The increasing complexity of sickle cell anemiaWARTH, J. A; RUCKNAGEL, D. L.Progress in hematology. 1983, Vol 13, pp 25-47, issn 0079-6301Article

IgG2 deficiency in sickle cell anaemiaNATTA, C. L; OUTSCHOORN, I. M.Scandinavian journal of haematology. 1984, Vol 33, Num 2, pp 129-134, issn 0036-553XArticle

Treatment of acute sickle cell crises with a vasopressin analogueCHARACHE, S; MOYER, M. A; WALKER, W. G et al.American journal of hematology. 1983, Vol 15, Num 4, pp 315-319, issn 0361-8609Article

Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the γ-δ-β-globin gene complexCHARACHE, S; DOVER, G; SMITH, K et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1983, Vol 80, Num 15, pp 4842-4846, issn 0273-1134Article

Sickle cell disease: current perspectives, conference, Bethesda MD, 11-13 April, 1988WHITTEN, C. F; BERTLES, J. F.Annals of the New York Academy of Sciences. 1989, Vol 565, pp XIV-477, issn 0077-8923, pConference Proceedings

Le syndrome de Moya-Moya dans la drépanocytose : notre expérience six ans aprèsBUISSON, G.G; VERNANT, J.C; FRANCOIS, M.A et al.XXe congrès international des médecins de langue française de l'hémisphère américain. 1986, pp 244-245Conference Paper

Sickle cell anemiaJOHNSON, C. S.JAMA, the journal of the American Medical Association. 1985, Vol 254, Num 14, pp 1958-1963, issn 0098-7484Article

Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemiaSTEINBERG, M. H; ROSENSTOCK, W; COLEMAN, M. B et al.Blood. 1984, Vol 63, Num 6, pp 1353-1360, issn 0006-4971Article

L'incidence clinique de la drépanocytose dans le milieu urbain de Kinshasa (Zaïre) = Clinical incidence of sicckle cell anemia an urban area of Knishiasa (Zaïre)MBENSA, M; NKUSU, K.Médecine d'Afrique Noire. 1984, Vol 31, Num 8-9, pp 461-462, issn 0465-4668Article

The haemoglobin pattern of sickle cell and haemoglobin Cβ⁺-thalassaemia in LiberiaWILLCOX, M.Journal of medical genetics. 1983, Vol 20, Num 6, pp 430-432, issn 0022-2593Article

Lymphokine and NK cell activity in sickle cell diseaseTAYLOR, S; SHACKS, S. J.Pediatric asthma, allergy & immunology. 1989, Vol 3, Num 4, pp 217-225, issn 0883-1874, 9 p.Article

Use of erythrocytopheresis in the treatment of patients with sickle cell anemiaKLEINMAN, S. H; HURVITZ, C. G; GOLDFINGER, D et al.Journal of clinical apheresis (Print). 1984, Vol 2, Num 2, pp 170-176, issn 0733-2459Article

Increased IgG molecules bound to the surface of red cells of patients with sickle cell anemiaPETZ, L. D; YAM, P; WILKINSON, L et al.Blood. 1984, Vol 64, Num 1, pp 301-304, issn 0006-4971Article

Effects of oxygen inhalation on endogeneous erythropoietin kinetics, erythropoiesis, and properties of blood cells in sickle-cell anemiaEMBURY, S. H; GARCIA, J. F; MOHANDAS, N et al.The New England journal of medicine. 1984, Vol 311, Num 5, pp 291-295, issn 0028-4793Article

Myocardial infarction in sickle cell anemiaBARRETT, ÓN. JR; SAUNDERS, D. E; MCFARLAND, D. E et al.American journal of hematology. 1984, Vol 16, Num 2, pp 139-147, issn 0361-8609Article

Static and dynamic rigidities of normal and sickle erythrocytes: major influence of cell hemoglobin concentrationEVANS, E; MOHANDAS, N; LEUNG, A et al.The Journal of clinical investigation. 1984, Vol 73, Num 2, pp 477-488, issn 0021-9738Article

La maladie drépanocytaireBEGUE, P.1984, 309 p.Book

La drépanocytoseCHETTAB, Laètitia.L'Aide soignante. 2005, Num 71-72, pp 31-32, issn 1166-3413, 2 p.Article

Antisickling effect of tellurite: a potent membrane-acting agent in vitroASAKURA, T; SHIBUTANI, Y; REILLY, M. P et al.Blood. 1984, Vol 64, Num 1, pp 305-307, issn 0006-4971Article

Erythrocyte density distribution in sickle cell anemiaWEEMS, H. B; LESSIN, L. S.Acta haematologica. 1984, Vol 71, Num 6, pp 361-370, issn 0001-5792Article

The relationship between fetal hemoglobin level and glycosylation in sickle cell diseaseELSEWEIDY, M. M; ABRAHAM, E. C.American journal of hematology. 1984, Vol 16, Num 4, pp 375-381, issn 0361-8609Article

Splenic function in Saudi children with sickel cell diseaseAHMAD MALLOUH; BURKE, G. M; SALAMAH, M et al.Annals of tropical paediatrics. 1984, Vol 4, Num 2, pp 87-91, issn 0272-4936Article

The approximate gene frequency of sickle haemoglobin in the Arabian PeninsulaWHITE, J. M.British journal of haematology. 1983, Vol 55, Num 3, pp 563-564, issn 0007-1048Article

EditorialGALACTEROS, F.Bulletin épidémiologique hebdomadaire. 2012, Num 27-28, pp 311-312, issn 0245-7466, 2 p.Article

Characteristics of I and i antigen receptors on the membrane of erythrocytes in sickle cell anemiaBASU, M. K; LEE, M. M; MANIATIS, A et al.The Journal of laboratory and clinical medicine. 1984, Vol 103, Num 5, pp 712-719, issn 0022-2143Article