Striking bone marrow plasmacytosis in a patient with sickle cell anaemia
Paraneoplastic pemphigus associated with follicular lymphoma
Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia
Optimal management of adults with ALL
A comparative study of bone marrow and peripheral blood CD34+ myeloblasts in acute myeloid leukaemia
Molecular and clinical features of chronic lymphocytic leukaemia with stereotyped B cell receptors : results from an Italian multicentre study
Expression and function of toll like receptors in chronic lymphocytic leukaemia cells
Monitoring minimal residual disease in acute myeloid leukaemia with NPM1 mutations by quantitative PCR : clonal evolution is a limiting factor
High-dose Ara-C and beam with autograft rescue in R-CHOP responsive mantle cell lymphoma patients
The Stanford V regimen is effective in patients with good risk Hodgkin lymphoma but radiotherapy is a necessary component
The role of X-inactivation in the gender bias of patients with acquired α-thalassaemia and myelodysplastic syndrome (ATMDS)
The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locus
Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP : identification of factors predictive of a sustained response
Long-term outcome of initially homogenously treated and relapsed childhood acute lymphoblastic leukaemia in Austria – A population-based report of the Austrian Berlin-Frankfurt-Münster (BFM) Study Group
Manufacturing of human placenta-derived mesenchymal stem cells for clinical trials
Compartmentalization regulates the interaction between the platelet integrin αIIbβ3 and ICln
Phosphatidylserine surface expression and integrin αIIbβ3 activity on thrombin/convulxin stimulated platelets/particles of different sizes
Expansion of haematopoietic stem cells from normal donors and bone marrow failure patients by recombinant hoxb4
The role of Epstein–Barr virus in Richter syndrome
The role of Epstein–Barr virus in Richter syndrome : response to Nourse et al
Complex inheritance of chronic haemolytic anaemia
Improving management of neutropenic sepsis in the emergency department
Immature platelet fraction as novel laboratory parameter predicting the course of neonatal thrombocytopenia
Anti-Fy3 in sickle cell disease : a difficult transfusion problem
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF
Corrigendum
Transfusion Microbiology