British Journal of Haematology: Vol 88, No 1

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British Journal of Haematology

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British Journal of Haematology: Volume 88, Issue 1

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PATHOGENESIS OF IDIOPATHIC MYELOFIBROSIS: PRESENT STATUS AND FUTURE DIRECTIONS

Transforming growth factor-β and megakaryocytes in the pathogenesis of idiopathic myelofibrosis

Tumour necrosis factor-α and interleukin 4 promote the differentiation of myeloma cell precursors in multiple myeloma

CD45 isoform expression on human haemopoietic cells at different stages of development

Myeloid haemopoietic cells of patients with chronic granulomatous disease are relatively resistant to TNF

Reducing erythropoietin in cultures of human erythroid precursors elevates the proportion of fetal haemoglobin

Recovery of T-lymphocytes for adoptive immunotherapy by lymphapheresis of HIV-infected patients without alterations of virological, immunological or clinical parameters

Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis

The effect of iron overload and iron reductive treatment on the serum concentration of carbohydrate-deficient transferrin

Human cytomegalovirus (HCMV) infection in paediatric patients given allogeneic bone allogeneic bone marrow transplantation: role of early antiviral treatment for HCMV antigenaemaia on Patients' outcome

Treatment of advanced acute leukaemia with allogeneic bone marrow transplantation from unrelated donors

Influence of donor lymphocytes on the incidence of primary graft failure after allogeneic bone marrow transplatition in a murine model

Estimatetd 8-year survival of more than 40% in a population-based study of 79 adult patients with acute lymphoblastic leukaemia

Acute lymphocytic leukaemia in the elderly: characteristics and outsome with the vincristine-adriamycin-dexamethasone (VAD) regimen

Unique immunophenotype of acute promyelocytic leukaemia as defined by CD9 and CD68 antibodies

The relationship between bcl-2 expression and response to chemotherapy in acute leukaemia

Molecular detection of clonally rearranged cells in peripheral blood progenitor cell harvests from multiple myeloma patients

Impact of response to treatment on survival in multiple myeloma: results in a series of 243 patients

Efficient gene transfer into human umbilical vein endothelial cells allows functional analysis of the human tissue factor gene promoter

A haemorrhagic platelet disorder associated with altered stimulus-response coupling and abnormal membrane phospholipid composition

Influence of combined thrombin stimulation, surface activation, and receptor occupancy on organization of GPIb/IX receptors on human platelets

Dissociation between the phospholipases C and A2 activities in stimulated platelets and their involvement in the arachidonic acid liberation

Factor IX Bm Kiryu: a Val-313-to-Asp substitution in the catalytic domain results in loss of function due to a conformational change of the surface loop: evidence obtained by chimaeric modelling

Epitope mapping of human factor IX inhibitor antibodies

Red blood cell aggregability in patients with a history of leg vein thrombosis: influence of post-thrombotic treatment

Characterization of human blood group scFv antibodies derived from a V gene phage-display library

Detection of herpesvirus type 6 by polymerase chain reaction in blood donors: random tests and prospective longitudinal studies

PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease

Acute myeloid leukaemia with +i(12p) shortly after treatment of mediastinal germ cell tumour

Predicting the severity of rhesus alloimmunization: monocyte-mediated chemiluminescence versus maternal anti-D antibody estimation

SHORT REPORT

Further evidence that activated protein C resistance can be misdiagnosed as inherited functional protein S deficiency

High-dose gamma-globulin therapy in the reactive haemophagocytic syndrome

Prenatal diagnosis of congenital dysgranulopoietic neutropenia

Immunoglobulin replacement in patients with chronic lymphocytic leukaemia: a comparison of two dose regimes

Fluctuating symptomatic cryofibrinogenaemia in a patient with left atrial myxoma

Cyclic haemopoiesis at 7- or 8-day intervals

High prevalence of a mutation in the factor V gene within the U.K. population: relationship to activated protein C resistance and familial thrombosis

Correspondence

CONSIDERATIONS ON THE TRUE VALUE OF THE INTERNATIONAL NORMALIZED RATIO IN THE CONTROL OF ORAL ANTICOAGULANT THERAPY

CONSIDERATIONS ON THE TRUE VALUE OF THE INTERNATIONAL NORMALIZED RATIO IN THE CONTROL OF ORAL ANTICOAGULANT THERAPY

A MUTATION IN THE POLYADENYLATION SIGNAL OF THE α2 GLOBIN GENE (AATAA→AATA–) AS A CAUSE OF α THALASSAEMIA IN ASIAN INDIANS

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A MUTATION IN THE POLYADENYLATION SIGNAL OF THE α₂ GLOBIN GENE (AATAA→AATA–) AS A CAUSE OF α THALASSAEMIA IN ASIAN INDIANS