Papers to be published in forthcoming issues
Superior vena cava syndrome from an intracardiac non-Hodgkin lymphoma
Nodular sclerosing Hodgkin disease presenting as a sternal mass
Down syndrome and acute lymphoblastic leukaemia
A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO
Guidelines on the management of massive blood loss
Haematological malignancies developing in previously healthy individuals who received haematopoietic growth factors
Possible harmful effects of short course granulocyte colony-stimulating factor in normal donors
The c-Jun-N-terminal-Kinase inhibitor SP600125 enhances the butyrate derivative D1-induced apoptosis via caspase 8 activation in Kasumi 1 t(8;21) acute myeloid leukaemia cells
Erythropoietin treatment in advanced multiple myeloma is associated with improved immunological functions
t(8;21) acute myeloid leukaemia cells are dependent on vascular endothelial growth factor (VEGF)/VEGF receptor type2 pathway and phosphorylation of Akt
Concurrent MPL515 and JAK2V617F mutations in myelofibrosis
Bortezomib reduces serum dickkopf-1 and receptor activator of nuclear factor-κB ligand concentrations and normalises indices of bone remodelling in patients with relapsed multiple myeloma
Preceding immunosuppressive therapy with antithymocyte globulin and ciclosporin increases the incidence of graft rejection in children with aplastic anaemia who underwent allogeneic bone marrow transplantation from HLA-identical siblings
ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk
Isolation of an adult blood-derived progenitor cell population capable of differentiation into angiogenic, myocardial and neural lineages
Stage specific gene expression of serpins and their cognate proteases during myeloid differentiation
Differential cell division history between neutrophils and macrophages in their development from granulocyte–macrophage progenitors
Carotid intima-media thickness is increased and related to arterial stiffening in patients with beta-thalassaemia major
Globin gene expression in Hb Lepore-BAC transgenic mice
Cell-free DNA levels in pregnancies at risk of sickle-cell disease and significant ethnic variation
Novel mutations in a child with congenital amegakaryocytic thrombocytopenia
Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the α2-globin gene polyadenylation signal mutation AATAAA→AATA– –
A four base pair insertion in exon 1 of the RPS19 gene is a common polymorphism in African-Americans
Novo Nordisk Haemophilia Foundation website
International Conference on Emerging Trends in Haematology and Immunohaematology