- Platelet activation and endothelial cell dysfunction in sickle cell disease is unrelated to reduced antioxidant capacity (2003) (30)
- Predictors of renal function progression in adults with homozygous sickle cell disease (2016) (29)
- Sexual development and fertility of Jamaican female patients with homozygous sickle cell disease. (1981) (29)
- Angioid streaks in Jamaican patients with homozygous sickle cell disease. (1981) (29)
- Portal vein thrombosis in a child with homozygous sickle-cell disease. (1993) (29)
- Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors. (2017) (29)
- Influence of genotype on the natural history of untreated proliferative sickle retinopathy--an angiographic study. (1991) (29)
- The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes. (1987) (29)
- Clinical presentation of sickle cell-hemoglobin C disease. (1986) (29)
- Detection of Alpha Thalassaemia in Negro Infants (1980) (29)
- Unusual chorioretinal degeneration in sickle cell disease. Possible sequelae of posterior ciliary vessel occlusion. (1973) (29)
- Neonatal screening for sickle cell disease in the Eastern Province of Saudi Arabia. (1984) (28)
- Topical antibiotics in chronic sickle cell leg ulcers. (1986) (28)
- Photocoagulation and diathermy in the treatment of proliferative sickle retinopathy. (1974) (28)
- Increased renal reflectivity in sickle cell disease: prevalence and characteristics. (1995) (28)
- Nocturnal enuresis in sickle cell haemoglobinopathies. (1990) (28)
- The mechanism of low testosterone levels in homozygous sickle-cell disease. (1994) (28)
- Sickle cell retinopathy in Jamaican children: a search for prognostic factors. (1983) (28)
- Body shape in young children with homozygous sickle cell disease. (1983) (28)
- Hb S-β-Thalassemia: Molecular, Hematological and Clinical Comparisons (2011) (27)
- The Determinants of Irreversibly Sickled Cells in Homozygous Sickle Cell Disease (1978) (26)
- Non-gouty arthritis in sickle cell disease: report of 37 consecutive cases. (1984) (26)
- Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease. (1979) (26)
- Sickle Cell and Altitude (1972) (26)
- A Randomized Clinical Trial of Feeder Vessel Photocoagulation of Proliferative Sickle Cell Retinonathy: II. Update and Analysis of Risk Factors (1984) (26)
- HURRICANE GILBERT ANAEMIA (1989) (26)
- Recommendations for neonatal screening for haemoglobinopathies (1988) (25)
- Choroidal neovascularisation induced by photocoagulation in sickle cell disease. (1981) (25)
- An update on techniques of photocoagulation treatment of proliferative sickle cell retinopathy (1991) (25)
- Clinical features of pulmonary lesions in sickle-cell anaemia. (1970) (25)
- A comparison of sickle cell syndromes in Northern Greece (1991) (25)
- Cholelithiasis in Jamaican patients with homozygous sickle cell disease (1977) (25)
- Peak expiratory flow rate and the acute chest syndrome in homozygous sickle cell disease. (1991) (25)
- The radiological features of avascular necrosis of the femoral head in homozygous sickle cell disease. (1981) (25)
- Social Effects of Leg Ulceration in Sickle Cell Anemia (1977) (24)
- Macular vasculature, visual acuity, and irreversibly sickled cells in homozygous sickle cell disease. (1982) (24)
- Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease. (1981) (24)
- INADEQUACY OF Hb BART'S AS AN INDICATOR OF α THALASSAEMIA (1982) (24)
- Urea kinetics in adults with homozygous sickle cell disease. (1988) (23)
- The internal auditory canel and sensori-neural hearing loss in homozygous sickle cell disease (1975) (23)
- Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work? (2017) (23)
- Testosterone deficiency and extreme retardation of puberty in homozygous sickle-cell disease. (1995) (23)
- Measurement of glomerular filtration rate in homozygous sickle cell disease: a comparison of 51Cr-EDTA clearance, creatinine clearance, serum creatinine and beta 2 microglobulin. (1990) (23)
- Systemic lupus erythematosus and sickle-cell anaemia. (1976) (23)
- HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HÆMOGLOBIN AND HOMOZYGOUS SICKLE-CELL DISEASE (1977) (22)
- Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease. (1995) (22)
- Normal pregnancy in a patient with multiple myeloma and sickle cell anaemia. (1971) (22)
- Neural tube defects in hurricane aftermath (1991) (22)
- Treatment and prevention of sickle-cell crisis. (1971) (22)
- Renal length in sickle cell disease: observations from a cohort study. (1996) (22)
- Is the painful crisis of sickle-cell disease due to sickling? (1991) (22)
- Pneumococcal and other infections in children with sickle-cell hemoglobin C (SC) disease. (1982) (22)
- Adolescent blood pressure in a cohort study of sickle cell disease. (1993) (22)
- Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers. (2000) (22)
- Heights and weights of Jamaican children with homozygous sickle cell disease. (1977) (22)
- The effect of splenectomy for hypersplenism on whole body protein turnover, resting metabolic rate and growth in sickle cell disease. (1996) (21)
- Focal echogenic lesions in the spleen in sickle cell disease. (1993) (21)
- Salmon-patch hemorrhages after central retinal artery occlusion in sickle cell disease. (1981) (21)
- Blood rheology and proliferative retinopathy in homozygous sickle cell disease. (1986) (21)
- The Chhattisgarh state screening programme for the sickle cell gene: a cost-effective approach to a public health problem (2015) (20)
- The in vivo sickle phenomenon: a reappraisal. (1973) (20)
- Photocoagulation in proliferative sickle retinopathy: results of a 5-year study. (1980) (20)
- Prevalence of antibodies to hepatitis C virus and other markers in Jamaica. (1995) (20)
- Foetal haemoglobin in homozygous sickle cell disease: a study of patients with low HBF levels. (2001) (20)
- The case for dedicated sickle cell centres (2006) (20)
- Iris atrophy in sickle cell disease. (1986) (20)
- CHRONIC TRANSFUSION PROGRAMMES IN SICKLE CELL DISEASE: PROBLEM OR PANACEA? (1997) (20)
- The Development of Haemoglobin A2 in Normal Negro Infants and in Sickle Cell Disease (1978) (20)
- Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions. (1991) (19)
- MAPPING OF ANTIGENIC SITES ON HUMAN HAEMOGLOBIN BY MEANS OF MONOCLONAL ANTIBODIES AND HAEMOGLOBIN VARIANTS (1981) (19)
- Blood transfusion in sickle cell disease: a cautionary tale (2003) (19)
- Observations on the epidemiology of sickle cell disease. (1981) (19)
- Cardio-pulmonary responses and gas exchange during exercise in adults with homozygous sickle-cell disease (sickle-cell anaemia). (1973) (19)
- Propionyl-L-carnitine in chronic leg ulcers of homozygous sickle cell disease: a pilot study. (1997) (19)
- Sickle Cell Disease in Central India: A Potentially Severe Syndrome (2016) (19)
- Haematological risk factors for pregnancy outcome in Jamaican women with homozygous sickle cell disease (1994) (19)
- Plasma haemoglobin and complement activation in sickle cell disease. (1981) (19)
- Pneumonia in young children with homozygous sickle cell disease: risk and clinical features (1985) (18)
- Airline travel in sickle-cell disease (1998) (18)
- Urographic findings in homozygous sickle cell disease. (1978) (18)
- Isoxsuprine hydrochloride in the therapy of sickle cell leg ulceration. (1977) (18)
- Glomerular function and hyperuricaemia in sickle cell disease. (1984) (17)
- Retinal and choroidal neovascularization in sickle cell disease. (1980) (17)
- Delayed menarche in homozygous sickle cell disease. (1986) (17)
- Antiphospholipid antibodies in homozygous sickle cell disease. (1992) (17)
- Serum urate concentrations in homozygous sickle cell disease (1981) (17)
- Outcome of iatrogenic choroidal neovascularisation in sickle cell disease. (1990) (16)
- A simple micromethod for the measurement of fetal haemoglobin. (1975) (16)
- Screening for the sickle cell gene in Gujarat, India: a village-based model (2012) (16)
- Radiological changes associated with leg ulcers in the tropics. (1972) (16)
- RBC transfusion in sickle cell anemia (HbSS):experience from the Jamaican Cohort Study (2001) (16)
- Delayed skeletal maturation in sickle cell anemia in Jamaica. (1973) (16)
- Blood rheology and proliferative retinopathy in sickle cell-haemoglobin C disease. (1984) (15)
- Body Habitus of Jamaican Adults with Sickle Cell Anemia (1972) (15)
- Genetical, Functional, and Physical Studies of Hemoglobins (1972) (15)
- The epidemiology of Sickle Cell Disorder: A challenge for Africa (2005) (15)
- Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease. (2004) (15)
- alpha thalassemia in black populations. (1980) (15)
- Treatment of sickle cell disease in early childhood in Jamaica. (1985) (15)
- Ocular findings in children with sickle cell haemoglobin C disease in Jamaica. (1974) (14)
- Leg ulcers in sickle-cell anaemia. (1970) (14)
- Interpretation of lung function tests in the sickle-cell haemoglobinopathies. (1978) (14)
- Cardiac performance in children with homozygous sickle cell disease. (1987) (14)
- Resolution of chronic hepatic sequestration in a patient with homozygous sickle cell disease receiving hydroxyurea. (2003) (14)
- Epiretinal membranes in sickle cell disease. (1987) (14)
- A survey of parasites in primary school children in Dominica, West Indies. (1981) (14)
- Influence of alpha thalassaemia on the retinopathy of homozygous sickle cell disease. (1993) (14)
- Haemoglobin spanish town α27 GLU – VAL (B8) (1976) (14)
- A randomized controlled trial of solcoseryl and duoderm in chronic sickle-cell ulcers. (1993) (14)
- ACUTE SPLENIC SEQUESTRATION IN JAMAICAN ADULTS WITH HOMOZYGOUS SICKLE CELL DISEASE: A ROLE OF ALPHA THALASSAEMIA (1991) (14)
- Laser photocoagulation for proliferative retinopathy in sickle haemoglobin C disease (1993) (14)
- Interaction of the ααα globin gene haplotype and sickle haemoglobin (1984) (14)
- Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia. (1976) (13)
- Erythropoietin and renal function in sickle-cell disease. (1982) (13)
- The Effect of Splenectomy on Whole Body Protein Turnover in Homozygous Sickle Cell Disease (1991) (13)
- Systemic Salmonella infections in sickle cell anaemia. (1989) (13)
- Ulcerative colitis in sickle cell disease. (1987) (13)
- General anesthesia in sickle cell disease. (1980) (13)
- Patterns of low‐affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease (2002) (13)
- Mass Spectral Analysis of Asymmetric Hemoglobin Hybrids: Demonstration of Hb FS (α2γβS) in Sickle Cell Disease (2001) (13)
- Red Cell Size and the Clinical and Haematological Features of Homozygous Sickle Cell Disease (1981) (12)
- The Politics of Sickle Cell and Thalassaemia (2001) (12)
- Fetal growth in women with homozygous sickle cell disease: an observational study. (2013) (12)
- Recurrent visual loss in homozygous sickle cell disease. (1985) (12)
- Elevated IL-1α and CXCL10 Serum Levels Occur in Patients with Homozygous Sickle Cell Disease and a History of Acute Splenic Sequestration (2012) (12)
- Recurrent infections in sickle cell disease: haematological and immune studies. (1985) (12)
- Alpha thalassaemia and the haematology of normal Jamaican children. (1985) (12)
- Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural History. (2015) (12)
- A whole blood solubility and centrifugation test for sickle cell hemoglobin: a clinical trial. (1972) (12)
- Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes. (2012) (12)
- Ocular findings in Saudi Arabian patients with sickle cell disease. (1995) (11)
- Recent advances in the treatment of proliferative sickle cell retinopathy (1992) (11)
- Haemoglobin SC disease in Jamaica. (1973) (11)
- Duodenal ulceration in sickle cell anaemia. (1973) (11)
- Sickle haemoglobin and pregnancy. (1983) (10)
- Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell disease and in normal subjects (1998) (10)
- Abnormal thyroid hormone and thyrotropin levels in homozygous sickle cell disease. (1989) (10)
- Corynebacterium diphtheriae in sickle cell leg ulcers in Jamaica. (1985) (10)
- Haemoglobin Variant Screening in Jamaica: Meeting Student's Request (2016) (10)
- The clinical features in adults sickle cell anaemia in Jamaica. (1970) (10)
- Neodymium-YAG laser vitreolysis in sickle cell retinopathy. (1987) (10)
- Sickle-cell and altitude. (1972) (10)
- Pregnancy in sickle cell-haemoglobin C (SC) disease. A retrospective study of birth size and maternal weight gain. (2016) (10)
- Sickle cell-hemoglobin D Iran: benign sickle cell syndrome. (1982) (10)
- Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers (2000) (9)
- The progression of sickle cell eye disease in Jamaica (1975) (9)
- The Role of Preventive Medicine in Sickle Cell Disease (1996) (9)
- Treatment of subretinal neovascularization associated with angioid streaks in sickle cell retinopathy. Case report. (1987) (9)
- Sickle cell trait and leg ulceration. (1970) (9)
- Raised Hb F levels in sickle cell disease are caused by a determinant linked to the beta globin gene cluster. (1987) (9)
- A randomized clinical trial of feeder vessel photocoagulation of proliferative sickle cell retinopathy. II. Update and analysis of risk factors. (1984) (9)
- PAINFUL CRISES IN SICKLE CELL DISEASE AFTER FLUORESCEIN ANGIOGRAPHY (1985) (9)
- Splenic opacification in homozygous sickle cell disease. (1981) (9)
- Determinants of Haemoglobin Level in Sickle Cell‐Haemoglobin C Disease (1979) (9)
- Evolving locally appropriate models of care for Indian sickle cell disease (2016) (9)
- Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome. (1983) (8)
- Body habirus of Jamaican adults with sickle cell anemia. (1972) (8)
- General anaesthesia in sickle-cell disease. (1979) (8)
- Painful crises in sickle-cell disease (1996) (8)
- Alpha thalassaemia and the macular vasculature in homozygous sickle cell disease. (1983) (8)
- Daily variability in resting levels of cardiovascular variables in normal subjects and those with homozygous sickle cell disease (1995) (8)
- Pulmonary artery pressure and the acute chest syndrome in homozygous sickle cell disease. (1993) (7)
- Management of sickle cell disease: challenges and risks of transfusion (2016) (7)
- Comparison of haematological features of the beta0 and beta+ thalassaemia traits in Jamaican Negroes. (1977) (7)
- Growth curves for normal Jamaican neonates. (2006) (7)
- Sickle cell anaemia in Nigeria: a comparison between Benin and Lagos. (1994) (7)
- Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry (2011) (7)
- Heights and weights of West Indian children with the sickle cell trait. (1978) (7)
- Alpha thalassemia and homozygous sickle cell disease. (1981) (7)
- Blood transfusion in sickle cell disease (1985) (7)
- The dilemma of defining clinical severity in homozygous sickle cell disease. (2004) (7)
- Mononuclear cells in sickle cell disease: subpopulations and in vitro response to mitogens. (1984) (7)
- Acceptability of antenatal diagnosis for sickle-cell disease among Jamaican mothers and female patients. (1988) (7)
- The Spleen in Sickle Cell Disease (2002) (7)
- Retained Placenta in Homozygous Sickle Cell Disease (2009) (6)
- The red cell distribution width in sickle cell disease--is it of clinical value? (2008) (6)
- World Sickle Cell Day: Lessons for India (2017) (6)
- Biliary surgery in patients with sickle-cell anaemia. (1992) (6)
- The metacarpal index in homozygous sickle-cell disease. (1988) (6)
- Pattern of pregnancy weight gain in homozygous sickle cell disease and effect on birth size. (2011) (6)
- Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica (2016) (6)
- Five-year follow-up of Jamaican adults with sickle cell anaemia. (1975) (6)
- Transfusion in Sickle Cell Disease: Experience from a Gujarat Centre (2014) (6)
- Awareness of sickle cell disease among high school students in Kingston, Jamaica. (1976) (6)
- Sickle cell beta thalassaemia in Jamaica. (1973) (6)
- Gall stones in homozygous sickle cell disease. (1989) (6)
- Homozygous sickle cell disease in Central India & Jamaica: A comparison of newborn cohorts (2020) (6)
- HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome. (1998) (5)
- Complement and immunoglobulin levels in early childhood in homozygous sickle cell disease. (1986) (5)
- Sickle Cell Disease in Saudi Arabia: The Asian Haplotype (2004) (5)
- Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene. (1979) (5)
- Serum immunoglobulin levels in children with homozygous sickle cell disease. (1982) (5)
- Sickle haemoglobin and haemoglobin Stanleyville II: possible confusion with sickle cell-haemoglobin C disease. (2005) (5)
- Haemophilus influenzae osteomyelitis complicating dactylitis in homozygous sickle cell disease (1990) (5)
- Clinical judgment and sickle cell disease. (1993) (5)
- Newborn Screening for Sickle Cell Disease in India: The Need for Defining Optimal Clinical Care (2014) (5)
- Ocular findings in sickle cell-haemoglobin O Arab disease. (1979) (5)
- Microchromatographic quantitation of hemoglobin A levels in phenotypes of sickle cell-beta(+) thalassemia. (1997) (5)
- Comparison of sickle cell beta o-thalassemia and sickle cell beta +-thalassemia in black populations. (1982) (5)
- Avascular necrosis of the femoral head in Saudi Arabians with homozygous sickle cell disease - risk factors. (1995) (5)
- Pregnancy outcome in homozygous sickle cell disease: observations from the Jamaican Birth Cohort (2021) (5)
- The Bone Pain Crisis of Sickle Cell Disease and Malaria: Observations from Gujarat, India (2017) (5)
- Testing for the random occurrence of sickle cell disease in a study of 100,000 Jamaican newborns. (1990) (5)
- Jamaica, the Caribbean and sickle cell disease. (2012) (5)
- The interaction of alpha thalassaemia with SS disease. (1978) (4)
- Cord blood screening for sickle hemoglobin: evidence against a female preponderance of hemoglobin S. (1981) (4)
- Use of blood specimens collected on filter paper in screening for abnormal hemoglobins. (1976) (4)
- A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin (2017) (4)
- Skeletal development of Jamaican children with homozygous sickle cell disease. (1978) (4)
- Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease. (1982) (4)
- Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples (2016) (4)
- Oral zinc sulphate treatment of chronic non-sickle cell ulcers in Jamaica. (1975) (4)
- Shortening of the digits in sickle cell anaemia: a sequela of the hand-foot syndrome. (1971) (3)
- Newborn Screening for Sickle Cell Disease: Jamaican Experience. (2015) (3)
- Peripheral retinal vasculature in normal Jamaican children. (1994) (3)
- Comparison of clinical, hematological and molecular findings of Jamaican and Sicilian patients with sickle cell disease. (1990) (3)
- Negro alpha-thalassaemia: genetic studies in homozygous sickle cell disease. (1980) (3)
- Sickle haemoglobin comes of age. (2014) (3)
- Sickle cell-hemoglobin Caribbean--a benign syndrome. (1982) (3)
- Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell disease. (2001) (3)
- The Challenge of Sickle Cell Disease in Saudi Arabia (1990) (3)
- Psychological distress among younger siblings of patients with homozygous sickle cell disease in the Jamaican cohort study. (2000) (3)
- The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia. (1988) (3)
- Treatment of iatrogenic choriovitreal neovascularisation in sickle cell disease. (1991) (3)
- Delayed diagnosis of homozygous sickle cell disease in Jamaica. (1992) (3)
- Haemoglobin Spanish Town alpha27 Glu replaced by Val (B8). (1976) (3)
- Iron Deficiency among Jamaican Adolescents. (2015) (3)
- Penicillin-resistant Streptococcus pneumoniae in a Jamaican patient with homozygous sickle-cell disease. (1996) (3)
- Intravenous oxpentifylline and the painful crisis of sickle cell disease (2016) (2)
- The red cell distribution width - is it of clinical value? (1991) (2)
- Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin. (1984) (2)
- Diabetic retinopathy and visual loss in a Jamaican population. (1987) (2)
- Fetal hemoglobin and the irreversibly sickled cell in sickle cell disease (1974) (2)
- Gamma chain variants in Jamaican newborns. (1976) (2)
- What's new in sickle cell disease? (1988) (2)
- Sickle Cell Disease: Thoughts for India From the Jamaican Cohort Study (2021) (2)
- Skinfold thickness and nutritional status in young Jamaican children. (1983) (2)
- 4 The clinical features of sickle cell disease (1993) (2)
- Sickle Cell Disease in Central India: High Prevalence of Sickle/Beta Thalassemia and Severe Dsiease Phenotype (2015) (2)
- Empyema of gallbladder in a child with homozygous sickle-cell disease. (1990) (2)
- β-Thalassemia Mutations in Jamaica: Geographic Variation in Small Communities (2018) (1)
- A Note on the Prevalence of Impaternity in Jamaica (2017) (1)
- Beta-chain variants in Jamaican newborns. (1978) (1)
- Counselling mothers of babies with the sickle cell trait: to be or not to be. (2011) (1)
- Letter: Fetal hemoglobin and the irreversibly sickled cell in sickle cell disease. (1974) (1)
- Odisha Revisited: A Personal Account (2021) (1)
- The sickle cell trait and leg ulceration. (1972) (1)
- Patterns of attendance at Jamaican sickle cell clinics 1952 to 1981. (1984) (1)
- The development of cardiomegaly in homozygous sickle cell disease. (1985) (1)
- Haemoglobin F Victoria Jubilee (alpha 2 A gamma 2 80 Asp-Try). (1975) (1)
- A second example of haemoglobin F Texas I (α2Aγ25Glu→Lys) in a Jamaican infant (1977) (1)
- Perinatal factors in students admitted to the University of the West Indies data from the Jamaican Perinatal Study. (2010) (1)
- Risk Factors for Proliferative Sickle Retinopathy (1990) (1)
- Pregnancy in Jamaican women with homozygous sickle cell disease. Fetal and maternal outcome (1986) (1)
- Sickle-cell anaemia before Herrick. (1972) (1)
- Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica (2015) (1)
- Determinants ofnocturnal enuresis inhomozygous sickle cell disease (1990) (0)
- disease . retinopathy of homozygous sickle cell Influence of alpha thalassaemia on the (2003) (0)
- British support for Caribbean research (1991) (0)
- 21.10.6 Sickle-cell disease and the kidney (2010) (0)
- Screening for the sickle cell gene in Gujarat, India: a village-based model (2012) (0)
- Renal function in patients over 40 with homozygous sickle-cell disease (1981) (0)
- Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work? (2017) (0)
- Sickle cell screening and its value in Jamaica (1989) (0)
- Gall-bladder sludge in sickle cell disease: A precursor of gall-stones? (1993) (0)
- homozygous sickle cell disease . with proliferative retinopathy in Haematological factors associated (0)
- Adolescent growth in homozygous sickle-cell disease is delayed but follows a normal pattern - abstract (1993) (0)
- Haemoglobin caribbean beta91 (F7) Leu replaced by Arg: a mildly haemoglobin with a low oxygen affinity. (1976) (0)
- Jamaican children . Peripheral retinal vasculature in normal (0)
- Early splenomegaly and septicaemia in homozygous sickle cell disease: A birth cohort study (2022) (0)
- Retinal changes insickle cell/hereditary persistence offetal haemoglobin syndrome (1983) (0)
- Iris atrophy in sickle cell disease Table 1 Crude prevalence rates of ' spontaneous ' iris atrophy Patients Eyes (0)
- Book Review: The Hemoglobinopathies (1950) (0)
- Author Index for Volume 69 (1998) (0)
- Uncommon Differential Diagnosis to Homozygous Sickle Cell Disease (2016) (0)
- Heart size and chest shape in homozygous sickle cell disease. (1983) (0)
- Leg ulcerationinsicklecell anemia (1974) (0)
- The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report (2019) (0)
- Neonatal screening for sickle hemoglobin. (1979) (0)
- with homozygous sickle cell disease . Angioid streaks in Jamaican patients (2004) (0)
- Megaloblastic change in sickle cell disease obscured by genetically determined microcytosis. (1986) (0)
- Sickle cell disease continued. (1985) (0)
- Jamaica and Research in Sickle Cell Disease (2017) (0)
- Ventilatory response to carbon dioxide in sickle-cell disease. (1977) (0)
- Alphathalassaemia andthemacular vasculature inhomozygous sickle cell disease (1983) (0)
- in Screening for Abnormal Hemoglobins (1976) (0)
- Effect of thermal stimuli on peripheral blood flow in homozygous sickle cell disease: A preliminary study (1996) (0)
- B19 Virus Infection and the Aplastic Crisis (2018) (0)
- ’ s response to reviews Title : The additional genetic diagnosis of homozygous Sickle Cell Disease in a patient with Waardenburg-Shah Syndrome : A Case Report (2018) (0)
- children in Jamaica . Sickle cell retinopathy in young (0)
- Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programme (2022) (0)
- Erectile dysfunction with chemotherapy (2000) (0)
- Epiretinal membranes in sickle cell disease Fig (0)
- Ocular findings inelderly casesofhomozygous sickle-cell disease inJamaica (1976) (0)
- Reply to R Apatu (1993) (0)
- Gamma Chain Variants in Jamaican Newborns (1976) (0)
- homozygous sickle cell disease . and irreversibly sickled cells in Macular vasculature , visual acuity , (0)
- disease . syndrome in homozygous sickle cell Peak expiratory flow rate and the acute chest (2007) (0)
- disease in Jamaica . sickle cell haemoglobin C Ocular findings in children with (2005) (0)
- Is hemoglobin C relevant to the genesis of proliferans retinopathy? (1976) (0)
- TheSickle-cell andAltitude (1971) (0)
- Immunoglobulin receptor polymorphisms in stroke and sickle cell disease (2000) (0)
- Epiretinal membranes insickle cell disease (1987) (0)
- Iris atrophy insickle cell disease (1986) (0)
- Sickle cell diseasecontinued. (1985) (0)
- Anassessment oflungvolumes andgastransfer in sickle-cell anaemia (1971) (0)
- GallstonesinJamaican children withhomozygous sickle cell disease (1989) (0)
- The Chhattisgarh state screening programme for the sickle cell gene: a cost-effective approach to a public health problem (2015) (0)
- Peakexpiratory flowrateandtheacutechest syndrome inhomozygous sickle cell disease (2011) (0)
- Hb F Kingston (G gamma 55 [D6] Met leads to Arg). (1982) (0)
- Nocturnal enuresis insickle cell haemoglobinopathies (1990) (0)
- Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples (2016) (0)
- Heights, Weights, andSkeletal AgeofJamaican Adolescents withSickle Cell Anaemia (1972) (0)
- Energy intake and resting metabolic rate in preschool Jamaican children with homozygous sickle cell disease 1 , 2 (0)
- Chapter 116 – Infections in sickle cell disease (2010) (0)
- Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS (2022) (0)
- RESTING METABOLIC RATE IN SICKLE CELL DISEASE. AUTHOR'S REPLY (1993) (0)
- and Clozapine: Report of a Homozygous Individual D4Valinel94Glycine, Is Insensitive to Dopamine (1996) (0)
- A second example of haemoglobin F Texas 1 (alpha2Agamma25Glu replaced by Lys) in a Jamaican infant. (1977) (0)
- Anthropometric measurements of school children in Dominica, West Indies. (1981) (0)
- Body habitus of Jamaican adults with sickle cell--haemoglobin C (SC) disease. (1979) (0)
- The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes (2022) (0)
- Antiphospholipid antibodies inhomozygous sickle cell disease (1992) (0)
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