Osteitis fibrosa cystica generalisata with adult T-cell leukaemia: a case report
THE HISTORY OF BLOOD TRANSFUSION
DYSKERATOSIS CONGENITA IN ALL ITS FORMS
THE CLINICAL AND CELLULAR PHARMACOLOGY OF VINCRISTINE, CORTICOSTEROIDS, L-ASPARAGINASE, ANTHRACYCLINES and CYCLOPHOSPHAMIDE IN RELATION TO CHILDHOOD ACUTE LYMPHOBLASTIC LEUKAEMIA
CLASSIFICATION OF EX VIVO METHOTREXATE RESISTANCE IN ACUTE LYMPHOBLASTIC AND MYELOID LEUKAEMIA
INVESTIGATION OF 9-O-ACETYLATED SIALOGLYCOCONJUGATES IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKAEMIA
In vitro drug resistance profiles of adult versus childhood acute lymphoblastic leukaemia
Activation of an ataxia telangiectasia mutation-dependent intra-S-phase checkpoint by anti-tumour drugs in HL-60 and human lymphoblastoid cells
Detection of different Ikaros isoforms in human leukaemias using real-time quantitative polymerase chain reaction
T-cell prolymphocytic leukaemia: antigen receptor gene rearrangement and a novel mode of MTCP1 B1 activation
The incidences of trisomy 8, trisomy 9 and D20S108 deletion in polycythaemia vera: an analysis of blood granulocytes using interphase fluorescence in situ hybridization
Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia
Diagnostic utility of fluorescence in situ hybridization in mantle-cell lymphoma
Primary myelosarcomas are associated with a high rate of relapse: report on 34 children from the acute myeloid leukaemia-Berlin-Frankfurt-Münster studies
Novel BCR-ABL transcript containing an intronic sequence insert in a patient with Philadelphia-positive acute lymphoblastic leukaemia
Acute leukaemia in acromegaly patients
Sight-threatening varicella zoster virus infection after fludarabine treatment
Involvement of natural killer cells in patients with myelodysplastic syndrome carrying monosomy 7 revealed by the application of fluorescence in situ hybridization to cells collected by means of fluorescence-activated cell sorting
Nephrotic syndrome caused by protein thrombi in glomerulocapillary lumen in Waldenström's macroglobulinaemia
Long-term remission after intensive chemotherapy in advanced myelodysplastic syndromes is generally associated with restoration of polyclonal haemopoiesis
Feasibility and recent improvement of autologous stem cell transplantation for acute myelocytic leukaemia in patients over 60 years of age: importance of the source of stem cells
Cytomegalovirus colitis after autologous transplantation for multiple myeloma
Allogeneic haematopoietic transplantation for Richter's syndrome
Two-step immunoablative treatment with autologous peripheral blood CD34+ cell transplantation in an 8-year-old boy with autoimmune haemolytic anaemia
Retrovirus-mediated transfer of the herpes simplex virus thymidine kinase and enhanced green fluorescence protein genes in primary T lymphocytes
Glycoprotein Ib/IX complex is the target in rifampicin-induced immune thrombocytopenia
Defective platelet response to arachidonic acid and thromboxane A2 in subjects with Pl A2 polymorphism of β3 subunit (glycoprotein IIIa)
Bernard-Soulier syndrome in a patient doubly heterozygous for two frameshift mutations in the glycoprotein Ibα gene
The central role of the P 2T receptor in amplification of human platelet activation, aggregation, secretion and procoagulant activity
Fibrinogen polymorphisms are not associated with the risk of myocardial infarction
Factor V Leiden: the venous thrombotic risk in thrombophilic families
Haemostatic screening and identification of zebrafish mutants with coagulation pathway defects: an approach to identifying novel haemostatic genes in man
Contrasting effects of HSP72 expression on apoptosis in human umbilical vein endothelial cells and an angiogenic cell line, ECV304
Relationship between bleeding time, aspirin and the PlA1/A2 polymorphism of platelet glycoprotein IIIa
Th1 and Th2 cytokines in a patient with Evans' syndrome and profound lymphopenia
Hepatic iron concentration combined with long-term monitoring of serum ferritin to predict complications of iron overload in thalassaemia major
Relationship between TNF-α and iron metabolism in differentiating human monocytic THP-1 cells
Chelator-induced iron excretion in iron-overloaded marmosets
A new PKLR gene mutation in the R-type promoter region affects the gene transcription causing pyruvate kinase deficiency
Erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS)
CHILDHOOD ESSENTIAL THROMBOCYTHAEMIA WITHOUT EVIDENCE OF MYELOPROLIFERATION: HOW MANY INVESTIGATIONS SHOULD BE DONE?
ANTENATAL TESTING FOR HAEMOGLOBINOPATHIES
ANTENATAL TESTING FOR HAEMOGLOBINOPATHIES
TRANSFECTION OF RECEPTOR TYROSINE KINASE axl INTO HUMAN HAEMATOPOIETIC CELLS DOES NOT CAUSE SPONTANEOUS CELLULAR AGGREGATION
PRERETINAL NEOVASCULARIZATION IN SOUTH-EAST ASIAN OVALOCYTOSIS
EFFECT OF ELITE CYCLING ON LEUCOCYTE COUNTS
ESSENTIAL THROMBOCYTHAEMIA IN CHILDREN: A REPORT OF NINE CASES
ALL-TRANS RETINOIC ACID (ATRA) AND TRANEXAMIC ACID: A POTENTIALLY FATAL COMBINATION IN ACUTE PROMYELOCYTIC LEUKAEMIA
AGGRESSIVE MULTIPLE MODALITY THERAPY FOR VARICELLA-ASSOCIATED PURPURA FULMINANS
RITUXIMAB SALVAGE FOLLOWING RELAPSE AFTER ALLOGENEIC BONE MARROW TRANSPLANTATION FOR NON-HODGKIN'S LYMPHOMA