Iron deficiency anaemia : an unusual presentation of lymphangioma
Faggot cells in an HIV-positive patient with inv(16)/therapy-related acute myeloid leukaemia
Current status of stem cell mobilization
Stem cell mobilization : the other side of the coin
Differential expression of HDAC3, HDAC7 and HDAC9 is associated with prognosis and survival in childhood acute lymphoblastic leukaemia
Clinical use of unfractionated heparin therapy in children : time for change?
IL1RN VNTR and IL2 −330 polymorphic genes are independently associated with chronic immune thrombocytopenia
Bleeding disorders in Lowe syndrome patients : evidence for a link between OCRL mutations and primary haemostasis disorders
Role of the cold shock domain protein A in the transcriptional regulation of HBG expression
Single nucleotide polymorphisms in the human TNF gene are associated with anaemia and neutropenia in a cohort of patients with de novo myelodysplastic syndrome
BCL3 translocation in CLL with typical phenotype : assessment of frequency, association with cytogenetic subgroups, and prognostic significance
PNH-phenotype cells in patients with idiopathic cytopenia of undetermined significance (ICUS) with megakaryocytic hypoplasia and thrombocytopenia
Pregnancy in PNH : another eculizumab baby
Low prevalence of coagulation F2 and F5 polymorphisms in mothers and children in a large cohort of patients with neonatal arterial ischemic stroke
Expansion of CD8+/perforin+ effector memory T cells in the bone marrow of patients with thymoma-associated pure red cell aplasia
Cyclic neutropenia associated with T cell immunity to granulocyte proteases and a double de novo mutation in GFI1 , a transcriptional regulator of ELANE
Incidence of leukaemia in patients with primary myelofibrosis and RBC–transfusion-dependence
Splenectomy after allogeneic haematopoietic stem cell transplantation in patients with primary myelofibrosis
CD23 expression in plasma cell leukaemia
Identification of TINF2 gene mutations in adult Japanese patients with acquired bone marrow failure syndromes
A novel assay for investigation of suspected familial haemophagocytic lymphohistiocytosis
Non-malignant haematology research in the UK : looking forward to new opportunities