TELOMERES AND HAEMOPOIESIS
DEVELOPMENTS IN ALLOGENEIC PERIPHERAL BLOOD PROGENITOR CELL TRANSPLANTATION
Composition and function of peripheral blood stem and progenitor cell harvests from patients with severe active rheumatoid arthritis
Evaluation of breast tumour cell contamination in the bone marrow and leukapheresis collections by RT-PCR for cytokeratin-19 mRNA
Extensive phenotypic analysis of CD34 subsets in successive collections of mobilized peripheral blood progenitors
Bone marrow transplantation for adults with acute leukaemia and 11q23 chromosomal abnormalities
Expansion of megakaryocyte progenitors from human umbilical cord blood using a new two-step separation procedure
Autologous bone marrow transplantation for non-Hodgkin's lymphoma resulting in long-term remission of coincidental Crohn's disease
Seasonal variation in the incidence of Hodgkin's disease
In-vivo immune responses to idiotypic VH complementarity-determining region 3 peptide vaccination in B-cell non-Hodgkin's lymphoma
Establishment of an IL-2-dependent cell line derived from 'nasal-type' NK/T-cell lymphoma of CD2+, sCD3-, CD3 epsilon+, CD56+ phenotype and associated with the Epstein-Barr virus
Paclitaxel plus high-dose cyclosphosphamide with G-CSF support in patients with relapsed and refractory aggressive non-Hodgkin's lymphoma
CD40 regulation of death domains containing receptors and their ligands on lymphoma B cells
Bolus administration of cladribine in the treatment of Waldenstrom macroglobulinaemia
Anticipation in familial plasma cell dyscrasias
Chromosomal abnormalities in systemic amyloidosis*
Expression of p210 and p190 BCR-ABL due to alternative splicing in chronic myelogenous leukaemia
The susceptibility of Philadelphia chromosome positive cells to FAS-mediated apoptosis is not linked to the tyrosine kinase activity of BCR-ABL
Arsenic trioxide inhibits growth of human T-cell leukaemia virus type I infected T-cell lines more effectively than retinoic acids
Ultrastructural characteristics and lysozyme content in hypergranular and variant type of acute promyelocytic leukaemia
Systemic mastocytosis associated with acute myeloid leukaemia : report of two cases and detection of the c-kit mutation Asp-816 to Val
Near-haploid common acute lymphoblastic leukaemia of childhood with a second hyperdiploid line : a DNA ploidy and fluorescence in-situ hybridization study
Longitudinal observation and outcome of nonfamilial childhood haemophagocytic syndrome receiving etoposide-containing regimens
The in-vitro generation of dendritic cells from blast cells in acute leukaemia
No treatment for low-risk thrombocythaemia : results from a prospective study
Plasma thrombopoietin (TPO) levels and expression of TPO receptor on platelets in patients with myelodysplastic syndromes
Poor response rate to a continuous schedule of Amifostine therapy for 'low/intermediate risk' myelodysplastic patients
Reactivation of Behcet's disease in the course of multicentric HHV8-positive Castleman's disease : long-term complete remission by a combined chemo/radiation and interferon-alpha therapy regimen
A novel BCR-ABL fusion gene (e2/1a) in a patient with Philadelphia-positive chronic myelogenous leukaemia and an aggressive clinical course
Cerebral candidiasis in a child 1 year after leukaemia
Mast cell recruitment after subcutaneous injection of RANTES in the sole of the rat paw
Effect of the interaction between fibronectin and VLA-4 on the proliferation of human B cells, especially a novel human B-cell line, OPM-3
The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelated
Iron status in pregnant women : which measurements are valid?
Effects of four species of interferon-alpha on cultured erythroid progenitors from congenital dyserythropoietic anaemia type I
Congenital dyserythropoiesis with intererythroblastic chromatin bridges and ultrastructurally-normal erythroblast heterochromatin : a new disorder
Activation of the human delta-globin gene promoter in primary adult erythroid cells
R411C mutation of the ALAS2 gene encodes a pyridoxine-responsive enzyme with low activity
Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany
The incidence and significance of fevers during treatment with antithymocyte globulin for aplastic anaemia
Anti-CD36 autoantibodies in thrombotic thrombocytopenic purpura and other thrombotic disorders : identification of an 85 kD form of CD36 as a target antigen
The P2Y1 receptor, necessary but not sufficient to support full ADP-induced platelet aggregation, is not the target of the drug clopidogrel
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R
Additional genetic risk factors for venous thromboembolism in carriers of the factor V Leiden mutation
Identification of new type 2B von Willebrand disease mutations : Arg543Gln, Arg545Pro and Arg578Leu
Two novel mutations (Pro864His, Val867Glu) causing type 2A von Willebrand disease and affecting a single restriction site in exon 28
Factor V Arg306 [arrow right] Thr (factor V Cambridge) and factor V Arg306 [arrow right] Gly mutations in venous thrombotic disease
Acute liver failure induced by alcohol and paracetamol in an HCV-infected haemophiliac
COMPLETE SPLENIC EMBOLIZATION IN THE TREATMENT OF IMMUNE THROMBOCYTOPENIC PURPURA