Extramedullary plasmocytoma with local amyloidosis presenting as a lump on the lip
Aortic thrombus with Aspergillus in a patient with refractory acute myelomonocytic leukaemia
Guidelines on the diagnosis and management of AL amyloidosis
Adverse prognostic significance of CD20 positive Reed–Sternberg cells in classical Hodgkin's disease*
Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome
Phenotypic and functional characterization of monocyte-derived dendritic cells in chronic lymphocytic leukaemia patients : influence of neoplastic CD19+ cells in vivo and in vitro
Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating marker
Either interleukin-12 or interferon-γ can correct the dendritic cell defect induced by transforming growth factor β1 in patients with myeloma
Haematopoetic stem cell transplantation for refractory autoimmune cytopenia
Etoposide, methylprednisolone, cytarabine and cisplatin successfully cytoreduces resistant myeloma patients and mobilizes them for transplant without adverse effects
Treatment of isolated central nervous system relapse in high-risk lymphoid malignancy with allogeneic bone marrow transplantation and extended intrathecal therapy
Interest of transjugular liver biopsy in adult patients with haemophilia or other congenital bleeding disorders infected with hepatitis C virus
Platelet degranulation and monocyte–platelet complex formation are increased in the acute and convalescent phases after ischaemic stroke or transient ischaemic attack
Anti-sickling effect of MX-1520, a prodrug of vanillin : an in vivo study using rodents
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome : association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction
Elevated circulating endothelial membrane microparticles in paroxysmal nocturnal haemoglobinuria
Biological and clinical features of T-biphenotypic acute leukaemia : report from a single centre
Association of the 1513C polymorphism in the P2X7 gene with familial forms of chronic lymphocytic leukaemia
Severe factor XI deficiency caused by compound heterozygosity
Long-term improvement of anaemia in a patient with aplastic anaemia by short-term administration of pegylated recombinant human megakaryocyte growth and development factor
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