Works matching IS 00071048 AND DT 2022 AND VI 199 AND IP 5
Results: 26
Diagnostic value of multigene sequencing for inherited thrombocytopenia.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 645, doi. 10.1111/bjh.18501
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Patients with sickle cell disease who develop end‐stage kidney disease continue to experience poor survival — A 19‐year United States Renal Data System study.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. e43, doi. 10.1111/bjh.18494
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Mantle cell lymphoma in human immunodeficiency virus‐infected patients.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 782, doi. 10.1111/bjh.18493
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Refractory/relapse thrombocytopenia in a patient with Evans' syndrome successfully treated with zanubrutinib.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. e37, doi. 10.1111/bjh.18490
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Allogeneic haematopoietic stem cell transplantation for VEXAS syndrome: UK experience.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 777, doi. 10.1111/bjh.18488
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Early‐salvage therapy with venetoclax‐based regimens for induction failure and poor early response acute lymphoblastic leukaemia: A retrospective case series of 13 patients.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 772, doi. 10.1111/bjh.18487
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Maternal gonosomal mosaicism in rare autosomal dominant SLFN14‐related thrombocytopenia.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 765, doi. 10.1111/bjh.18481
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Differentiation therapy using low‐dose venetoclax in a variant acute promyelocytic leukaemia carrying ZBTB16‐RARA.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 768, doi. 10.1111/bjh.18476
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Mixed chimerism post haematopoietic stem cell transplantation in JMML: Interventions and outcome.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. e34, doi. 10.1111/bjh.18474
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Cauda equina syndrome secondary to extramedullary erythropoiesis in a transfusion‐dependent thalassemia patient following treatment with luspatercept: A case report.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. e30, doi. 10.1111/bjh.18470
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Germline ERCC excision repair 6 like 2 (ERCC6L2) mutations lead to impaired erythropoiesis and reshaping of the bone marrow microenvironment.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 754, doi. 10.1111/bjh.18466
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Morphological characterization of acute myeloid leukaemia with t(11;17)(q23;q21)/ZBTB16::RARA fusion.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 638, doi. 10.1111/bjh.18463
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Biological, clinical features and modelling of heterozygous variants of glycoprotein Ib platelet subunit alpha (GP1BA) and glycoprotein Ib platelet subunit beta (GP1BB) genes responsible for constitutional thrombocytopenia.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 744, doi. 10.1111/bjh.18462
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Acute myeloid leukaemia presenting with Sweet syndrome.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 637, doi. 10.1111/bjh.18439
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Obinutuzumab as consolidation after chemo‐immunotherapy: Results of the UK National Cancer Research Institute phase II/III GALACTIC trial.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 707, doi. 10.1111/bjh.18427
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De novo NUF2 variant in a novel inherited bone marrow failure syndrome including microcephaly and renal hypoplasia.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 739, doi. 10.1111/bjh.18461
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- Article
Hyperinflammatory syndrome resembling haemophagocytic lymphohistiocytosis following axicabtagene ciloleucel and brexucabtagene autoleucel.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 720, doi. 10.1111/bjh.18454
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Vascular thrombotic events in the era of modern myeloma therapy.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 642, doi. 10.1111/bjh.18452
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Irradiation‐free, T‐cell replete haploidentical transplant for Fanconi anaemia, weighing the benefits.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 639, doi. 10.1111/bjh.18446
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Incidence, prevalence and survival in patients with Langerhans cell histiocytosis: A national registry study from England, 2013–2019.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 728, doi. 10.1111/bjh.18459
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Clinical outcomes and immune responses to SARS‐CoV‐2 vaccination in severe aplastic anaemia.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 679, doi. 10.1111/bjh.18456
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The impact of histological grade on outcomes in follicular lymphoma: An analysis of patients in the SEER database in the context of evolving disease classification and treatment.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 696, doi. 10.1111/bjh.18404
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Quality of end‐of‐life care in multiple myeloma: A 13‐year analysis of a population‐based cohort in Ontario, Canada.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 688, doi. 10.1111/bjh.18401
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Treatment of blast phase chronic myeloid leukaemia: A rare and challenging entity.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 665, doi. 10.1111/bjh.18370
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Diversity in the bone marrow niche: Classic and novel strategies to uncover niche composition.
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- British Journal of Haematology, 2022, v. 199, n. 5, p. 647, doi. 10.1111/bjh.18355
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Issue Information.
- Published in:
- British Journal of Haematology, 2022, v. 199, n. 5, p. 633, doi. 10.1111/bjh.17605
- Publication type:
- Article