Works matching IS 00071048 AND DT 2020 AND VI 189 AND IP 5
Results: 40
COVID‐19 infection in patients with sickle cell disease.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 851, doi. 10.1111/bjh.16734
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SARS‐CoV‐2: a new aetiology for atypical lymphocytes.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 845, doi. 10.1111/bjh.16730
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Thromboembolic risk and anticoagulant therapy in COVID‐19 patients: emerging evidence and call for action.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 846, doi. 10.1111/bjh.16727
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Management of COVID‐19‐related paediatric blood samples in a clinical haematology laboratory.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 848, doi. 10.1111/bjh.16721
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Reactive lymphocytes in patients with COVID‐19.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 844, doi. 10.1111/bjh.16690
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A special type of chromosome 1 abnormality in myelodysplastic syndrome patients: duplication 1q.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e218, doi. 10.1111/bjh.16643
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Treosulfan conditioning for allogeneic transplantation in multiple myeloma – improved overall survival in first line haematopoietic stem cell transplantation – a large retrospective study by the Chronic Malignancies Working Party of the EBMT.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e213, doi. 10.1111/bjh.16642
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Haemophagocytic lymphohistiocytosis associated with immune checkpoint inhibitors: a descriptive case study and literature review.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 985, doi. 10.1111/bjh.16630
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Safety, feasibility and preliminary efficacy of single agent combretastatin A1 diphosphate (OXi4503) in patients with relapsed or refractory acute myeloid leukemia or myelodysplastic syndromes.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e211, doi. 10.1111/bjh.16629
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NPM1 mutation with DNMT3A wild type defines a subgroup of MDS with particularly favourable outcomes after decitabine therapy.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 982, doi. 10.1111/bjh.16628
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Genotype‐phenotype correlation of unusual BCR‐ABL1 transcripts in Philadelphia chromosome‐positive leukaemia.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e207, doi. 10.1111/bjh.16627
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Analysis of saliva samples and cluster of differentiation 3 (CD3)+ lymphocytes as a source of germline DNA in myeloproliferative neoplasms.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e204, doi. 10.1111/bjh.16624
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Efficacy of venetoclax in combination with azacitidine followed by haploidentical transplantation in refractory acute myeloid leukaemia and mixed phenotype acute leukaemia.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e200, doi. 10.1111/bjh.16622
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Catheter associated thromboses in patients with sickle cell anaemia and dual lumen Vortex apheresis ports are common and can be clinically asymptomatic.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e198, doi. 10.1111/bjh.16619
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Distinct bone marrow morphologic features discriminate myelodysplastic syndromes patients with and without an early platelet response to decitabine.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. e194, doi. 10.1111/bjh.16615
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Leishmaniasis with cryoglobulinaemia and Leishmania infantum in peripheral blood neutrophils.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 801, doi. 10.1111/bjh.16538
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Numerous abnormal mitoses in parvovirus B19‐infected proerythroblasts.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 800, doi. 10.1111/bjh.16520
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Analysing therapeutic responses in immune thrombocytopaenia: shifting the focus towards immune characteristics.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 811, doi. 10.1111/bjh.16482
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Distinctive and common features of moderate aplastic anaemia.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 967, doi. 10.1111/bjh.16460
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Outcomes of allogeneic stem cell transplantation for patients with t(6:9) AML‐ A strong case for allogeneic stem cell transplantation in first complete remission.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 806, doi. 10.1111/bjh.16478
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PNH phenotypes and their genesis.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 802, doi. 10.1111/bjh.16473
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Primary analysis of JUMP, a phase 3b, expanded‐access study evaluating the safety and efficacy of ruxolitinib in patients with myelofibrosis, including those with low platelet counts.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 888, doi. 10.1111/bjh.16462
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Treatment of relapsed/refractory paediatric aggressive B‐cell non‐Hodgkin lymphoma.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 826, doi. 10.1111/bjh.16461
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Immunoglobulin heavy variable somatic hyper mutation status in chronic lymphocytic leukaemia: on the threshold of a new era?
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 809, doi. 10.1111/bjh.16480
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Platelet and immune characteristics of immune thrombocytopaenia patients non‐responsive to therapy reveal severe immune dysregulation.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 943, doi. 10.1111/bjh.16459
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An alpha‐defensin gene single nucleotide polymorphism modulates the gut microbiota and may alter the risk of acute graft‐versus‐host disease.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 926, doi. 10.1111/bjh.16458
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Dissecting the role of the CXCL12/CXCR4 axis in acute myeloid leukaemia.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 815, doi. 10.1111/bjh.16456
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Induction therapy with the MATRix regimen in patients with newly diagnosed primary diffuse large B‐cell lymphoma of the central nervous system – an international study of feasibility and efficacy in routine clinical practice.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 879, doi. 10.1111/bjh.16451
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ASXL1 mutations, previous vascular complications and age at diagnosis predict survival in 85 WHO‐defined polycythaemia vera patients.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 913, doi. 10.1111/bjh.16450
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Long‐term efficacy and safety of 2CdA (cladribine) in extra‐pulmonary adult‐onset Langerhans cell histiocytosis: analysis of 23 cases from the French Histiocytosis Group and systematic literature review.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 869, doi. 10.1111/bjh.16449
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Second‐line treatment trends and long‐term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 931, doi. 10.1111/bjh.16448
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The derived neutrophil‐to‐lymphocyte ratio is an independent prognostic factor in patients with angioimmunoblastic T‐cell lymphoma.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 908, doi. 10.1111/bjh.16447
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Comparison of efficacy from two different dosing regimens of bortezomib: an exposure–response analysis.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 860, doi. 10.1111/bjh.16446
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Androgen therapy in inherited bone marrow failure syndromes: analysis from the Canadian Inherited Marrow Failure Registry.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 976, doi. 10.1111/bjh.16445
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Comparison of MALDI‐TOF mass spectrometry analysis of peripheral blood and bone marrow‐based flow cytometry for tracking measurable residual disease in patients with multiple myeloma.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 904, doi. 10.1111/bjh.16443
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Redefining the prognostic likelihood of chronic lymphocytic leukaemia patients with borderline percentage of immunoglobulin variable heavy chain region mutations.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 853, doi. 10.1111/bjh.16434
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Allogeneic stem cell transplantation in AML with t(6;9)(p23;q34);DEK‐NUP214 shows a favourable outcome when performed in first complete remission.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 920, doi. 10.1111/bjh.16433
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In search for a haemoglobin threshold in myelodysplastic syndromes.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 813, doi. 10.1111/bjh.16392
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Issue Information.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 791, doi. 10.1111/bjh.16027
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Presentation clinical, haematological and immunophenotypic features of 1081 patients with GPI‐deficient (paroxysmal nocturnal haemoglobinuria) cells detected by flow cytometry.
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- British Journal of Haematology, 2020, v. 189, n. 5, p. 954, doi. 10.1111/bjh.16427
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