Fanconi's anaemia
Wolman's disease in an infant
FLT3 MUTATIONS AND LEUKAEMIA
THE HISTORY OF ACUTE PROMYELOCYTIC LEUKAEMIA
EARLY HISTORY OF IRON DEFICIENCY
Acute promyelocytic leukaemia in patients originating in Latin America is associated with an increased frequency of the bcr1 subtype of the PML/RARα fusion gene
Aberrant gene promoter methylation in acute promyelocytic leukaemia : profile and prognostic significance
CXCR4 chemokine receptors (CD184) and α4β1 integrins mediate spontaneous migration of human CD34+ progenitors and acute myeloid leukaemia cells beneath marrow stromal cells (pseudoemperipolesis)
A 2·6 Mb interval on chromosome 6q25.2–q25.3 is commonly deleted in human nasal natural killer/T-cell lymphoma
Disease activity and pretreatment, rather than hypogammaglobulinaemia, are major risk factors for infectious complications in patients with chronic lymphocytic leukaemia
Hyperfractionated cyclophosphamide in combination with pulsed dexamethasone and thalidomide (HyperCDT) in primary refractory or relapsed multiple myeloma
Severe and selective deficiency of interferon-γ-producing invariant natural killer T cells in patients with myelodysplastic syndromes
Kinetics of haematopoietic recovery after dose-intensive chemo/radiotherapy in mice : optimized erythroid support with darbepoetin alpha
Graft-versus-host disease (GVHD)-specific survival and duration of systemic immunosuppressive treatment in patients who developed chronic GVHD following allogeneic haematopoietic cell transplantation
Does sticky blood predict a sticky end? Associations of blood viscosity, haematocrit and fibrinogen with mortality in the West of Scotland
Activation of platelets in whole blood by recombinant factor VIIa by a thrombin-dependent mechanism
Expression of Plasmodium falciparum G6PD-6PGL in laboratory parasites and in patient isolates in G6PD-deficient and normal Nigerian children
Simultaneous (AC)n microsatellite polymorphism analysis and single-stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin-1 mutations in dominant hereditary spherocytosis
Increasing oxygen tension improves filtration of sickle trait donor blood
McLeod syndrome resulting from a novel XK mutation
TRANSIENT LEUKAEMIA IN NEWBORN INFANTS WITH TRISOMY 21
SUCCESSFUL USE OF GEMTUZUMAB OZOGAMICIN IN A CHILD WITH RELAPSED CD33-POSITIVE ACUTE LYMPHOBLASTIC LEUKAEMIA
ISOLATED EPIDURAL CHLOROMA WITH TRANSLOCATION T(15; 17) SUCCESSFULLY TREATED WITH CHEMOTHERAPY AND ALL-TRANS-RETINOIC ACID
RITUXIMAB EFFECTIVE IN A PATIENT WITH REFRACTORY AUTOIMMUNE HAEMOLYTIC ANAEMIA AND CD20-NEGATIVE MULTIPLE MYELOMA