Works matching IS 00071048 AND DT 2022 AND VI 197 AND IP 3
Results: 25
Does recipient body mass index inform donor selection for allogeneic haematopoietic cell transplantation?
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 326, doi. 10.1111/bjh.18108
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Association of metformin treatment and outcome in adult patients with ITP and pre‐existing T2DM.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 367, doi. 10.1111/bjh.18121
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Resolving sticky relationships between platelets and lymphocytes in COVID‐19: A role for checkpoint inhibitors?
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 247, doi. 10.1111/bjh.18095
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British Society for Haematology guidelines for the laboratory diagnosis of malaria.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 271, doi. 10.1111/bjh.18092
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Impact of chronic lymphocytic leukaemia on melanoma outcomes: A retrospective case‐control study.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 320, doi. 10.1111/bjh.18090
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Immunophenotypic changes in juvenile myelomonocytic leukaemia after treatment with hypomethylating agent: Do they help to evaluate dept of response?
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 339, doi. 10.1111/bjh.18089
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The impact of B‐cell‐directed therapy on SARS‐CoV‐2 vaccine efficacy in chronic lymphocytic leukaemia.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 306, doi. 10.1111/bjh.18088
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Adults with immune thrombocytopenia who switched to avatrombopag following prior treatment with eltrombopag or romiplostim: A multicentre US study.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 359, doi. 10.1111/bjh.18081
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Von Willebrand factor assays in patients with acquired immune thrombotic thrombocytopenia purpura treated with caplacizumab.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 349, doi. 10.1111/bjh.18080
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Optimizing transfusion therapy for survivors of Haemoglobin Bart's hydrops fetalis syndrome: Defining the targets for haemoglobin‐H fraction and "functional" haemoglobin level.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 373, doi. 10.1111/bjh.18077
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Inherited platelet disorders: From new variants to new knowledge.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 245, doi. 10.1111/bjh.18074
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Third dose of COVID‐19 vaccine restores immune response in patients with haematological malignancies after loss of protective antibody titres.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 302, doi. 10.1111/bjh.18073
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Immune response to COVID‐19 vaccination is attenuated by poor disease control and antimyeloma therapy with vaccine driven divergent T‐cell response.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 293, doi. 10.1111/bjh.18066
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Incidence and outcomes of post‐transplant lymphoproliferative disease after 5365 solid‐organ transplants over a 20‐year period at two UK transplant centres.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 310, doi. 10.1111/bjh.18065
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Platelets modulate CD4<sup>+</sup> T‐cell function in COVID‐19 through a PD‐L1 dependent mechanism.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 283, doi. 10.1111/bjh.18062
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Gelatinous transformation as a result of starvation.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 244, doi. 10.1111/bjh.18056
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- Article
Novel RASGRP2 variants in platelet function defects: Indian study.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 377, doi. 10.1111/bjh.18049
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Management of haemostatic complications of chimaeric antigen receptor T‐cell therapy.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 250, doi. 10.1111/bjh.18045
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Neurocognitive risk in sickle cell disease: Utilizing neuropsychology services to manage cognitive symptoms and functional limitations.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 260, doi. 10.1111/bjh.18041
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Very late extramedullary relapse of acute myeloid leukaemia as prostatic myeloid sarcoma occurring 24 years post‐allograft.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 243, doi. 10.1111/bjh.18038
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Checklist Individual Strength to measure severe fatigue in immune thrombocytopenia.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. e41, doi. 10.1111/bjh.18031
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Risk of febrile neutropenia in very elderly patients aged ≥80 years receiving their first cycle of R‐CHOP regimen: a nationwide real‐world study in Japan.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. e37, doi. 10.1111/bjh.18028
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What does the term 'sickle cell disease' mean?
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- British Journal of Haematology, 2022, v. 197, n. 3, p. 381, doi. 10.1111/bjh.18024
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Assessing the impact of the 2017 European LeukemiaNet recommendations on FLT3 allelic ratio calculation and reporting in acute myeloid leukaemia.
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- British Journal of Haematology, 2022, v. 197, n. 3, p. e35, doi. 10.1111/bjh.18023
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Issue Information.
- Published in:
- British Journal of Haematology, 2022, v. 197, n. 3, p. 239, doi. 10.1111/bjh.17591
- Publication type:
- Article