Acute myeloblastic leukaemia with differentiation to myeloblasts and mast cell blasts
Heparin-induced skin necrosis
CHRONIC MYELOGENOUS LEUKAEMIA
Pure red cell aplasia
Historical aspects of chronic lymphocytic leukaemia
Multiple myeloma: an odyssey of discovery
Haematologists' approaches to the management of adolescents and young adults with acute leukaemia
Cytogenetically cryptic AML1–ETO and CBFβ–MYH11 gene rearrangements: incidence in 412 cases of acute myeloid leukaemia
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cells
Myeloperoxidase gene expression in non-infant pro-B acute lymphoblastic leukaemia with or without ALL1/AF4 transcript
Analysis of ETV6/AML1 abnormalities in acute lymphoblastic leukaemia: incidence, alternative spliced forms and minimal residual disease value
Minimal residual disease studies are beneficial in the follow-up of TEL/AML1 patients with B-precursor acute lymphoblastic leukaemia
Antisense oligonucleotides complementary to immunoglobulin sequences of BCL-2/immunoglobulin fusion transcript induce apoptosis of t(14;18) lymphoma cells
Procalcitonin in paediatric cancer patients: its diagnostic relevance is superior to that of C-reactive protein, interleukin 6, interleukin 8, soluble interleukin 2 receptor and soluble tumour necrosis factor receptor II
Molecular remission without blood product support using all-trans retinoic acid (ATRA) induction and combined arsenic trioxide/ATRA consolidation in a Jehovah's Witness with de novo acute promyelocytic leukaemia
BCL10 deletions in haematological malignancies: a cloning artefact?
Are aberrant BCR–ABL transcripts more common than previously thought?
Novel association of haemophagocytic syndrome with Kaposi's sarcoma-associated herpesvirus-related primary effusion lymphoma
Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13
Bone sialoprotein mRNA and protein expression in human multiple myeloma cell lines and patients
Defibrotide for the treatment of hepatic veno-occlusive disease: results of the European compassionate-use study
Is there a graft-versus-leukaemia effect in the absence of graft-versus-host disease in patients undergoing bone marrow transplantation for acute leukaemia?
The phenotypic profile of CD34-positive peripheral blood stem cells in different mobilization regimens
Purging of acute myeloid leukaemia cells from stem cell grafts by hyperthermia: enhancement of the therapeutic index by the tetrapeptide AcSDKP and the alkyl-lysophospholipid ET-18-OCH 3
Stem cell transplantation for the treatment of Fanconi anaemia using a fludarabine-based cytoreductive regimen and T-cell-depleted related HLA-mismatched peripheral blood stem cell grafts
PNH cells are as sensitive to T-cell-mediated lysis as their normal counterparts: implications for the pathogenesis of paroxysmal nocturnal haemoglobinuria
Mechanisms of bone marrow progenitor cell apoptosis in aplastic anaemia and the effect of anti-thymocyte globulin: examination of the role of the Fas–Fas‐L interaction
Cytokine requirement for the development of T-lymphoid lineage potential in clonal lymphohaematopoietic progenitors in vitro
Megakaryocyte maturation is associated with expression of the CXC chemokine connective tissue‐activating peptide CTAP III
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis
Hypofibronectinaemia and severity of sickle cell anaemia in Nigeria
Affordable CD4 + T-cell counts on ‘single-platform’ flow cytometers I. Primary CD4 gating
Age-dependent variations in the expression of PLC isoforms upon mitogenic stimulation of peripheral blood T cells from healthy donors
von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura
The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or both
The importance of locally derived reference ranges and standardized calculation of dilute Russell's viper venom time results in screening for lupus anticoagulant
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
A novel two base pair deletion in the factor V gene associated with severe factor V deficiency
Genetic linkage of Kozak sequence polymorphism of the platelet glycoprotein Ibα with human platelet antigen-2 and variable number of tandem repeats polymorphism, and its relationship with coronary artery disease
Systemic inflammation increases shear stress-induced platelet plug formation measured by the PFA-100
A comparison of polymorphism in the 3′-untranslated region of the prothrombin gene between Chinese and Caucasians in Australia
Identification of a new CA dinucleotide repeat in the human factor VIII gene
DDAVP (desmopressin; 1-deamino-cys-8- D -arginine-vasopressin) treatment in children with haemophilia B
Haematopoietic and lymphoid cell culture.