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    Sickle Cell Bibiography for Sickle Cell Trust Web Site

    1 Serjeant GR, Richards R, Barbor PRH, Milner PF. Relatively benign sickle-cell anaemia in 60 patients aged over 30 in the West Indies. Br Med J 1968;3:86-91.

    2 Serjeant GR, Serjeant BE, Milner PF. The irreversibly sickled cell: a determinant of haemolysis in sickle cell anaemia. Br J Haematol 1969;17:527-33.

    3 Milner PF, Serjeant GR. Laboratory studies in sickle cell anemia. Blood 1969;34: 729-30 (abs).

    4 Serjeant GR. The natural history of sickle cell anemia in adults. Blood 1969;34: 730-1 (abs).

    5 Serjeant GR. The clinical features of adults with sickle cell anaemia in Jamaica. West Indian Med J 1970;19:1-8.

    6 Petch MC, Serjeant GR. Clinical features of pulmonary lesions in sickle cell anaemia. Br Med J 1970;3:31.

    7 Gueri M, Serjeant GR. Leg ulcers in sickle cell anaemia. Trop Geogr Med 1970; 22:155-60.

    8 Serjeant GR, Gueri M. Sickle cell trait and leg ulceration. Br Med J 1970;1:820 (letter).

    9 Serjeant GR. Irreversibly sickled cells and splenomegaly in sickle-cell anaemia. Br J Haematol 1970;19:635-41.

    10 Serjeant GR, Galloway RE, Gueri M. Oral zinc sulphate in sickle-cell ulcers. Lancet 1970;2:891-3.

    11 Miller GJ, Serjeant GR. An assessment of lung volumes and gas transfer in sickle cell anaemia. Thorax 1971;26:309-15.

    12 Talerman A, Serjeant GR, Milner PF. Normal pregnancy in a patient with multiple myeloma and sickle cell anaemia. West Indian Med J 1971;20:97-100.

    13 Serjeant GR, Ashcroft MT. Shortening of the digits in sickle cell anaemia. A sequela of the hand-foot syndrome. Trop Geogr Med 1971;23:341-6.

    14 Green RL, Huntsman RG, Serjeant GR. The sickle-cell and altitude. Br Med J 1971;4:593-5.

    15 Serjeant GR, White JM. Treatment and prevention of sickle cell crisis. Lancet 1971;2:1255-6 (letter).

    16 Ennis JT, Gueri MC, Serjeant GR. Radiological changes associated with leg ulcers in the tropics. Br J Radiol 1972;45:8-14.

    17 Serjeant GR, Serjeant BE, Condon PI. The conjunctival sign in sickle cell anemia. A relationship with irreversibly sickled cells. JAMA 1972;219:1428-31.

    18 Condon PI, Serjeant GR. Ocular findings in homozygous sickle cell disease in Jamaica. Am J Ophthalmol 1972;73:533-43.

    19 Serjeant GR, Serjeant BE. Sickle-cell anaemia before Herrick. Lancet 1972;i: 746-7.

    20 Ashcroft MT, Serjeant GR. Body habitus of Jamaican adults with sickle cell anemia. Southern Med J 1972;65:579-82.

    21 Serjeant BE, Serjeant GR. A whole blood solubility and centrifugation test for sickle cell hemoglobin: a clinical trial. Am J Clin Pathol 1972;58:11-3.

    22 Ashcroft MT, Serjeant GR, Desai P. Height, weights, and skeletal age of Jamaican adolescents with sickle cell anaemia. Arch Dis Child 1972;47:519-24.

    23 Serjeant GR, Serjeant BE. A comparison of erythrocyte characteristics in sickle cell syndromes in Jamaica. Br J Haematol 1972;23:205-13.

    24 Gueri M, Gueri MV, Serjeant GR. The sickle cell trait and leg ulceration. J Trop Med Hyg 1972;75:193-4.

    25 Green RL, Huntsman RG, Serjeant GR. Sickle-cell and altitude. Br Med J 1972;1: 803-4.

    26 Condon PI, Serjeant GR. Ocular findings in hemoglobin SC disease in Jamaica. Am J Ophthalmol 1972:74:921-31.

    27 Condon PI, Serjeant GR. Ocular findings in sickle cell thalassemia in Jamaica. Am J Ophthalmol 1972;74:1105-9.

    28 Serjeant GR, May H, Patrick A, Slifer ED. Duodenal ulceration in sickle cell anaemia. Trans Roy Soc Trop Med Hyg 1973;67:59-63.

    29 Miller GJ, Serjeant GR, Sivapragasam S, Petch MC. Cardio-pulmonary responses and gas exchange during exercise in adults with homozygous sickle cell disease (sickle cell anaemia). Clin Sci 1973;44:113-28.

    30 Serjeant GR, Ashcroft MT. Delayed skeletal maturation in sickle cell anemia in Jamaica. Johns Hopk Med J 1973;132:95-102.

    31 Serjeant GR. Sickle cell anemia: clinical features in adulthood and old age. In: Abramson H, Bertles JF, Wethers DL, eds. Sickle Cell Disease - Diagnosis, Management, Education and Research. CV Mosby, St Louis 1973; 252-63.

    32 Condon PI, Serjeant GR, Ikeda H. Unusual chorioretinal degeneration in sickle cell disease. Possible sequelae of posterior ciliary vessel occlusion. Br J Ophthalmol 1973;57:81-8.

    33 Serjeant GR, Ashcroft MT, Serjeant BE, Milner PF. The clinical features of sickle-cell b thalassaemia in Jamaica. Br J Haematol 1973;24:19-30.

    34 Serjeant GR, Ashcroft MT, Serjeant BE. The clinical features of haemoglobin SC disease in Jamaica. Br J Haematol 1973;24:491-501.

    35 Serjeant GR, Petch MC, Serjeant BE. The in-vivo sickle phenomenon: a reappraisal. J Lab Clin Med 1973;81:850-6.

    36 Serjeant GR, Ennis JT, Middlemiss H. Haemoglobin SC disease in Jamaica. Br J Radiol 1973;46:935-42.

    37 Ennis JT, Serjeant GR, Middlemiss H. Homozygous sickle cell disease in Jamaica. Br J Radiol 1973;46:943-50.

    38 Serjeant GR, Ennis JT, Middlemiss JH. Sickle cell b thalassaemia in Jamaica. Br J Radiol 1973;46:951-959.

    39 Todd GB, Serjeant GR, Larson MR. Sensori-neural hearing loss in Jamaicans with SS disease. Acta Otolaryngol 1973;76:268-72.

    40 Condon PI, Gray R, Serjeant GR. Ocular findings in children with sickle cell haemoglobin C disease in Jamaica. Br J Ophthalmol 1974;58:644-9.

    41 Serjeant BE, Forbes M, Williams LL, Serjeant GR. Screening cord bloods for detection of sickle cell disease in Jamaica. Clin Chem 1974;20:666-9.

    42 Serjeant GR. Leg ulceration in sickle cell anemia. Arch Intern Med 1974;133: 690-4.

    43 Condon PI, Serjeant GR. Photocoagulation and diathermy in the treatment of proliferative sickle retinopathy. Br J Ophthalmol 1974;58: 650-62.

    44 Serjeant GR. The Clinical Features of Sickle Cell Disease. North Holland Publishing Co., Amsterdam 1974, (book).

    45 McCormack MK, Bresson VL, Serjeant GR. Fetal hemoglobin and the irreversibly sickled cell in sickle cell disease. J Pediatr 1974;85:435-6 (letter).

    46 Leslie J, Langler D, Serjeant GR, Serjeant BE, Desai P, Gordon YB. Coagulation changes during the steady state in homozygous sickle-cell disease in Jamaica. Br J Haematol 1975;30:159-66.

    47 Serjeant GR, Norman W, Todd GB. The internal auditory canal and sensori-neural hearing loss in homozygous sickle cell disease. J Laryngol Otol 1975;89:453-5.

    48 Serjeant GR. Fetal haemoglobin in homozygous sickle cell disease. Clin Haematol 1975;4:109-22.

    49 Gueri M, Van Devanter S Serjeant BE, Serjeant GR. Oral zinc sulphate treatment of chronic non-sickle cell ulcers in Jamaica. West Indian Med J 1975;24:26-9.

    50 Ahern E, Holder W, Ahern V, Serjeant GR, Serjeant BE, Forbes M, Brimhall B, Jones RT. Haemoglobin F Victoria Jubilee (a2Ag280 Asp-gTyr). Biochim Biophys Acta 1975;393:188-94.

    51 Serjeant GR. A five year follow up of Jamaican adults with sickle cell anaemia. Br Med J 1975;3:20-1.

    52 Serjeant BE, Clarke JM, Desai R, Serjeant GR. A simple micromethod for the measurement of fetal haemoglobin. J Clin Pathol 1975;28:761-4.

    53 Condon PI, Serjeant GR. The progression of sickle cell eye disease in Jamaica. Docum Ophthalmol 1975;39:203-10.

    54 Redwood AM, Williams EM, Desai P, Serjeant GR. Climate and the painful crisis of sickle-cell disease in Jamaica. Br Med J 1976;1:66-8.

    55 Weatherall DJ, Clegg JB, Milner PF, Marsh GW, Bolton FG, Serjeant GR. Linkage relationships between b-and d-structural loci and the African forms of b thalassaemia. J Med Genet 1976;13:20-6.

    56 Wilson WA, Nicholson GD, Hughes GRV, Amin S, Alleyne GAO, Serjeant GR. Systemic lupus erythematosus and sickle-cell anaemia. Br Med J 1976;2:813.

    57 Ahern E, Ahern V, Holder W, Palomino E, Serjeant GR, Serjeant BE, Forbes M, Brimhall B, Jones RT. Haemoglobin Spanish Town a27 GLU→VAL (B8). Biochim Biophys Acta 1976;427:530-5.

    58 Desai P, Serjeant GR. Awareness of sickle cell disease among high school students in Kingston, Jamaica. Public Health Reports 1976;91:265-7.

    59 Ashcroft MT, Desai P, Richardson SA, Serjeant GR. Growth, behaviour, and educational achievement of Jamaican children with the sickle-cell trait. Br Med J 1976;1:1371-3.

    60 Schmidt RM, Brossius EM, Holland S, Wright JM, Serjeant GR. Use of blood specimens collected on filter paper in screening for abnormal hemoglobins. Clin Chem 1976;22:685-7.

    61 Condon PI, Serjeant GR. Ocular findings in elderly cases of homozygous sickle-cell disease in Jamaica. Br J Ophthalmol 1976;60:361-4.

    62 Serjeant GR. Sickle Cell Haemoglobinopathies. In: Cruickshank R, Standard KL, Russell HBL, eds. Epidemiology and Community Health in Warm Climate Countries. Churchill-Livingstone, Edinburgh 1976;384-405.

    63 Alleyne SI, Wint E, Serjeant GR. Psychosocial aspects of sickle cell disease. Health and Social Work 1976;1:104-19.

    64 Ahern E, Ahern V, Hilton T, Serjeant GR, Serjeant BE, Seakins M, Lang A, Middleton A, Lehmann H. Haemoglobin Caribbean b91 (F7) LeugArg: a mildly unstable haemoglobin with a low oxygen affinity. FEBS Letters 1976;69:99-102.

    65 Condon PI, Serjeant GR, Archer D. Is hemoglobin C relevant to the genesis of proliferans retinopathy? In: Bergsma D, Bron AJ, Cotlier E, eds. The Eye and Inborn Errors of Metabolism. Birth Defects: original article series, volume 12. Alan R Liss Inc., New York 1976;517-20.

    66 Ahern E, Ahern V, Holder W, Palomino E, Serjeant GR, Clarke J, Brimhall B, Jones RT. Gamma chain variants in Jamaican newborns. Hemoglobin 1977;1: 153-69.

    67 Serjeant GR. Sickle cell conditions. In: Conn HF, ed. Current Therapy. Saunders, London 1977;269-73.

    68 Millard DP, Mason K, Serjeant BE, Serjeant GR. Comparison of the haematological features of the bo and b+ thalassaemia traits in Jamaican Negroes. Br J Haematol 1977;36:161-70.

    69 Alleyne SI, Wint E, Serjeant GR. Social effects of leg ulceration in sickle cell anemia. Southern Med J 1977;70:213-4.

    70 Serjeant GR, Serjeant BE, Mason K. Heterocellular hereditary persistence of fetal haemoglobin and homozygous sickle-cell disease. Lancet 1977;1; 795-6 (letter).

    71 Lowry MR, Desai P, Ashcroft MT, Serjeant BE, Serjeant GR. Heights and weights of Jamaican children with homozygous sickle cell disease. Human Biol 1977;49: 429-36.

    72 Miller GJ, Serjeant GR. Ventilatory response to carbon dioxide in sickle-cell disease. Br J Anaesth 1977;49:391 (letter).

    73 Serjeant GR, Howard C. Isoxsuprine hydrochloride in the therapy of sickle cell ulceration. West Indian Med J 1977;26:164-6.

    74 Ahern E, Serjeant GR. A second example of haemoglobin F Texas I (a2Ag25GlugLys) in a Jamaican infant. Biochim Biophys Acta 1977;292:241-4.

    75 McCall IW, Desai P, Serjeant BE, Serjeant GR. Cholelithiasis in Jamaican patients with homozygous sickle cell disease. Am J Hematol 1978;3:15-21.

    76 Miller GJ, Serjeant GR, Saunders MJ, Richardson C, Gilson RJC. Interpretation of lung function tests in the sickle-cell haemoglobinopathies. Thorax 1978;33:85-8.

    77 McCall IW, Moule N, Desai P, Serjeant GR. Urographic findings in homozygous sickle cell disease. Radiology 1978;126:99-104.

    78 Serjeant BE, Mason KP, Serjeant GR. The development of HbA2 in normal Negro infants and in sickle cell disease. Br J Haematol 1978;39:259-65.

    79 Serjeant GR, Serjeant BE, Desai P, Mason KP, Sewell A, England JM. The determinants of irreversibly sickled cells in homozygous sickle cell disease. Br J Haematol 1978;40:431-8.

    80 Lowry MF, Desai P, Ashcroft MT, McCall IW, Serjeant GR. Skeletal development of Jamaican children with homozygous sickle cell disease. Human Biol 1978;50; 115-9.

    81 Rogers DW, Clarke JM, Cupidore L, Ramlal AM, Sparke BR, Serjeant GR. Early deaths in Jamaican children with sickle cell disease. Br Med J 1978;1:1515-6.

    82 Serjeant GR. International Perspectives. In: Proceedings of the First National Sickle Cell Educational Symposium. Washington: DHEW Publication No. (NIH) 78-1084:135-42.

    83 Sewell A, Millard D, Serjeant GR. The Interaction of Alpha Thalassemia with SS Disease. In: Brewer GJ, ed. The Red Cell. Alan R Liss Inc., New York, 1978;93-102.

    84 Ashcroft MT, Desai P, Grell GAC, Serjeant BE, Serjeant GR. Heights and weights of West Indian children with sickle cell trait. Arch Dis Child 1978;53:596-8.

    85 Rogers DW, Vaidya S, Serjeant GR. Early splenomegaly in homozygous sickle-cell disease: an indicator of susceptibility to infection. Lancet 1978;2:963-5.

    86 Serjeant GR, Sommereux A-M, Stevenson M, Mason K, Serjeant BE. Comparison of sickle cell-bo thalassaemia with homozygous sickle cell disease. Br J Haematol 1979;41:83-93.

    87 Ahern E, Ahern V, Serjeant GR, Serjeant BE, Seakins M, Darbre P, Middleton A, Lehmann H. b-chain variants in Jamaican newborns. Hemoglobin 1978;2:495-502.

    88 Bannerman RM, Serjeant BE, Seakins M, England JM, Serjeant GR. Determinants of haemoglobin level in sickle cell-haemoglobin C disease. Br J Haematol 1979;43: 49-56.

    89 Homi J, Reynolds J, Skinner A, Hannah W, Serjeant GR. General anaesthesia in sickle-cell disease. Br Med J 1979;1:1599-1601.

    90 Juarez C, Jampol LM, Serjeant GR. Choroidal amyloidosis: a case report. Perspectives in Ophthalmology 1979;3:141-5.

    91 Higgs DR, Pressley L, Old JM, Hunt DM, Clegg JB, Weatherall DJ, Serjeant GR. Negro alpha-thalassaemia is caused by the deletion of a single alpha-globin gene. Lancet 1979;2:272-6.

    92 Condon PI, Serjeant GR. Ocular findings in sickle cell-haemoglobin O Arab disease. Br J Haematol 1979;63:839-41.

    93 Ashcroft MT, Serjeant GR. Body habitus of Jamaican adults with sickle cell-haemoglobin (SC) disease. West Indian Med J 1979;28:218-21.

    94 Serjeant GR. Natural History of Sickle Cell Disease in the Caribbean. In: Scott RB, ed. International Aspects of Sickle Cell Disease. Howard University Press, Washington 1979;48-53.

    95 Serjeant GR. Leg Ulceration in Homozygous Sickle Cell Disease in Jamaica. In: Scott RB, ed. International Aspects of Sickle Cell Disease. Howard University Press, Washington 1979;103-105.

    Serjeant G, Serjeant B. Neonatal screening for sickle hemoglobin. Am J Clin Pathol 1979;72:251 (letter).





    97 Condon PI, Serjeant GR. Behaviour of untreated proliferative sickle cell retinopathy. Br J Ophthalmol 1980;64:404-11.

    98 Emond A, Holman R, Hayes RJ, Serjeant GR. Priapism and impotence in homozygous sickle cell disease. Arch Intern Med 1980;140:1434-7.

    99 Serjeant GR, Mason KP, Serjeant BE. Negro a-thalassaemia: genetic studies in homozygous sickle cell disease. J Med Genet 1980;17:281-4.

    100 Gibbs WN, Wardle J, Serjeant GR. Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Jamaica. Br J Haematol 1980; 45:73-80.

    101 Wood WG, Pembrey ME, Serjeant GR, Perrine RP, Weatherall DJ. HbF synthesis in sickle cell anaemia: a comparison of Saudi Arabian cases with those of African origin. Br J Haematol 1980;45:431-45.

    102 Higgs DR, Pressley L, Clegg JB, Weatherall DJ, Higgs S, Carey P, Serjeant GR. Detection of alpha thalassaemia in Negro infants. Br J Haematol 1980;46:39-46.

    103 Serjeant GR, Grandison Y, Mason K, Serjeant B, Sewell A, Vaidya S. Haematological indices in normal Negro children: a Jamaican cohort from birth to five years. J Clin Lab Haematol 1980;2:169-78.

    104 Condon PI, Serjeant GR. Photocoagulation in proliferative sickle retinopathy: results of a 5-year study. Br J Ophthalmol 1980;54:832-40.

    105 Higgs DR, Pressley L, Clegg JB, Weatherall DJ, Serjeant GR. a-thalassemia in Black populations. Johns Hopk Hosp Med J 1980;146:300-10.

    106 Condon PI, Hayes RJ, Serjeant GR. Retinal and choroidal neovascularization in sickle cell disease. Trans Ophthalmol Soc UK 1980;100:434-9.

    107 Homi J, Serjeant GR. General anesthesia in sickle cell disease. Pediatrics 1980; 65:861 (letter).

    108 Serjeant BE. Sickle cell research in Jamaica. Gazette Inst Med Lab Sci 1980;24: 309-11.

    108a Little PFR, Whitelaw E, Annison G, Williamson R, Kooter JM, Flavell RA, Goossens M, Serjeant GR, Montgomery D. The detection and use of hemoglobin mutants in the direct analysis of globin genes. Blood 1980;55:1060-2.

    109 Serjeant GR, Higgs DR, Aldridge B, Hayes RJ, Weatherall DJ. Alpha Thalassemia and Homozygous Sickle Cell Disease. In: The Red Cell, Fifth Ann Arbor Conference, Alan R Liss, New York 1981, pp 781-6.

    110 Hayes RJ, Condon PI, Serjeant GR. Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease. Br J Ophthalmol 1981; 65:29-35.

    111 Stevens MCG, Hayes RJ, Vaidya S, Serjeant GR. Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. J Pediatr 1981;98:37-41.

    112 Foster K, Forbes M, Hayes R, Serjeant GR. Cord blood screening for sickle hemoglobin: Evidence against a female preponderance of hemoglobin S. J Pediatr 1981;98:79-81.

    113 Higgs DR, Pressley L, Serjeant GR, Clegg JB, Weatherall DJ. The genetics and molecular basis of alpha thalassaemia in association with HbS in Jamaican Negroes. Br J Haematol 1981;47:43-56.

    114 Lee REJ, Golding JSR, Serjeant GR. The radiological features of avascular necrosis of the femoral head in homozygous sickle cell disease. Clin Radiol 1981;32:205-14.

    115 Serjeant GR. Observations on the epidemiology of sickle cell disease. Trans Roy Soc Trop Med Hyg 1981;75:228-33.

    116 Jampol LM, Condon P, Dizon-Moore R, Serjeant GR, Schulman JA. Salmon-patch hemorrhages after central retinal artery occlusion in sickle cell disease. Arch Ophthalmol 1981;99:237-40.

    117 De Ceulaer K, Wilson WA, Morgan AG, Serjeant GR. Plasma haemoglobin and complement activation in sickle cell disease. J Clin Lab Immunol 1981;6:57-60.

    118 Condon PI, Jampol LM, Ford S, Serjeant GR. Choroidal neovascularisation induced by photocoagulation in sickle cell disease. Br J Ophthalmol 1981;65:192-7.

    119 Stevens MCG, Padwick M, Serjeant GR. Observations on the natural history of dactylitis in homozygous sickle cell disease. Clin Pediatr 1981;20:311-7.

    120 Hamilton AM, Pope FM, Condon PI, Slavin G, Sowter C, Ford S, Hayes RJ, Serjeant GR. Angioid streaks in Jamaican patients with homozygous sickle cell disease. Br J Ophthalmol 1981;65:341-7.

    121 De Ceulaer K, Morgan AG, Choo-Kang E, Wilson WA, Serjeant GR. Serum urate concentrations in homozygous sickle cell disease. J Clin Pathol 1981;34:965-9.

    122 Serjeant GR, Foster K, Serjeant BE. Red cell size and the clinical and haematological features of homozygous sickle cell disease. Br J Haematol 1981;48:445-9.

    123 Alleyne SI, D'Hereux Rauseo R, Serjeant GR. Sexual development and fertility of Jamaican female patients with homozygous sickle cell disease. Arch Intern Med 1981;141:1295-7.

    124 Topley JM, Rogers DW, Stevens MCG, Serjeant GR. Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. Arch Dis Child 1981;56:765-9.

    125 Morgan AG, Serjeant GR. Renal function in patients over 40 with homozygous sickle cell disease. Br Med J 1981;282:1181-3.

    126 Serjeant GR, Grandison Y, Lowrie Y, Mason K, Phillips J, Serjeant BE, Vaidya S. The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to six years. Br J Haematol 1981;48:533-43.

    127 Serjeant GR, Topley JM, Mason K, Serjeant BE, Pattison JR, Jones SE, Mohamed R. Outbreak of aplastic crises in sickle cell anaemia associated with parvovirus-like agent. Lancet 1981;2:595-7.

    128 Stamatoyannopoulos G, Farquhar M, Lindsley D, Brice M, Papayannopoulou Th, Nute PE, Serjeant GR, Lehmann H. Mapping of antigenic sites on human haemoglobin by means of monoclonal antibodies and haemoglobin variants. Lancet 1981;2:952-4.

    129 Grell GAC, Alleyne GAO, Serjeant GR. Blood pressure in adults with homozygous sickle cell disease. Lancet 1981;2:1166 (letter).

    130 Hayes RJ, CondonPI, Serjeant GR. Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease. Br J Ophthalmol 1981;65:712-7.

    131 McCall IW, Vaidya S, Serjeant GR. Splenic opacification in homozygous sickle cell disease. Clin Radiol 1981;32:611-5.

    132 Ashcroft MT, Serjeant GR. Growth, morbidity and mortality in a cohort of Jamaican adolescents with homozygous sickle cell disease. West Indian Med J 1981;30:197-201.

    133 Grell GAC, Desai P, Watty E, Muller R, Serjeant GR. A survey of parasites in primary school children in Dominica, West Indies. Ann Trop Pediatr 1981;1:155-60.

    134 Grell GAC, Desai P, Serjeant GR, Muller R. Anthropometric measurements of school children in Dominica, West Indies. Ann Trop Paediatr 1981;1:241-3.

    135 Stevens MCG, Lehmann H, Mason KP, Serjeant BE, Serjeant GR. Sickle cell-hemoglobin Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease. Am J Dis Child 1982;136:19-22.

    136 Hawker H, Neilson H, Hayes RJ, Serjeant GR. Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease. Br J Haematol 1982;50:29-34.

    137 Talbot JF, Bird AC, Serjeant GR, Hayes RJ. Sickle cell retinopathy in young children in Jamaica. Br J Ophthalmol 1982;66:149-54.

    138 Marsh RJ, Ford SM, Rabb MF, Hayes RJ, Serjeant GR. Macular vasculature, visual acuity, and irreversibly sickled cells in homozygous sickle cell disease. Br J Ophthalmol 1982;66:155-60.

    139 Anderson MJ, Davis LR, Jones SE, Pattison JR, Serjeant GR. The development and use of an antibody capture radioimmunoassay for specific IgM to a human parvovirus-like agent. J Hyg (Camb) 1982;88:309-24.

    140 Condon PI, Serjeant GR. The Eye in Sickle Cell Disease: In Ophthalmology. Jonxis Lectures Vol 8. Excerpta Medica, Amsterdam 1982;147-58.

    141 Serjeant BE, Myerscough E, Serjeant GR, Higgs DR, Moo-Penn WF. Sickle cell-hemoglobin D Iran: a benign sickle cell syndrome. Hemoglobin 1982;6:57-9.

    142 Higgs DR, Lamb J, Aldridge BE, Clegg JB, Weatherall DJ, Serjeant BE, Serjeant GR. Inadequacy of Hb Barts as an indicator of a-thalassaemia. Br J Haematol 1982;50:177-8.

    143 Klein ML, Jampol LM, Condon PI, Rice TA, Serjeant GR. Central retinal artery occlusion without retrobulbar hemorrhage after retrobulbar anesthesia. Am J Ophthalmol 1982;93:573-7.

    144 Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR. The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med 1982;306:1441-6.

    145 Rogers DW, Serjeant BE, Serjeant GR. Early rise in 'pitted' red cell counts as a guide to susceptibility to infection in childhood sickle cell anaemia. Arch Dis Child 1982;57:338-42.

    146 Topley JM, Cupidore L, Vaidya S, Hayes RJ, Serjeant GR. Pneumococcal and other infections in children with sickle cell-hemoglobin C (SC) disease. J Pediatr 1982; 101: 176-9.

    147 Rabb L, Serjeant GR. Sickle cell-hemoglobin Caribbean - a benign syndrome. Hemoglobin 1982;6:403-5.

    148 Serjeant GR, Serjeant BE. The natural history of sickle cell disease. Medicine Digest 1982;8:5-15.

    149 Mason KP, Grandison Y, Hayes RJ, Serjeant BE, Serjeant GR, Vaidya S, Wood WG. Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parental HbF levels. Br J Haematol 1982;52:455-63.

    150 De Ceulaer K, Gruber C, Hayes RJ, Serjeant GR. Medroxyprogesterone acetate and homozygous sickle-cell disease. Lancet 1982;2:299-31.

    151 Millard D, De Ceulaer K, Vaidya S, Serjeant GR. Serum immunoglobulin levels in children with homozygous sickle cell disease. Clin Chim Acta 1982;125:81-7.

    152 Thomas AN, Pattison C, Serjeant GR. Causes of death in sickle-cell disease in Jamaica. Br Med J 1982;285:633-5.

    153 Morgan AG, Gruber CA, Serjeant GR. Erythropoietin and renal function in sickle-cell disease. Br Med J 1982;285:1686-8.

    154 Serjeant GR, Serjeant BE, Lehmann H, Dukes M, Rabb L. HbF Kingston (Gg55 (D6) Met gArg). FEBS Letters 1982;150:77-80.

    155 Serjeant GR, Serjeant BE. Comparison of Sickle Cell-bo Thalassemia and Sickle Cell-b+ Thalassemia in Black Populations. In: Birth Defects; Original Article Series, vol 18 1982, Alan R Liss Inc., New York. pp 223-229.

    156 Serjeant GR. Interaction of alpha-thalassemia and homozygous sickle cell disease. N Engl J Med 1982;307:1349-50 (letter).

    157 Stevens MCG, Hayes RJ, Serjeant GR. Body shape in young children with homozygous sickle cell disease. Pediatrics 1983;71:610-4.

    158 Jampol LM, Condon P, Farber M, Rabb M, Ford S, Serjeant GR. A randomised clinical trial of feeder vessel photocoagulation of proliferative sickle cell retinopathy. I. Preliminary results. Ophthalmology 1983;90:540-5.

    159 Klein ML, Jampol LM, Condon PI, Serjeant GR, Rice TA. Complications of retrobulbar photocoagulation. In: Management of Retinal Vascular and Macular Disorders, Chapter 33. Eds. Fine SL, Owens SL. Williams and Wilkins, Baltimore 1983; pp 208-212.

    160 De Ceulaer K, Higgs DR, Weatherall DJ, Hayes RJ, Serjeant BE, Serjeant GR. a-thalassemia reduces the hemolytic rate in homozygous sickle cell disease. N Engl Med J 1983;309:189-90. (letter)

    161 Rabb LM, Grandison Y, Mason K, Hayes RJ, Serjeant BE, Serjeant GR. A trial of folate supplementation in children with homozygous sickle cell disease. Br J Haematol 1983;54:589-94.

    162 Morais PV, Clarke WF, Hayes RJ, Serjeant GR. Heart size and chest shape in homozygous sickle cell disease. West Indian Med J 1983;32:157-60.

    163 Stevens MCG, Landman J, Hayes RJ, Serjeant GR. Skin fold thickness and nutritional status in young Jamaican children. West Indian Med J 1983;32:161-7.

    164 Serjeant GR. Sickle haemoglobin and pregnancy. Br Med J 1983;187:628-30.

    165 Serjeant BE, Mason KP, Kenny MW, Stuart J, Higgs D, Weatherall DJ, Hayes RJ, Serjeant GR. Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease. Br J Haematol 1983;55:479-86.

    166 Talbot JF, Bird AC, Serjeant GR. Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome. Br J Ophthalmol 1983;67:777-8.

    167 Condon PI, Marsh RJ, Maude GH, Higgs DR, Weatherall DJ, Serjeant GR. Alpha thalassaemia and the macular vasculature in homozygous sickle cell disease. Br J Ophthalmol 1983;67:779-81.

    168 Talbot JF, Bird AC, Rabb LM, Maude GH, Serjeant GR. Sickle cell retinopathy in Jamaican children - a search for prognostic factors. Br J Ophthalmol 1983;67:782-5.

    169 Wainscoat JS, Bell JI, Thein SL, Higgs DR, Serjeant GR, Peto TEA, Weatherall DJ. Multiple origins of the sickle mutation: evidence for bs globin gene cluster polymorphisms. Mol Biol Med 1983;1:191-7.

    170 Emond AM, Morais, Venugopal S, Carpenter R, Serjeant GR. Role of splenectomy in homozygous sickle cell disease in childhood. Lancet 1984;1:88-91.

    171 Hendricks J, De Ceulaer K, Williams E, Serjeant GR. Mononuclear cells in sickle cell disease - subpopulations and in vitro response to mitogens. J Clin Lab Immunol 1984;13:129-32.

    172 John AB, Ramlal A, Jackson H, Maude GH, Waight-Sharma A, Serjeant GR. Prevention of pneumococcal infection in children with homozygous sickle cell disease. Br Med J 1984;288:1567-70.

    173 Antonarakis SE, Boehm CD, Serjeant GR, Theisen CE, Dover GJ, Kazazian HH. Origin of the bs-globin gene in Blacks: the contribution of recurrent mutation or gene conversion or both. Proc Natl Acad Sci USA 1984;81:853-6.

    174 Serjeant BE, Mason KP, Condon PI, Hayes RJ, Kenny MW, Stuart J, Serjeant GR. Blood rheology and proliferative retinopathy in sickle-cell haemoglobin C disease. Br J Ophthalmol 1984;68:325-8.

    175 Higgs DR, Clegg JB, Weatherall DJ, Serjeant BE, Serjeant GR. Interaction of the aaa globin gene haplotype and sickle haemoglobin. Br J Haematol 1984;58:671-8.

    176 De Ceulaer K, Forbes M, Roper D, Serjeant GR. Non-gouty arthritis in sickle cell disease: report of 37 consecutive cases. Ann Rheum Dis 1984;43:599-603.

    177 Collins FS, Stoeckert CJ, Serjeant GR, Forget BG, Weissman SM. Ggb+ Hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the Gg gene. Proc Natl Acad Sci USA 1984; 81: 4894-4898.

    178 Morgan AG, De Ceulaer K, Serjeant GR. Glomerular function and hyperuricaemia in sickle cell disease. J Clin Pathol 1984; 37: 1046-1049.

    179 Boyer SH, Dover GJ, Serjeant GR, Smith KD, Antonarakis SE, Embury SH, Margolet L, Noyes AN, Boyer ML, Bias WB. Production of F cells in sickle cell anemia: regulation by a genetic locus of loci

    180 Serjeant GR, Hutson C. Patterns of attendance at Jamaican sickle cell clinics 1952-1981. Trans Roy Soc Trop Med Hyg 1984;78:648-52.

    181 Al-Awamy BH, Al-Muzan M, Al-Turki M, Serjeant GR. Neonatal screening for sickle cell disease in the Eastern Province of Saudi Arabia. Trans Roy Soc Trop Med Hyg 1984;78:792-4.

    182 Condon P, Jampol LM, Farber MD, Rabb M, Serjeant GR. A randomized clinical trial of feeder vessel photocoagulation of proliferative sickle cell retinopathy. II. Update and analysis of risk factors. Ophthalmology 1984;91:1496-8.

    183 Hayes RJ, Beckford M, Grandison Y, Mason K, Serjeant BE, Serjeant GR. The haematology of steady state homozygous sickle cell disease. Frequency distributions, variation with age and sex, longitudinal observations. Br J Haematol 1985;59:369-82.

    184 Baum KF, MacFarlane DE, Cupidore L, Serjeant GR. Corynebacterium diphtheriae in sickle cell leg ulcers in Jamaica. West Indian Med J 1985;34:24-8.

    185 Serjeant GR. Sickle Cell Disease. In: Current Therapy in Hematology/Oncology. Brain MG, Carbone PP Eds. BC Decker, Inc., 1985, 39-43.

    186 Wainscoat JS, Thein SL, Higgs DR, Bell JI, Weatherall DJ, Al-Awamy BH, Serjeant GR. A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease? Br J Haematol 1985;60:261-8.

    187 Noguchi CT, Dover GJ, Rodgers GP, Serjeant GR, Antonarakis SE, Anagnou NP, Higgs DR, Weatherall DJ, Schechter AN. Alpha-thalassemia changes erythrocyte heterogeneity in sickle cell disease. J Clin Invest 1985;75:1632-7.

    188 Bainbridge R, Higgs DR, Maude GH, Serjeant GR. Clinical presentation of homozygous sickle cell disease. J Pediatr 1985;106:881-5.

    189 Stevens MCG, Beckford M, Grandison Y, Mason K, Taylor B, Maude GH, Serjeant BE, Serjeant GR. Haematological changes in sickle cell-haemoglobin C disease and in sickle cell-b thalassaemia. Br J Haematol 1985;60:279-92.

    190 Acheson RW, Serjeant GR. Painful crises in sickle cell disease after fluorescein angiography. Lancet 1985;1:1222 (letter).

    191 De Ceulaer K. Pagliucca A, Forbes M, Maude GH, Serjeant BE, Serjeant GR. Recurrent infections in sickle cell disease - haematological and immune studies. Clin Chim Acta 1985;148:161-5.

    192 Serjeant GR. The Sickling Haemoglobinopathies. In Epidemiology and Community control of Disease in Warm Climate Countries. Churchill Livingstone - 2nd Edition 1985,644-57.

    193 Emond AM, Collis R, Darvill D, Higgs DR, Maude GH, Serjeant GR. Acute splenic sequestration in homozygous sickle cell disease: natural history and management. J Pediatr 1985;107:201-6.

    194 Serjeant GR. Sickle Cell Disease. In: Recent Advances in Haematology 4. Ed. Hoffbrand AV. Churchill Livingstone 1985;88-108.

    195 Serjeant GR. Blood transfusion in sickle cell disease. In: Supportive Therapy in Haematology. Eds. Das PC, Smit Sibinga C Th, Halie MR, Martinus Nijhoff Publishing Co., Boston. 1985;199-208.

    196 Condon PI, Whitelocke RAF, Bird AC, Talbot JF, Serjeant GR. Recurrent visual loss in homozygous sickle cell disease. Br J Ophthalmol 1985;69:700-6.

    197 De Ceulaer K, McMullen KW, Maude GH, Keatinge R, Serjeant GR. Pneumonia in young children with homozygous sickle cell disease: risk and clinical features. Europ J Pediatr 1985;144:255-8.

    198 Stevens MCG, Crooks GW, Serjeant GR. The development of cardiomegaly in homozygous sickle cell disease. West Indian Med J 1985;34:253-6.

    199 Serjeant GR, De Ceulaer K, Maude GH. Stilboestrol and stuttering priapism in homozygous sickle cell disease. Lancet 1985;11:1274-6.

    200 Serjeant GR. Treatment of sickle cell disease in early childhood in Jamaica. Am J Pediatr Hematol/Oncol 1985;7:235-9.

    201 Serjeant GR. Sickle Cell Disease. Oxford University Press, Oxford 1985.

    202 Maude GH, Higgs DR, Beckford M, Grandison Y, Mason K, Taylor B, Serjeant BE, Serjeant GR. Alpha thalassaemia and the haematology of normal Jamaican children. Clin Lab Haematol 1985;7:289-95.

    203 Graham C, Maude GH, Serjeant GR. Delayed menarche in homozygous sickle cell disease - a search for prognostic factors. West Indian Med J 1986;35:18-22.

    204 Stevens MCG, Maude GH, Beckford M, Grandison Y, Mason K, Taylor B, Serjeant BE, Higgs DR, Teal H, Weatherall DJ, Serjeant GR. Alpha thalassemia and the hematology of homozygous sickle cell disease in childhood. Blood 1986;67:411-4.

    205 Emond AM, Walters JP, Serjeant GR. Megaloblastic change in sickle cell disease obscured by genetically determined microcytosis. West Indian Med J 1986;35:63-5.

    206 Serjeant GR, Serjeant BE. Progress in care of sickle cell anaemia in Jamaica - present and future. In: Beuzard Y, Charache S, Galacteros F, Eds. Approaches to the Therapy of Sickle Cell Anaemia. Inserm, Paris 1986;499-507.

    207 Poddar D, Maude GH, Plant MJ, Scorer H, Serjeant GR. Pregnancy in Jamaican women with homozygous sickle cell disease. Fetal and maternal outcome. Br J Obstet Gynaecol 1986;93:727-32.

    208 Acheson RW, Ford SM, Maude GH, Lyness RW, Serjeant GR. Iris atrophy in sickle cell disease. Br J Ophthalmol 1986;70:516-21.

    209 Serjeant BE, Mason KP, Acheson RW, Maude GH, Stuart J, Serjeant GR. Blood rheology and proliferative retinopathy in homozygous sickle cell disease. Br J Ophthalmol 1986;70:522-5.

    210 Stevens MCG, Maude GH, Cupidore L, Jackson H, Hayes RJ, Serjeant GR. Prepubertal growth and skeletal maturation in sickle cell disease. Pediatrics 1986; 78:124-32.

    211 MacFarlane DE, Baum KF, Serjeant GR. Bacteriology of sickle cell leg ulcers. Trans Roy Soc Trop Med Hyg 1986;80:553-6.

    212 Serjeant GR. Pain-relief in sickle cell. (Editorial). Lancet 1986;ii:320-2.

    213 Kulozik AE, Wainscoat JS, Serjeant GR, Kar BC, Al-Awamy B, Esan F, Falusi Y, Haque SK, Hilali AM, Kate S, Ranasinghe WAEP, Weatherall DJ. Geographical survey of bs-globin gene haplotypes: Evidence for an independent Asian origin of the sickle-cell mutation. Am J Hum Genet 1986;39:239-44.

    214 Serjeant GR, Serjeant BE, Forbes M, Hayes RJ, Higgs DR, Lehmann H. Haemoglobin gene frequencies in the Jamaican population: a study of 100,000 newborns. Br J Haematol 1986;64:253-62.

    215 Williams S, Maude GH, Serjeant GR. Clinical presentation of sickle cell-hemoglobin C disease. J Pediatr 1986;109:586-9.

    216 Kar BC, Satapathy RK, Kulozik AE, Kulozik M, Sirr S, Serjeant BE, Serjeant GR. Sickle cell disease in Orissa State, India. Lancet 1986;ii:1198-201.

    217 Serjeant GR. Hemoglobinopathies in the Caribbean. Hemoglobin Variants in Human Populations. 1986. Vol 1, CRC PRESS, 91-9.

    218 De Ceulaer K, Forbes M, Maude GH, Pagliucca A, Serjeant GR. Complement and immunoglobulin levels in early childhood in homozygous sickle cell disease. J Clin Lab Immunol 1986;21:37-41.

    219 Dover GJ, Chang VT, Boyer SH, Serjeant GR, Antonarakis S, Higgs DR. The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three and four alpha globin genes. Blood 1987;69:341-4.

    220 Jampol LM, Acheson RW, Eagle RC, Serjeant GR, O'Grady RB. Calcification of Bruch's membrane in angioid streaks with homozygous sickle cell disease. Arch Ophthalmol 1987;105:93-8.

    221 Serjeant GR. Sickle Cell Disease. In: Current Therapy in Internal Medicine - 2. Eds. Bayliss TM, Brain MC, Cherniak RM. BC Decker, Inc., Toronto 1987, pp 316-319.

    222 Terry SI, Rajendran A, Hanchard B, Serjeant GR. Ulcerative colitis in sickle cell disease. J Clin Gastroenterol 1987;9:55-7.

    223 Chung EE, Dianzumba SB, Morais P, Serjeant GR. Cardiac performance in children with homozygous sickle cell disease. J Am Coll Cardiol 1987;9:1038-42.

    224 Kulozik AE, Kar BC, Satapathy RK, Serjeant BE, Serjeant GR, Weatherall DJ. Fetal hemoglobin levels and bs globin haplotypes in an Indian population with sickle cell disease. Blood 1987;69:1742-6.

    225 Moriarty BJ, Acheson RW, Serjeant GR. Epiretinal membranes in sickle cell disease. Br J Ophthalmol 1987;71:466-9.

    226 Goldstein AR, Anderson MJ, Serjeant GR. Parvovirus associated aplastic crisis in homozygous sickle cell disease. Arch Dis Child 1987;62:585-8.

    227 Baum KF, Dunn DT, Maude GH, Serjeant GR. The painful crisis of homozygous sickle cell disease: a study of risk factors. Arch Int Med 1987;147:1231-4.

    228 Moriarty BJ, Acheson RW, Char JN, Serjeant GR. Diabetic retinopathy and visual loss in a Jamaican population. West Indian Med J 1987;36:14-6.

    229 Condon PI, Serjeant GR. Haematological Disorders. Chapter 21 - Systemic Diseases of the Eye (Ed. Sir Stephen Miller), John Wright, London 1987; 552-561.

    230 Maude GH, Hayes RJ, Serjeant GR. The haematology of steady state homozygous sickle cell disease: interrelationships between haematological indices. Br J Haematol 1987;66:549-58.

    231 Hrisomalos NF, Jampol LM, Moriarty BJ, Serjeant GR, Acheson R, Goldberg MF. Neodymium-YAG laser vitreolysis in sickle cell retinopathy. Arch Ophthalmol 1987; 105:1087-91.

    232 Moriarty BJ, Webb DK, Serjeant GR. Treatment of subretinal neovascularization associated with angioid streaks in sickle cell retinopathy. Arch Ophthalmol 1987; 105:1327-8.

    233 Baum KF, MacFarlane DE, Maude GH, Serjeant GR. Topical antibiotics in chronic sickle leg ulcers. Trans Roy Soc Trop Med Hyg 1987;81:847-9.

    234 Serjeant GR. Lessons from Hemoglobinopathy Screening in Jamaica. In: Advances on Neonatal Screening. Excerpta Medica, International Congress Series, 741 Elsevier 1987;401-5.

    235 Kulozik AE, Thein SL, Kar BC, Wainscoat JS, Serjeant GR, Weatherall DJ. Raised HbF levels in sickle cell disease are caused by a determinant linked to the b globin gene cluster. In: Hemoglobin Switching V, ed. Stamatoyannopoulos G, Alan R Liss, New York 1987, pp 427-39.

    236 Noguchi CT, Rodgers GP, Serjeant GR, Schechter AN. Levels of fetal hemoglobin necessary for treatment of sickle cell disease. N Engl J Med 1988;318:96-9.

    237 Kulozik AE, Kar BC, Serjeant GR, Serjeant BE, Weatherall DJ. The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. Blood 1988;71:467-72.

    238 Jones S, Shickle DA, Goldstein AR, Serjeant GR. Acceptability of antenatal diagnosis for sickle cell disease among Jamaican mothers and female patients. West Indian Med J 1988;37:12-15.

    239 Serjeant GR, Goldstein AR. B19 virus infection and the aplastic crisis. In: Human Parvoviruses and Disease, Ed. Pattison JR, CRC PRESS INC. 1988,85-92.

    240 Walker TM, Dunn DT, Serjeant GR. The metacarpal index in homozygous sickle cell disease. Br J Radiol 1988;61:280-1.

    241 Murray N, Serjeant BE, Serjeant GR. Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes. Br J Haematol 1988;69:89-92.

    242 Serjeant GR. What's new in sickle cell disease? Trans Roy Soc Trop Med Hyg 1988;82:177-8.

    243 Jackson AA, Landman JP, Stevens MCG, Serjeant GR. Urea kinetics in adults with homozygous sickle cell disease. Europ J Clin Nutrition 1988;42:491-6.

    244 Moriarty BJ, Acheson RW, Condon PI, Serjeant GR. Patterns of visual loss in untreated sickle cell retinopathy. Eye 1988;2:330-5.

    245 Talbot JF, Bird AC, Maude GH, Acheson RW, Moriarty BJ, Serjeant GR. Sickle cell retinopathy in Jamaican children: further observations from a cohort study. Br J Ophthalmol 1988;72:727-32.

    246 Marti H, Stephens AD, Baine RM, Rucknagel DL, Schneider RG, Serjeant GR. ICHS Recommendations for neonatal screening for haemoglobinopathies. Clin Lab Haematol 1988;10:335-45.

    247 Vyas P, Higgs DR, Weatherall DJ, Dunn DT, Serjeant BE, Serjeant GR. The interaction of alpha thalassaemia and sickle cell-betao thalassaemia. Br J Haematol 1988;70:449-54.

    248 Webb DKH, Darby JS, Dunn DT, Terry SI, Serjeant GR. Gallstones in Jamaican children with homozygous sickle cell disease. Arch Dis Child 1989;64:693-6.

    249 Serjeant GR. Geography and the clinical picture of sickle cell disease. Ann NY Acad Sci 1989;565:109-19.

    250 Readett DRJ, Serjeant BE, Serjeant GR. Hurricane Gilbert anaemia. Lancet 1989; 2:101-2.

    251 Lee MG, Thirumalai CHR, Terry SI, Serjeant GR. Endoscopic and gastric acid studies in homozygous sickle cell disease and upper abdominal pain. Gut 1989;30:569-72.

    252. Dunn DT, Poddar D, Serjeant BE, Serjeant GR. Fetal haemoglobin and pregnancy in homozygous sickle cell disease. Br J Haematol 1989;72: 434-8.

    253 Webb DKH, Serjeant GR. Systemic salmonella infections in homozygous sickle cell disease in Jamaica. Ann Trop Paediatr 1989;9:169-72.

    254 Webb DKH, Dunn DT, Serjeant GR. Gallstones in homozygous sickle cell disease. Arch Dis Child 1989;64:1342 (letter).

    255 Serjeant GR. Sickle Cell Screening and its Value in Jamaica. Chapter 15 in: Ethnic Factors in Health and Disease, Eds Cruickshank JK, Beavers DG. Butterworths, London 1989, pp 131-5.

    256 Parshad O, Stevens MCG, Hudson C, Rosenthal J, Melville GN, Dunn DT, Serjeant GR. Abnormal thyroid hormone and thryotropin levels in homozygous sickle cell disease. Clin Lab Haematol 1989;11:309-16.

    257 De Ceulaer K, Serjeant GR, Nagel RL, Billett HH, Christakis J, Loukopoulos D, Bellingham AJ, Lucas GS, Stuart J. Intravenous oxpentifylline and the painful crisis of sickle cell disease. Clin Hemorrheol 1990;10:35-42.

    258 Readett DRJ, Morris JS, Serjeant GR. Nocturnal enuresis in sickle haemoglobinopathies. Arch Dis Child 1990;65:290-3.

    259 Serjeant GR. The spleen in sickle cell disease. Chapter 16 in: The Spleen. Structure, Function, and Clinical Significance. Ed. Bowdler AJ. Chapman and Hall Medical, London 1990, pp 387-397.

    260 Christakis J, Vavatsi N, Hassapopoulou H, Papadopoulou M, Mandraveli K, Loukopoulos D, Morris J, Serjeant BE, Serjeant GR. Comparison of homozygous sickle cell disease in Northern Greece and Jamaica. Lancet 1990;335:637-40.

    261 Fox PD, Dunn DS, Morris JS, Serjeant GR. Risk factors for proliferative sickle retinopathy. Br J Ophthalmol 1990;74:172-6.

    262 Hayes RJ, Serjeant GR. Testing for the random occurrence of sickle cell disease in a study of 100,000 Jamaican newborns. J Trop Med Hyg 1990;93:127-32.

    263 Aparicio SAJR, Mojimimiyi S, Kay JDS, Shepstone BJ, De Ceulaer K, Serjeant GR. Measurement of glomerular filtration rate in homozygous sickle cell disease: a comparison of 51Cr EDTA clearance, creatinine clearance, serum creatinine and b2 microglobulin. J Clin Pathol 1990;43:370-1.

    264 Douglas L, Fletcher H, Serjeant GR. Penile prostheses in the management of impotence in sickle cell disease. Br J Urol 1990;65:533-5.

    265 Readett DRJ, Morris J, Serjeant GR. Determinants of nocturnal enuresis in homozygous sickle cell disease. Arch Dis Child 1990;65:615-8.

    266 Serjeant GR. The challenge of sickle cell disease in Saudi Arabia. Ann Saudi Med 1990;10:443-8.

    267 Webb DKW, Serjeant GR. Haemophilus influenzae osteomyelitis complicating dactylitis in homozygous sickle cell disease. Eur J Paediatr 1990;149:613-4.

    268 Fox PD, Acheson RW, Serjeant GR. The outcome of iatrogenic choroidal neovascularisation in sickle cell disease. Br J Ophthalmol 1990;74:417-20.

    269 Serjeant GR, Chalmers RM. Is the painful crisis of sickle cell disease a "steal" syndrome? J Clin Pathol 1990;43:789-91.

    270 Singhal A, Raju N, Serjeant GR. Empyema of gall bladder in a child with homozygous sickle cell disease. West Indian Med J 1990;39:243-4.

    271 Schiliro G, Russo MG, Kulozik AE, Serjeant BE, Serjeant GR. Comparison of clinical, haematological, and molecular findings in Jamaican and Sicilian patients with sickle cell disease in Sicily. Haematologica 1990;75 (suppl. 5),42-56.

    272 Economou EP, Antonorakis SE, Kazazian HH, Serjeant GR, Dover GJ. Variation in hemoglobin-F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma-promoter regions. Blood 1991;77:174-7.

    273 Kulozik AE, Bail S, Kar BC, Serjeant BE, Serjeant GR. Sickle cell-beta+ thalassaemia in Orissa State, India. Br J Haematol 1991;77:215-20.

    274 Duff EMW, Cooper ES, Danbury CM, Johnson BE, Serjeant GR. Neural tube defects in hurricane aftermath. Lancet 1991;337:120-1 (letter)

    275 Badaloo A, Emond A, Venugopal S, Serjeant GR, Jackson AA. The effect of splenectomy on whole body protein turnover in homozygous sickle cell disease. Acta Paediatr Scand 1991;80:103-5.

    276 Morris J, Dunn D, Beckford M, Grandison Y, Mason K, Higgs DR, De Ceulaer K, Serjeant BE, Serjeant GR. The haematology of homozygous sickle cell disease after the age of forty years. Br J Haematol 1991;77:382-5.

    277 Christakis J, Vavatsi N, Hassapopoulou H, Papadopoulou M, Loukopoulos D, Morris J, Serjeant BE, Serjeant GR. A comparison of sickle cell syndromes in Northern Greece. Br J Haematol 1991;77:386-91.

    278 Bailey S, Higgs DR. Morris J, Serjeant GR. Is the painful crisis of sickle cell disease due to sickling? Lancet 1991;337:735 (letter).

    279 Farber MD, Jampol LM, Fox PD, Moriarty BJ, Acheson RW, Rabb MF, Serjeant GR. A randomized clinical trial of scatter photocoagulation of proliferative sickle cell retinopathy. Arch Ophthalmol 1991;109:363-7.

    280 De Ceulaer K, Serjeant GR. Acute splenic sequestration in Jamaican adults with homozygous sickle cell disease: a role of alpha thalassaemia. Br J Haematol 1991; 77:563-4.

    281 Bowen FE, Crowston JG, De Ceulaer K, Serjeant GR. Peak expiratory flow rate and the acute chest syndrome in homozygous sickle cell disease. Arch Dis Child 1991; 66:330-2.

    282 Fox PD, Vessey SJR, Forshaw ML, Serjeant GR. The influence of genotype on the natural history of untreated proliferative sickle retinopathy - an angiographic study. Br J Ophthalmol 1991;75:229-31.

    283 Serjeant GR. British support for Caribbean research. Lancet 1991;337:1352 (letter)

    284 Jampol LM, Farber M, Rabb MF, Serjeant GR. An update on techniques of photocoagulation treatment of proliferative sickle cell retinopathy. Eye 1991;5:260-3.

    285 Padmos MA, Roberts GT, Sackey K, Kulozik A, Bail S, Morris JS, Serjeant BE, Serjeant GR. Two different forms of homozygous sickle cell disease occur in Saudi Arabia. Br J Haematol 1991;79:93-8.

    286 Thame M, Grandison Y, Mason K, Thompson M, Higgs DR, Morris J, Serjeant BE, Serjeant GR. The red cell distribution width in sickle cell disease - is it of clinical value? Clin Lab Haematol 1991;13:229-37.

    287 Serjeant GR. The geography of sickle cell disease. Gematologija I Transfusiologija 1991;36:27-30.

    288 Acheson RW, Fox PD, Chuang EL, Serjeant GR. Treatment of iatrogenic chorio-vitreal neovascularisation in sickle cell disease. Br J Ophthalmol 1991;75:729-30.

    289 Readett DRJ, Bamigbade T, Serjeant GR. Nocturnal enuresis in normal Jamaican children - implications for therapy. West Indian Med J 1991;40:181-4.

    290 Balkaran B, Char G, Morris JS, Serjeant BE, Serjeant GR. Stroke in a cohort study of patients with homozygous sickle cell disease. J Pediatr 1992;120:360-6.

    291 Bailey K, Morris JS, Serjeant GR. Fetal haemoglobin and early manifestations of homozygous sickle cell disease. Arch Dis Child 1992;67:517-20.

    292 De Ceulaer K, Khamashta MA, Harris EN, Serjeant GR, Hughes GRV. Antiphospholipid antibodies in homozygous sickle cell disease. Ann Rheum Dis 1992;51:671-2.

    293 Singhal A, Jones R, David S, Serjeant GR. Delayed diagnosis in homozygous sickle cell disease in Jamaica. In Perinatal Problems of Islands in Relation to Prevention of Handicaps. Eds. C Bercgel, E Papiernik, F de Caunes 1992, 268-75.

    294 Penman AD, Serjeant GR. Recent advances in the treatment of proliferative sickle cell retinopathy. Current Opinion in Ophthalmology 1992;3:379-88.

    295 Dover GJ, Smith KD, Chang YC, Purvis S, Mays A, Meyers DA, Sheils C, Serjeant GR. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp 22.2. Blood 1992;80:816-24.

    296 Duncan ND, DePaz H, Serjeant GR. Biliary surgery in patients with homozygous sickle cell (SS) disease - experience and recommendations. West Indian Med J 1992; 41:96-8.

    297 Serjeant GR. Sickle Cell Disease, 2nd Edition, Oxford University Press, Oxford 1992.

    298 Singhal A, Davies P, Sahota A, Thomas PW, Serjeant GR. Resting metabolic rate in homozygous sickle cell disease. Am J Clin Nutr. 1993;57:32-4.

    299 Fox PD, Higgs DR, Serjeant GR. The influence of alpha thalassaemia on the retinopathy of homozygous sickle cell disease. Br J Ophthalmol. 1993;77:89-90.

    300 Singhal A, Doherty JF, Raynes JG, McAdam KPWJ, Thomas PW, Serjeant BE, Serjeant GR. Is there an acute phase response in steady state sickle cell disease? Lancet 1993;341:651-3.

    301 Walker TM, Serjeant GR. Focal echogenic lesions in the spleen in sickle cell disease. Clin Radiol 1993;47:114-6.

    302 Serjeant GR. The Clinical Features of Sickle Cell Disease. In The Haemoglobinopathies (Eds DJ Weatherall, DR Higgs), Bailliere's Clinical Haematology, Bailliere Tindall, London 1993,6:93-115.

    303 Arnold KE, Char G, Serjeant GR. Portal vein thrombosis in a child with homozygous sickle cell disease. West Indian Med J. 1993;42:27-8.

    304 Denbow CE, Chung EE, Serjeant GR. Pulmonary artery pressure and the acute chest syndrome in homozygous sickle cell disease. Br Heart J 1993;69:536-8.

    305 Singhal A, Cook JD, Skikne BS, Thomas P, Serjeant B, Serjeant G. The clinical significance of serum transferrin receptor levels in homozygous sickle cell disease. Br J Haematol 1993;84:301-4.

    306 Homi J, Homi-Levee L, Gentles S, Thomas P, Serjeant G. Adolescent blood pressure in a cohort study of sickle cell disease. Arch Intern Med. 1993;153:1233-6.

    307 Serjeant GR, Serjeant BE, Thomas P, Anderson MJ, Patou G, Pattison JR. Human parvovirus infection in homozygous sickle cell disease. Lancet 1993;341:1237-40.

    308 Serjeant GR, Serjeant BE. Management of Sickle Cell Disease: Lessons from the Jamaican Cohort Study. Blood Reviews 1993;7;137-45.

    309 La Grenade L, Thomas PW, Serjeant GR. A randomized controlled trial of Solcoseryl and Duoderm in chronic sickle cell leg ulcers. West Ind Med J 1993;42: 121-3.

    310 Serjeant GR. Recent advances in sickle cell disease. Ch. 10 in Recent Advances in Paediatrics, Churchill-Livingstone 1993;12:141-54.

    311 Serjeant GR. Ulcers in Haematological Disorders. Chapter 12 in; Leg Ulcers - Diagnosis and Treatment. Ed W Westerhof, Elsevier 1993;199-211.

    312 Fox PD, Minninger K, Forshaw ML, Vessey SJR, Morris JS, Serjeant GR. Laser photocoagulation for proliferative retinopathy in sickle haemoglobin C disease. Eye 1993;7:703-6.

    313 Serjeant GR. Clinical judgement and sickle cell disease. N Engl J Med 1993;329: 501-2 (Editorial)

    314 Parshad O, Stevens MCG, Preece MA, Serjeant GR. The mechanism of low testosterone levels in homozygous sickle cell disease. W Ind Med J 1994;43:12-4

    315 Serjeant GR. The geography of sickle cell disease: opportunities for understanding its diversity. Ann Saudi Med 1994;14:237-46

    316 Serjeant GR, De Ceulaer C, Lethbridge R, Morris JS, Singhal A, Thomas PW. The painful crisis of homozygous sickle cell disease - clinical features. Br J Haematol 1994;87:586-91.

    317 Morris JS, Dunn DT, Poddar D, Serjeant GR. Haematological risk factors for pregnancy outcome in Jamaican women with homozygous sickle cell disease. Br J Obstet Gynaecol 1994;101:770-3.

    318 Penman A, Talbot JF, Chuang EL, Bird AC, Serjeant GR. Peripheral retinal vasculature in normal Jamaican children. Br J Ophthalmol 1994;78:615-7.

    319 Penman AD, Talbot JF, Chuang EL, Thomas P, Serjeant GR, Bird AC. A new classification of peripheral retinal vascular changes in sickle cell disease. Br J Ophthalmol 1994;78:681-9.

    320 Seeman P, Ulpian C, Chouinard G, Van Tol HHM, Dwosh H, Lieberman JA, Siminovitch K, Liu ISC, Waye J, Voruganti P, Hudson C, Serjeant GR, Masibay AS, Seeman MV. Dopamine D4 receptor variant, D4glycine 194, in African, but not in Caucasians: no association with schizophrenia. Am J Med Genet 1994;52:1-8.

    321 Singhal A, Thomas P, Cook R, Wierenga K, Serjeant G. Delayed adolescent growth in homozygous sickle cell disease. Arch Dis Child 1994;71:404-8.

    322 Akenzua G, Akinyanju O, Kulozik A, Whitehead S, Morris J, Serjeant BE, Serjeant GR. Homozygous sickle cell disease in Nigeria: a comparison between Benin and Lagos. Afr J Med Sci 1994;23:101-7.

    323 Padmos A, Roberts G, Lindahl S, Kulozik A, Thomas P, Serjeant BE, Serjeant GR. Avascular necrosis of the femoral head in Saudi Arabians with homozygous sickle cell disease - risk factors. Ann Saudi Med 1995;15:21-4.

    324 Singhal A, Thomas P, Kearney T, Venugopal S, Serjeant G. Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease. Arch Dis Child 1995;72:227-9.

    325 Singhal A, Gabay L, Serjeant GR. Testosterone deficiency and extreme retardation of puberty in homozygous sickle cell disease. W Ind Med J 1995;44:20-3.

    326 Serjeant GR. Natural history and determinants of clinical severity of sickle cell disease. Current Science 1995;2:103-8.

    327 Serjeant GR, Serjeant BE, Homi J, Knight S, Mohan J, Singhal AS, Wierenga KJJ. Recent research developments in sickle cell disease in Jamaica. In: Sickle cell disease and thalassaemias: new trends in therapy (Eds. Y Beuzard, B Lubin, J Rosa), Colloque INSERM/John Libbey, 1995;234:427-30.

    328 Chang YC, Smith KD, Moore RD, Serjeant GR, Dover GJ. An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, b-globin haplotypes, a-globin gene number, gender and age. Blood 1995;85: 1111-7.

    329 King SD, Dodd RY, Haynes G, Wynter HH, Sullivan MT, Serjeant GR, Choo-Kang E, Michael E. Prevalence of antibodies to hepatitis C virus and other markers in Jamaica. West Ind Med J 1995;44:55-7.

    330 Al-Hazzaa S, Bird AC, Kulozik A, Serjeant BE, Serjeant GR, Thomas P, Padmos A. Ocular findings in Saudi Arabian patients with sickle cell disease. Br J Ophthalmol 1995;79:457-61.

    331 Mohan JS, Marshall JMM, Reid HL, Serjeant GR. Daily variability in resting levels of cardiovascular variables in normal subjects and those with homozygous sickle cell disease. Clin Autonomic Research 1995;5:1-6.

    332 Walker TM, Serjeant GR. Increased renal reflectivity in sickle cell disease: Prevalence and characteristics. Clin Radiol 1995;50:566-9.

    333 Wierenga KJJ, Pattison JR, Brink N, Griffiths M, Miller M, Shah DJ, Williams W, Serjeant BE, Serjeant GR. Glomerulonephritis after human parvovirus infection in homozygous sickle cell disease. Lancet 1995;346:475-6.

    334 Knight S, Singhal A, Thomas P, Serjeant G. Factors associated with lowered intelligence in homozygous sickle cell disease. Arch Dis Child 1995;73:316-20.

    335 Lee A, Thomas P, Cupidore L, Serjeant B, Serjeant G. Improved survival in homozygous sickle cell disease: lessons from a cohort study. Br Med J 1995; 311:160-2.

    336 Serjeant G, Serjeant B, Stephens A, Roper D, Higgs D, Beckford M, Cook J, Thomas P. Determinants of haemoglobin level in steady-state homozygous sickle cell disease. Br J Haematol 1996;92:143-9.

    337 Serjeant GR. The role of preventive medicine in sickle cell disease. J Roy Coll Physicians London 1996;30:37-41.

    338 Mohan JS, Reid HL, Serjeant GR. Effect of thermal stimuli on peripheral blood flow in homozygous sickle cell disease: a preliminary study. Int J Angiology 1996;5:19-23.

    339 Liu ISC, Seeman P, Sanyal S, Ulpian C, Rodgers-Johnson PEB, Serjeant GR, Van Tool HHM. Dopamine D4 receptor variant in Africans, D4 valine 194gglutamine, is insensitive to dopamine and clozapine: report of a homozygous individual. Am J Med Genet 1996;61:277-82.

    340 Serjeant GR, Serjeant BE. Painful crises in sickle-cell disease. Lancet 1996;347: 1190-1 (letter)

    341 Singhal A, Morris J, Thomas P, Dover G, Higgs D, Serjeant G. Factors affecting prepubertal growth in homozygous sickle cell disease. Arch Dis Child 1996;74:502-6

    342 Serjeant GR. Sickle Cell Disease in: Illustrated History of Tropical Diseases (Ed Prof FEG Cox), The Wellcome Trust, London 1996, pp 340-7

    343 Wierenga KJJ, Moosdeen F, Thomas S, Serjeant GR. Penicillin-resistant Streptococcus pneumoniae in a Jamaican patient with homozygous sickle-cell disease. W Ind Med J 1996;45:95-6.

    344 Walker TM, Serjeant GR. Biliary sludge in sickle cell disease. J Pediatr 1996; 129:443-5

    345 Badaloo AV, Singhal A, Forrester TE, Serjeant GR, Jackson AA. The effect of splenectomy for hypersplenism on whole body protein turnover, resting metabolic rate and growth in sickle cell disease. Eur J Clin Nutr 1996;50:672-5

    346 Serjeant GR. Sickle Cell Disease in Renal Manifestations of Systemic Diseases, Oxford Textbook of Medicine, 3rd Edition, Oxford University Press, 1996;3194-5

    347 Walker TM, Beardsall K, Thomas PW, Serjeant GR. Renal length in sickle cell disease: observations from a cohort study. Clin Radiol 1996;46:384-8.

    348 Hilton C, Osborn M, Knight S, Singhal A, Serjeant GR. Psychiatric complications of homozygous sickle cell disease amongst young adults in the Jamaican Cohort Study. Br J Psychiatr 1997;170:69-76

    349 Homi J, Levee L, Higgs D, Thomas P, Serjeant G. Pulse oximetry in a cohort study of sickle cell disease. Clin Lab Haematol 1997;19:17-22.

    350 Wright JG, Cooper P, Malia RG, Kulozik AE, Vetter B, Thomas P, Preston FE, Serjeant GR. Activated protein-C resistance in homozygous sickle cell disease. Br J Haematol 1997;96:854-6.

    351 Mohan JS, Marshall JM, Reid HL, Thomas PW, Serjeant GR. Postural vasoconstriction and leg ulceration in homozygous sickle cell disease. Clin Sci 1997; 92:153-8.

    352 Wright J, Thomas P, Serjeant GR. Septicemia caused by salmonella infection; an overlooked complication of sickle cell disease. J Pediatr 1997;130:394-9.

    353 Thomas PW, Higgs DR, Serjeant GR. Benign clinical course of homozygous sickle cell disease - a search for predictors. J Clin Epidemiol 1997;50:121-6.

    354 Serjeant GR. Chronic transfusion programmes in sickle cell disease: problem or panacea. Br J Haematol 1997;97:253-5 (Annotation)

    355 Serjeant GR. Sickle-Cell Disease. Seminar, Lancet 1997;350:725-30.

    356 Wright JG, Malia R, Cooper P, Thomas P, Preston FE, Serjeant GR. Protein C and protein S in homozygous sickle cell disease: does hepatic dysfunction contribute to low levels? Br J Haematol 1997;98:627-31.

    357 Singhal A, Wierenga KJJ, Byford S, Adab N, Thomas PW, Serjeant GR. Is there an energy deficiency in homozygous sickle cell disease? Am J Clin Nutr 1997;66:386-90.

    358 Serjeant BE, Harris J, Thomas P, Serjeant GR. Propionyl-L-carnitine in chronic leg ulcers of homozygous sickle cell disease; a pilot study. J Am Acad Dermatol 1997; 37:491-3.

    359 Sweeting I, Serjeant BE, Thomas PW, Serjeant GR. Microchromatographic quantitation of HbA levels in phenotypes of sickle cell-b+ thalassemia. J Chromatogr 1997;700:269-74.

    360 Serjeant GR. Understating the morbidity of sickle cell disease. Reply to Dr. Vichinsky. Br J Haematol 1997;99:976-7 (letter)

    361 Hilton C, Osborn M, Serjeant GR. Psychiatric disorder in young adults in Jamaica. Internat J Soc Psychiatr 1997;43:257-68.

    362 Cooper ES, Randath DD, Whyte-Alleng C, Howell S, Serjeant BE. Plasma proteins in children with trichuris dysentery syndrome. J Clin Pathol 1997;50:236-240.

    363 Serjeant GR. Sickle Cell Disease. Chapter for 50th Anniversary Edition of Conn's Current Therapy, WB Saunders Company, Philadelphia, 1998; pp 363-370.

    364 Mohan JS, Marshall JM, Reid HL, Thomas PW, Hambleton I, Serjeant GR. Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell (SS) disease and in normal subjects. Clin Auton Res 1998;8:25-30.

    365 Mohan JS, Marshall JM, Reid HL, Thomas PW, Serjeant GR. Peripheral vascular response to mild indirect cooling in patients with homozygous sickle cell (SS) disease and the frequency of painful crisis. Clin Sci. 1998;94:111-120.

    366 Sweeting I, Serjeant BE, Serjeant GR, Kulozik AE, Vetter B. Sickle cell-Hb Monroe; a sickle cell -b thalassemia syndrome. Hemoglobin 1998;22:153-156.

    367 Serjeant GR. Sickle Cell Disease. Chapter in Haemoglobinopathies, Néstles Nutrition Services, Annales Nestlé 1998;56:53-63.

    368 Ware ME, Tyghter D, Staniforth S, Serjeant GR. Airline travel in sickle cell disease. Lancet 1998;352:652 (letter)

    369 Serjeant GR. Sickle Cell Disease. Chapter in Conn's Current Therapy, Ed Robert E Rakel, WB Saunders, Philadelphia, 1999,375-382.

    370 Ware ME, Hambleton I, Ochaya I, Serjeant GR. Sickle cell painful crises in Jamaica:

    a day care approach to management. Br J Haematol. 1999;104:93-96.

    371 Serjeant GR. Sickle Crisis. Chapter 10.6.1 Pathophysiology. Oxford Textbook of Critical Care, Oxford University Press, Oxford, 1999, pp699-701.

    372 Serjeant GR, Singer M. Sickle Crisis. Chapter 10.6.2 Prevention and Management of Complications. Oxford Textbook of Critical Care, Oxford University Press, Oxford, 1999, pp702-704..

    373 Wright JG, Hambleton IR, Thomas PW, Duncan ND, Venugopal S, Serjeant GR. Postsplenectomy course in homozygous sickle cell disease? J Pediatr 1999;134:304-309.

    374 Magnus SA, Hambleton IR, Moosdeen F, Serjeant GR. Recurrent infections in homozygous sickle cell disease. Arch Dis Child 1999;80:537-541.

    375 Serjeant GR. Infections in Sickle Cell Disease. Chapter 6.31 in Infectious Diseases, textbook edited by D. Armstrong & J. Cohen, Mosby International, 1999,

    376 Serjeant GR. Sickle Cell Disease. Section 2 Red Cell Disorders, Chapter 11 Sickle Cell Disease in Pediatric Hematology, Churchill Livingstone, London 1999;219-30.

    377 Cumming AM, Olujohungbe A, Keeney S, Singh H, Hay CRM, Serjeant GR. The methylenetetrahydro-folate reductase gene C677T polymorphism in patients with homozygous sickle cell disease and stroke. Br J Haematol 1999;107:569-71.

    378 Walker TM, Hambleton IR, Serjeant GR. Gallstones in sickle cell disease: observations from the Jamaican Cohort Study. J Pediatr 2000;136:80-5.

    379 Donaldson A, Old J, Fisher C, Serjeant BE, Serjeant GR. Jamaican Sb+ thalassaemia: mutations and haematology. Br J Haematol 2000;108:290-4.

    380 Foster-Williams K, Hambleton IR, Hilton C, Serjeant GR. Psychiatric distress among younger siblings of patients with homozygous sickle cell disease in the Jamaican cohort study. W Indian Med J 2000;49:52-4.

    381 Thomas PW, Singhal A, Hemmings-Kelly M, Serjeant GR. Height and weight reference curves for homozygous sickle cell disease. Arch Dis Child 2000;82:204-8.

    382 Mohan JS, Vigilance JE, Marshall JM, Hambleton IR, Reid HL, Serjeant GR. Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers. Clin Sci 2000;98:667-72.

    383 Serjeant GR. Screening for sickle-cell disease in Brazil. Lancet 2000;356:168-9 (letter).

    384 Serjeant GR. Sickle-cell disease and the kidney. Chapter 12.16 in the Concise Oxford Textbook of Medicine, 2000, pp 1164-1165.

    385 Serjeant GR. Sickle cell disease in the Caribbean. Caribbean Health, 2000;3:9-13.

    386 Knight-Madden J, Serjeant GR. Invasive pneumococcal disease in homozygous sickle cell disease: Jamaican experience 1973-1997. J Pediatr 2001;138:65-70.

    387 Wierenga KJJ, Hambleton IR, Wilson RM, Alexander H, Serjeant BE, Serjeant GR. Significance of fever in Jamaican children with homozygous sickle cell disease. Arch Dis Child 2001;84:156-9.

    388 Serjeant GR. A Guide to Sickle Cell Disease. Handbook for the Caribbean. 2001

    389 Thame JR, Hambleton IR, Serjeant GR. Red cell transfusion in homozygous sickle cell disease: experience from the Jamaican Cohort Study. Transfusion 2001;41:596-601.

    390 Serjeant GR. The emerging understanding of sickle cell disease. Br J Haematol 2001;112:3-18.

    391 Serjeant GR. Geographic heterogeneity of homozygous sickle cell disease. Chapter 33 in: Disorders of Hemoglobin, Eds Steinberg MH, Forget BG, Higgs DR, Nagel RL, Cambridge University Press, 2001, pp 895-905.

    392 Serjeant GR, Serjeant BE. Sickle Cell Disease. Oxford University Press, 3rd edition, 2001.

    393 Thomas VJ, Hambleton I, Serjeant GR. Psychological distress and coping in sickle cell disease: comparison of British and Jamaican attitudes. Ethn Health 2001;6:129-36.

    394 Olujohungbe A, Hambleton IR, Stephens L, Serjeant BE, Serjeant GR. Red cell antibodies in patients with homozygous sickle cell disease: a comparison of patients in Jamaica and the United Kingdom. Br J Haematol 2001;113:661-5.

    395 Wierenga KJJ, Serjeant BE, Serjeant GR. Cerebrovascular complications and parvovirus infection in homozygous sickle cell disease. J Pediatr 2001;139:438-42.

    396 Serjeant GR, Singhal A, Hambleton IR. Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study. Arch Dis Child 2001;85:375-8.

    397 Ofori-Acquah SF, Green BN, Davies SC, Nicolaides KH, Serjeant GR, Layton DM. Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha (2) gammabeta(S)) in sickle cell disease. Anal Biochem 2001;298:76-82.

    398 Donaldson A, Thomas P, Serjeant BE, Serjeant GR. Fetal haemoglobin in homozygous sickle cell disease: a study of patients with low HbF levels. Clin Lab Haematol 2001;23:285-9.

    399 Serjeant BE, Hambleton IR, Kerr S, Kilty CG, Serjeant GR. Haematological response to parvovirus B19 infection in sickle-cell disease. Lancet 2001;358:1779-80.

    400 Serjeant GR, Serjeant BE. The epidemiology of sickle cell disease: a challenge for Africa. Ibadan Med J 2001;2:46-52.

    401 Serjeant GR. The spleen in sickle cell disease. Ch. 15 in The Complete Spleen: Structure, Function and Clinical Disorders. 2nd edition, Humana Press 2002, pp251-7.

    402 Taylor JG, Tang D, Foster CB, Serjeant GR, Rodgers GP, Chanock SJ. Patterns of low affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease. Am J Hematol 2002;69:109-14.

    403 Singhal A, Parker S, Linsell L, Serjeant GR. Energy intake and resting metabolic rate in pre-school Jamaican children with homozygous sickle cell disease. Am J Clin Nutr. 2002;75:1093-7.

    404 Taylor JG, Tang D, Savage SA, Leitman SF, Heller S, Serjeant GR, Rodgers GP, Chanock SJ. Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease. Blood 2002;100:3403-9.

    405 Clare A, FitzHenley M, Harris J, Hambleton I, Serjeant GR. Chronic leg ulceration in homozygous sickle cell disease: a role of venous incompetence. Br J Haematol 2002;119:567-71.

    406 Jeng MR, Rieman MD, Naidu PE, Kaste SC, Jenkins JJ, Ware M, Serjeant GR, Wang WC. Case Report: Resolution of chronic hepatic sequestration in a patient with homozygous sickle cell disease receiving hydroxyurea. Am J Pediat Hematol/Oncol 2003;25:257-60.

    407 Serjeant GR. Sickle-cell disease and the kidney. Chapter 20.10.7 in the Oxford Textbook of Medicine, 4th edition. 2003, 411-12.

    408 Blann AD, Marwah S, Serjeant G, Bareford D, Wright J. Platelet activation and endothelial cell dysfunction in sickle disease is unrelated to reduced antioxidant capacity. Blood Coagul Fibrinolysis 2003;14:255-9.

    409 Serjeant GR. Blood transfusion in homozygous sickle cell disease – a cautionary tale. Lancet 2003;361:1659-60.

    410 Sanderson PJ, Serjeant GR. Infections in orthopaedic surgery. Ch 16 in Infection in Surgical Practice, Arnold, 2003, 151-162.

    411 Serjeant GR, Ndugwa CM. Sickle cell disease in Uganda: a time for action. E Afr Med J 2003;81:384-7.

    412 Brandelise S, Pinheiro V, Gabetta CS, Hambleton I, Serjeant B, Serjeant G. Newborn screening for sickle cell disease in Brazil: the Campinas experience. Clin Lab Haematol 2004;26:15-19.

    413 Serjeant GR, Serjeant BE. Sickle cell disease in Saudi Arabia: the Asian haplotype. Reflections on a meeting at Hofuf, September 2003. Ann Saudi Med 2004;24;166-8.

    414 Ofori-Acquah SF, Lalloz MR, Serjeant G, Layton DM. Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease. Cell Mol Biol 2004;50:35-42.

    415 Serjeant GR. Infections in Sickle Cell Disease. Chapter 171 in Infectious Disease (eds Cohen J, Powderly I) Elsevier Science, 2nd Edition, 2004, 1615-9.

    416 Serjeant GR, Look Loy L, Crowther M, Hambleton IR, Thame M. The outcome of pregnancy in homozygous sickle cell disease. Obstet Gynecol 2004;103:1278-85.

    417 Alexander N, Higgs D, Dover G, Serjeant GR. Are there clinical phenotypes of homozygous sickle cell disease? Br J Haematol 2004;126:606-11.

    418 Serjeant GR. The dilemma of defining clinical severity in homozygous sickle cell disease. Current Hematology Reports 2004;3:307-9.

    419 Ndugwa C, Kiggundu M, Cohen B, Serjeant GR. Aplastic crises and acute anaemic episodes in homozygous sickle cell disease. E Afr Med J 2004;81:493-4.

    420 Haverfield EV, McKenzie CA, Forrester T, Bouzekri N, Harding R, Serjeant GR, Walker T, Peto TE, Ward R, Weatherall DJ. UGT1A1 variation and gallstone formation in sickle cell disease. Blood 2005;105:968-972.

    421 Serjeant GR. Mortality from sickle cell disease in Africa. Br Med J 2005;330:432-3.

    422 Serjeant GR, Hambleton IR, Thame M. Fecundity and pregnancy outcome in a cohort with sickle cell-haemoglobin C (SC) disease followed from birth. Br J Obstet Gynaecol 2005;112:1308-14.

    423 Serjeant GR, Serjeant BE, Mohan JS, Clare A. Leg ulceration in sickle cell disease: Medieval medicine in a modern world. Hematol Oncol Clinics North Am 2005;19:943-56.

    424 Serjeant GR, Wild B, Tebasulwa S, Mason K, Serjeant BE, Ndugwa CM. Sickle haemoglobin and haemoglobin Stanleyville II: possible confusion with sickle cell-haemoglobin C disease. East Afr Med J 2005;82:367-70.

    425 Downes SM, Hambleton IR Chuang EL, Serjeant GR, Bird AC. Incidence and natural history of proliferative sickle retinopathy: Observations from a cohort study. Ophthalmology 2005;112:1869-75

    426 Weatherall MW, Higgs DR, Weiss H, Weatherall DJ, Serjeant GR. Genotype/phenotype relationships in sickle cell disease: a pilot twin study. Clin Lab Haematol 2005;27:384-90.

    427 Serjeant GR. The case for dedicated Sickle Cell Centres. Ind J Hum Genet 2006;12:148-151.

    428 Samms-Vaughan M, Thame M, Osmond C, Hambleton IR, McCaw-Binns A, Ashley DE, Serjeant GR. Growth curves for normal Jamaican neonates. W Ind Med J. 2006;55:368-74.

    429 Etima-Kizito M, Mworozi E, Ndugwa C, Serjeant GR. Bacteraemia in homozygous sickle cell disease in Africa: Is pneumococcal prophylaxis justified? Arch Dis Child 2007;92:21-3.

    430 Serjeant GR, Higgs DR, Hambleton IR. Elderly survivors with homozygous sickle cell disease. N Engl J Med 2007;356:642-3. (letter)

    431 Serjeant GR. The case for dedicated sickle cell centers. BMJ 2007;334:477 (Personal view).

    432 Thompson J, Hambleton IR, Reid M, Serjeant GR. Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study. Arch Intern Med 2007;167:701-8.

    433 Thame M, Lewis J, Trotman H, Hambleton I, Serjeant G. The mechanisms of low birth weight in infants of mothers with homozygous sickle cell disease. Pediatr. 2007;120: e686-93.

    434 Al Hajeri A, Serjeant GR, Fedorowicz Z. Inhaled nitric oxide for acute chest syndrome in people with sickle cell disease. Cochrane Database Syst Rev. 2008 Jan 23;CD006957.

    435 Cumming V, King L, Fraser R, Serjeant G, Reid M. Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia.

    Br J Haematol. 2008 Jul;142:119-25.

    436 Serjeant GR, Serjeant BE, Mason KP, Hambleton IR, Fisher C, Higgs DR. The changing face of homozygous sickle cell disease: 102 patients over the age of 60 years. Int J Lab Hematol 2008; July 15 epub.

    437 Serjeant GR. Setting up a comprehensive care facility for sickle cell disease. In: Control and Management of Thalassemia and other Hemoglobinopathies in the Indian Subcontinent – Synoptic Views, Eds. Kanjaksha Ghosh, Roshan Colah. National Institute of Immunohaematology, Mumbai 2008, pp 125-130.

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