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Hematological and molecular characterization of beta-thalassemia/Hb Tak compound heterozygoteCHAROENKWAN, Pimlak; THANARATTANAKORN, Pattra; CHAOVALUKSAKUL, Siriporn et al.Southeast Asian journal of tropical medicine and public health. 2003, Vol 34, Num 2, pp 415-419, issn 0125-1562, 5 p.Article
Bone marrow transplantationHONG, R.Advances in pediatrics. 1993, Vol 40, pp 101-124, issn 0065-3101Article
Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuriaWIEDMER, T; HALL, S. E; ORTEL, T. L et al.Blood. 1993, Vol 82, Num 4, pp 1192-1196, issn 0006-4971Article
Pain measurement in hospitalized adults with sickle cell painful episodesBALLAS, S. K; DELENGOWSKI, A.Annals of clinical and laboratory science. 1993, Vol 23, Num 5, pp 358-361, issn 0091-7370Article
Transient erythroblastopenia of childhood in Sweden : incidence and findings at the time of diagnosisSKEPPNER, G; WRANNE, L.Acta paediatrica (Oslo). 1993, Vol 82, Num 6-7, pp 574-578, issn 0803-5253Article
Human parvovirus infection in homozygous sickle cell diseaseSERJEANT, G. R; SERJEANT, B; THOMAS, P. W et al.Lancet (British edition). 1993, Vol 341, Num 8855, pp 1237-1240, issn 0140-6736Article
Prevalence of heterozygous β-thalassemia in northern areas of PakistanMOHAMMAD FAROOQ KHATTAK; MOHAMMAD SALEEM.Journal of the Pakistan Medical Association. 1992, Vol 42, Num 2, pp 32-34, issn 0030-9982Article
A study of erythropoiesis and iron metabolism in the rabbit in vivo. II: Dependence of the response on iron storage and transportALBA LOIS, L; MAINERO, A; VALDES-LOPEZ, V. M et al.Archives of medical research. 1992, Vol 23, Num 1, pp 7-11, issn 0188-4409Article
Prevalance of hemoglobinopathies in North JordanBASHIR, N; BARKAWI, M; SHARIF, L et al.Tropical and geographical medicine. 1992, Vol 44, Num 1-2, pp 122-125, issn 0041-3232Article
Polycythemia vera and other polycythemic statesLANDAW, S. A.Clinics in laboratory medicine. 1990, Vol 10, Num 4, pp 857-871, issn 0272-2712Article
Characterization of a new GGPD variant: GGPD TitusvilleCSEPREGHY, M; HALL, M. K; BERKOW, R. L et al.The American journal of the medical sciences. 1989, Vol 297, Num 2, pp 114-117, issn 0002-9629Article
High frequencies of a rearrangement (+ATA; -T) at -530 to the β-globin gene in different populations indicate the absence of a correlation with a silent β-thalassemia determinantWONG, S. C; STOMING, T. A; EFREMOV, G. D et al.Hemoglobin. 1989, Vol 13, Num 1, pp 1-5, issn 0363-0269Article
Myelofibrosis and aplastic anemia: first report of the two disorders occurring sequentially in the same personANTONUCCI, R; WALKER, R; HERION, J et al.The American journal of medicine. 1989, Vol 86, Num 3, pp 352-355, issn 0002-9343Article
Haplotypes of alpha-globin-gene in the Saudi population, the triplicated gene (αααanti3.7/)EL-HAZMI, M. A. F.Human heredity. 1987, Vol 37, Num 5, pp 314-318, issn 0001-5652Article
Bone marrow and peripheral blood globin chain synthesis in sickle cell β° thalassaemiaCOSTA, F. F; ZAGO, M. A.Journal of medical genetics. 1986, Vol 23, Num 3, pp 252-255, issn 0022-2593Article
Functional activity of the triplicated ααα4.2/gene rearrangementTRENT, R. J; YAKAS, J; BROCK, P. E et al.Hemoglobin. 1986, Vol 10, Num 5, pp 507-517, issn 0363-0269Article
Specific cognitive effects of mild iron deficiency and assosications with blood polymorphisms in Young adultsFOLEY, D; HAY, D. A; MITCHELL, R. J et al.Annals of human biology. 1986, Vol 13, Num 5, pp 417-425, issn 0301-4460Article
Presence of the Tn antigen on hematopoietic progenitors from patients with the Tn symdromeVAINCHENKER, W; VINCI, G; TESTA, U et al.The Journal of clinical investigation. 1985, Vol 75, Num 2, pp 541-546, issn 0021-9738Article
Electrophoretic and chromatographic techniques for the differential diagnosis of a haemoglobin abnormality: Hb E heterozygosityBIANCHI BOSISIO, A; ROCHETTE, J; WAJCMAN, H et al.Journal of chromatography. 1985, Vol 330, Num 2, pp 299-306, issn 0021-9673Article
Glutathione reductase deficiency in association with sickle cell and Thalassaemia genes in Saudi populationsEL-HAZMI, M. A. F; WARSY, A. S.Human heredity. 1985, Vol 35, Num 5, pp 326-332, issn 0001-5652Article
αααanti-4.2haplotype and heterozygous β° thalassemia in a sicilian familyACUTO, S; BUTTICE, G; SAITTA, B et al.Human genetics. 1985, Vol 70, Num 4, pp 318-320, issn 0340-6717Article
Accumulation and drainage of hemin in the red cell membraneSHAKLAI, N; SHVIRO, Y; RABIZADEH, E et al.Biochimica et biophysica acta. 1985, Vol 821, Num 2, pp 355-366, issn 0006-3002Article
Iron metabolism and «sports anemia». II: A hematological comparison of elite runners and control subjectsMAGNUSSON, B; HALLBERG, L; ROSSANDER, L et al.Acta medica Scandinavica. 1984, Vol 216, Num 2, pp 157-164, issn 0001-6101Article
Analysis of lymphocyte subsets in patients with aplastic anaemiaZOUMBOS, N. C; FERRIS, W. O; SU-MING HSU et al.British journal of haematology. 1984, Vol 58, Num 1, pp 95-105, issn 0007-1048Article
Distributions of hemoglobins a and S among erythrocytes of heterozygotesANYAIBE, S; CASTRO, O; HEADINGS, V et al.Hemoglobin. 1983, Vol 9, Num 2, pp 137-155, issn 0363-0269Article