Works matching IS 00071048 AND DT 2020 AND VI 191 AND IP 5
Results: 52
BSH guidelines for the use of irradiated blood components: guidance that is needed.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 658, doi. 10.1111/bjh.17150
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Cerebral MRI findings predict the risk of cognitive impairment in thrombotic thrombocytopenic purpura.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 868, doi. 10.1111/bjh.17126
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Long‐term cognitive impairments following recovery in the patients with immune‐mediated thrombotic thrombocytopenic purpura.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 671, doi. 10.1111/bjh.17124
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British Society for Haematology Guidelines on transfusion for fetuses, neonates and older children (Br J Haematol. 2016;175:784–828). Addendum August 2020.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 725, doi. 10.1111/bjh.17109
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British Society of Haematology Guidelines on the spectrum of fresh frozen plasma and cryoprecipitate products: their handling and use in various patient groups in the absence of major bleeding (Br J Haematol. 2018;181:54–67). Addendum August 2020.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 728, doi. 10.1111/bjh.17104
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F cell numbers are associated with an X‐linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 888, doi. 10.1111/bjh.17102
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Investigating the missing heritability of fetal haemoglobin level in Africa.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 668, doi. 10.1111/bjh.17101
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Clinical features of vitamin B12 deficiency mimicking thrombotic microangiopathy.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 938, doi. 10.1111/bjh.17099
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Microcytosis in patients with haemoglobin C trait: is α‐thalassaemia trait to blame?
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e129, doi. 10.1111/bjh.17095
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The evolution of clinical research in thalassaemia: where has all the funding gone?
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 666, doi. 10.1111/bjh.17094
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Adjuvant tyrosine kinase inhibitor therapy improves outcome for children and adolescents with acute lymphoblastic leukaemia who have an ABL‐class fusion.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 844, doi. 10.1111/bjh.17093
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Co‐morbidities and mortality associated with transfusion‐dependent beta‐thalassaemia in patients in England: a 10‐year retrospective cohort analysis.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 897, doi. 10.1111/bjh.17091
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A Sardinian founder mutation in glycoprotein Ib platelet subunit beta (GP1BB) that impacts thrombocytopenia.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e124, doi. 10.1111/bjh.17090
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Venetoclax plus hypomethylating agent in blast‐phase myeloproliferative neoplasm: preliminary experience with 12 patients.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e120, doi. 10.1111/bjh.17084
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Rapid fluorescence in situ hybridisation optimises induction therapy for acute myeloid leukaemia.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 935, doi. 10.1111/bjh.17082
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Loss‐of‐function mutations in CSF3R cause moderate neutropenia with fully mature neutrophils: two novel pedigrees.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 930, doi. 10.1111/bjh.17081
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A real‐world study of panobinostat, weekly bortezomib and dexamethasone in a very heavily pretreated population of multiple‐myeloma patients.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 927, doi. 10.1111/bjh.17076
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Autologous stem cell transplant in first remission for transformed indolent non‐Hodgkin lymphoma: additional data to guide practice.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 663, doi. 10.1111/bjh.17075
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Autologous stem cell transplantation for untreated transformed indolent B‐cell lymphoma in first remission: an international, multi‐centre propensity‐score‐matched study.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 806, doi. 10.1111/bjh.17072
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High infiltration of CD20<sup>+</sup> B lymphocytes in extranodal natural killer/T‐cell lymphoma is associated with better prognosis.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e116, doi. 10.1111/bjh.17069
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Dynamic evolution of ponatinib‐resistant mutations in BCR–ABL1‐positive leukaemias revealed by next‐generation sequencing.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e113, doi. 10.1111/bjh.17068
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Indomethacin is an effective treatment in adults and children with bone Langerhans cell histiocytosis (LCH).
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e109, doi. 10.1111/bjh.17067
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Reporting of race and ethnicity at an international haematology conference.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e107, doi. 10.1111/bjh.17065
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Severe airport malaria complicated by macrophage activation syndrome.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 652, doi. 10.1111/bjh.17064
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A high TP53 mutation burden is a strong predictor of primary refractory mantle cell lymphoma.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e103, doi. 10.1111/bjh.17063
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Paraneoplastic acute demyelinating disease with monoclonal gammopathy of unknown significance expressing aquaporin‐4.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. e101, doi. 10.1111/bjh.17057
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Guideline for diagnosis and management of hairy cell leukaemia (HCL) and hairy cell variant (HCL‐V).
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 730, doi. 10.1111/bjh.17055
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Direct‐acting antiviral agents in lymphoproliferative disorders: more complex than expected.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 661, doi. 10.1111/bjh.17037
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Direct‐acting antiviral agents for hepatitis C virus‐mixed cryoglobulinaemia: dissociated virological and haematological responses.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 775, doi. 10.1111/bjh.17036
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p53 is associated with high‐risk and pinpoints TP53 missense mutations in mantle cell lymphoma.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 796, doi. 10.1111/bjh.17023
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Oropharyngeal psychogenic purpura.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 651, doi. 10.1111/bjh.17021
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Characteristics and outcomes of adults with cytomegalovirus‐associated thrombocytopenia: a case series and literature review.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 863, doi. 10.1111/bjh.17017
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Preventing transfusion‐associated graft‐versus‐host disease with blood component irradiation: indispensable guidance for a deadly disorder.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 653, doi. 10.1111/bjh.17016
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Guidelines on the use of irradiated blood components.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 704, doi. 10.1111/bjh.17015
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Body weight is negatively associated with direct oral anticoagulant trough concentrations in dabigatran and apixaban users.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 941, doi. 10.1111/bjh.17009
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Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 835, doi. 10.1111/bjh.17006
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Hydroxycarbamide exposure and ovarian reserve in women with sickle cell disease in the Multicenter Study of Hydroxycarbamide.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 880, doi. 10.1111/bjh.16976
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The Kg‐antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newborn.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 920, doi. 10.1111/bjh.16955
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Role of bone marrow‐derived mesenchymal stem cell defects in CD8<sup>+</sup>CD28<sup>–</sup> suppressor T‐lymphocyte induction in patients with immune thrombocytopenia and associated mechanisms.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 852, doi. 10.1111/bjh.16953
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Long‐term follow‐up of children with risk organ‐negative Langerhans cell histiocytosis after 2‐chlorodeoxyadenosine treatment.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 825, doi. 10.1111/bjh.16944
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Benefits of risk‐adapted and mould‐specific antifungal prophylaxis in childhood leukaemia.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 816, doi. 10.1111/bjh.16931
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Cumulative outcome of pre‐implantation genetic diagnosis for sickle cell disease: a 5‐year review.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 875, doi. 10.1111/bjh.16930
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Lenalidomide and pomalidomide potently interfere with induction of myeloid‐derived suppressor cells in multiple myeloma.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 784, doi. 10.1111/bjh.16881
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All‐trans‐retinoic acid shifts Th1 towards Th2 cell differentiation by targeting NFAT1 signalling to ameliorate immune‐mediated aplastic anaemia.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 906, doi. 10.1111/bjh.16871
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The role of high‐dose melphalan with autologous stem‐cell transplant in multiple myeloma: is it time for a paradigm shift?
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 692, doi. 10.1111/bjh.16764
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Real‐world non‐interventional long‐term post‐authorisation safety study of ruxolitinib in myelofibrosis.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 764, doi. 10.1111/bjh.16729
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Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 755, doi. 10.1111/bjh.16720
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How we treat older patients with acute myeloid leukaemia.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 682, doi. 10.1111/bjh.16701
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Antibody‐based immunotherapy for treatment of immunoglobulin light‐chain amyloidosis.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 673, doi. 10.1111/bjh.16697
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Anticoagulation prophylaxis reduces venous thromboembolism rate in adult acute lymphoblastic leukaemia treated with asparaginase‐based therapy.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 748, doi. 10.1111/bjh.16695
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