Works matching IS 00071048 AND DT 2012 AND VI 157 AND IP 2
Results: 23
Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acids.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 249, doi. 10.1111/j.1365-2141.2011.08937.x
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Growth factor-associated graft-versus-host disease and mortality 10 years after allogeneic bone marrow transplantation.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 220, doi. 10.1111/j.1365-2141.2012.09034.x
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Romiplostim for the early management of severe immune thrombocytopenia unresponsive to conventional treatment.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 256, doi. 10.1111/j.1365-2141.2011.08950.x
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De Novo polycythaemia vera arising 5 years following acute myeloid leukemia remission: suggestion of a chemotherapy resistant JAK2 clone.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 266, doi. 10.1111/j.1365-2141.2011.08972.x
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Early relapse and refractory disease remain risk factors in the anthracycline and autologous transplant era for patients with relapsed/refractory classical Hodgkin lymphoma: a single centre intention-to-treat analysis.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 201, doi. 10.1111/j.1365-2141.2011.08993.x
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Transcriptional regulation of MIR29B by PU.1 ( SPI1) and MYC during neutrophil differentiation of acute promyelocytic leukaemia cells.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 270, doi. 10.1111/j.1365-2141.2011.08964.x
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Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 240, doi. 10.1111/j.1365-2141.2012.09061.x
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An acquired CSF3R mutation in an adult chronic idiopathic neutropenia patient who developed acute myeloid leukaemia.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 264, doi. 10.1111/j.1365-2141.2011.08968.x
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Perinephric extramedullary haematopoiesis in primary myelofibrosis.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 157, doi. 10.1111/j.1365-2141.2012.09053.x
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Eltrombopag named patient programme for patients with chronic immune thrombocytopenia.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 259, doi. 10.1111/j.1365-2141.2011.08954.x
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Treatment of the elderly patient with diffuse large B cell lymphoma.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 159, doi. 10.1111/j.1365-2141.2011.09011.x
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Acute myeloid leukaemia with inv(3)(q21q26).
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 158, doi. 10.1111/j.1365-2141.2012.09062.x
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Human erythrocyte remodelling during Plasmodium falciparum malaria parasite growth and egress.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 171, doi. 10.1111/j.1365-2141.2012.09044.x
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T cell depletion utilizing CD34<sup>+</sup> stem cell selection and CD3<sup>+</sup> addback from unrelated adult donors in paediatric allogeneic stem cell transplantation recipients.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 205, doi. 10.1111/j.1365-2141.2012.09048.x
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Improved outcome of allogeneic haemopoietic stem cell transplantation for children with philadelphia positive acute lymphoblastic leukaemia.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 261, doi. 10.1111/j.1365-2141.2011.08953.x
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Increased natural killer cells and decreased CD3<sup>+</sup>CD8<sup>+</sup>CD62L<sup>+</sup> T cells in CML patients who sustained complete molecular remission after discontinuation of imatinib.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 254, doi. 10.1111/j.1365-2141.2011.08939.x
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Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 230, doi. 10.1111/j.1365-2141.2011.09025.x
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Pyrosequencing of BRAF V600E in routine samples of Hairy Cell Leukaemia identifies CD5+ variant Hairy Cell Leukaemia that lacks V600E.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 267, doi. 10.1111/j.1365-2141.2011.08963.x
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Amplified segment in the 'Down Syndrome critical region' on HSA21 shared between Down syndrome and euploid AML-M0 excludes RUNX1, ERG and ETS2.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 197, doi. 10.1111/j.1365-2141.2011.08985.x
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Treatment of primary intraocular lymphoma with rituximab, high dose methotrexate, procarbazine, and vincristine chemotherapy, reduced whole-brain radiotherapy, and local ocular therapy.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 252, doi. 10.1111/j.1365-2141.2011.08938.x
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Incidence, risk factors and outcome of histological transformation in follicular lymphoma.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 188, doi. 10.1111/j.1365-2141.2012.09054.x
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The uptake of recombinant glucocerebrosidases by blood monocytes from type 1 Gaucher disease patients is variable.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 274, doi. 10.1111/j.1365-2141.2011.08989.x
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A 15q24 microdeletion in transient myeloproliferative disease ( TMD) and acute megakaryoblastic leukaemia ( AMKL) implicates PML and SUMO3 in the leukaemogenesis of TMD/ AMKL.
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- British Journal of Haematology, 2012, v. 157, n. 2, p. 180, doi. 10.1111/j.1365-2141.2012.09028.x
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