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Results 1 to 25 of 180811

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Clinical and molecular correlations in the sickle/β+-thalassemia syndromeATWEH, G. F; FORGET, B. G.American journal of hematology. 1987, Vol 24, Num 1, pp 31-36, issn 0361-8609Article

Clinical presentation of sickle cell-hemoglobin C diseaseWILLIAMS, S; MAUDE, G. H; SERJEANT, G. R et al.The Journal of pediatrics. 1986, Vol 109, Num 4, pp 586-589, issn 0022-3476Article

Sardinian δβ°-thalassemia: a further example of a C to T substitution at position -196 of the Aγ globin gene promoterOTTOLENGHI, S; GIGLIONI, B; PULAZZINI, A et al.Blood. 1987, Vol 69, Num 4, pp 1058-1061, issn 0006-4971Article

Symposium on immunodeficiency and cancerFILIPOVICH, A. H.The American journal of pediatric hematology/oncology. 1987, Vol 9, Num 2, issn 0192-8562, 178Article

Avidity of radiogallium for bone in thalassemiaGRIMMOND, A. P; SPENCER, R. P.Clinical nuclear medicine. 1987, Vol 12, Num 9, pp 758-759, issn 0363-9762Article

Amoxapine-associated agranulocytosis with thrombocytosis occurring early during recoverySEDLACEK, S. M; RUDOLF, P. M; KAEHNY, W. D et al.The American journal of medicine. 1986, Vol 80, Num 3, pp 533-536, issn 0002-9343Article

HB F-albaicin or Gγ8(A5)Lys→Glu or GlnDE PABLOS, J. M; WILSON, J. B; KUTLAR, A et al.Hemoglobin. 1986, Vol 10, Num 6, pp 655-659, issn 0363-0269Article

L'association hémoglobinose E-thalassémie (E-thal) = HbE-thalassemiaSCHAISON, G; LEVERGER, G; VIDAUD, M et al.Archives françaises de pédiatrie. 1985, Vol 42, Num 8, pp 709-711, issn 0003-9764Article

Fibrinogen Giessen. I: A congenital homozygously expressed dysfibrinogenemia with Aα 16 Arg→His substitutionALVING, B. M; HENSCHEN, A. H.American journal of hematology. 1987, Vol 25, Num 4, pp 479-482, issn 0361-8609Article

Hb F-Oakland or α2GγI226(B8)Glu→LysKLEMAN, K; LUBIN, B; WILSON, J. B et al.Hemoglobin. 1987, Vol 11, Num 2, pp 181-183, issn 0363-0269Article

The thalassemia repositoryKUTLAR, A; LANCLOS, K. D.Hemoglobin. 1987, Vol 11, Num 2, pp 191-198, issn 0363-0269Article

Le syndrome osseux dans le myélome (étude rétrospective de 113 cas) = Bone lesions in myeloma (113 cases)MOALLA, M; BERGAOUI, N; BEN AYED, H et al.Revue internationale de rhumatologie. 1987, Vol 17, Num 1, pp 19-26, issn 0294-474XArticle

Pneumothorax associated with lymphomaYELLIN, A; BENFIELD, J. R.The American review of respiratory disease. 1986, Vol 134, Num 3, pp 590-592, issn 0003-0805Article

Les thrombocythémies: étude rétrospective à propos de 93 dossiers = Thrombocythemia: retrospective study based upon 93 medical recordsJANVIER, M; BELLUCCI, S; TOBELEM, G et al.Actualités hématologiques. 1984, Vol 18, pp 129-141, issn 0567-8757Article

Radiological features of systemic mast-cell diseaseTSUNG-YAO HUANG; YAM, L. T; CHIN-YANG LI et al.British journal of radiology. 1987, Vol 60, Num 716, pp 765-770, issn 0007-1285Article

A critical evaluation of the clinical diagnosis of anemiaGJØRUP, T; BUGGE, P. M; HENDRIKSEN, C et al.American journal of epidemiology. 1986, Vol 124, Num 4, pp 657-665, issn 0002-9262Article

Hemoglobin La Desirade αA2β2129(H7)Ala→Val: a new unstable hemoglobinMERAULT, G; KECLARD, L; GARIN, J et al.Hemoglobin. 1986, Vol 10, Num 6, pp 593-605, issn 0363-0269Article

The thalassemia repositoryLANCLOS, K. D; KUTLAR, A.Hemoglobin. 1986, Vol 10, Num 5, pp 533-558, issn 0363-0269Article

HB Himeji or β 140 (H18) Ala→Asp. A slightly unstable hemoglobin with increased βN-terminal glycationOHBA, Y; MIYAJI, T; IMAI, K et al.Hemoglobin. 1986, Vol 10, Num 2, pp 109-125, issn 0363-0269Article

HB Saint Luis or α2β2 28(B10)Leu→Gln in a Czechoslovakian maleWIEDERMANN, B. F; INDRAK, K; WILSON, J. B et al.Hemoglobin. 1986, Vol 10, Num 6, pp 673-676, issn 0363-0269Article

Evolution of coagulation abnormalities following Russell's viper bite in BurmaTHAN THAN; KHIN EI HAN; HUTTON, R. A et al.British journal of haematology. 1987, Vol 65, Num 2, pp 193-198, issn 0007-1048Article

Minor components of Hb Bart'sABRAHAM, E. C; ABRAHAM, A; KASTEN-JOLLY, J et al.Hemoglobin. 1987, Vol 11, Num 4, pp 329-339, issn 0363-0269Article

Paghogenesis of thrombotic: thrombocytopenic purpuraLIAN, E. C.-Y.Seminars in hematology. 1987, Vol 24, Num 2, pp 82-100, issn 0037-1963Article

Functional studies, anion-binding and effects of bezafibrate on three high affinity hemoglobin variants: HB Olympia, HB Great Lakes and HB North ChicagoRAHBAR, S; ASMEROM, Y.Hemoglobin. 1986, Vol 10, Num 6, pp 643-649, issn 0363-0269Article

Care of the young hemophiliac: new socioeconomic demands and the changing patient-physician relationshipSMITH, P. S; GOLDMAN, D. S.The American journal of pediatric hematology/oncology. 1985, Vol 7, Num 2, pp 165-174, issn 0192-8562Article

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