Cardiac involvement in non-Hodgkin's lymphoma
Haemopoietic and neuroglial progenitors are promoted during cord blood ex vivo expansion
RED CELL AGGLUTINATION
HISTORICAL ASPECTS AND PRESENT KNOWLEDGE OF IDIOPATHIC THROMBOCYTOPENIC PURPURA
FANCONI AND GLANZMANN
Investigatory and analytical approaches to differential gene expression profiling in mantle cell lymphoma
Intrasinusoidal bone marrow infiltration
Acquired immunodeficiency syndrome-associated lymphomas are efficiently lysed through complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity by rituximab
A study on 289 consecutive Korean patients with acute leukaemias revealed fluorescence in situ hybridization detects the MLL translocation without cytogenetic evidence both initially and during follow-up
Altered expression of retinoblastoma protein-interacting zinc finger gene, RIZ, in human leukaemia
The naive T-lymphocyte compartment is well preserved in patients with chronic myelogenous leukaemia in chronic phase
Etoposide-mediated deregulation of the G2M checkpoint in myeloid leukaemic cell lines results in loss of cell survival
Histone deacetylase inhibitors potently repress CXCR4 chemokine receptor expression and function in acute lymphoblastic leukaemia
Novel flow-cytometric analysis based on BCD5+ subpopulations for the evaluation of minimal residual disease in chronic lymphocytic leukaemia
Fludarabine, cyclophosphamide and mitoxantrone in the treatment of resistant or relapsed chronic lymphocytic leukaemia
Genetic polymorphisms in the tumour necrosis factor locus in childhood acute lymphoblastic leukaemia
Infrequent hypermethylation of CEBPA promotor in acute myeloid leukaemia
Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti-glycoprotein IIb–IIIa antibodies
Dissociation between fibrinogen and fibrin interaction with platelets in patients with different subtypes of Glanzmann's thrombasthenia
Anticardiolipin antibodies as a risk factor for venous thromboembolism in a population-based prospective study
Impaired circadian variations of haemostatic and fibrinolytic parameters in tetraplegia
Increased resistance to activated protein C after short-term oral hormone replacement therapy in healthy post-menopausal women
Activation of integrin αIIbβ3 expressed in Chinese hamster ovary cells is required for interaction with solid-phase von Willebrand factor
Mechanisms involved in the antiplatelet activity of magnesium in human platelets
Activation and inactivation of human factor X by proteases derived from Ficus carica
Two double heterozygous mutations in the F7 gene show different manifestations
Clonal T cell-mediated cyclic thrombocytopenia
Does isochromosome 7q mandate bone marrow transplant in children with Shwachman–Diamond syndrome?
Expression and function of pituitary tumour transforming gene for T-lymphocyte activation
Results and follow-up of a phase III randomized study of recombinant human-granulocyte stimulating factor as support for immunosuppressive therapy in patients with severe aplastic anaemia
Human bone marrow angiogenesis
Treatment of adult systemic mastocytosis with interferon-α
Hydroxyurea exerts bi-modal dose-dependent effects on erythropoiesis in human cultured erythroid cells via distinct pathways
A 3′UTR mutation affects β-globin expression without altering the stability of its fully processed mRNA
Comparison of outcome following allogeneic bone marrow transplantation with cyclophosphamide–total body irradiation versus busulphan–cyclophosphamide conditioning regimens for acute myelogenous leukaemia in first remission
Respiratory virus infections in transplant recipients after reduced-intensity conditioning with Campath-1H
The TNFd4 allele is correlated to moderate-to-severe acute graft-versus-host disease after allogeneic stem cell transplantation
ORAL ANTICOAGULATION AND DENTAL EXTRACTIONS
LOW-GRADE RECTAL MALT LYMPHOMA OCCURRING IN A PATIENT WITH CHRONIC LYMPHOCYTIC LEUKAEMIA
HOW FREQUENT IS MUTATION IN THE MITOCHONDRIAL CYTOCHROME C OXIDASE GENE IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES?
REPLY TO GATTERMANN ET AL
RECURRENT THROMBOEMBOLISM IN A FAMILIAL PSEUDOHYPERKALAEMIA PATIENT WITH AN INTACT SPLEEN
Human Blood Groups