Works matching IS 00071048 AND DT 1999 AND VI 106 AND IP 3
Results: 43
MLL REARRANGEMENTS IN HAEMATOLOGICAL MALIGNANCIES: LESSONS FROM CLINICAL AND BIOLOGICAL STUDIES.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 614, doi. 10.1046/j.1365-2141.1999.01439.x
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THE PATHOGENESIS OF ACUTE PROMYELOCYTIC LEUKAEMIA: EVALUATION OF THE ROLE OF MOLECULAR DIAGNOSIS AND MONITORING IN THE MANAGEMENT OF THE DISEASE.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 591, doi. 10.1046/j.1365-2141.1999.01501.x
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DETECTION OF MINIMAL RESIDUAL DISEASE IN ACUTE MYELOID LEUKAEMIA: METHODOLOGIES, CLINICAL AND BIOLOGICAL SIGNIFICANCE.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 578, doi. 10.1046/j.1365-2141.1999.01522.x
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Incompatibility for CD31 and human platelet antigens and acute graft-versus-host disease after bone marrow transplantation.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 723, doi. 10.1046/j.1365-2141.1999.01585.x
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FADD expression and caspase activation in B-cell lymphomas resistant to Fas-mediated apoptosis.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 652, doi. 10.1046/j.1365-2141.1999.01586.x
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Additional translocation (8;21)(q22;q22) in a patient with Philadelphia-positive chronic myelogenous leukaemia in the blastic phase.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 720, doi. 10.1046/j.1365-2141.1999.01588.x
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Defective functional activity and accelerated apoptosis in neutrophils from children with cancer are differentially corrected by granulocyte and granulocyte-macrophage colony stimulating factors in vitro.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 756, doi. 10.1046/j.1365-2141.1999.01589.x
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Substitution of Arg[sup 527] and Arg[sup 531] in factor VIII associated with mild haemophilia A: characterization in terms of subunit interaction and cofactor function.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 792, doi. 10.1046/j.1365-2141.1999.01590.x
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Clonal immunoglobulin light chain variable region germline gene use in AL amyloidosis: association with dominant amyloid-related organ involvement and survival after stem cell transplantation.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 744, doi. 10.1046/j.1365-2141.1999.01591.x
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Hepatosplenic candidiasis in patients with acute leukaemia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 697, doi. 10.1046/j.1365-2141.1999.01592.x
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Monoclonal Epstein-Barr virus-related lymphoproliferative disorder following adult acute lymphoblastic leukaemia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 713, doi. 10.1046/j.1365-2141.1999.01593.x
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Fas ligand-induced apoptosis of hepatocytes in natural killer cell leukaemia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 709, doi. 10.1046/j.1365-2141.1999.01594.x
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Mutational analysis of the DNA mismatch repair gene hMLH1 in myeloid leukaemias.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 706, doi. 10.1046/j.1365-2141.1999.01595.x
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Lipid composition of seven APTT reagents in relation to heparin sensitivity.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 801, doi. 10.1046/j.1365-2141.1999.01596.x
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The GPIa C807T dimorphism associated with platelet collagen receptor density is not a risk factor for myocardial infarction.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 771, doi. 10.1046/j.1365-2141.1999.01597.x
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Bone marrow effects of anagrelide therapy in patients with myelofibrosis with myeloid metaplasia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 682, doi. 10.1046/j.1365-2141.1999.01598.x
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Production and characterization of anti-Kell monoclonal antibodies using transfected cells as the immunogen.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 817, doi. 10.1046/j.1365-2141.1999.01599.x
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Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 752, doi. 10.1046/j.1365-2141.1999.01600.x
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Effect of factor VIII concentrate on leucocyte cytokine production: characterization of TGF-beta as an immunomodulatory component in plasma-derived factor VIII concentrate.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 784, doi. 10.1046/j.1365-2141.1999.01601.x
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Phenotypic and molecular analysis of six human cell lines derived from patients with plasma cell dyscrasia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 669, doi. 10.1046/j.1365-2141.1999.01602.x
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The relationship between monoclonal myeloma precursor B cells in the peripheral blood stem cell harvests and the clinical response of multiple myeloma patients.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 737, doi. 10.1046/j.1365-2141.1999.01603.x
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Therapeutic monitoring of von Willebrand disease: interest and limits of a platelet function analyser at high shear rates.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 777, doi. 10.1046/j.1365-2141.1999.01604.x
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Quantification of minimal residual disease in patients with BCR-ABL-positive acute lymphoblastic leukaemia using quantitative competitive polymerase chain reaction.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 634, doi. 10.1046/j.1365-2141.1999.01605.x
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Phase III efficacy study of interleukin-3 after autologous bone marrow transplantation in patients with malignant lymphoma.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 730, doi. 10.1046/j.1365-2141.1999.01609.x
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Myelodysplastic syndrome in a patient with adult T-cell leukaemia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 702, doi. 10.1046/j.1365-2141.1999.01610.x
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High levels of lung resistance related protein mRNA in leukaemic cells from patients with acute myelogenous leukaemia are associated with inferior response to chemotherapy and prior treatment with mitoxantrone.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 627, doi. 10.1046/j.1365-2141.1999.01611.x
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Measurement of endogenous and exogenous alpha-granular platelet proteins in patients with immune and nonimmune thrombocytopenia.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 762, doi. 10.1046/j.1365-2141.1999.01612.x
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A family with hereditary factor X deficiency with a point mutation Gla[sup 32] to Gln in the Gla domain (factor X Tokyo).
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 809, doi. 10.1046/j.1365-2141.1999.01614.x
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P53 deletion is not a frequent event in multiple myeloma.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 717, doi. 10.1046/j.1365-2141.1999.01615.x
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Is there a correlation between degree of splenomegaly, symptoms and hypersplenism? A study of 218 patients with Gaucher disease.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 812, doi. 10.1046/j.1365-2141.1999.01616.x
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The cyclin-dependent kinase inhibitors p18[sup INK4c] and p19[sup INK4d] are highly expressed in CD34[sup +] progenitor and acute myeloid leukaemic cells but not in normal differentiated myeloid cells.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 644, doi. 10.1046/j.1365-2141.1999.01617.x
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A prospective study of routine antenatal enzyme antibody screening demonstrates lack of clinical value in predicting haemolytic disease of the newborn.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 824, doi. 10.1046/j.1365-2141.1999.01618.x
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Leucocyte transfusions from rhG-CSF or prednisolone stimulated donors for treatment of severe infections in immunocompromised neutropenic patients.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 689, doi. 10.1046/j.1365-2141.1999.01619.x
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Telomerase activity in chronic lymphoproliferative disorders of B-cell lineage.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 662, doi. 10.1046/j.1365-2141.1999.01620.x
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Functional expression of TRAIL by lymphoid and myeloid tumour cells.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 827, doi. 10.1046/j.1365-2141.1999.01630.x
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Malaria in an African penguin.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 577, doi. 10.1046/j.1365-2141.1999.01652.x
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THE MANAGEMENT OF ‘LOW-RISK’ AND ‘INTERMEDIATE-RISK’ PATIENTS WITH PRIMARY THROMBOCYTHAEMIA.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 833, doi. 10.1046/j.1365-2141.1999.01653.x
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THE MANAGEMENT OF ‘LOW-RISK’ AND ‘INTERMEDIATE-RISK’ PATIENTS WITH PRIMARY THROMBOCYTHAEMIA.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 834, doi. 10.1046/j.1365-2141.1999.1653a.x
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DOES ANTI-D PROTECT PLATELETS FROM ANTI-HPA 1A MEDIATED DESTRUCTION?
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 835, doi. 10.1046/j.1365-2141.1999.01654.x
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ERYTHROPHAGOCYTOSIS BY RHABDOMYOSARCOMA.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 835, doi. 10.1046/j.1365-2141.1999.01655.x
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ANTICIPATION IN FAMILIAL PLASMA CELL DISEASE.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 836, doi. 10.1046/j.1365-2141.1999.01656.x
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PROBABLE AUTOIMMUNE NEUTROPENIA INDUCED BY FLUDARABINE TREATMENT FOR CHRONIC LYMPHOCYTIC LEUKAEMIA.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 836, doi. 10.1046/j.1365-2141.1999.01682.x
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C-KIT ACTIVATING MUTATION IN A NEONATE WITH IN-UTERO PRESENTATION OF SYSTEMIC MASTOCYTOSIS ASSOCIATED WITH MYELOPROLIFERATIVE DISORDER.
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- British Journal of Haematology, 1999, v. 106, n. 3, p. 838, doi. 10.1046/j.1365-2141.1999.01683.x
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