Malignant sarcoma masquerading as a pseudotumour in a patient with mild haemophilia
Atypical large granular lymphocytes in a child
THE ROLE OF HAPLOIDENTICAL STEM CELL TRANSPLANTATION IN THE MANAGEMENT OF CHILDREN WITH HAEMATOLOGICAL DISORDERS
HAEMATOLOGY AT THE HAMMERSMITH HOSPITAL AND ROYAL POSTGRADUATE MEDICAL SCHOOL 1934–1994
Cytogenetic findings in adult de novo acute myeloid leukaemia. A population-based study of 303/337 patients
Possible regulation of Wilms' tumour gene 1 (WT1) expression by the paired box genes PAX2 and PAX8 and by the haematopoietic transcription factor GATA-1 in human acute myeloid leukaemias
Clinical significance of residual disease during treatment in childhood acute myeloid leukaemia
Occurrence of dysregulated oncogenes in primary plasma cells representing consecutive stages of myeloma pathogenesis : indications for different disease entities
Enhanced production of osteopontin in multiple myeloma : clinical and pathogenic implications
Chlorambucil in combination with induction and maintenance rituximab is feasible and active in indolent non-Hodgkin's lymphoma
Successful treatment of refractory pure red cell aplasia associated with lymphoproliferative disorders with the anti-CD52 monoclonal antibody alemtuzumab (Campath-1H)
Predictive value of early 18F-fluoro-deoxyglucose positron emission tomography in chemosensitive relapsed lymphoma
DNA microarray analysis of stage progression mechanism in myelodysplastic syndrome
Granulomatous slack skin disease – disease features and response to pentostatin
Plasma levels of tumour necrosis factor alpha and interleukin-6 predict progression-free survival following thalidomide therapy in patients with previously untreated multiple myeloma
T- and B-cell immune reconstitution and clinical outcome in patients with multiple myeloma receiving T-cell-depleted, reduced-intensity allogeneic stem cell transplantation with an alemtuzumab-containing conditioning regimen followed by escalated donor lymphocyte infusions
T-cell alloreactivity dominates natural killer cell alloreactivity in minimally T-cell-depleted HLA-non-identical paediatric bone marrow transplantation
Pregnancy-associated venous thromboembolism (VTE) in combined heterozygous factor V Leiden (FVL) and prothrombin (FII) 20210 A mutation and in heterozygous FII single gene mutation alone
A multicentre assessment of the endogenous thrombin potential using a continuous monitoring amidolytic technique
Two novel factor V null mutations associated with activated protein C resistance phenotype-genotype discrepancy
Familial polycythemia vera with Budd–Chiari syndrome in childhood
Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of β-thalassaemia trait
Causes of death in sickle cell disease : an autopsy study
CONCOMITANT MYELODYSPLASTIC SYNDROME AND CHRONIC MYELOID LEUKAEMIA : TREATMENT OUTCOMES WITH IMATINIB MESYLATE
SEVERE ACUTE RESPIRATORY SYNDROME AND LUPUS ANTICOAGULANTS IN CHILDREN
MALIGNANCIES IN SICKLE CELL DISEASE PATIENTS TREATED WITH HYDROXYUREA
LITHIUM EFFECTS ON NEUTROPHIL MOTILITY IN SHWACHMAN–DIAMOND SYNDROME : EVALUATION BY COMPUTER-ASSISTED IMAGE ANALYSIS
PROGNOSTIC FEATURES OF SPLENIC LYMPHOMA WITH VILLOUS LYMPHOCYTES
ERYTHROCYTOSIS AND THE CHUVASH VON HIPPEL-LINDAU MUTATION
ENDOTHELIAL CELLS EXPRESS NORMAL CELLULAR PRION PROTEIN
HEPARIN-INDUCED THROMBOCYTOPENIA : PATHOGENESIS AND MANAGEMENT
HEPARIN-INDUCED THROMBOCYTOPENIA : PATHOGENESIS AND MANAGEMENT – RESPONSE TO RASHEED SAAD