A WHOLE BLOOD SOLUBILITY AND CENTRIFUGATION TEST FOR SICKLE CELL HEMOGLOBIN: A CLINICAL TRIAL = UNE EPREUVE DE SOLUBILITE ET DE CENTRIFUGATION DU SANG ENTIER POUR L'EMOGLOBINE S. EXPERIMENTATION CLINIQUESERJEANT BE; SERJEANT GR.1972; AMER. J. CLIN. PATHOL.; U.S.A.; DA. 1972; VOL. 58; NO 1; PP. 11-13; BIBL. 2 REF.Serial Issue

NEGRO ALPHA -THALASSAEMIA: GENETIC STUDIES IN HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; MASON KP; SERJEANT BE et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 4; PP. 281-284; BIBL. 4 REF.Article

RED CELL SIZE AND THE CLINICAL AND HAEMATOLOGICAL FEATURES OF HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; FOSTER K; SERJEANT BE et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 48; NO 3; PP. 445-449; BIBL. 7 REF.Article

THE DEVELOPMENT OF HAEMOGLOBIN A₂ IN NORMAL NEGRO INFANTS AND IN SICKLE CELL DISEASESERJEANT BE; MASON KP; SERJEANT GR et al.1978; BRIT. J. HAEMATOL.; GBR; DA. 1978; VOL. 39; NO 2; PP. 259-265; BIBL. 11 REF.Article

A SIMPLE MICROMETHOD FOR THE MEASUREMENT OF FETAL HAEMOGLOBIN = UNE MICROMETHODE SIMPLE POUR LE DOSAGE L'HEMOGLOBINE FOETALESERJEANT BE; CLARKE JM; DESAI P et al.1975; J. CLIN. PATHOL.; G.B.; DA. 1975; VOL. 28; NO 9; PP. 761-764; BIBL. 16 REF.Article

CHOLELITHIASIS IN JAMAICAN PATIENTS WITH HOMOZYGOUS SICKLE CELLE DISEASE.MCCALL IW; DESAI P; SERJEANT BE et al.1977; AMER. J. HEMATOL.; U.S.A.; DA. 1977; VOL. 3; PP. 15-21; BIBL. 14 REF.Article

COMPARISON OF HAEMATOLOGICAL FEATURES OF THE BETA ⁰ AND BETA ⁺ THALASSAEMIA TRAITS IN JAMAICAN NEGROES.MILLARD DP; MASON K; SERJEANT BE et al.1977; BRIT. J. HAEMATOL.; G.B.; DA. 1977; VOL. 36; NO 2; PP. 161-170; BIBL. 1 P. 1/2Article

HEIGHTS AND WEIGHTS OF WEST INDIAN CHILDREN WITH THE SICKLE CELL TRAITASHCROFT MT; DESAI P; GRELL GAC et al.1978; ARCH. DIS. CHILDH.; GBR; DA. 1978; VOL. 53; NO 7; PP. 596-598; BIBL. 4 REF.Article

COMPARISON OF SICKLE CELL-BETA ^O THALASSAEMIA WITH HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; SOMMEREUX AM; STEVENSON M et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 41; NO 1; PP. 83-93; BIBL. 14 REF.Article

HEIGHTS AND WEIGHTS OF JAMAICAN CHILDREN WITH HOMOZYGOUS SICKLE CELL DISEASE.LOWRY MF; DESAI P; ASHCROFT MT et al.1977; HUM. BIOL.; U.S.A.; DA. 1977; VOL. 49; NO 3; PP. 429-436; BIBL. 1 P.Article

HAEMOGLOBIN F VICTORIA JUBILEE (A₂^A GAMMA ₂ 80 ASP -> TYR)AHERN E; HOLDER W; AHERN V et al.1975; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1975; VOL. 393; NO 1; PP. 188-194; BIBL. 17 REF.Article

OUTBREAK OF APLASTIC CRISES IN SICKLE CELL ANAEMIA ASSOCIATED WITH PARVOVIRUS-LIKE AGENTSERJEANT GR; MASON K; TOPLEY JM et al.1981; LANCET (BR. ED.); ISSN 0140-6736; GBR; DA. 1981; NO 8247; PP. 595-597; BIBL. 6 REF.Article

THE DETERMINANTS OF IRREVERSIBLY SICKLED CELLS IN HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; SERJEANT BE; DESAI P et al.1978; BRIT. J. HAEMATOL.; GBR; DA. 1978; VOL. 40; NO 3; PP. 431-438; BIBL. 16 REF.Article

Management of sickle cell disease; Lessons from the Jamaican cohort studySERJEANT, G. R; SERJEANT, B. E.Blood reviews. 1993, Vol 7, Num 3, pp 137-145, issn 0268-960XArticle

Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromesMURRAY, N; SERJEANT, B. E; SERJEANT, G. R et al.British journal of haematology. 1988, Vol 69, Num 1, pp 89-92, issn 0007-1048Article

One hundred years of sickle cell diseaseSERJEANT, Graham R.British journal of haematology. 2010, Vol 151, Num 5, pp 425-429, issn 0007-1048, 5 p.Article

Hadramawt to Zanzibar: The Pilot-Poem of the Nakhudha Said Ba Tayi of al-Hami in From Zinj to Zanzibar: Studies in History, Trade and Society on the Eastern Coast of Africa in honour of James Kirkman on the occasion of his seventy-fifth birthdaySERJEANT, R. B.Paideuma. Mitteilungen zur Kulturkunde Wiesbaden. 1982, Vol 28, pp 109-127Article

Chronic transfusion programmes in sickle cell disease: Problem or panacea?SERJEANT, G. R.British journal of haematology. 1997, Vol 97, Num 2, pp 253-255, issn 0007-1048Article

Sickle-cell diseaseSERJEANT, G. R.Lancet (British edition). 1997, Vol 350, Num 9079, pp 725-730, issn 0140-6736Article

What's new in sickle cell disease?SERJEANT, G. R.Transactions of the Royal Society of Tropical Medicine and Hygiene. 1988, Vol 82, Num 2, pp 177-178, issn 0035-9203Article

Propionyl-L-carnitine in chronic leg ulcers of homozygous sickle cell disease : A pilot studySERJEANT, B. E; HARRIS, J; THOMAS, P et al.Journal of the American Academy of Dermatology. 1997, Vol 37, Num 3, pp 491-493, issn 0190-9622, 1Article

Red cell antibodies in patients with homozygous sickle cell disease : a comparison of patients in Jamaica and the United KingdomOLUJOHUNGBE, Ade; HAMBLETON, Ian; STEPHENS, Lorna et al.British journal of haematology. 2001, Vol 113, Num 3, pp 661-665, issn 0007-1048Article

Improved survival in homozygous sickle cell disease : lessons from a cohort studyLEE, A; THOMAS, P; CUPIDORE, L et al.BMJ. British medical journal (International ed.). 1995, Vol 311, Num 7020, pp 1600-1602, issn 0959-8146Article

FIVE-YEAR FOLLOW-UP OF JAMAICAN ADULTS WITH SICKLE CELL ANAEMIA = ETUDE SUR 5 ANS D'ADULTES ORIGINAIRES DE LA JAMAIQUE, PORTEURS D'ANEMIE FALCIFORMESERJEANT GR.1975; BRIT. MED. J.; G.B.; DA. 1975; NO 5974; PP. 20-21; BIBL. 5REF.Article

Acute splenic sequestration in Jamaican adults with homozygous sickle cell disease : a role of alpha thalassaemiaDE CEULAER, K; SERJEANT, G. R.British journal of haematology. 1991, Vol 77, Num 4, pp 563-564, issn 0007-1048Article