Patients with Sickle Cell Disease have Reduced Blood Antioxidant ProtectionHONGMEI REN; GHEBREMESKEL, Kebreab; OKPALA, Iheanyi et al.International journal for vitamin and nutrition research. 2008, Vol 78, Num 3, pp 139-147, issn 0300-9831, 9 p.Article

Le point sur... La dréponocytose : une maladie génétique fréquente et méconnueBiofutur (Puteaux). 2008, Num 294, pp 58-60, issn 0294-3506, 3 p.Article

Macrocytic anemia in cirrhotic patients : a preliminary clinical reportCOLLE, R; CESCHIA, T.Current therapeutic research. 1992, Vol 52, Num 6, pp 929-934, issn 0011-393XArticle

Lymphome primitif vésical chez le transplanté rénal : à propos d'un cas = Primary lymphoma of the bladder in renal transplant patients based upon one caseBITKER, M.-O; BAGNIS, C; MOUQUET, C et al.Progrès en urologie. 1992, Vol 2, Num 5, pp 908-921Article

Influence of crisis on haemoglobin F level in adult Nigerian sickle cell anaemia patientsOLATUNJI, P. O; FALUSI, A. G; ESIEN, E. M et al.Central african journal of medicine. 1992, Vol 38, Num 6, pp 242-246, issn 0008-9176Article

Translocation (12;17)(p11-12;q11-12) : a recurrent primary rearrangement in acute leukemiaLIU, H. W; WAN, S. K; CHING, L. M et al.Cancer genetics and cytogenetics. 1992, Vol 64, Num 1, pp 27-29, issn 0165-4608Article

Endotoxic shock after transfusion of contaminated red blood cells in a child with sickle cell diseaseFOREMAN, N. K; WANG, W. C; CULLEN, E. J et al.The Pediatric infectious disease journal. 1991, Vol 10, Num 8, pp 624-626, issn 0891-3668Article

Inhibition by 1,25 dihydroxyvitamin D₃ of chemically induced erythroid differentiation of K562 leukemia cellsMOORE, D. C; CARTER, D. L; BHANDAL, A. K et al.Blood. 1991, Vol 77, Num 7, pp 1452-1461, issn 0006-4971Article

Nucleation and growth of fibres and gel formation in sickle cell haemoglobinSAMUEL, R. E; SALMON, E. D; BRIEHL, R. W et al.Nature (London). 1990, Vol 345, Num 6278, pp 833-835, issn 0028-0836Article

A search for anomalies in the ζ, α, β and γ globin gene arrangements in normal black, italian, turkish, and spania newbornsFEI, Y. J; KUTLAR, F; GURGEY, A et al.Hemoglobin. 1989, Vol 13, Num 1, pp 45-65, issn 0363-0269Article

Recherche de l'anomalie génétique dans une forme hémolytique d'elliptocytose héréditaire avec homozygotie pour le variant spectrine alpha I/74 = Search for the genetic abnormality in a case of hemolytic hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variantGARBARZ, M; DEVAUX, I; GRANDHCAMP, B et al.Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie. 1989, Vol 308, Num 2, pp 43-48, issn 0764-4469Article

Comparison of unitages for total free erythrocyte protoporphyrin (total EP) in anemia screeningHARADA, K; OMORI, S; UENO, T et al.Clinica chimica acta. 1989, Vol 180, Num 1, pp 87-92, issn 0009-8981Article

Persistance héréditaire de l'hémoglobine foetale associée à une mutation en amont d'un gène γ = A case of hereditary persistence of fetal hemoglobin due to a mutation in 5' of the Gγ geneVIDAUD-RAPHANAUD, D; BADOUAL, J; LABIE, D et al.Archives françaises de pédiatrie. 1988, Vol 45, Num 5, pp 315-317, issn 0003-9764Article

Glomerular annular-tubular immune deposits in adult hemolytic uremic syndromeSCHWARTZMANN, M. S; D'AGATI, V.Nephron. 1988, Vol 50, Num 4, pp 371-375, issn 0028-2766Article

The relationship of models of the mind to clinical work: object relations theoryMICHELS, R; OLDHAM, J. M.Journal of the American Psychoanalytic Association. 1988, Vol 36, Num 3, pp 749-757, issn 0003-0651Article

Distribution of Gd- alleles in some ethnic of the USSRKRASNOPOLSKAYA, X. D; SHATSKAYA, T. L.Human genetics. 1987, Vol 75, Num 3, pp 258-263, issn 0340-6717Article

Abnormal arrangements in the α- and γ-globin gene clusters in a relatively large group of japanese newbornsSHIMIZU, K; HARANO, T; HARANO, K et al.American journal of human genetics. 1986, Vol 38, Num 1, pp 45-58, issn 0002-9297Article

Different ζ globin gene deletions among black AmericansFELICE, A. E; CLEEK, M. P; MARINO, E. M et al.Human genetics. 1986, Vol 73, Num 3, pp 221-224, issn 0340-6717Article

Peripheral nerve involvement in familial chorea-acanthocytosisSOBUE, G; MUKAI, E; FUJII, K et al.Journal of the neurological sciences. 1986, Vol 76, Num 2-3, pp 347-356, issn 0022-510XArticle

Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and α and β thalassaemiaWHITE, J. M; BYRNE, M; RICHARDS, R et al.Journal of medical genetics. 1986, Vol 23, Num 3, pp 245-251, issn 0022-2593Article

HB Fort Worth or α₂27(B8) Glu-Glyβ₂ in a black family from CanadaCARSTAIRS, K. C; RAULFS, A; KUTLAR, A et al.Hemoglobin. 1985, Vol 9, Num 2, pp 201-205, issn 0363-0269Article

Growth and cytogenetic characteristics of bone marrow colonies from patients with 5q-syndromeCARBONELL, F; HEIMPEL, H; KUBANEK, B et al.Blood. 1985, Vol 66, Num 2, pp 463-465, issn 0006-4971Article

Acquired iron-deficiency anemia caused by an antibody against the transferrin receptorLARRICK, J. W; HYMAN, E. S.The New England journal of medicine. 1984, Vol 311, Num 4, pp 214-218, issn 0028-4793Article

The flow behavior of lysolecithin-induced echinocytesROGAUSCH, H.Biorheology (Oxford). 1984, Vol 21, Num 6, pp 757-765, issn 0006-355XArticle

Erythrocyte enzymopathies, hemolytic anemia, and multisystem disease: an annoteated reviewVALENTINE, W. N; PAGLIA, D. E.Blood. 1984, Vol 64, Num 3, pp 583-591, issn 0006-4971Article